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Article

Identification and Expressional Analysis of Putative PRDI-BF1 and RIZ Homology Domain-Containing Transcription Factors in Mulinia lateralis

by
Feng Zhao
1,†,
Xiaolin Guo
1,†,
Xixi Li
1,
Fang Liu
1,
Yifan Fu
1,
Xiaohan Sun
1,
Zujing Yang
1,
Zhifeng Zhang
1,2 and
Zhenkui Qin
1,*
1
Ministry of Education Key Laboratory of Marine Genetics and Breeding, College of Marine Life Sciences, Ocean University of China, Qingdao 266003, China
2
Key Laboratory of Tropical Aquatic Germplasm of Hainan Province, Sanya Oceanographic Institution, Ocean University of China, Sanya 572000, China
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Biology 2023, 12(8), 1059; https://doi.org/10.3390/biology12081059
Submission received: 22 May 2023 / Revised: 24 July 2023 / Accepted: 25 July 2023 / Published: 27 July 2023
(This article belongs to the Section Marine Biology)
Browse Figures
Versions Notes

Abstract

:

Simple Summary

The formation of primordial germ cells (PGCs) is the basis of molluskan reproduction, but limited information is reported on this topic. PRDI-BF1 and RIZ homology domain-containing proteins (PRDMs), especially PRDM1 (also known as BLIMP1) and PRDM14, have been reported to be essential for the formation of PGCs. In this study, we systematically characterized the putative PRDMs in a bivalve mollusk species, Mulinia lateralis, and analyzed their sequence structures, phylogenetic relationships, and expressional profiles. Furthermore, we analyzed the temporal–spatial expression patterns of Ml-prdm1 and Ml-prdm14 RNA in early embryos and larvae. Our study suggests that Ml-prdm1 may function as an important regulator of PGC formation in M. lateralis.

Abstract

Mollusca represents one of the ancient bilaterian groups with high morphological diversity, while the formation mechanisms of the precursors of all germ cells, primordial germ cells (PGCs), have not yet been clarified in mollusks. PRDI-BF1 and RIZ homology domain-containing proteins (PRDMs) are a group of transcriptional repressors, and PRDM1 (also known as BLIMP1) and PRDM14 have been reported to be essential for the formation of PGCs. In the present study, we performed a genome-wide retrieval in Mulinia lateralis and identified 11 putative PRDMs, all of which possessed an N-terminal PR domain. Expressional profiles revealed that all these prdm genes showed specifically high expression levels in the given stages, implying that all PRDMs played important roles during early development stages. Specifically, Ml-prdm1 was highly expressed at the gastrula stage, the key period when PGCs arise, and was specifically localized in the cytoplasm of two or three cells of blastula, gastrula, or trochophore larvae, matching the typical characteristics of PGCs. These results suggested that Ml-prdm1-positive cells may be PGCs and that Ml-prdm1 could be a candidate marker for tracing the formation of PGCs in M. lateralis. In addition, the expression profiles of Ml-prdm14 hinted that it may not be associated with PGCs of M. lateralis. The present study provides insights into the evolution of the PRDM family in mollusks and offers a better understanding of the formation of PGCs in mollusks.

1. Introduction

Germline cells transmit genetic and epigenetic information across generations in all sexually reproducing animals to ensure the survival of the species [1,2]. Primordial germ cells (PGCs) that separated from somatic cells during early embryogenesis are common precursors of both sperms and eggs [3,4], and the segregating of germ cells from somatic cells is the first diversification step in the evolution of metazoans [5]. Under the initial determination of germ cell fate, there are two generally accepted theories of PGC specification: preformation, in which the specification of PGCs is determined by maternally inherited determinants in early development, and epigenesis, in which PGCs arise by inductive signals in late development [3,6]. These two mechanisms are not mutually exclusive and are inevitably used simultaneously at a certain stage of germ cell development [6]. So far, the PGC specification modes are different among different species, and both theories are reported in mollusks [7,8,9,10].
PRDM proteins comprise an N-terminal PR (PRDI-BF1 and RIZ1 homology) domain derived from the SET (suppressor of variegation 3–9, enhancer of zeste, and trithorax) domain and a variable number of C-terminal Zn-finger repeats [11,12]. As important transcription factors, PRDMs modulate different cellular processes, including the regulation of germ cell development. For example, PRDM1 and PRDM14 are essential for PGC development in several species. Notably, PRDM1 is functionally conserved across vertebrates and invertebrates. In mice (Mus musculus), PRDM1 and PRDM14 have been identified as the key regulators of PGC specification. PRDM1 is a key transcriptional regulator and is primarily responsible for the repression of somatic genes in PGCs [13,14]. The deletion of prdm1 led to the failure of normal proliferation and migration of mouse PGCs [13], and prdm1 homozygous mutants lacked PGCs [15]. PRDM14 is critical for the reacquisition of potential pluripotency and successful epigenetic reprogramming during PGC specification [14,16]. Embryos with the complete deletion of prdm14 generated impaired PGCs with reduced numbers and lower mobility [16]. In 11-week-old prdm14 mutant females and males, germ cells in the ovaries and testes were completely lacking [16]. The simultaneous overexpression of prdm1, prdm14, and tfap2c could rapidly and efficiently induce epiblast-like cells (EpiLCs) to enter a PGC state in vitro [17]. Notably, prdm14 alone was sufficient to direct the PGC state in EpiLCs [17]. In humans (Homo sapiens), PRDM1 functions as a repressor of somatic genes, which might allow SOX17, the key regulator of PGC-like cells’ (hPGCLCs) fate, to specify hPGCLCs [18]. The loss of prdm14 significantly reduced the specification efficiency of hPGCLCs [19]. In chickens (Gallus gallus), both PRDM1 and PRDM14 play pivotal roles in the post-specification of PGC development and are involved in PGC self-renewal [20]. In crickets (Gryllus bimaculatus), prdm1 is required for PGC formation and/or maintenance [21]. PRDM2 plays a potential tumor suppressor role in the formation of testicular germ cell tumors (TGCTs), which derive from PGCs [22]. PRDM8 participates in the regulation of mouse testis development [23]. And PRDM9 is a key determinant of meiotic recombination hotspots in both humans and mice [24,25]. Moreover, PRDMs are also involved in the proliferation and differentiation of embryonic stem cells [26,27,28,29], hematopoietic stem cells [30,31,32,33], and neurons [34,35,36,37,38,39]. Systematic identifications, expressive analyses, and functional studies of the PRDM gene family have been well conducted in vertebrates, but little information is available on invertebrates, especially on mollusks. This lack of information has prevented the elucidation of the evolution and conservation of the PRDM family, as well as the PGC development mechanisms in mollusks.
Mollusks are one of the most diverse groups in the animal kingdom; most of them are aquaculture species with important economic value. As they are an ancestral bilaterian group, studies on PGC specification in mollusks can help to elucidate the evolution of metazoan germ cell specification. Furthermore, understanding the molecular mechanisms of germ cells will facilitate the development of propagation control techniques and promote the aquaculture industry [40,41,42]. However, studies on the origin and development of PGCs in mollusks are scarce, and currently only three genes, vasa, nanos, and piwi, are used in related studies [7,8,9,43,44].
In the present study, we systematically identified and characterized PRDMs in M. lateralis, a promising model organism for bivalve mollusks. We then conducted a functional domain prediction, and sequence, phylogenetic, and expression level analyses of PRDMs. Moreover, we investigated the distribution of Ml-prdm1 and Ml-prdm14 transcripts in embryonic and larval stages. This study provided insights into the evolution of PRDMs and their potential involvement in PGC development in mollusks, laying a theoretical foundation for further functional investigations.

2. Materials and Methods

2.1. Identification of M. lateralis PRDMs

To identify PRDM members (Ml-PRDMs), we firstly searched the annotation files of the M. lateralis genome (unpublished data), and then combined the data with a protein-based sequence alignment and a domain-based sequence analysis. For the sequence alignment, orthologous PRDM sequences of vertebrates and invertebrates downloaded from databases including NCBI (https://www.ncbi.nlm.nih.gov/, accessed on 20 October 2022) and Uniprot (https://www.uniprot.org/, accessed on 23 October 2022) (Table S1) were used as query sequences for blastp using BioEdit 7.0.9 software [45] with an E-value threshold of 1 × 10−5. For the domain analysis, both hmmbuild and hmmsearch programs in HMMER v.3.0 [46] were used. Firstly, on the basis of sequence alignments with ClustalW (https://www.genome.jp/tools-bin/clustalw, accessed on 5 November 2022) among all Ml-PRDMs identified by blastp, the hmmbuild was carried out to generate a hidden Markov model (HMM) profile. The hmmsearch program (E-value < 1 × 10−5) was performed according to the HMM profiles for genome-wide domain analysis in M. lateralis. The candidate sequences obtained using these three methods were re-evaluated manually using CD-Search and Protein BLAST in the NCBI database with default parameters. Moreover, to better enrich the data on the PRDM gene family in shellfish for a more comprehensive phylogenetic analysis, the same identification procedure was applied to sequences from the Chlamys farreri genome [47].

2.2. PRDMs Sequence Analysis

The isoelectric point (pI) and molecular weight (Mw) were predicted using the Expasy Compute pI/MW tool (https://www.expasy.org/, accessed on 12 November 2022). The functional domains of Ml-PRDMs were visualized using IBS 1.0.3 [48] according to the prediction information from SMART (http://smart.embl-heidelberg.de/, accessed on 12 November 2022) and NCBI CD-Search. Multiple alignments of the PR domains among M. lateralis, H. sapiens, M. musculus, and D. rerio were performed using Clustal Omega on the EMBL-EBI website (https://www.ebi.ac.uk/, accessed on 12 November 2022), and the results were displayed using Jalview2.11.2.6 software [49].

2.3. Phylogenetic Analysis

The PR domains of sequences were extracted to perform a multiple sequence alignment using ClustalW with default parameters, and a phylogenetic tree was constructed using the maximum likelihood algorithm with default parameters in MEGA-X [50]. Finally, the tree was modified using the online software EvolView v3 (https://www.evolgenius.info/evolview, accessed on 10 March 2023).

2.4. Gene Expression Analysis of M. lateralis prdms

The HeatMap function of TBtools [51] was used to conduct heatmap and clustering analyses of M. lateralis prdm genes based on the published RNASeq datasets of four developmental stages: blastula, gastrula, trochophore, and D-shaped larvae (NCBI accession numbers SRR17520079–SRR17520090) [52].

2.5. Collection of Embryos and Larvae

Adult M. lateralis were provided by the MOE Key Laboratory of Marine Genetics and Breeding. Mature males and females were stimulated with seawater at 27 °C to lay eggs or to release sperms after cooling in a dry and dark environment for 1.5 h. Artificial insemination was then carried out based on a ratio of 1 egg to 10 sperms, and the fertilized eggs were incubated at 24 °C. Collected embryos and larvae were washed twice with PBS at room temperature and fixed with 4% paraformaldehyde overnight at 4 °C. Then, gradient dehydration was performed with serial methanol (25, 50, 75%, and 100%) after washing with PBS. Finally, the samples were stored in 100% methanol at −30 °C for whole-mount in situ hybridization analysis. Samples of the same developmental stages were also snap-frozen in liquid nitrogen and then stored at −80 °C for total RNA extraction.

2.6. Quantitative RT-PCR Analysis of Ml-prdm1 and Ml-prdm14

The expression patterns of Ml-prdm1 and Ml-prdm14 during early development stages were detected. Briefly, the total RNA of the fertilized egg, multicellular embryo, blastula, gastrula, trochophore, D-shaped larva, and umbo larva were extracted with the MicroElute Total RNA Kit (Omega, Norcross, GA, USA). The RNA’s integrity and quality were assessed by performing 1.2% agarose gel electrophoresis and spectrophotometry, and the first-strand cDNAs were reverse-transcribed using the SuperScript First-Strand Synthesis System (Invitrogen, Carlsbad, CA, USA). Quantitative RT-qPCR was conducted using the LightCycler 480 real-time fluorescence quantitative PCR instrument (Roche, Basel, Switzerland) with specific primers (Table 1), and ef-1b was utilized as an internal reference [52]. The 2−ΔΔCt method [53] was used to calculate relative gene expression with three biological replicates and three technical replicates. The statistical analysis was tested using one-way ANOVA followed by Duncan’s test (SPSS 22.0, IBM Corp., Armonk, NY, USA), and the statistically significant difference was set as p < 0.05.

2.7. Whole-Mount In Situ Hybridization of Ml-prdm1 and Ml-prdm14

Specific fragments of Ml-prdm1 and Ml-prdm14 were amplified using gastrula cDNA and gene-specific primers (Table 2) containing T7 or SP6 promoter sequences. The resultant PCR products were used as templates for in vitro transcription to synthesize digoxigenin-labeled RNA probes according to the manufacturer’s instructions for the DIG RNA labeling kit (Roche, Mannheim, Germany). In addition, the labeled probes were precipitated using ethanol and lithium chloride, and dissolved in RNase-free water.
Whole-mount in situ hybridization was performed as previously described [54] with slight modifications. The rehydrated samples were treated with proteinase K (1 μg/mL for embryos and 4 μg/mL for trochophore larvae) at 37 °C for 20 min before incubation in TAE buffer. After treatment with acetic anhydride, samples were post-fixed in 4% paraformaldehyde for 30 min. Samples were pre-hybridized in hybridization buffer (50% deionized formamide, 5% dextran sulfate, 0.1% tween-20, 5 × SSC, 50 μg/mL heparin, 500 μg/mL yeast total RNA, 18 mM citric acid) at 60 °C for three hours, followed by being hybridized with 6 μg/mL denatured RNA probe at 60 °C overnight and then washed in gradient saline sodium citrate buffer at 60 °C. After treatment in blocking buffer for 1 h, samples were incubated with 1:2500 diluted alkaline phosphatase-conjugated digoxigenin antibody (Roche, Mannheim, Germany) overnight at 4 °C. Samples were finally incubated with NBT-BCIP in staining buffer (100 mM Tris-HCl, 100 mM NaCl, 10% PVA, 50 mM MgCl2, 0.1% Tween-20, pH 9.5) in darkness at 37 °C for color development.

3. Results

3.1. Identification and Sequence Analysis of M. lateralis Putative PRDMs

Eleven members of the PRDM family were identified in the genome of M. lateralis. All of these Ml-PRDMs had one PR domain and several zinc fingers (0–20), and their protein lengths varied from 283 to 1969 aa (Figure 1; Table 3). The members identified with both SMART and NCBI CD-Search were named Ml-PRDM, whereas those recognized by only one algorithm were designated as Ml-PRDM-like. The predicted physical and chemical properties, molecular weights, and isoelectric points of all PRDM members were presented in Table 3.
Four highly conserved residues (G, I, and E-L) in both PR and SET domains [55] were observed in the PR domains of all the Ml-PRDMs, except for the Ml-PRDM16-like, of which the G and L were not conserved (Figure 2). In addition, six well-conserved and unique residues (W, A) and motifs (F-G-P, E-Q-N-L, Y/F-Y/F, L-V-W), which were almost exclusive to the PR domains [55,56,57], were partially or completely identified in Ml-PRDMs (Figure 2). Notably, most of these residues and motifs were less conserved in Ml-PRDM13-like and Ml-PRDM16-like proteins. A multiple sequence alignment of 44 sequences between M. lateralis and three vertebrates showed that the identity of 14 residues was higher than 80%, and there was a residue (E) exhibiting great conservation in all sequences (Figure 3).

3.2. Phylogenetic Analysis of Putative M. lateralis PRDMs

The putative PRDM proteins of M. lateralis were further confirmed using phylogenetic analysis (Figure 4). In the phylogenetic tree constructed, Ml-PRDM1 and Ml-PRDM14 displayed the closest phylogenetic relationships with other bivalves. Ml-PRDM9 and Ml-PRDM15 displayed the closest phylogenetic relationships with C. farreri. Ml-PRDM10 exhibited the closest clustering relationship with Crassostrea gigas and Ml-PRDM4 clustered with Crassostrea virginica and C. gigas. In short, M. lateralis PRDMs were closely clustered with different molluskan PRDMs and then grouped with vertebrate PRDMs in each family member clade.

3.3. Temporal Expression Pattern of Putative M. lateralis prdms during Early Development Stages

M. lateralis prdms exhibited dynamic expression patterns during embryonic and larval stages, which were obtained from the published RNASeq datasets (NCBI accession numbers SRR17520079–SRR17520090) (Figure 5). Three family members (Ml-prdm9, Ml-prdm13-like, Ml-prdm16-like) were highly expressed in the blastula; two family members (Ml-prdm1, Ml-prdm2) showed the highest expression levels in the gastrula stage; and the highest expression of five members (Ml-prdm14, Ml-prdm10, Ml-prdm4-like, Ml-prdm12, and Ml-prdm15) occurred in the trochophore larva stage, whereas only Ml-prdm8-like had the highest expression level in the D-shaped larva stage. According to the heatmap, the expression profiles of Ml-prdm1 and Ml-prdm14 exhibited a similar trend: the expression level initially increased and then subsequently decreased. However, the highest expression of Ml-prdm1 occurred earlier than that of Ml-prdm14.
With the RT-qPCR analysis, it was shown that Ml-prdm1 started to express at the multicellular stage and reached a peak value when developed to the gastrula stage. The expression decreased at the trochophore larva stage and declined sharply after that (Figure 6). A similar pattern could be seen in Ml-prdm14, with the exception that the trochophore larva occupied the highest expression level and the D-shaped larva was second to that.

3.4. Spatial Expression Pattern of M. lateralis prdm1 and prdm14 in Embryo and Larva

To reveal the potential relevance of PRDMs to PGC specification, the spatial distribution of Ml-prdm1 and Ml-prdm14 mRNA from fertilized egg to trochophore larva was investigated by carrying out whole-mount in situ hybridization. According to the results, no signals of Ml-prdm1 or Ml-prdm14 transcripts were detected in fertilized eggs and multicellular embryos. The signals of Ml-prdm1 were initially detected in the blastula, but those of Ml-prdm14 were observed firstly in the gastrula, which was consistent with the temporal expression pattern that Ml-prdm14 exhibited, with higher expression in later stages compared to Ml-prdm1. The signals of Ml-prdm1 were specifically concentrated in the cytoplasm of two adjacent cells in the blastula and gastrula (Figure 7 and Figure S1). And then, in the trochophore larva, Ml-prdm1 transcripts were localized in three cells in the middle of the body, and the signals were still mainly located in the cytoplasm. In contrast, the positive signals of Ml-prdm14 appeared as two or three dots scattered in cell clusters at the edge of the gastrula or trochophore larva, respectively (Figure 7). These two genes displayed quite distinct expression patterns, implying that they may have different functions.

4. Discussion

The number of prdm genes identified per species is significantly different, ranging from 2 in the sponge Oscarella carmela to 19 in teleosteans [55]. Such differences of gene numbers also exist within each main animal lineage [55]. In lophotrochozoans, 6 to 8 genes can be found in platyhelminthes, whereas in mollusks, the number of prdm genes ranges from 8 in Pinctada fucata to 13 in C. gigas [55]. In the present study, we identified 11 putative PRDMs in both the M. lateralis and C. farreri genomes. The identified Ml-PRDM13-like lacked zinc fingers in this study because of the non-integral nature of its DNA sequence in the genome. However, its deduced amino acid sequences and PR domain were conserved with the PRDM13 of other species, and this member was retained in the present study.
In vertebrates, several PRDM proteins have been shown to possess intrinsic HMTase activity similar to that of SET proteins [23,31,58,59,60,61], whereas others that lack this intrinsic activity can participate in epigenetic regulation by interacting with enzymes capable of methylating histones or catalyzing other post-translational modifications of chromatin [30,62,63,64]. Four highly conserved residues shared in the PR and SET domains as well as six well-conserved and unique residues and motifs that are exclusive to the PR domains [55,56,57] were identified in Ml-PRDMs (Figure 2). Furthermore, fourteen residues showed an identity of higher than 80% between M. lateralis and vertebrates (Figure 3). These conserved residues and motifs suggest that Ml-PRDMs may exert molecular functions similar to those of their vertebrate homologous proteins.
PRDMs are transcriptional factors that regulate many fundamental aspects of cellular differentiation [65]. Transcriptomic analysis revealed that M. lateralis prdm genes exhibited dynamic expression patterns during embryonic and larval development (Figure 5). It is worth mentioning that nearly half of the M. lateralis prdm genes had the highest expression levels in the trochophore larva, including Ml-prdm4-like, Ml-prdm10, Ml-prdm12, Ml-prdm14, and Ml-prdm15. In many mollusks, the trochophore stage is the beginning of neurogenesis [66,67,68,69]. It has been reported that prdm4, prdm12, and prdm14 are involved in vertebrate neurological development [36,70,71,72]. Therefore, we can presume that these members of the PRDM gene family may have important functions in larval nervous system development.
It was speculated that Ml-prdm1-positive cells are putative PGCs or their progenitors in M. lateralis. PGCs in mollusks can be recognized in mesodermal tissues around the time of gastrulation [73,74]. In the transcriptomic and quantitative RT-PCR analysis results, we observed the highest expression of Ml-prdm1 at the gastrula stage (Figure 5 and Figure 6), suggesting that Ml-prdm1 may be involved in PGC formation in M. lateralis. The specific expression patterns of prdm1 orthologs have been revealed in many organisms, including Drosophila melanogaster [75], G. bimaculatus [21], Petromyzon marinus [76], Strongylocentrotus purpuratus [77], D. rerio [78], X. laevis [79], Ambystoma mexicanum [80], G. gallus [81], and M. musculus [13,82], and prdm1 was identified as the PGC marker in most of these animals. Usually, a subset of cells labeled by marker genes, such as vasa and nanos, are identified as putative PGCs or their precursors in mollusks. Although the expression patterns of these markers throughout embryonic development are not completely the same, the bivalve blastula and gastrula shared a similar subcellular localization of markers, which were restricted to two cells or cell clumps [7,8,9,43]. In the present study, Ml-prdm1 exhibited a restricted expression in the embryos and larvae of M. lateralis. In the blastula and gastrula, we observed two hybridization signals restricted to only two cells (Figure 7). In the trochophore larva, hybridization signals specifically appeared in three cells without any signals elsewhere (Figure 7). The distribution of Ml-prdm1 transcripts around the gastrula stage was remarkably similar to some of the putative PGC markers, especially nanos, in other bivalves [8,9]. In addition, Ml-prdm1-positive cells exhibited slow cell cycles from the blastula to the trochophore larva, and this was also consistent with observations in other mollusks in which PGCs were mitotically quiescent for a period [73,74]. Therefore, we hypothesized that Ml-prdm1 is a candidate PGC marker gene.
In mice, the expression of Ml-prdm1 preceded Ml-prdm14 [16,83,84], and a similar expression pattern was detected in the present study. However, the expression of prdm14 has been detected in presumptive prdm1-positive cells representing PGCs and their precursors in mice [16,85]. In contrast, the spatial expression patterns of these two genes in M. lateralis were completely different and did not seem to be co-expressed (Figure 7). It has been reported that prdm14 in G. bimaculatus is absent, although prdm1 has been shown to play an essential role in PGC development, indicating the different roles of prdm14 [21]. Moreover, we failed to identify an ortholog of the vertebrate tfap2c gene either in the transcriptome or in the genome, which is another regulator cooperating with prdm1 in the specification of murine PGCs [1,84]. Therefore, we assumed that Ml-prdm14 was probably not expressed in M. lateralis PGCs and was dispensable for their specification. This distinction suggested the divergence of the molecular network for PGC formation between vertebrates and invertebrates. Further functional validations should be performed to elucidate the mechanisms of PGC formation in mollusks.

5. Conclusions

In the present study, we identified 11 PRDM gene family members in M. lateralis based on genome-wide screening. The functional domain compositions, sequence identities, phylogenetic relationships, and expression profiles of the M. lateralis PRDMs were uncovered. Furthermore, we investigated the distribution of Ml-prdm1 and Ml-prdm14 transcripts during the early developmental stages, ranging from fertilized eggs to trochophore larvae. The results suggested that Ml-prdm1 may present functional conservation in terms of PGC specification similar to that in vertebrates. This study provides insights into the evolution of PRDMs in mollusks and offers clues for the further investigation of prdm1 in the formation of PGCs in mollusks.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/biology12081059/s1, Table S1: Accession numbers of PRDM protein sequences. Figure S1: The visualization of Ml-prdm1 expressing cells in early development stages of M. lateralis.

Author Contributions

F.Z. contributed to the investigation, data curation, formal analysis, and writing—original draft; X.G. contributed to the data curation and writing—original draft; Z.Q. contributed to funding acquisition; Z.Q. and Z.Z. contributed to supervision, conceptualization, methodology, project administration, validation, and writing—review and editing; X.L. and F.L. contributed to visualization; Y.F., X.S. and Z.Y. contributed to resources. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Natural Science Foundation of China (32070516).

Institutional Review Board Statement

The animal study was performed in accordance with the Institutional Animal Care and Use Committee of the Ocean University of China (OUC-IACUC) and the local government.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available in this article or in the Supplementary Materials.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Magnúsdóttir, E.; Surani, M.A. How to make a primordial germ cell. Development 2014, 141, 245–252. [Google Scholar] [CrossRef] [Green Version]
  2. Zeng, F.; Huang, F.; Guo, J.; Hu, X.; Liu, C.; Wang, H. Emerging methods to generate artificial germ cells from stem cells. Biol. Reprod. 2015, 92, 89. [Google Scholar] [CrossRef] [PubMed]
  3. Extavour, C.G.; Akam, M. Mechanisms of germ cell specification across the metazoans: Epigenesis and preformation. Development 2003, 130, 5869–5884. [Google Scholar] [CrossRef] [Green Version]
  4. Juliano, C.E.; Swartz, S.Z.; Wessel, G.M. A conserved germline multipotency program. Development 2010, 137, 4113–4126. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Rebscher, N.; Zelada-González, F.; Banisch, T.U.; Raible, F.; Arendt, D. Vasa unveils a common origin of germ cells and of somatic stem cells from the posterior growth zone in the polychaete Platynereis dumerilii. Dev. Biol. 2007, 306, 599–611. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Extavour, C.G. Evolution of the bilaterian germ line: Lineage origin and modulation of specification mechanisms. Integr. Comp. Biol. 2007, 47, 770–785. [Google Scholar] [CrossRef]
  7. Fabioux, C.; Huvet, A.; Lelong, C.; Robert, R.; Pouvreau, S.; Daniel, J.Y.; Minguant, C.; Le Pennec, M. Oyster vasa-like gene as a marker of the germline cell development in Crassostrea gigas. Biochem. Biophys. Res. Commun. 2004, 320, 592–598. [Google Scholar] [CrossRef] [Green Version]
  8. Kranz, A.M.; Tollenaere, A.; Norris, B.J.; Degnan, B.M.; Degnan, S.M. Identifying the germline in an equally cleaving mollusc: Vasa and Nanos expression during embryonic and larval development of the vetigastropod Haliotis asinina. J. Exp. Zool. B Mol. Dev. Evol. 2010, 314, 267–279. [Google Scholar] [CrossRef]
  9. Liu, L.; Liu, T.; Wu, S.; Li, Y.; Wei, H.; Zhang, L.; Shu, Y.; Yang, Y.; Xing, Q.; Wang, S.; et al. Discovery of nanos1 and nanos2/3 as germ cell markers during scallop gonadal development. Mar. Biotechnol. 2022, 24, 408–416. [Google Scholar] [CrossRef]
  10. Xu, R.; Li, Q.; Yu, H.; Kong, L. Oocyte maturation and origin of the germline as revealed by the expression of Nanos-like in the Pacific oyster Crassostrea gigas. Gene 2018, 663, 41–50. [Google Scholar] [CrossRef]
  11. Huang, S.; Shao, G.; Liu, L. The PR domain of the Rb-binding zinc finger protein RIZ1 is a protein binding interface and is related to the SET domain functioning in chromatin-mediated gene expression. J. Biol. Chem. 1998, 273, 15933–15939. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Fumasoni, I.; Meani, N.; Rambaldi, D.; Scafetta, G.; Alcalay, M.; Ciccarelli, F.D. Family expansion and gene rearrangements contributed to the functional specialization of PRDM genes in vertebrates. BMC Evol. Biol. 2007, 7, 187. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Ohinata, Y.; Payer, B.; O’Carroll, D.; Ancelin, K.; Ono, Y.; Sano, M.; Barton, S.C.; Obukhanych, T.; Nussenzweig, M.; Tarakhovsky, A.; et al. Blimp1 is a critical determinant of the germ cell lineage in mice. Nature 2005, 436, 207–213. [Google Scholar] [CrossRef] [PubMed]
  14. Kurimoto, K.; Yamaji, M.; Seki, Y.; Saitou, M. Specification of the germ cell lineage in mice: A process orchestrated by the PR-domain proteins, Blimp1 and Prdm14. Cell Cycle 2008, 7, 3514–3518. [Google Scholar] [CrossRef] [PubMed]
  15. Vincent, S.D.; Dunn, N.R.; Sciammas, R.; Shapiro-Shalef, M.; Davis, M.M.; Calame, K.; Bikoff, E.K.; Robertson, E.J. The zinc finger transcriptional repressor Blimp1/Prdm1 is dispensable for early axis formation but is required for specification of PGCs in the mouse. Development 2005, 132, 1315–1325. [Google Scholar] [CrossRef] [Green Version]
  16. Yamaji, M.; Seki, Y.; Kurimoto, K.; Yabuta, Y.; Yuasa, M.; Shigeta, M.; Yamanaka, K.; Ohinata, Y.; Saitou, M. Critical function of Prdm14 for the establishment of the germ cell lineage in mice. Nat. Genet. 2008, 40, 1016–1022. [Google Scholar] [CrossRef]
  17. Nakaki, F.; Hayashi, K.; Ohta, H.; Kurimoto, K.; Yabuta, Y.; Saitou, M. Induction of mouse germ-cell fate by transcription factors In Vitro. Nature 2013, 501, 222–226. [Google Scholar] [CrossRef] [Green Version]
  18. Irie, N.; Weinberger, L.; Tang, W.W.; Kobayashi, T.; Viukov, S.; Manor, Y.S.; Dietmann, S.; Hanna, J.H.; Surani, M.A. SOX17 is a critical specifier of human primordial germ cell fate. Cell 2015, 160, 253–268. [Google Scholar] [CrossRef] [Green Version]
  19. Sybirna, A.; Tang, W.W.C.; Pierson Smela, M.; Dietmann, S.; Gruhn, W.H.; Brosh, R.; Surani, M.A. A critical role of PRDM14 in human primordial germ cell fate revealed by inducible degrons. Nat. Commun. 2020, 11, 1282. [Google Scholar] [CrossRef] [Green Version]
  20. Okuzaki, Y.; Kaneoka, H.; Suzuki, T.; Hagihara, Y.; Nakayama, Y.; Murakami, S.; Murase, Y.; Kuroiwa, A.; Iijima, S.; Nishijima, K.I. PRDM14 and BLIMP1 control the development of chicken PGCs. Dev. Biol. 2019, 455, 32–41. [Google Scholar] [CrossRef]
  21. Nakamura, T.; Extavour, C.G. The transcriptional repressor Blimp-1 acts downstream of BMP signaling to generate PGCs in the cricket Gryllus bimaculatus. Development 2016, 143, 255–263. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Di Zazzo, E.; Porcile, C.; Bartollino, S.; Moncharmont, B. Critical function of PRDM2 in the neoplastic growth of testicular germ cell tumors. Biology 2016, 5, 54. [Google Scholar] [CrossRef]
  23. Eom, G.H.; Kim, K.; Kim, S.M.; Kee, H.J.; Kim, J.Y.; Jin, H.M.; Kim, J.R.; Kim, J.H.; Choe, N.; Kim, K.B.; et al. Histone methyltransferase PRDM8 regulates mouse testis steroidogenesis. Biochem. Biophys. Res. Commun. 2009, 388, 131–136. [Google Scholar] [CrossRef] [PubMed]
  24. Baudat, F.; Buard, J.; Grey, C.; Fledel-Alon, A.; Ober, C.; Przeworski, M.; Coop, G.; de Massy, B. PRDM9 is a major determinant of meiotic recombination hotspots in humans and mice. Science 2010, 327, 836–840. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Parvanov, E.D.; Petkov, P.M.; Paigen, K. Prdm9 controls activation of mammalian recombination hotspots. Science 2010, 327, 835. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Cheedipudi, S.; Puri, D.; Saleh, A.; Gala, H.P.; Rumman, M.; Pillai, M.S.; Sreenivas, P.; Arora, R.; Sellathurai, J.; Schrøder, H.D.; et al. A fine balance: Epigenetic control of cellular quiescence by the tumor suppressor PRDM2/RIZ at a bivalent domain in the cyclin a gene. Nucleic Acids Res. 2015, 43, 6236–6256. [Google Scholar] [CrossRef] [Green Version]
  27. Mzoughi, S.; Zhang, J.; Hequet, D.; Teo, S.X.; Fang, H.; Xing, Q.R.; Bezzi, M.; Seah, M.K.Y.; Ong, S.L.M.; Shin, E.M.; et al. PRDM15 safeguards naive pluripotency by transcriptionally regulating WNT and MAPK-ERK signaling. Nat. Genet. 2017, 49, 1354–1363. [Google Scholar] [CrossRef]
  28. Bogani, D.; Morgan, M.A.; Nelson, A.C.; Costello, I.; McGouran, J.F.; Kessler, B.M.; Robertson, E.J.; Bikoff, E.K. The PR/SET domain zinc finger protein Prdm4 regulates gene expression in embryonic stem cells but plays a nonessential role in the developing mouse embryo. Mol. Cell. Biol. 2013, 33, 3936–3950. [Google Scholar] [CrossRef] [Green Version]
  29. Galli, G.G.; Honnens de Lichtenberg, K.; Carrara, M.; Hans, W.; Wuelling, M.; Mentz, B.; Multhaupt, H.A.; Fog, C.K.; Jensen, K.T.; Rappsilber, J.; et al. Prdm5 regulates collagen gene transcription by association with RNA polymerase II in developing bone. PLoS Genet. 2012, 8, e1002711. [Google Scholar] [CrossRef] [Green Version]
  30. Davis, C.A.; Haberland, M.; Arnold, M.A.; Sutherland, L.B.; McDonald, O.G.; Richardson, J.A.; Childs, G.; Harris, S.; Owens, G.K.; Olson, E.N. PRISM/PRDM6, a transcriptional repressor that promotes the proliferative gene program in smooth muscle cells. Mol. Cell. Biol. 2006, 26, 2626–2636. [Google Scholar] [CrossRef] [Green Version]
  31. Wu, Y.; Ferguson, J.E.; Wang, H.; Kelley, R.; Ren, R.; McDonough, H.; Meeker, J.; Charles, P.C.; Wang, H.; Patterson, C. PRDM6 is enriched in vascular precursors during development and inhibits endothelial cell proliferation, survival, and differentiation. J. Mol. Cell. Cardiol. 2008, 44, 47–58. [Google Scholar] [CrossRef] [Green Version]
  32. Zhang, Y.; Stehling-Sun, S.; Lezon-Geyda, K.; Juneja, S.C.; Coillard, L.; Chatterjee, G.; Wuertzer, C.A.; Camargo, F.; Perkins, A.S. PR-domain-containing Mds1-Evi1 is critical for long-term hematopoietic stem cell function. Blood 2011, 118, 3853–3861. [Google Scholar] [CrossRef] [PubMed]
  33. Konantz, M.; Alghisi, E.; Müller, J.S.; Lenard, A.; Esain, V.; Carroll, K.J.; Kanz, L.; North, T.E.; Lengerke, C. Evi1 regulates Notch activation to induce zebrafish hematopoietic stem cell emergence. EMBO J. 2016, 35, 2315–2331. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Zhang, Y.; Liu, X.; Xue, H.; Liu, X.; Dai, A.; Song, Y.; Ke, K.; Cao, M. Upregulation of PRDM5 is associated with astrocyte proliferation and neuronal apoptosis caused by lipopolysaccharide. J. Mol. Neurosci. 2016, 59, 146–157. [Google Scholar] [CrossRef] [PubMed]
  35. Eguchi, R.; Yoshigai, E.; Koga, T.; Kuhara, S.; Tashiro, K. Spatiotemporal expression of Prdm genes during Xenopus development. Cytotechnology 2015, 67, 711–719. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Chen, Y.C.; Auer-Grumbach, M.; Matsukawa, S.; Zitzelsberger, M.; Themistocleous, A.C.; Strom, T.M.; Samara, C.; Moore, A.W.; Cho, L.T.; Young, G.T.; et al. Transcriptional regulator PRDM12 is essential for human pain perception. Nat. Genet. 2015, 47, 803–808. [Google Scholar] [CrossRef]
  37. Mona, B.; Uruena, A.; Kollipara, R.K.; Ma, Z.; Borromeo, M.D.; Chang, J.C.; Johnson, J.E. Repression by PRDM13 is critical for generating precision in neuronal identity. Elife 2017, 6, e25787. [Google Scholar] [CrossRef]
  38. Shimada, I.S.; Acar, M.; Burgess, R.J.; Zhao, Z.; Morrison, S.J. Prdm16 is required for the maintenance of neural stem cells in the postnatal forebrain and their differentiation into ependymal cells. Genes Dev. 2017, 31, 1134–1146. [Google Scholar] [CrossRef] [Green Version]
  39. Su, L.; Lei, X.; Ma, H.; Feng, C.; Jiang, J.; Jiao, J. PRDM16 orchestrates angiogenesis via neural differentiation in the developing brain. Cell Death Differ. 2020, 27, 2313–2329. [Google Scholar] [CrossRef]
  40. Lannan, J.E.; Robinson, A.; Breese, W.P. Broodstock management of Crassostrea gigas: II. Broodstock conditioning to maximize larval survival. Aquaculture 1980, 21, 337–345. [Google Scholar] [CrossRef]
  41. de Siqueira-Silva, D.H.; Saito, T.; Dos Santos-Silva, A.P.; da Silva Costa, R.; Psenicka, M.; Yasui, G.S. Biotechnology applied to fish reproduction: Tools for conservation. Fish. Physiol. Biochem. 2018, 44, 1469–1485. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Rivers, N.; Daly, J.; Temple-Smith, P. New directions in assisted breeding techniques for fish conservation. Reprod. Fertil. Dev. 2020, 32, 807–821. [Google Scholar] [CrossRef] [PubMed]
  43. Kakoi, S.; Kin, K.; Miyazaki, K.; Wada, H. Early development of the Japanese spiny oyster (Saccostrea kegaki): Characterization of some genetic markers. Zool. Sci. 2008, 25, 455–464. [Google Scholar] [CrossRef] [Green Version]
  44. Rui, X.; Qi, L.; Hong, Y. Expression pattern of Piwi-like gene implies the potential role in germline development in the Pacific oyster Crossosrea gigas. Aquac. Rep. 2020, 18, 100486. [Google Scholar] [CrossRef]
  45. Hall, T.A. BioEdit: A user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp. Ser. 1999, 41, 95–98. [Google Scholar] [CrossRef]
  46. Eddy, S.R. A new generation of homology search tools based on probabilistic inference. Genome Inform. 2009, 23, 205–211. [Google Scholar] [CrossRef] [Green Version]
  47. Li, Y.; Sun, X.; Hu, X.; Xun, X.; Zhang, J.; Guo, X.; Jiao, W.; Zhang, L.; Liu, W.; Wang, J.; et al. Scallop genome reveals molecular adaptations to semi-sessile life and neurotoxins. Nat. Commun. 2017, 8, 1721. [Google Scholar] [CrossRef] [Green Version]
  48. Liu, W.; Xie, Y.; Ma, J.; Luo, X.; Nie, P.; Zuo, Z.; Lahrmann, U.; Zhao, Q.; Zheng, Y.; Zhao, Y.; et al. IBS: An illustrator for the presentation and visualization of biological sequences. Bioinformatics 2015, 31, 3359–3361. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Waterhouse, A.M.; Procter, J.B.; Martin, D.M.; Clamp, M.; Barton, G.J. Jalview Version 2--a multiple sequence alignment editor and analysis workbench. Bioinformatics 2009, 25, 1189–1191. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  50. Kumar, S.; Stecher, G.; Li, M.; Knyaz, C.; Tamura, K. MEGA X: Molecular evolutionary genetics analysis across computing platforms. Mol. Biol. Evol. 2018, 35, 1547–1549. [Google Scholar] [CrossRef]
  51. Chen, C.; Chen, H.; Zhang, Y.; Thomas, H.R.; Frank, M.H.; He, Y.; Xia, R. TBtools: An integrative toolkit developed for interactive analyses of big biological data. Mol. Plant 2020, 13, 1194–1202. [Google Scholar] [CrossRef] [PubMed]
  52. Guo, X.; Li, X.; Zhao, F.; Liu, D.; Yang, Z.; Li, M.; Li, Y.; Wei, H.; Wang, H.; Qin, Z.; et al. Full-length transcriptome analysis provides insights into larval shell formation in Mulinia lateralis. Front. Mar. Sci. 2023, 9, 1111241. [Google Scholar] [CrossRef]
  53. Livak, K.J.; Schmittgen, T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 2001, 25, 402–408. [Google Scholar] [CrossRef] [PubMed]
  54. Wang, S.; Zhang, J.; Jiao, W.; Li, J.; Xun, X.; Sun, Y.; Guo, X.; Huan, P.; Dong, B.; Zhang, L.; et al. Scallop genome provides insights into evolution of bilaterian karyotype and development. Nat. Ecol. Evol. 2017, 1, 120. [Google Scholar] [CrossRef] [Green Version]
  55. Vervoort, M.; Meulemeester, D.; Béhague, J.; Kerner, P. Evolution of Prdm genes in animals: Insights from comparative genomics. Mol. Biol. Evol. 2016, 33, 679–696. [Google Scholar] [CrossRef] [Green Version]
  56. Huang, S. Histone methyltransferases, diet nutrients and tumour suppressors. Nat. Rev. Cancer. 2002, 2, 469–476. [Google Scholar] [CrossRef]
  57. Hohenauer, T.; Moore, A.W. The Prdm family: Expanding roles in stem cells and development. Development 2012, 139, 2267–2282. [Google Scholar] [CrossRef] [Green Version]
  58. Derunes, C.; Briknarová, K.; Geng, L.; Li, S.; Gessner, C.R.; Hewitt, K.; Wu, S.; Huang, S.; Woods, V.I., Jr.; Ely, K.R. Characterization of the PR domain of RIZ1 histone methyltransferase. Biochem. Biophys. Res. Commun. 2005, 333, 925–934. [Google Scholar] [CrossRef]
  59. Pinheiro, I.; Margueron, R.; Shukeir, N.; Eisold, M.; Fritzsch, C.; Richter, F.M.; Mittler, G.; Genoud, C.; Goyama, S.; Kurokawa, M.; et al. Prdm3 and Prdm16 are H3K9me1 methyltransferases required for mammalian heterochromatin integrity. Cell 2012, 150, 948–960. [Google Scholar] [CrossRef] [Green Version]
  60. Gewies, A.; Castineiras-Vilarino, M.; Ferch, U.; Jährling, N.; Heinrich, K.; Hoeckendorf, U.; Przemeck, G.K.; Munding, M.; Groß, O.; Schroeder, T.; et al. Prdm6 is essential for cardiovascular development in vivo. PLoS ONE 2013, 8, e81833. [Google Scholar] [CrossRef] [Green Version]
  61. Koh-Stenta, X.; Joy, J.; Poulsen, A.; Li, R.; Tan, Y.; Shim, Y.; Min, J.H.; Wu, L.; Ngo, A.; Peng, J.; et al. Characterization of the histone methyltransferase PRDM9 using biochemical, biophysical and chemical biology techniques. Biochem. J. 2014, 461, 323–334. [Google Scholar] [CrossRef]
  62. Gyory, I.; Wu, J.; Fejér, G.; Seto, E.; Wright, K.L. PRDI-BF1 recruits the histone H3 methyltransferase G9a in transcriptional silencing. Nat. Immunol. 2004, 5, 299–308. [Google Scholar] [CrossRef]
  63. Duan, Z.; Person, R.E.; Lee, H.H.; Huang, S.; Donadieu, J.; Badolato, R.; Grimes, H.L.; Papayannopoulou, T.; Horwitz, M.S. Epigenetic regulation of protein-coding and microRNA genes by the Gfi1-interacting tumor suppressor PRDM5. Epigenetic regulation of protein-coding and microRNA genes by the Gfi1-interacting tumor suppressor PRDM5. Mol. Cell Biol. 2007, 27, 6889–6902. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Yu, J.; Angelin-Duclos, C.; Greenwood, J.; Liao, J.; Calame, K. Transcriptional repression by blimp-1 (PRDI-BF1) involves recruitment of histone deacetylase. Mol. Cell. Biol. 2000, 20, 2592–2603. [Google Scholar] [CrossRef] [Green Version]
  65. Fog, C.K.; Galli, G.G.; Lund, A.H. PRDM proteins: Important players in differentiation and disease. Bioessays 2012, 34, 50–60. [Google Scholar] [CrossRef]
  66. Voronezhskaya, E.E.; Tyurin, S.A.; Nezlin, L.P. Neuronal development in larval chiton Ischnochiton hakodadensis (Mollusca: Polyplacophora). J. Comp. Neurol. 2002, 444, 25–38. [Google Scholar] [CrossRef] [PubMed]
  67. Dyachuk, V.; Odintsova, N. Development of the larval muscle system in the mussel Mytilus trossulus (Mollusca, Bivalvia). Dev. Growth Differ. 2009, 51, 69–79. [Google Scholar] [CrossRef] [PubMed]
  68. Pavlicek, A.; Schwaha, T.; Wanninger, A. Towards a ground pattern reconstruction of bivalve nervous systems: Neurogenesis in the zebra mussel Dreissena polymorpha. Org. Divers. Evol. 2018, 18, 101–114. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  69. Yurchenko, O.V.; Skiteva, O.I.; Voronezhskaya, E.E.; Dyachuk, V.A. Nervous system development in the Pacific oyster, Crassostrea gigas (Mollusca: Bivalvia). Front. Zool. 2018, 15, 10. [Google Scholar] [CrossRef] [Green Version]
  70. Liu, C.; Ma, W.; Su, W.; Zhang, J. Prdm14 acts upstream of islet2 transcription to regulate axon growth of primary motoneurons in zebrafish. Development 2012, 139, 4591–4600. [Google Scholar] [CrossRef] [Green Version]
  71. Chittka, A.; Nitarska, J.; Grazini, U.; Richardson, W.D. Transcription factor positive regulatory domain 4 (PRDM4) recruits protein arginine methyltransferase 5 (PRMT5) to mediate histone arginine methylation and control neural stem cell proliferation and differentiation. J. Biol. Chem. 2012, 287, 42995–43006. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  72. Kinameri, E.; Inoue, T.; Aruga, J.; Imayoshi, I.; Kageyama, R.; Shimogori, T.; Moore, A.W. Prdm proto-oncogene transcription factor family expression and interaction with the Notch-Hes pathway in mouse neurogenesis. PLoS ONE 2008, 3, e3859. [Google Scholar] [CrossRef] [Green Version]
  73. Woods, F.H. History of the germ cells in Sphaerium striatinum (Lam.). Int. J. Morphol. 1931, 51, 545–595. [Google Scholar] [CrossRef]
  74. Lyons, D.C.; Perry, K.J.; Lesoway, M.P.; Henry, J.Q. Cleavage pattern and fate map of the mesentoblast, 4d, in the gastropod Crepidula: A hallmark of spiralian development. Evodevo 2012, 3, 21. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  75. Akagi, K.; Ueda, H. Regulatory mechanisms of ecdysone-inducible Blimp-1 encoding a transcriptional repressor that is important for the prepupal development in Drosophila. Dev. Growth Differ. 2011, 53, 697–703. [Google Scholar] [CrossRef] [PubMed]
  76. Nikitina, N.; Tong, L.; Bronner, M.E. Ancestral network module regulating prdm1 expression in the lamprey neural plate border. Dev. Dyn. 2011, 240, 2265–2271. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  77. Livi, C.B.; Davidson, E.H. Expression and function of blimp1/krox, an alternatively transcribed regulatory gene of the sea urchin endomesoderm network. Dev. Biol. 2006, 293, 513–525. [Google Scholar] [CrossRef] [Green Version]
  78. Wilm, T.P.; Solnica-Krezel, L. Essential roles of a zebrafish prdm1/blimp1 homolog in embryo patterning and organogenesis. Development 2005, 132, 393–404. [Google Scholar] [CrossRef] [Green Version]
  79. de Souza, F.S.; Gawantka, V.; Gómez, A.P.; Delius, H.; Ang, S.L.; Niehrs, C. The zinc finger gene Xblimp1 controls anterior endomesodermal cell fate in Spemann’s organizer. EMBO J. 1999, 18, 6062–6072. [Google Scholar] [CrossRef] [Green Version]
  80. Chatfield, J.; O’Reilly, M.A.; Bachvarova, R.F.; Ferjentsik, Z.; Redwood, C.; Walmsley, M.; Patient, R.; Loose, M.; Johnson, A.D. Stochastic specification of PGCs from mesoderm precursors in axolotl embryos. Development 2014, 141, 2429–2440. [Google Scholar] [CrossRef] [Green Version]
  81. Wan, Z.; Rui, L.; Li, Z. Expression patterns of prdm1 during chicken embryonic and germline development. Cell Tissue Res. 2014, 356, 341–356. [Google Scholar] [CrossRef] [Green Version]
  82. Saitou, M.; Yamaji, M. Primordial germ cells in mice. Cold Spring Harb. Perspect. Biol. 2012, 4, a008375. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  83. Saitou, M.; Yamaji, M. Germ cell specification in mice: Signaling, transcription regulation, and epigenetic consequences. Reproduction 2010, 139, 931–942. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  84. Magnúsdóttir, E.; Dietmann, S.; Murakami, K.; Günesdogan, U.; Tang, F.; Bao, S.; Diamanti, E.; Lao, K.; Gottgens, B.; Azim Surani, M. A tripartite transcription factor network regulates primordial germ cell specification in mice. Nat. Cell Biol. 2013, 15, 905–915. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  85. Yabuta, Y.; Kurimoto, K.; Ohinata, Y.; Seki, Y.; Saitou, M. Gene expression dynamics during germline specification in mice identified by quantitative single-cell gene expression profiling. Biol. Reprod. 2006, 75, 705–716. [Google Scholar] [CrossRef] [PubMed]
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Figure 1. Conserved domain identification of PRDM proteins of M. lateralis.
Figure 1. Conserved domain identification of PRDM proteins of M. lateralis.
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Figure 2. Multiple sequence alignment of the PR domains in M. lateralis. Blue boxes indicate shared conserved residues in the PR and SET domains, and red boxes indicate exclusively conserved residues in the PR domains.
Figure 2. Multiple sequence alignment of the PR domains in M. lateralis. Blue boxes indicate shared conserved residues in the PR and SET domains, and red boxes indicate exclusively conserved residues in the PR domains.
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Figure 3. Multiple sequence alignment of the PR domains in different species. Asterisks indicate residues with more than 80% identity, blue boxes indicate shared conserved residues in the PR and SET domains, and red boxes indicate exclusively conserved residues in the PR domains.
Figure 3. Multiple sequence alignment of the PR domains in different species. Asterisks indicate residues with more than 80% identity, blue boxes indicate shared conserved residues in the PR and SET domains, and red boxes indicate exclusively conserved residues in the PR domains.
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Figure 4. Phylogenetic analysis of M. lateralis PRDM proteins. Hs: Homo sapiens; Mm: M. musculus; Gg: G. gallus; Xl: Xenopus laevis; Dr: Danio rerio; Sa: Sparus aurata; My: M. yessoensis; Mc: Mytilus coruscus; Cv: C. virginica; Cg: C. gigas; Pm: Pecten maximus; Mg: Mytilus galloprovincialis; Pc: Pomacea canaliculate; Cf: C. farreri. Blue dots indicate M. lateralis PRDMs.
Figure 4. Phylogenetic analysis of M. lateralis PRDM proteins. Hs: Homo sapiens; Mm: M. musculus; Gg: G. gallus; Xl: Xenopus laevis; Dr: Danio rerio; Sa: Sparus aurata; My: M. yessoensis; Mc: Mytilus coruscus; Cv: C. virginica; Cg: C. gigas; Pm: Pecten maximus; Mg: Mytilus galloprovincialis; Pc: Pomacea canaliculate; Cf: C. farreri. Blue dots indicate M. lateralis PRDMs.
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Figure 5. Expression profiles of prdm genes during early development stages of M. lateralis.
Figure 5. Expression profiles of prdm genes during early development stages of M. lateralis.
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Figure 6. Expression of Ml-prdm1 and Ml-prdm14 during early development stages of M. lateralis. (A,B) represented Ml-prdm1 and Ml-prdm14, respectively. Genes expression level of trochophore or gastrula was set as standard 1, respectively, and the expression levels in other stages were indicated as relative fold-change. All data were represented as mean ± SD (n = 3). Different letters indicated statistically significant differences (p < 0.05).
Figure 6. Expression of Ml-prdm1 and Ml-prdm14 during early development stages of M. lateralis. (A,B) represented Ml-prdm1 and Ml-prdm14, respectively. Genes expression level of trochophore or gastrula was set as standard 1, respectively, and the expression levels in other stages were indicated as relative fold-change. All data were represented as mean ± SD (n = 3). Different letters indicated statistically significant differences (p < 0.05).
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Figure 7. The localization of Ml-prdm1 and Ml-prdm14 transcripts in early development stages of M. lateralis detected by whole-mount in situ hybridization.
Figure 7. The localization of Ml-prdm1 and Ml-prdm14 transcripts in early development stages of M. lateralis detected by whole-mount in situ hybridization.
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Table
Table 1. Primer sequences used for quantitative RT-qPCR.
Table 1. Primer sequences used for quantitative RT-qPCR.
Gene NameForward Primer (5′-3′)Reverse Primer (5′-3′)
Ml-prdm1AGGAGAGGAAATGTTACAAGCAGGCAGGAGTAGGTGGAGTCTTA
Ml-prdm14ACTGACGCCTCGGTTTTATCGTCGGACTCGGTGTTTCTGA
Ml-ef1bGGGCATTACTTCACTCTAAATTGTGCTATCTGAGGGTCTACT
Table
Table 2. Primer sequences used for the synthesis of RNA probes of in situ hybridization.
Table 2. Primer sequences used for the synthesis of RNA probes of in situ hybridization.
Gene NameForward Primer (5′-3′)Reverse Primer (5′-3′)
Ml-prdm1ATTTAGGTGACACTATAGAAGCG 1
CATTTAAGAGCCCGAAGT		TAATACGACTCACTATAGGGAGACA 2
CATAGGAGGGTAAGGTGG
Ml-prdm14ATTTAGGTGACACTATAGAAGCG 1
GATTGGTTTCCCATTTC		TAATACGACTCACTATAGGGAGACA 2
TCGTGCTCCTCTGACTT
1 The underlined sequence represents the SP6 promoter. 2 The underlined sequence represents the T7 promoter.
Table
Table 3. Summary of M. lateralis PRDMs properties.
Table 3. Summary of M. lateralis PRDMs properties.
ProteinProtein LengthDomain NumberPR Domain LengthpIMw (Da)
PRZinc Finger
Ml-PRDM1837151226.9695,462.42
Ml-PRDM219691111226.04221,527.46
Ml-PRDM4-like881141355.7498,698.34
Ml-PRDM8-like746131187.9684,010.47
Ml-PRDM97101101218.5481,667.44
Ml-PRDM1014811121196.25165,430.32
Ml-PRDM12283131209.232,469.99
Ml-PRDM13-like54210988.5460,496.27
Ml-PRDM14524161248.9159,197.42
Ml-PRDM1516191201185.96181,519.82
Ml-PRDM16-like87919496.7698,759.51
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Zhao, F.; Guo, X.; Li, X.; Liu, F.; Fu, Y.; Sun, X.; Yang, Z.; Zhang, Z.; Qin, Z. Identification and Expressional Analysis of Putative PRDI-BF1 and RIZ Homology Domain-Containing Transcription Factors in Mulinia lateralis. Biology 2023, 12, 1059. https://doi.org/10.3390/biology12081059

AMA Style

Zhao F, Guo X, Li X, Liu F, Fu Y, Sun X, Yang Z, Zhang Z, Qin Z. Identification and Expressional Analysis of Putative PRDI-BF1 and RIZ Homology Domain-Containing Transcription Factors in Mulinia lateralis. Biology. 2023; 12(8):1059. https://doi.org/10.3390/biology12081059

Chicago/Turabian Style

Zhao, Feng, Xiaolin Guo, Xixi Li, Fang Liu, Yifan Fu, Xiaohan Sun, Zujing Yang, Zhifeng Zhang, and Zhenkui Qin. 2023. "Identification and Expressional Analysis of Putative PRDI-BF1 and RIZ Homology Domain-Containing Transcription Factors in Mulinia lateralis" Biology 12, no. 8: 1059. https://doi.org/10.3390/biology12081059

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