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Molecular cloning and mRNA expression pattern of Sox10 in Paramisgurnus dabryanus

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Abstract

A number of genetic studies have established that Sox10 involved in a wide range of developmental processes including sex differentiation and neurogenesis in vertebrates. A Sox10 homologue was cloned from brain of Paramisgurnus dabryanus by using homologous cloning and RACE method, designated as PdSox10. The full-length cDNA of PdSox10 contains a 312 bp 5′ UTR, a 1,476 bp open reading frame (ORF) encoding 492 amino acids and a 262 bp 3′ UTR (Accession no.: JQ217143). The overall topology of the phylogenetic tree shows that the PdSox10 fits within the Sox10 clade. During embryogenesis, PdSox10 gene seemed to be de novo synthesized in the embryos from gastrulae stage. From the somitogenesis stage and thereafter, distinct expression of PdSox10 was observed in the medial neural tube, extending from the hindbrain through the posterior trunk. In adult, PdSox10 mRNA was detected primarily in the gonads, as well as in brain and heart by RT-PCR. In situ hybridization on gonadal sections further demonstrated that PdSox10 is expressed especially in premature germ cells, in early perinucleolus stage oocytes and cortical–alveolar stage oocytes in ovaries and in spermatogonia and spermatocytes in testes. These preliminary findings suggested that PdSox10 is highly conserved during vertebrate evolution and involved in a wide range of developmental processes including neurogenesis and sex differentiation in vertebrates.

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References

  1. Gubbay J, Collignon J, Koopman P, Capel B, Economou A, Münsterberg A, Vivian N, Goodfellow P, Lovell-Badge R (1990) A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes. Nature 346:245–250

    Article  CAS  PubMed  Google Scholar 

  2. Harley VR, Lovell-Badge R, Goodfellow PN (1994) Definition of a consensus DNA binding site for SRY. Nucleic Acids Res 22:1500–1501

    Article  CAS  PubMed  Google Scholar 

  3. Guth SIE, Wegner M (2008) Having it both ways: Sox protein function between conservation and innovation. Cell Mol Life Sci 65:3000–3018

    Article  CAS  PubMed  Google Scholar 

  4. Pevny LH, Lovell-Badge R (1997) Sox genes find their feet. Curr Opin Genet Dev 7:338–344

    Article  CAS  PubMed  Google Scholar 

  5. Soullier S, Jay P, Poulat F, Vanacker JM, Berta P, Laudet V (1999) Diversification pattern of the HMG and SOX family members during evolution. J Mol Evol 48:517–527

    Article  CAS  PubMed  Google Scholar 

  6. Kiefer JC (2007) Back to basics: Sox genes. Dev Dyn 236:2356–2366

    Article  CAS  PubMed  Google Scholar 

  7. Polanco JC, Wilhelm D, Davidson TL, Knight D, Koopman P (2010) Sox10 gain-of-function causes XX sex reversal in mice: implications for human 22q-linked disorders of sex development. Hum Mol Genet 19:506–516

    Article  CAS  PubMed  Google Scholar 

  8. Stolt CC, Wegner M (2010) SoxE function in vertebrate nervous system development. Int J Biochem Cell Biol 42:437–440

    Article  CAS  PubMed  Google Scholar 

  9. Pingault V, Bondurand N, Kuhlbrodt K, Goerich DE, Préhu MO, Puliti A, Herbarth B, Hermans-Borgmeyer I, Legius E, Matthijs G, Amiel J, Lyonnet S, Ceccherini I, Romeo G, Smith JC, Read AP, Wegner M, Goossens M (1998) Sox10 mutations in patients with Waardenburg–Hirschsprung disease. Nat Genet 18:171–173

    Article  CAS  PubMed  Google Scholar 

  10. Bondurand N, Kuhlbrodt K, Pingault V, Enderich J, Sajus M, Tommerup N, Warburg M, Hennekam RC, Read AP, Wegner M, Goossens M (1999) A molecular analysis of the Yemenite deaf–blind hypopigmentation syndrome: Sox10 dysfunction causes different neurocristopathies. Hum Mol Genet 8:1785–1789

    Article  CAS  PubMed  Google Scholar 

  11. Pingault V, Guiochon-Mantel A, Bondurand N, Faure C, Lacroix C, Lyonnet S, Goossens M, Landrieu P (2000) Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: a developmental “neural crest syndrome” related to a Sox10 mutation. Ann Neurol 48:671–676

    Article  CAS  PubMed  Google Scholar 

  12. Kapur RP (1999) Early death of neural crest cells is responsible for total enteric aganglionosis in Sox10(Dom)/Sox10(Dom) mouse embryos. Pediatr Dev Pathol 2:559–569

    Article  CAS  PubMed  Google Scholar 

  13. Kim J, Lo L, Dormand E, Anderson DJ (2003) SOX10 maintains multipotency and inhibits neuronal differentiation of neural crest stem cells. Neuron 38:17–31

    Article  CAS  PubMed  Google Scholar 

  14. Britsch S, Goerich DE, Riethmacher D, Peirano RI, Rossner M, Nave KA, Birchmeier C, Wegner M (2001) The transcription factor Sox10 is a key regulator of peripheral glial development. Genes Dev 15:66–78

    Article  CAS  PubMed  Google Scholar 

  15. Reiprich S, Stolt CC, Schreiner S, Parlato R, Wegner M (2008) SoxE proteins are differentially required in mouse adrenal gland development. Mol Biol Cell 19:1575–1586

    Article  CAS  PubMed  Google Scholar 

  16. Southard-Smith EM, Kos L, Pavan WJ (1998) Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model. Nat Genet 18:60–64

    Article  CAS  PubMed  Google Scholar 

  17. Dutton KA, Pauliny A, Lopes SS, Elworthy S, Carney TJ, Rauch J, Geisler R, Haffter P, Kelsh RN (2001) Zebrafish colourless encodes Sox10 and specifies non-ectomesenchymal neural crest fates. Development 128:4113–4125

    CAS  PubMed  Google Scholar 

  18. Deng Si-Ping, Chen Song-Lin (2009) cDNA cloning, tissues, embryos and larvae expression analysis of Sox10 in half-smooth tongue-sole, Cynoglossus semilaevis. Mar Genomics 1:109–114

    Article  Google Scholar 

  19. Liu Qiongyou, Huijie Lu, Zhang Lihong, Xie Jun, Shen Wenying, Zhang Weimin (2012) Homologues of sox8 and sox10 in the orange-spotted grouper Epinephelus coioides: sequences, expression patterns, and their effects on cyp19a1a promoter activities in vitro. Comp Biochem Physiol B Biochem Mol Biol 163:86–95

    Article  CAS  PubMed  Google Scholar 

  20. Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2 (-delta delta C (T)) method. Methods 25:402–408

    Article  CAS  PubMed  Google Scholar 

  21. Wilkinson DG (1992) In situ hybridization: a practical approach. Oxford University Press, Oxford

    Google Scholar 

  22. Zhou L, Wang Y, Yao B, Li CJ, Ji GD, Gui JF (2005) Molecular cloning and expression pattern of 14 kDa apolipoprotein in orange-spotted grouper, Epinephelus coioides. Comp Biochem Physiol B Biochem Mol Biol 142:432–437

    Article  PubMed  Google Scholar 

  23. Bertwistle D (1999) In situ hybridization to sections of Xenopus embryos. Methods Mol Biol 127:69–76

    CAS  PubMed  Google Scholar 

  24. Wang Y, Zhou L, Yao B, Li CJ, Gui JF (2004) Differential expression of thyroid-stimulating hormone beta subunit in gonads during sex reversal of orange-spotted and red-spotted groupers. Mol Cell Endocrinol 220:77–88

    Article  CAS  PubMed  Google Scholar 

  25. Bondurand N, Kobetz A, Pingault V, Lemort N, Encha-Razavi F, Couly G, Goerich DE, Wegner M, Abitbol M, Goossens M (1998) Expression of the SOX10 gene during human development. FEBS Lett 432:168–172

    Article  CAS  PubMed  Google Scholar 

  26. Stella M Honoré, Manuel J Aybar, Roberto Mayor (2003) Sox10 is required for the early development of the prospective neural crest in Xenopus embryos. Dev Biol 260:79–96

    Article  Google Scholar 

  27. Kuhlbrodt K, Herbarth B, Sock E, Hermans-Borgmeyer I, Wegner M (1998) Sox10, a novel transcriptional modulator in glial cells. J Neurosci 18:237–250

    CAS  PubMed  Google Scholar 

  28. Cory AT, Boyer A, Pilon N, Lussier JG, Silversides DW (2007) Presumptive pre-Sertoli cells express genes involved in cell proliferation and cell signalling during a critical window in early testis differentiation. Mol Reprod Dev 74:1491–1504

    Article  CAS  PubMed  Google Scholar 

  29. Herbarth B, Pingault V, Bondurand N, Kuhlbrodt K, Hermans-Borgmeyer I, Puliti A, Lemort N, Goossens M, Wegner M (1998) Mutation of the Sry-related Sox10 gene in dominant megacolon, a mouse model for human Hirschsprung disease. Proc Natl Acad Sci U S A 95:5161–5165

    Article  CAS  PubMed  Google Scholar 

  30. Stolt CC, Rehberg S, Ader M, Lommes P, Riethmacher D, Schachner M, Bartsch U, Wegner M (2002) Terminal differentiation of myelin-forming oligodendrocytes depends on the transcription factor Sox10. Genes Dev 16:165–170

    Article  CAS  PubMed  Google Scholar 

  31. Cheng YC, Cheung M, Abu-Elmagd MM, Orme A, Scotting PJ (2000) Chick sox10, a transcription factor expressed in both early neural crest cells and central nervous system. Brain Res Dev Brain Res 121:233–241

    Article  CAS  PubMed  Google Scholar 

  32. Aoki Yoichiro, Saint-Germain Natasha, Gyda Michael, Magner-Fink Emily, Lee Young-Hoon, Credidio Christine, Saint-Jeannet Jean-Pierre (2003) Sox10 regulates the development of neural crest-derived melanocytes in Xenopus. Dev Biol 259:19–33

    Article  CAS  PubMed  Google Scholar 

  33. Cossais François, Sock Elisabeth, Hornig Julia, Schreiner Silke, Kellerer Susanne, Bösl Michael R, Russell Steven, Wegner Michael (2010) Replacement of mouse Sox10 by the Drosophila ortholog Sox100B provides evidence for co-option of SoxE proteins into vertebrate-specific gene-regulatory networks through altered expression. Dev Biol 341:267–281

    Article  CAS  PubMed  Google Scholar 

  34. Foster JW, Dominguez-Steglich MA, Guioli S, Kwok C, Weller PA, Stevanovic M, Weissenbach J, Mansour S, Young ID, Goodfellow PN, Brook JD, Schafer AJ (1994) Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene. Nature 372:525–530

    Article  CAS  PubMed  Google Scholar 

  35. Wagner T, Wirth J, Meyer J, Zabel B, Held M, Zimmer J, Pasantes J, Bricarelli FD, Keutel J, Hustert E, Wolf U, Tommerup N, Schempp W, Scherer G (1994) Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9. Cell 79:1111–1120

    Article  CAS  PubMed  Google Scholar 

  36. Chaboissier MC, Kobayashi A, Vidal VIP, Lützkendorf S, Kant HJGV, Wegner M, Rooij DGD, Behringer RR, Schedl A (2004) Functional analysis of Sox8 and Sox9 during sex determination in the mouse. Development 131:1891–1901

    Article  CAS  PubMed  Google Scholar 

  37. Maka M, Stolt CC, Wegner M (2005) Identification of Sox8 as a modifier gene in a mouse model of Hirschsprung disease reveals underlying molecular defect. Dev Biol 277:155–169

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

This work is supported by grants from the National Natural Science Foundation of China (No. 31200923), Tianjin Key Laboratory of Animal and Plant Resistance Open Fund (No. 01046651012), Scientific Research Key Project Fund of the Education department of Henan Province (No. 12B180011) and Doctor Subject Foundation of Henan Normal University (No. 01046500109).

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Correspondence to Zhongjie Chang.

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Xia, X., Chen, J., Zhang, L. et al. Molecular cloning and mRNA expression pattern of Sox10 in Paramisgurnus dabryanus . Mol Biol Rep 40, 3123–3134 (2013). https://doi.org/10.1007/s11033-012-2386-1

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  • DOI: https://doi.org/10.1007/s11033-012-2386-1

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