SOX13 exhibits a distinct spatial and temporal expression pattern during chondrogenesis, neurogenesis, and limb development

Journal of Histochemistry and Cytochemistry

Volumn 54, Issue 12, 2006, Pages 1327-1333

  Wang, Yi ^a,b   Ristevski, Sika ^c   Harley, Vincent R ^a  

^a HUDSON INSTITUTE OF MEDICAL RESEARCH   (Australia)

^b UNIVERSITY OF MELBOURNE   (Australia)

^c MONASH UNIVERSITY   (Australia)

Author keywords

Endochondral bone; Expression pattern; Mouse embryonic development; Neural tube; Sclerotome; SOX13; Spongiotrophoblast; Visceral mesoderm

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR SOX13; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; CARTILAGE CELL; CELL LINEAGE; CHONDROGENESIS; CONTROLLED STUDY; EMBRYO; EMBRYO CELL; LIMB DEVELOPMENT; MESENCHYME; MESODERM; MOUSE; NERVOUS SYSTEM DEVELOPMENT; NEURAL TUBE; NONHUMAN; OSSIFICATION; PLACENTA; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; SCLEROTOME; SOMITE; YOLK SAC;

ANIMALS; AUTOANTIGENS; CENTRAL NERVOUS SYSTEM; CHONDROCYTES; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HIGH MOBILITY GROUP PROTEINS; IMMUNOHISTOCHEMISTRY; LIMB BUD; MICE; MICE, INBRED C57BL; MICE, INBRED CBA; PLACENTA; SOMITES; SPINAL CORD; YOLK SAC;

EID: 33751257788     PISSN: 00221554     EISSN: None     Source Type: Journal    
DOI: 10.1369/jhc.6A6923.2006     Document Type: Article

References (46)

1. Akiyama H, Chaboissier MC, Martin JF, Schedl A, de Crombrugghe B (2002) The transcription factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6. Genes Dev 16:2813-2828
2. Argentaro A, Olsson J, Critcher R, McDowall SG, Harley VR (2000) Genomic characterisation and fine mapping of the human SOX13 gene. Gene 250:181-189
3. Bahabri SA, Suwairi WM, Laxer RM, Polinkovsky A, Dalaan AA, Warman ML (1998) The camptodactyly-arthropathy-coxa vara-pericarditis syndrome: clinical features and genetic mapping to human chromosome 1. Arthritis Rheum 41:730-735
4. Bell DM, Leung KK, Wheatley SC, Ng LJ, Zhou S, Ling KW, Sham MH, et al. (1997) SOX9 directly regulates the type-II collagen gene. Nat Genet 16:174-178
5. Benitez J, Osorio A, Barroso A, Arranz E, Diaz-Guillen MA, Robledo M, Rodriguez de Cordoba S, et al. (1997) A region of allelic imbalance in 1q31-32 in primary breast cancer coincides with a recombination hot spot. Cancer Res 57:4217-4220
6. Bi W, Deng JM, Zhang Z, Behringer RR, de Crombrugghe B (1999) Sox9 is required for cartilage formation. Nat Genet 22:85-89
7. Bylund M, Andersson E, Novitch BG, Muhr J (2003) Vertebrate neurogenesis is counteracted by Sox1-3 activity. Nat Neurosci 6:1162-1168
8. Canto P, de la Chesnaye E, Lopez M, Cervantes A, Chavez B, Vilchis F, Reyes E, et al. (2000) A mutation in the 5′ non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism. J Clin Endocrinol Metab 85:1908-1911
9. Chimal-Monroy J, Rodriguez-Leon J, Montero JA, Ganan Y, Macias D, Merino R, Hurle JM (2003) Analysis of the molecular cascade responsible for mesodermal limb chondrogenesis: Sox genes and BMP signaling. Dev Biol 257:292-301
10. Collignon J, Sockanathan S, Hacker A, Cohen-Tannoudji M, Norris D, Rastan S, Stevanovic M, et al. (1996) A comparison of the properties of Sox-3 with Sry and two related genes, Sox-1 and Sox-2. Development 122:509-520
11. Cornelis F, Faure S, Martinez M, Prud'homme JF, Fritz P, Dib C, Alves H, et al. (1998) New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study. Proc Natl Acad Sci USA 95:10746-10750
12. Cross JC, Anson-Cartwright L, Scott IC (2002a) Transcription factors underlying the development and endocrine functions of the placenta. Recent Prog Horm Res 57:221-234
13. Cross JC, Hemberger M, Lu Y, Nozaki T, Whiteley K, Masutani M, Adamson SL (2002b) Trophoblast functions, angiogenesis and remodeling of the maternal vasculature in the placenta. Mol Cell Endocrinol 187:207-212
14. Durand JB, Bachinski LL, Bieling LC, Czernuszewicz GZ, Abchee AB, Yu QT, Tapscott T, et al. (1995) Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32. Circulation 92:3387-3389
15. Enomoto-Iwamoto M, Iwamoto M, Mukudai Y, Kawakami Y, Nohno T, Higuchi Y, Takemoto S, et al. (1998) Bone morphogenetic protein signaling is required for maintenance of differentiated phenotype, control of proliferation, and hypertrophy in chondrocytes. J Cell Biol 140:409-418
16. Ferrari S, Harley VR, Pontiggia A, Goodfellow PN, Lovell-Badge R, Bianchi ME (1992) SRY, like HMG1, recognizes sharp angles in DNA. EMBO J 11:4497-4506
17. Fogt F, Zhuang Z, Linehan WM, Merino MJ (1998) Collecting duct carcinomas of the kidney: a comparative loss of heterozygosity study with clear cell renal cell carcinoma. Oncol Rep 5:923-926
18. Foster JW, Graves JA (1994) An SRY-related sequence on the marsupial X chromosome: implications for the evolution of the mammalian testis-determining gene. Proc Natl Acad Sci USA 91:1927-1931
19. Graham V, Khudyakov J, Ellis P, Pevny L (2003) SOX2 functions to maintain neural progenitor identity. Neuron 39:749-765
20. Harley VR, Jackson DI, Hextall PJ, Hawkins JR, Berkovitz GD, Sockanathan S, Lovell-Badge R, et al. (1992) DNA binding activity of recombinant SRY from normal males and XY females. Science 255:453-456
21. Houdayer C, Soupre V, Rosenberg-Bourgin M, Martinez H, Tredano M, Feldmann D, Feingold J, et al. (1999) Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait. Ann Genet 42:69-74
22. Inoue K, Shilo K, Boerkoel CF, Crowe C, Sawady J, Lupski JR, Agamanolis DP (2002) Congenital hypomyelinating neuropathy, central dysmyelination, and Waardenburg-Hirschsprung disease: phenotypes linked by SOX10 mutation. Ann Neurol 52:836-842
23. Kasimiotis H, Myers MA, Argentaro A, Mertin S, Fida S, Ferraro T, Olsson J, et al. (2000) Sex-determining region Y-related protein SOX13 is a diabetes autoantigen expressed in pancreatic islets. Diabetes 49:555-561
24. Kido S, Hiraoka Y, Ogawa M, Sakai Y, Yoshimura Y, Aiso S (1998) Cloning and characterization of mouse mSox13 cDNA. Gene 208:201-206
25. Kraus JA, Albrecht S, Wiestler OD, von Schweinitz D, Pietsch T (1996a) Loss of heterozygosity on chromosome 1 in human hepatoblastoma. Int J Cancer 67:467-471
26. Kraus JA, Koch A, Albrecht S, Von Deimling A, Wiestler OD, Pietsch T (1996b) Loss of heterozygosity at locus F13B on chromosome 1q in human medulloblastoma. Int J Cancer 67:11-15
27. Laudet V, Stehelin D, Clevers H (1993) Ancestry and diversity of the HMG box superfamily. Nucleic Acids Res 21:2493-2501
28. Lefebvre V, Li P, de Crombrugghe B (1998) A new long form of Sox5 (L-Sox5), Sox6 and Sox9 are coexpressed in chondrogenesis and cooperatively activate the type II collagen gene. EMBO J 17: 5718-5733
29. Mizuseki K, Kishi M, Matsui M, Nakanishi S, Sasai Y (1998) Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction. Development 125:579-587
30. Paratore C, Eichenberger C, Suter U, Sommer L (2002) Sox10 haplo-insufficiency affects maintenance of progenitor cells in a mouse model of Hirschsprung disease. Hum Mol Genet 11:3075-3085
31. Pevny LH, Lovell-Badge R (1997) Sox genes find their feet. Curr Opin Genet Dev 7:338-344
32. Pevny LH, Sockanathan S, Placzek M, Lovell-Badge R (1998) A role for SOX1 in neural determination. Development 125:1967-1978
33. Rabin DU, Pleasic SM, Palmer-Crocker R, Shapiro JA (1992) Cloning and expression of IDDM-specific human autoantigens. Diabetes 41:183-186
34. Rex M, Uwanogho DA, Orme A, Scotting PJ, Sharpe PT (1997) cSox21 exhibits a complex and dynamic pattern of transcription during embryonic development of the chick central nervous system. Mech Dev 66:39-53
35. Roose J, Korver W, Oving E, Wilson A, Wagenaar G, Markman M, Lamers W, et al. (1998) High expression of the HMG box factor sox-13 in arterial walls during embryonic development. Nucleic Acids Res 26:469-476
36. Scherer G, Held M, Erdel M, Meschede D, Horst J, Lesniewicz R, Midro AT (1998) Three novel SRY mutations in XY gonadal dysgenesis and the enigma of XY gonadal dysgenesis cases without SRY mutations. Cytogenet Cell Genet 80:188-192
37. Schmitt-Ney M, Thiele H, Kaltwasser P, Bardoni B, Cisternino M, Scherer G (1995) Two novel SRY missense mutations reducing DNA binding identified in XY females and their mosaic fathers. Am J Hum Genet 56:862-869
38. Smits P, Li P, Mandel J, Zhang Z, Deng JM, Behringer RR, de Crombrugghe B, et al. (2001) The transcription factors L-Sox5 and Sox6 are essential for cartilage formation. Dev Cell 1:277-290
39. Southard-Smith EM, Kos L, Pavan WJ (1998) Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model. Nat Genet 18:60-64
40. Steiner G, Cairns P, Polascik TJ, Marshall FF, Epstein JI, Sidransky D, Schoenberg M (1996) High-density mapping of chromosomal arm 1q in renal collecting duct carcinoma: region of minimal deletion at 1q32.1-32.2. Cancer Res 56:5044-5046
41. Uehara S, Hashiyada M, Sato K, Nata M, Funato T, Okamura K (2002) Complete XY gonadal dysgenesis and aspects of the SRYgenotype and gonadal tumor formation. J Hum Genet 47: 279-284
42. Uwanogho D, Rex M, Cartwright EJ, Pearl G, Healy C, Scotting PJ, Sharpe PT (1995) Embryonic expression of the chicken Sox2, Sox3 and Sox11 genes suggests an interactive role in neuronal development. Mech Dev 49:23-36
43. Vollmer M, Jung M, Ruschendorf F, Ruf R, Wienker T, Reis A, Krapf R, et al. (1998) The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster. Am J Hum Genet 63:1724-1731
44. Wagner T, Wirth J, Meyer J, Zabel B, Held M, Zimmer J, Pasantes J, et al. (1994) Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9. Cell 79:1111-1120
45. Wang Y, Bagheri-Fam S, Harley VR (2005) SOX13 is up-regulated in the developing mouse neutoepithelium and identifies a sub-population of differentiating neurons. Brain Res Dev Brain Res 157:201-208
46. Wegner M (1999) From head to toes: the multiple facets of Sox proteins. Nucleic Acids Res 27:1409-1420