SOX5

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SRY (sex determining region Y)-box 5
PDB rendering based on 1i11.
Available structures: 1i11
Identifiers
Symbol(s) SOX5; L-SOX5; MGC35153
External IDs OMIM: 604975 MGI98367 HomoloGene21378
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 6660 20678
Ensembl ENSG00000134532 ENSMUSG00000041540
Uniprot P35711 Q3TVF9
Refseq NM_006940 (mRNA)
NP_008871 (protein)
NM_011444 (mRNA)
NP_035574 (protein)
Location Chr 12: 23.58 - 23.99 Mb Chr 6: 143.79 - 144.16 Mb
Pubmed search [1] [2]

SRY (sex determining region Y)-box 5, also known as SOX5, is a human gene.[1]

This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. The encoded protein may play a role in chondrogenesis. A pseudogene of this gene is located on chromosome 8. Multiple transcript variants encoding distinct isoforms have been identified for this gene.[1]

[edit] See also

[edit] References

[edit] Further reading

  • Kamachi Y, Uchikawa M, Kondoh H (2000). "Pairing SOX off: with partners in the regulation of embryonic development.". Trends Genet. 16 (4): 182-7. PMID 10729834. 
  • Bowles J, Schepers G, Koopman P (2001). "Phylogeny of the SOX family of developmental transcription factors based on sequence and structural indicators.". Dev. Biol. 227 (2): 239-55. doi:10.1006/dbio.2000.9883. PMID 11071752. 
  • Wilson M, Koopman P (2003). "Matching SOX: partner proteins and co-factors of the SOX family of transcriptional regulators.". Curr. Opin. Genet. Dev. 12 (4): 441-6. PMID 12100890. 
  • Schepers GE, Teasdale RD, Koopman P (2002). "Twenty pairs of sox: extent, homology, and nomenclature of the mouse and human sox transcription factor gene families.". Dev. Cell 3 (2): 167-70. PMID 12194848. 
  • Denny P, Swift S, Brand N, et al. (1992). "A conserved family of genes related to the testis determining gene, SRY.". Nucleic Acids Res. 20 (11): 2887. PMID 1614875. 
  • Connor F, Cary PD, Read CM, et al. (1994). "DNA binding and bending properties of the post-meiotically expressed Sry-related protein Sox-5.". Nucleic Acids Res. 22 (16): 3339-46. PMID 8078769. 
  • Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". Gene 138 (1-2): 171-4. PMID 8125298. 
  • Wunderle VM, Critcher R, Ashworth A, Goodfellow PN (1997). "Cloning and characterization of SOX5, a new member of the human SOX gene family.". Genomics 36 (2): 354-8. doi:10.1006/geno.1996.0474. PMID 8812465. 
  • Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery.". Genome Res. 6 (9): 791-806. PMID 8889548. 
  • Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.". Gene 200 (1-2): 149-56. PMID 9373149. 
  • 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 (19): 5718-33. doi:10.1093/emboj/17.19.5718. PMID 9755172. 
  • Uusitalo H, Hiltunen A, Ahonen M, et al. (2002). "Accelerated up-regulation of L-Sox5, Sox6, and Sox9 by BMP-2 gene transfer during murine fracture healing.". J. Bone Miner. Res. 16 (10): 1837-45. PMID 11585348. 
  • Zafarana G, Gillis AJ, van Gurp RJ, et al. (2002). "Coamplification of DAD-R, SOX5, and EKI1 in human testicular seminomas, with specific overexpression of DAD-R, correlates with reduced levels of apoptosis and earlier clinical manifestation.". Cancer Res. 62 (6): 1822-31. PMID 11912161. 
  • Ikeda T, Zhang J, Chano T, et al. (2003). "Identification and characterization of the human long form of Sox5 (L-SOX5) gene.". Gene 298 (1): 59-68. PMID 12406576. 
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899-903. doi:10.1073/pnas.242603899. PMID 12477932. 
  • Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40-5. doi:10.1038/ng1285. PMID 14702039.