SOX8

SOX8
Identifiers
Aliases	SOX8, SRY-box 8, SRY-box transcription factor 8
External IDs	OMIM: 605923 MGI: 98370 HomoloGene: 7950 GeneCards: SOX8
Gene location (Human)
Chr.	Chromosome 16 (human)[1]
End	986,979 bp[1]
Gene location (Mouse)
Chr.	Chromosome 17 (mouse)[2]
End	25,570,686 bp[2]
Gene ontology
Molecular function	• DNA binding; • sequence-specific DNA binding; • GO:0001131, GO:0001151, GO:0001130, GO:0001204 DNA-binding transcription factor activity; • transcription factor binding; • protein heterodimerization activity; • RNA polymerase II core promoter sequence-specific DNA binding; • GO:0001200, GO:0001133, GO:0001201 DNA-binding transcription factor activity, RNA polymerase II-specific; • GO:0001077, GO:0001212, GO:0001213, GO:0001211, GO:0001205 DNA-binding transcription activator activity, RNA polymerase II-specific;
Cellular component	• cytoplasm; • cell nucleus;
Biological process	• positive regulation of osteoblast proliferation; • cell fate commitment; • negative regulation of myoblast differentiation; • positive regulation of branching involved in ureteric bud morphogenesis; • male gonad development; • peripheral nervous system development; • regulation of transcription, DNA-templated; • morphogenesis of a branching epithelium; • ureter morphogenesis; • regulation of hormone levels; • oligodendrocyte differentiation; • negative regulation of apoptotic process; • in utero embryonic development; • cell maturation; • Sertoli cell development; • transcription, DNA-templated; • metanephric nephron tubule formation; • positive regulation of transcription, DNA-templated; • negative regulation of photoreceptor cell differentiation; • enteric nervous system development; • renal vesicle induction; • positive regulation of kidney development; • positive regulation of gene expression; • retina development in camera-type eye; • astrocyte fate commitment; • osteoblast differentiation; • neural crest cell migration; • spermatogenesis; • retinal rod cell differentiation; • skeletal muscle cell differentiation; • adipose tissue development; • negative regulation of transcription, DNA-templated; • fat cell differentiation; • signal transduction; • positive regulation of transcription from RNA polymerase II promoter; • positive regulation of gliogenesis; • morphogenesis of an epithelium; • central nervous system development;
	Sources:Amigo / QuickGO
Orthologs
	30812
	20681
	ENSG00000005513
	ENSMUSG00000024176
	P57073
	Q04886
	NM_014587
	NM_011447
	NP_055402
	NP_035577
	Wikidata
View/Edit Human	View/Edit Mouse

Transcription factor SOX-8 is a protein that in humans is encoded by the SOX8 gene.[5][6][7]

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 activator after forming a protein complex with other proteins. This protein may be involved in brain development and function. Haploinsufficiency for this protein may contribute to the mental retardation found in haemoglobin H-related mental retardation (ATR-16 syndrome).[7]

References

GRCh38: Ensembl release 89: ENSG00000005513 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000024176 - Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Pfeifer D, Poulat F, Holinski-Feder E, Kooy F, Scherer G (Apr 2000). "The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome". Genomics. 63 (1): 108–16. doi:10.1006/geno.1999.6060. PMID 10662550.
Schepers GE, Bullejos M, Hosking BM, Koopman P (Apr 2000). "Cloning and characterisation of the Sry-related transcription factor gene Sox8". Nucleic Acids Res. 28 (6): 1473–80. doi:10.1093/nar/28.6.1473. PMC 111037. PMID 10684944.
"Entrez Gene: SOX8 SRY (sex determining region Y)-box 8".

Daniels RJ, Peden JF, Lloyd C, et al. (2001). "Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16". Hum. Mol. Genet. 10 (4): 339–52. doi:10.1093/hmg/10.4.339. PMID 11157797.
Cheng YC, Lee CJ, Badge RM, et al. (2001). "Sox8 gene expression identifies immature glial cells in developing cerebellum and cerebellar tumours". Brain Res. Mol. Brain Res. 92 (1–2): 193–200. doi:10.1016/S0169-328X(01)00147-4. PMID 11483257.
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. PMC 139241. PMID 12477932.
Gevaert K, Goethals M, Martens L, et al. (2004). "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides". Nat. Biotechnol. 21 (5): 566–9. doi:10.1038/nbt810. PMID 12665801. S2CID 23783563.
Schepers G, Wilson M, Wilhelm D, Koopman P (2003). "SOX8 is expressed during testis differentiation in mice and synergizes with SF1 to activate the Amh promoter in vitro". J. Biol. Chem. 278 (30): 28101–8. doi:10.1074/jbc.M304067200. PMID 12732652.
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.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Martin J, Han C, Gordon LA, et al. (2005). "The sequence and analysis of duplication-rich human chromosome 16" (PDF). Nature. 432 (7020): 988–94. doi:10.1038/nature03187. PMID 15616553. S2CID 4362044.
Wissmüller S, Kosian T, Wolf M, et al. (2006). "The high-mobility-group domain of Sox proteins interacts with DNA-binding domains of many transcription factors". Nucleic Acids Res. 34 (6): 1735–44. doi:10.1093/nar/gkl105. PMC 1421504. PMID 16582099.

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[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000005513 - Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000024176 - Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid10662550-5] Pfeifer D, Poulat F, Holinski-Feder E, Kooy F, Scherer G (Apr 2000). "The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome". Genomics. 63 (1): 108–16. doi:10.1006/geno.1999.6060. PMID 10662550.

[pmid10684944-6] Schepers GE, Bullejos M, Hosking BM, Koopman P (Apr 2000). "Cloning and characterisation of the Sry-related transcription factor gene Sox8". Nucleic Acids Res. 28 (6): 1473–80. doi:10.1093/nar/28.6.1473. PMC 111037. PMID 10684944.

[entrez-7] "Entrez Gene: SOX8 SRY (sex determining region Y)-box 8".

SOX8

See also

References

Further reading