SIX1

SIX1
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	4EGC
Identifiers
Aliases	SIX1, BOS3, DFNA23, TIP39, SIX homeobox 1
External IDs	MGI: 102780 HomoloGene: 4360 GeneCards: SIX1
Gene location (Human)
Chr.	Chromosome 14 (human)[1]
End	60,658,259 bp[1]
Gene location (Mouse)
Chr.	Chromosome 12 (mouse)[2]
End	73,053,887 bp[2]
RNA expression pattern
	More reference expression data
Gene ontology
Molecular function	• DNA binding; • sequence-specific DNA binding; • transcription factor activity, sequence-specific DNA binding; • transcriptional activator activity, RNA polymerase II core promoter proximal region sequence-specific binding; • chromatin binding; • RNA polymerase II core promoter proximal region sequence-specific DNA binding; • protein binding; • transcription regulatory region DNA binding; • RNA polymerase II transcription factor activity, sequence-specific DNA binding; • transcription coactivator binding; • transcription regulatory region sequence-specific DNA binding; • transcriptional activator activity, RNA polymerase II distal enhancer sequence-specific binding;
Cellular component	• cytoplasm; • transcription factor complex; • nucleolus; • cell nucleus;
Biological process	• pattern specification process; • negative regulation of neuron apoptotic process; • regulation of neuron differentiation; • embryonic skeletal system morphogenesis; • mesonephric tubule formation; • neurogenesis; • animal organ development; • ureteric bud development; • myoblast migration; • positive regulation of branching involved in ureteric bud morphogenesis; • renal system development; • regulation of transcription, DNA-templated; • epithelial cell differentiation; • olfactory placode formation; • regulation of skeletal muscle cell differentiation; • tongue development; • organ induction; • kidney development; • anatomical structure development; • thymus development; • ureter smooth muscle cell differentiation; • neuron fate specification; • myotome development; • skeletal system morphogenesis; • outflow tract morphogenesis; • trigeminal ganglion development; • negative regulation of apoptotic process; • negative regulation of transcription from RNA polymerase II promoter; • sensory perception of sound; • aorta morphogenesis; • regulation of branch elongation involved in ureteric bud branching; • fungiform papilla morphogenesis; • transcription, DNA-templated; • generation of neurons; • otic vesicle development; • regulation of protein localization; • positive regulation of transcription, DNA-templated; • multicellular organism development; • branching involved in ureteric bud morphogenesis; • thyroid gland development; • inner ear morphogenesis; • cochlea morphogenesis; • positive regulation of ureteric bud formation; • positive regulation of mesenchymal cell proliferation involved in ureter development; • middle ear morphogenesis; • regulation of synaptic growth at neuromuscular junction; • protein localization to nucleus; • regulation of gene expression; • embryonic cranial skeleton morphogenesis; • inner ear development; • positive regulation of secondary heart field cardioblast proliferation; • negative regulation of branching involved in ureteric bud morphogenesis; • cell proliferation; • regulation of epithelial cell proliferation; • regulation of skeletal muscle satellite cell proliferation; • skeletal muscle tissue development; • metanephric mesenchyme development; • facial nerve morphogenesis; • positive regulation of transcription from RNA polymerase II promoter; • pharyngeal system development; • apoptotic process; • transcription from RNA polymerase II promoter; • cellular response to 3,3',5-triiodo-L-thyronine; • negative regulation of transcription, DNA-templated;
	Sources:Amigo / QuickGO
Orthologs
	6495
	20471
	ENSG00000126778
	ENSMUSG00000051367
	Q15475
	Q62231
	NM_005982
	NM_009189
	NP_005973
	NP_033215
	Wikidata
View/Edit Human	View/Edit Mouse

Homeobox protein SIX1 (Sineoculis homeobox homolog 1) is a protein that in humans is encoded by the SIX1 gene.^[5]^[6]^[7]

Function

The vertebrate SIX genes are homologs of the Drosophila 'sine oculis' (so) gene, which is expressed primarily in the developing visual system of the fly. Members of the SIX gene family encode proteins that are characterized by a divergent DNA-binding homeodomain and an upstream SIX domain, which may be involved both in determining DNA-binding specificity and in mediating protein–protein interactions. Genes in the SIX family have been shown to play roles in vertebrate and insect development or have been implicated in maintenance of the differentiated state of tissues.[supplied by OMIM]^[7]

Interactions

SIX1 has been shown to interact with EYA1,^[8] DACH, GRO and MDFI.^[9]

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000126778 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000051367 - Ensembl, May 2017
↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ Boucher CA, Carey N, Edwards YH, Siciliano MJ, Johnson KJ (April 1996). "Cloning of the human SIX1 gene and its assignment to chromosome 14". Genomics. 33 (1): 140–2. doi:10.1006/geno.1996.0172. PMID 8617500.
↑ Ruf RG, Xu PX, Silvius D, Otto EA, Beekmann F, Muerb UT, Kumar S, Neuhaus TJ, Kemper MJ, Raymond RM, Brophy PD, Berkman J, Gattas M, Hyland V, Ruf EM, Schwartz C, Chang EH, Smith RJ, Stratakis CA, Weil D, Petit C, Hildebrandt F (May 2004). "SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes". Proceedings of the National Academy of Sciences of the United States of America. 101 (21): 8090–5. doi:10.1073/pnas.0308475101. PMC 419562. PMID 15141091.
1 2 "Entrez Gene: SIX1 sine oculis homeobox homolog 1 (Drosophila)".
↑ Buller C, Xu X, Marquis V, Schwanke R, Xu PX (November 2001). "Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome". Human Molecular Genetics. 10 (24): 2775–81. doi:10.1093/hmg/10.24.2775. PMID 11734542.
↑ Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (October 2005). "Towards a proteome-scale map of the human protein–protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.

Oliver G, Wehr R, Jenkins NA, Copeland NG, Cheyette BN, Hartenstein V, Zipursky SL, Gruss P (March 1995). "Homeobox genes and connective tissue patterning". Development. 121 (3): 693–705. PMID 7720577.
Adrados, I., Larrasa-Alonso, J., Galarreta, A., López-Antona, I., Menéndez, C., Abad, M., ... & Palmero, I. (2015). The homeoprotein SIX1 controls cellular senescence through the regulation of p16INK4A and differentiation-related genes. Oncogene. doi:10.1038/onc.2015.408
Ford HL, Kabingu EN, Bump EA, Mutter GL, Pardee AB (October 1998). "Abrogation of the G2 cell cycle checkpoint associated with overexpression of HSIX1: a possible mechanism of breast carcinogenesis". Proceedings of the National Academy of Sciences of the United States of America. 95 (21): 12608–13. doi:10.1073/pnas.95.21.12608. PMC 22878. PMID 9770533.
Salam AA, Häfner FM, Linder TE, Spillmann T, Schinzel AA, Leal SM (June 2000). "A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred". American Journal of Human Genetics. 66 (6): 1984–8. doi:10.1086/302931. PMC 1378045. PMID 10777717.
Ford HL, Landesman-Bollag E, Dacwag CS, Stukenberg PT, Pardee AB, Seldin DC (July 2000). "Cell cycle-regulated phosphorylation of the human SIX1 homeodomain protein". The Journal of Biological Chemistry. 275 (29): 22245–54. doi:10.1074/jbc.M002446200. PMID 10801845.
Fan X, Brass LF, Poncz M, Spitz F, Maire P, Manning DR (October 2000). "The alpha subunits of Gz and Gi interact with the eyes absent transcription cofactor Eya2, preventing its interaction with the six class of homeodomain-containing proteins". The Journal of Biological Chemistry. 275 (41): 32129–34. doi:10.1074/jbc.M004577200. PMID 10906137.
Buller C, Xu X, Marquis V, Schwanke R, Xu PX (November 2001). "Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome". Human Molecular Genetics. 10 (24): 2775–81. doi:10.1093/hmg/10.24.2775. PMID 11734542.
Li CM, Guo M, Borczuk A, Powell CA, Wei M, Thaker HM, Friedman R, Klein U, Tycko B (June 2002). "Gene expression in Wilms' tumor mimics the earliest committed stage in the metanephric mesenchymal-epithelial transition". The American Journal of Pathology. 160 (6): 2181–90. doi:10.1016/S0002-9440(10)61166-2. PMC 1850829. PMID 12057921.
Ikeda K, Watanabe Y, Ohto H, Kawakami K (October 2002). "Molecular interaction and synergistic activation of a promoter by Six, Eya, and Dach proteins mediated through CREB binding protein". Molecular and Cellular Biology. 22 (19): 6759–66. doi:10.1128/MCB.22.19.6759-6766.2002. PMC 134036. PMID 12215533.
López-Ríos J, Tessmar K, Loosli F, Wittbrodt J, Bovolenta P (January 2003). "Six3 and Six6 activity is modulated by members of the groucho family". Development. 130 (1): 185–95. doi:10.1242/dev.00185. PMID 12441302.
Ruf RG, Berkman J, Wolf MT, Nurnberg P, Gattas M, Ruf EM, Hyland V, Kromberg J, Glass I, Macmillan J, Otto E, Nurnberg G, Lucke B, Hennies HC, Hildebrandt F (July 2003). "A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3". Journal of Medical Genetics. 40 (7): 515–9. doi:10.1136/jmg.40.7.515. PMC 1735534. PMID 12843324.
Zheng W, Huang L, Wei ZB, Silvius D, Tang B, Xu PX (September 2003). "The role of Six1 in mammalian auditory system development". Development. 130 (17): 3989–4000. doi:10.1242/dev.00628. PMC 3873880. PMID 12874121.
Li X, Oghi KA, Zhang J, Krones A, Bush KT, Glass CK, Nigam SK, Aggarwal AK, Maas R, Rose DW, Rosenfeld MG (November 2003). "Eya protein phosphatase activity regulates Six1-Dach-Eya transcriptional effects in mammalian organogenesis". Nature. 426 (6964): 247–54. doi:10.1038/nature02083. PMID 14628042.
Coletta RD, Christensen K, Reichenberger KJ, Lamb J, Micomonaco D, Huang L, Wolf DM, Müller-Tidow C, Golub TR, Kawakami K, Ford HL (April 2004). "The Six1 homeoprotein stimulates tumorigenesis by reactivation of cyclin A1". Proceedings of the National Academy of Sciences of the United States of America. 101 (17): 6478–83. doi:10.1073/pnas.0401139101. PMC 404070. PMID 15123840.
Grifone R, Laclef C, Spitz F, Lopez S, Demignon J, Guidotti JE, Kawakami K, Xu PX, Kelly R, Petrof BJ, Daegelen D, Concordet JP, Maire P (July 2004). "Six1 and Eya1 expression can reprogram adult muscle from the slow-twitch phenotype into the fast-twitch phenotype". Molecular and Cellular Biology. 24 (14): 6253–67. doi:10.1128/MCB.24.14.6253-6267.2004. PMC 434262. PMID 15226428.
Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (October 2005). "Towards a proteome-scale map of the human protein–protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
Ito T, Noguchi Y, Yashima T, Kitamura K (May 2006). "SIX1 mutation associated with enlargement of the vestibular aqueduct in a patient with branchio-oto syndrome". The Laryngoscope. 116 (5): 796–9. doi:10.1097/01.mlg.0000209096.40400.96. PMID 16652090.

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[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000126778 - Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000051367 - Ensembl, May 2017

[3] "Human PubMed Reference:".

[4] "Mouse PubMed Reference:".

[pmid8617500-5] Boucher CA, Carey N, Edwards YH, Siciliano MJ, Johnson KJ (April 1996). "Cloning of the human SIX1 gene and its assignment to chromosome 14". Genomics. 33 (1): 140–2. doi:10.1006/geno.1996.0172. PMID 8617500.

[pmid15141091-6] Ruf RG, Xu PX, Silvius D, Otto EA, Beekmann F, Muerb UT, Kumar S, Neuhaus TJ, Kemper MJ, Raymond RM, Brophy PD, Berkman J, Gattas M, Hyland V, Ruf EM, Schwartz C, Chang EH, Smith RJ, Stratakis CA, Weil D, Petit C, Hildebrandt F (May 2004). "SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes". Proceedings of the National Academy of Sciences of the United States of America. 101 (21): 8090–5. doi:10.1073/pnas.0308475101. PMC 419562. PMID 15141091.

[entrez-7] 1 2 "Entrez Gene: SIX1 sine oculis homeobox homolog 1 (Drosophila)".

[pmid11734542-8] Buller C, Xu X, Marquis V, Schwanke R, Xu PX (November 2001). "Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome". Human Molecular Genetics. 10 (24): 2775–81. doi:10.1093/hmg/10.24.2775. PMID 11734542.

[pmid16189514-9] Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (October 2005). "Towards a proteome-scale map of the human protein–protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.

SIX1

Function

Interactions

References

Further reading