POU3F1
POU domain, class 3, transcription factor 1 (also known as Oct-6) is a protein that in humans is encoded by the POU3F1 gene.[1][2]
See also
References
- ↑ Tobler A, Schreiber E, Fontana A (Feb 1993). “The human Oct-6 POU transcription factor lacks the first 50 amino acids of its murine counterpart”. Nucleic Acids Research. 21 (4): 1043. doi:10.1093/nar/21.4.1043. PMC 309249. PMID 8451175.
- ↑ “Entrez Gene: POU3F1 POU domain, class 3, transcription factor 1”.
Further reading
- Monuki ES, Kuhn R, Weinmaster G, Trapp BD, Lemke G (Sep 1990). “Expression and activity of the POU transcription factor SCIP”. Science. 249 (4974): 1300–3. doi:10.1126/science.1975954. PMID 1975954.
- Suzuki N, Rohdewohld H, Neuman T, Gruss P, Schöler HR (Nov 1990). “Oct-6: a POU transcription factor expressed in embryonal stem cells and in the developing brain”. The EMBO Journal. 9 (11): 3723–32. PMC 552128. PMID 1976514.
- Zwilling S, König H, Wirth T (Mar 1995). “High mobility group protein 2 functionally interacts with the POU domains of octamer transcription factors”. The EMBO Journal. 14 (6): 1198–208. PMC 398197. PMID 7720710.
- Leger H, Sock E, Renner K, Grummt F, Wegner M (Jul 1995). “Functional interaction between the POU domain protein Tst-1/Oct-6 and the high-mobility-group protein HMG-I/Y”. Molecular and Cellular Biology. 15 (7): 3738–47. doi:10.1128/mcb.15.7.3738. PMC 230612. PMID 7791781.
- Faus I, Hsu HJ, Fuchs E (May 1994). “Oct-6: a regulator of keratinocyte gene expression in stratified squamous epithelia”. Molecular and Cellular Biology. 14 (5): 3263–75. doi:10.1128/mcb.14.5.3263. PMC 358693. PMID 7909356.
- Abdel-Rahman B, Fiddler M, Rappolee D, Pergament E (Oct 1995). “Expression of transcription regulating genes in human preimplantation embryos”. Human Reproduction. 10 (10): 2787–92. doi:10.1093/oxfordjournals.humrep.a135792. PMID 8567814.
- Jaegle M, Mandemakers W, Broos L, Zwart R, Karis A, Visser P, Grosveld F, Meijer D (Jul 1996). “The POU factor Oct-6 and Schwann cell differentiation”. Science. 273 (5274): 507–10. doi:10.1126/science.273.5274.507. PMID 8662541.
- Sock E, Enderich J, Rosenfeld MG, Wegner M (Jul 1996). “Identification of the nuclear localization signal of the POU domain protein Tst-1/Oct6”. The Journal of Biological Chemistry. 271 (29): 17512–8. doi:10.1074/jbc.271.29.17512. PMID 8663425.
- Malik KF, Jaffe H, Brady J, Young WS (Apr 1997). “The class III POU factor Brn-4 interacts with other class III POU factors and the heterogeneous nuclear ribonucleoprotein U”. Brain Research. Molecular Brain Research. 45 (1): 99–107. doi:10.1016/S0169-328X(96)00238-0. PMID 9105675.
- Sumiyama K, Washio-Watanabe K, Ono T, Yoshida MC, Hayakawa T, Ueda S (Feb 1998). “Human class III POU genes, POU3F1 and POU3F3, map to chromosomes 1p34.1 and 3p14.2”. Mammalian Genome. 9 (2): 180–1. doi:10.1007/s003359900721. PMID 9457692.
- Arroyo EJ, Bermingham JR, Rosenfeld MG, Scherer SS (Oct 1998). “Promyelinating Schwann cells express Tst-1/SCIP/Oct-6”. The Journal of Neuroscience. 18 (19): 7891–902. PMID 9742157.
- Kawasaki T, Oka N, Tachibana H, Akiguchi I, Shibasaki H (Mar 2003). “Oct6, a transcription factor controlling myelination, is a marker for active nerve regeneration in peripheral neuropathies”. Acta Neuropathologica. 105 (3): 203–8. doi:10.1007/s00401-002-0630-9. PMID 12557005.
- Beck IM, Müller M, Mentlein R, Sadowski T, Mueller MS, Paus R, Sedlacek R (May 2007). “Matrix metalloproteinase-19 expression in keratinocytes is repressed by transcription factors Tst-1 and Skn-1a: implications for keratinocyte differentiation”. The Journal of Investigative Dermatology. 127 (5): 1107–14. doi:10.1038/sj.jid.5700674. PMID 17195013.
- Ryu EJ, Wang JY, Le N, Baloh RH, Gustin JA, Schmidt RE, Milbrandt J (Oct 2007). “Misexpression of Pou3f1 results in peripheral nerve hypomyelination and axonal loss”. The Journal of Neuroscience. 27 (43): 11552–9. doi:10.1523/JNEUROSCI.5497-06.2007. PMID 17959798.
External links
- POU3F1+protein,+human at the US National Library of Medicine Medical Subject Headings (MeSH)
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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