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Contents

   



(Top)
 


1 Function  





2 Interactive pathway map  





3 Interactions  





4 References  





5 Further reading  





6 External links  














MYT1






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From Wikipedia, the free encyclopedia
 


MYT1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMYT1, C20orf36, MTF1, MYTI, NZF2, PLPB1, ZC2HC4A, ZC2H2C1, myelin transcription factor 1
External IDsOMIM: 600379; MGI: 1100535; HomoloGene: 3332; GeneCards: MYT1; OMA:MYT1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004535

NM_001171615
NM_001171616
NM_001171680
NM_008665

RefSeq (protein)

NP_004526

NP_001165086
NP_001165087
NP_001165151
NP_032691

Location (UCSC)Chr 20: 64.1 – 64.24 MbChr 2: 181.76 – 181.83 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Myelin transcription factor 1 is a protein that in humans is encoded by the MYT1 gene.[5][6][7]

Function[edit]

The protein encoded by this gene is a member of a family of neural specific, zinc finger-containing DNA-binding proteins. The protein binds to the promoter regions of proteolipid proteins of the central nervous system and plays a role in the developing nervous system.[7]

Interactive pathway map[edit]

Click on genes, proteins and metabolites below to visit related articles. [§ 1]

[[File:

MECP2_and_Associated_Rett_Syndrome_WP3584Go to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to WikiPathwaysGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to article

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MECP2_and_Associated_Rett_Syndrome_WP3584Go to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to WikiPathwaysGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to article

|alt=MECP2 and associated Rett Syndrome edit]] MECP2 and associated Rett Syndrome edit
  1. ^ The interactive pathway map can be edited at WikiPathways: "WP3584".

Interactions[edit]

MYT1 has been shown to interact with PIN1.[8]

References[edit]

  • ^ "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.
  • ^ Kim JG, Hudson LD (December 1992). "Novel member of the zinc finger superfamily: A C2-HC finger that recognizes a glia-specific gene". Molecular and Cellular Biology. 12 (12): 5632–9. doi:10.1128/mcb.12.12.5632. PMC 360502. PMID 1280325.
  • ^ Booher RN, Holman PS, Fattaey A (August 1997). "Human Myt1 is a cell cycle-regulated kinase that inhibits Cdc2 but not Cdk2 activity". The Journal of Biological Chemistry. 272 (35): 22300–6. doi:10.1074/jbc.272.35.22300. PMID 9268380.
  • ^ a b "Entrez Gene: MYT1 myelin transcription factor 1".
  • ^ Wells NJ, Watanabe N, Tokusumi T, Jiang W, Verdecia MA, Hunter T (October 1999). "The C-terminal domain of the Cdc2 inhibitory kinase Myt1 interacts with Cdc2 complexes and is required for inhibition of G(2)/M progression". Journal of Cell Science. 112 (19): 3361–71. doi:10.1242/jcs.112.19.3361. PMID 10504341.
  • Further reading[edit]

  • Armstrong RC, Kim JG, Hudson LD (August 1995). "Expression of myelin transcription factor I (MyTI), a "zinc-finger" DNA-binding protein, in developing oligodendrocytes". Glia. 14 (4): 303–21. doi:10.1002/glia.440140407. PMID 8530187. S2CID 38779689.
  • Liu F, Stanton JJ, Wu Z, Piwnica-Worms H (February 1997). "The human Myt1 kinase preferentially phosphorylates Cdc2 on threonine 14 and localizes to the endoplasmic reticulum and Golgi complex". Molecular and Cellular Biology. 17 (2): 571–83. doi:10.1128/mcb.17.2.571. PMC 231782. PMID 9001210.
  • Kim JG, Armstrong RC, v Agoston D, Robinsky A, Wiese C, Nagle J, Hudson LD (October 1997). "Myelin transcription factor 1 (Myt1) of the oligodendrocyte lineage, along with a closely related CCHC zinc finger, is expressed in developing neurons in the mammalian central nervous system". Journal of Neuroscience Research. 50 (2): 272–90. doi:10.1002/(SICI)1097-4547(19971015)50:2<272::AID-JNR16>3.0.CO;2-A. PMID 9373037. S2CID 37120295.
  • Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (December 1998). "Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Research. 5 (6): 355–64. doi:10.1093/dnares/5.6.355. PMID 10048485.
  • Kikuno R, Nagase T, Ishikawa K, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (June 1999). "Prediction of the coding sequences of unidentified human genes. XIV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Research. 6 (3): 197–205. doi:10.1093/dnares/6.3.197. PMID 10470851.
  • Hirayama A, Oka A, Ito M, Tanaka F, Okoshi Y, Takashima S (January 2003). "Myelin transcription factor 1 (MyT1) immunoreactivity in infants with periventricular leukomalacia". Brain Research. Developmental Brain Research. 140 (1): 85–92. doi:10.1016/S0165-3806(02)00585-0. PMID 12524179.
  • Nielsen JA, Berndt JA, Hudson LD, Armstrong RC (January 2004). "Myelin transcription factor 1 (Myt1) modulates the proliferation and differentiation of oligodendrocyte lineage cells". Molecular and Cellular Neurosciences. 25 (1): 111–23. doi:10.1016/j.mcn.2003.10.001. PMID 14962745. S2CID 28151272.
  • Vana AC, Lucchinetti CF, Le TQ, Armstrong RC (May 2007). "Myelin transcription factor 1 (Myt1) expression in demyelinated lesions of rodent and human CNS". Glia. 55 (7): 687–97. doi:10.1002/glia.20492. PMC 2789289. PMID 17330875.
  • External links[edit]

    This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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    This page was last edited on 31 January 2024, at 15:49 (UTC).

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