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MED17 information


MED17
Identifiers
AliasesMED17, CRSP6, CRSP77, DRIP80, TRAP80, mediator complex subunit 17, SRB4
External IDsOMIM: 603810; MGI: 2182585; HomoloGene: 3151; GeneCards: MED17; OMA:MED17 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004268

NM_144933
NM_001364533

RefSeq (protein)

NP_004259

NP_659182
NP_001351462

Location (UCSC)Chr 11: 93.78 – 93.81 MbChr 9: 15.17 – 15.19 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Mediator of RNA polymerase II transcription subunit 17 is an enzyme that in humans is encoded by the MED17 gene.[5][6][7]

The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors.[7]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000042429 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000031935 – 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.
  5. ^ Ryu S, Zhou S, Ladurner AG, Tjian R (Feb 1999). "The transcriptional cofactor complex CRSP is required for activity of the enhancer-binding protein Sp1". Nature. 397 (6718): 446–50. Bibcode:1999Natur.397..446R. doi:10.1038/17141. hdl:11858/00-001M-0000-0019-A36A-8. PMID 9989412. S2CID 4405569.
  6. ^ Ito M, Yuan CX, Malik S, Gu W, Fondell JD, Yamamura S, Fu ZY, Zhang X, Qin J, Roeder RG (Apr 1999). "Identity between TRAP and SMCC complexes indicates novel pathways for the function of nuclear receptors and diverse mammalian activators". Mol Cell. 3 (3): 361–70. doi:10.1016/S1097-2765(00)80463-3. PMID 10198638.
  7. ^ a b "Entrez Gene: CRSP6 cofactor required for Sp1 transcriptional activation, subunit 6, 77kDa".

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injection Management V6: Bosch I4 2.0: Bosch MED17 with CAN-Bus and individual cylinder knock control I4 1.6: Bosch MED17 with CAN-Bus and individual cylinder...

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cerebral and cerebellar atrophy with postnatal progressive microcephaly MED17 recessive Ischiopatellar dysplasia TBX4 dominant Isodicentric 15 15q11–14...

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BRCA1

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CDK2 DHX9 ELK4 EP300 ESR1 FANCA FANCD2 FHL2 H2AFX JUNB JunD LMO4 MAP3K3 MED17 MED21 MRE11A MSH2 MSH3 MSH6 Myc NBN NMI NPM1 NCOA2 NUFIP1 P53 PALB2 POLR2A...

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Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly

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descent. The genetic cause was found to be a homozygous mutation of the MED17 gene, located in chromosome 11, this mutation is called L371P. In vitro...

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PPARGC1A

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receptor gamma (ERR-γ). Farnesoid X receptor FBXW7 MED1, MED12, MED14, MED17, NRF1 Peroxisome proliferator-activated receptor gamma Retinoid X receptor...

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C11orf54

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consists 13 exons and spans 23730 bp. C11orf54 is flanked by TAF1D and MED17. The protein ester hydrolase c11orf54 exists as a monomer and is composed...

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USF1

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ERK1/2, DNA-PK Acetylation PCAF Methylation' SET7/92 USF1-interacting proteins Transcription co-factors USF2, SP1, PEA3, MTF1, SREBP1-c, MED17, BAF60...

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