Cyclin-dependent kinase 9

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Cyclin-dependent kinase 9

Rendering based on PDB 1PF6.
Available structures
PDB Ortholog search: PDBe, RCSB
Identifiers
Symbols CDK9; C-2k; CDC2L4; CTK1; PITALRE; TAK
External IDs OMIM603251 MGI1328368 HomoloGene55566 ChEMBL: 3116 GeneCards: CDK9 Gene
EC number 2.7.11.22, 2.7.11.23
RNA expression pattern
PBB GE CDK9 203198 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 1025 107951
Ensembl ENSG00000136807 ENSMUSG00000009555
UniProt P50750 Q99J95
RefSeq (mRNA) NM_001261 NM_130860
RefSeq (protein) NP_001252 NP_570930
Location (UCSC) Chr 9:
130.55 – 130.55 Mb
Chr 2:
32.71 – 32.71 Mb
PubMed search [1] [2]

Cyclin-dependent kinase 9 or CDK9 is a cyclin-dependent kinase associated with P-TEFb. The protein encoded by this gene is a member of the cyclin-dependent protein kinase (CDK) family. CDK family members are highly similar to the gene products of S. cerevisiae cdc28, and S. pombe cdc2, and known as important cell cycle regulators. This kinase was found to be a component of the multiprotein complex TAK/P-TEFb, which is an elongation factor for RNA polymerase II-directed transcription and functions by phosphorylating the C-terminal domain of the largest subunit of RNA polymerase II. This protein forms a complex with and is regulated by its regulatory subunit cyclin T or cyclin K. HIV-1 Tat protein was found to interact with this protein and cyclin T, which suggested a possible involvement of this protein in AIDS.[1] CDK9 is also known to associate with other proteins such as TRAF2, and be involved in differentiation of skeletal muscle.[2]

Interactions[edit]

CDK9 has been shown to interact with Cyclin K,[3] Cyclin T2,[4] RELA,[5] Cyclin T1,[3][4][6][7][8][9][10][11][12] Retinoblastoma protein,[13] Androgen receptor,[14] SKP1A,[10] MYBL2,[11] CDC34[10] and SUPT5H.[12]

References[edit]

  1. ^ "Entrez Gene: CDK9 cyclin-dependent kinase 9 (CDC2-related kinase)". 
  2. ^ MacLachlan TK, Sang N, De Luca A, Puri PL, Levrero M, Giordano A., et al. (1998). "Binding of CDK9 to TRAF2.". J. Cell. Biochem. 71 (4): 467–78. doi:10.1002/(SICI)1097-4644(19981215)71:4<467::AID-JCB2>3.0.CO;2-G. PMID 9827693. 
  3. ^ a b Fu, T J; Peng J, Lee G, Price D H, Flores O (December 1999). "Cyclin K functions as a CDK9 regulatory subunit and participates in RNA polymerase II transcription". J. Biol. Chem. (UNITED STATES) 274 (49): 34527–30. doi:10.1074/jbc.274.49.34527. ISSN 0021-9258. PMID 10574912. 
  4. ^ a b Peng, J; Zhu Y, Milton J T, Price D H (March 1998). "Identification of multiple cyclin subunits of human P-TEFb". Genes Dev. (UNITED STATES) 12 (5): 755–62. doi:10.1101/gad.12.5.755. ISSN 0890-9369. PMC 316581. PMID 9499409. 
  5. ^ Amini, Shohreh; Clavo Anaira, Nadraga Yuri, Giordano Antonio, Khalili Kamel, Sawaya Bassel E (August 2002). "Interplay between cdk9 and NF-kappaB factors determines the level of HIV-1 gene transcription in astrocytic cells". Oncogene (England) 21 (37): 5797–803. doi:10.1038/sj.onc.1205754. ISSN 0950-9232. PMID 12173051. 
  6. ^ Cabart, Pavel; Chew Helen K, Murphy Shona (July 2004). "BRCA1 cooperates with NUFIP and P-TEFb to activate transcription by RNA polymerase II". Oncogene (England) 23 (31): 5316–29. doi:10.1038/sj.onc.1207684. ISSN 0950-9232. PMID 15107825. 
  7. ^ Young, Tara M; Wang Qi, Pe'ery Tsafi, Mathews Michael B (September 2003). "The human I-mfa domain-containing protein, HIC, interacts with cyclin T1 and modulates P-TEFb-dependent transcription". Mol. Cell. Biol. (United States) 23 (18): 6373–84. doi:10.1128/MCB.23.18.6373-6384.2003. ISSN 0270-7306. PMC 193714. PMID 12944466. 
  8. ^ Michels, Annemieke A; Nguyen Van Trung, Fraldi Alessandro, Labas Valérie, Edwards Mia, Bonnet François, Lania Luigi, Bensaude Olivier (July 2003). "MAQ1 and 7SK RNA interact with CDK9/cyclin T complexes in a transcription-dependent manner". Mol. Cell. Biol. (United States) 23 (14): 4859–69. doi:10.1128/MCB.23.14.4859-4869.2003. ISSN 0270-7306. PMC 162212. PMID 12832472. 
  9. ^ Hoque, Mainul; Young Tara M, Lee Chee-Gun, Serrero Ginette, Mathews Michael B, Pe'ery Tsafi (March 2003). "The growth factor granulin interacts with cyclin T1 and modulates P-TEFb-dependent transcription". Mol. Cell. Biol. (United States) 23 (5): 1688–702. doi:10.1128/MCB.23.5.1688-1702.2003. ISSN 0270-7306. PMC 151712. PMID 12588988. 
  10. ^ a b c Kiernan, R E; Emiliani S, Nakayama K, Castro A, Labbé J C, Lorca T, Nakayama Ki K, Benkirane M (December 2001). "Interaction between cyclin T1 and SCF(SKP2) targets CDK9 for ubiquitination and degradation by the proteasome". Mol. Cell. Biol. (United States) 21 (23): 7956–70. doi:10.1128/MCB.21.23.7956-7970.2001. ISSN 0270-7306. PMC 99964. PMID 11689688. 
  11. ^ a b De Falco, G; Bagella L, Claudio P P, De Luca A, Fu Y, Calabretta B, Sala A, Giordano A (January 2000). "Physical interaction between CDK9 and B-Myb results in suppression of B-Myb gene autoregulation". Oncogene (ENGLAND) 19 (3): 373–9. doi:10.1038/sj.onc.1203305. ISSN 0950-9232. PMID 10656684. 
  12. ^ a b Garber, M E; Mayall T P, Suess E M, Meisenhelder J, Thompson N E, Jones K A (September 2000). "CDK9 autophosphorylation regulates high-affinity binding of the human immunodeficiency virus type 1 tat-P-TEFb complex to TAR RNA". Mol. Cell. Biol. (UNITED STATES) 20 (18): 6958–69. doi:10.1128/MCB.20.18.6958-6969.2000. ISSN 0270-7306. PMC 88771. PMID 10958691. 
  13. ^ Simone, Cristiano; Bagella Luigi, Bellan Cristiana, Giordano Antonio (June 2002). "Physical interaction between pRb and cdk9/cyclinT2 complex". Oncogene (England) 21 (26): 4158–65. doi:10.1038/sj.onc.1205511. ISSN 0950-9232. PMID 12037672. 
  14. ^ Lee, D K; Duan H O, Chang C (March 2001). "Androgen receptor interacts with the positive elongation factor P-TEFb and enhances the efficiency of transcriptional elongation". J. Biol. Chem. (United States) 276 (13): 9978–84. doi:10.1074/jbc.M002285200. ISSN 0021-9258. PMID 11266437. 

Further reading[edit]

External links[edit]