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pubmed-article:18483222pubmed:issue10lld:pubmed
pubmed-article:18483222pubmed:dateCreated2008-5-16lld:pubmed
pubmed-article:18483222pubmed:abstractTextThe positive transcription elongation factor b (P-TEFb), consisting of Cdk9 and cyclin T, stimulates RNA polymerase II elongation and cotranscriptional pre-mRNA processing. To accommodate different growth conditions and transcriptional demands, a reservoir of P-TEFb is kept in an inactive state in the multisubunit 7SK snRNP. Under certain stress or disease conditions, P-TEFb is released to activate transcription, although the signaling pathway(s) that controls this is largely unknown. Here, through analyzing the UV- or hexamethylene bisacetamide (HMBA)-induced release of P-TEFb from 7SK snRNP, an essential role for the calcium ion (Ca2+)-calmodulin-protein phosphatase 2B (PP2B) signaling pathway is revealed. However, Ca2+ signaling alone is insufficient, and PP2B must act sequentially and cooperatively with protein phosphatase 1alpha (PP1alpha) to disrupt 7SK snRNP. Activated by UV/HMBA and facilitated by a PP2B-induced conformational change in 7SK snRNP, PP1alpha releases P-TEFb through dephosphorylating phospho-Thr186 in the Cdk9 T-loop. This event is also necessary for the subsequent recruitment of P-TEFb by the bromodomain protein Brd4 to the preinitiation complex, where Cdk9 remains unphosphorylated and inactive until after the synthesis of a short RNA. Thus, through cooperatively dephosphorylating Cdk9 in response to Ca2+ signaling, PP2B and PP1alpha alter the P-TEFb functional equilibrium through releasing P-TEFb from 7SK snRNP for transcription.lld:pubmed
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pubmed-article:18483222pubmed:authorpubmed-author:ZhuYingYlld:pubmed
pubmed-article:18483222pubmed:authorpubmed-author:LiuMinMlld:pubmed
pubmed-article:18483222pubmed:authorpubmed-author:LiHuanHlld:pubmed
pubmed-article:18483222pubmed:authorpubmed-author:ZhouQiangQlld:pubmed
pubmed-article:18483222pubmed:authorpubmed-author:ZhouNanNlld:pubmed
pubmed-article:18483222pubmed:authorpubmed-author:ChenRuichuanRlld:pubmed
pubmed-article:18483222pubmed:authorpubmed-author:HeNanhaiNlld:pubmed
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pubmed-article:18483222pubmed:authorpubmed-author:AiNanpingNlld:pubmed
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