Inhibition of CDK9 activity compromises global splicing in prostate cancer cells

Cyclin-dependent kinase 9 (CDK9) phosphorylates RNA polymerase II to promote productive transcription elongation. Here we show that short-term CDK9 inhibition affects the splicing of thousands of mRNAs. CDK9 inhibition impairs global splicing and there is no evidence for a coordinated response betwe...

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Main Authors: Hu, Q, Poulose, N, Girmay, S, Helevä, A, Doultsinos, D, Gondane, A, Steele, RE, Liu, X, Loda, M, Liu, S, Tang, D, Mills, IG, Itkonen, HM
Format: Journal article
Language:English
Published: Taylor and Francis 2021
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author Hu, Q
Poulose, N
Girmay, S
Helevä, A
Doultsinos, D
Gondane, A
Steele, RE
Liu, X
Loda, M
Liu, S
Tang, D
Mills, IG
Itkonen, HM
author_facet Hu, Q
Poulose, N
Girmay, S
Helevä, A
Doultsinos, D
Gondane, A
Steele, RE
Liu, X
Loda, M
Liu, S
Tang, D
Mills, IG
Itkonen, HM
author_sort Hu, Q
collection OXFORD
description Cyclin-dependent kinase 9 (CDK9) phosphorylates RNA polymerase II to promote productive transcription elongation. Here we show that short-term CDK9 inhibition affects the splicing of thousands of mRNAs. CDK9 inhibition impairs global splicing and there is no evidence for a coordinated response between the alternative splicing and the overall transcriptome. Alternative splicing is a feature of aggressive prostate cancer (CRPC) and enables the generation of the anti-androgen resistant version of the ligand-independent androgen receptor, AR-v7. We show that CDK9 inhibition results in the loss of AR and AR-v7 expression due to the defects in splicing, which sensitizes CRPC cells to androgen deprivation. Finally, we demonstrate that CDK9 expression increases as PC cells develop CRPC-phenotype both in vitro and also in patient samples. To conclude, here we show that CDK9 inhibition compromises splicing in PC cells, which can be capitalized on by targeting the PC-specific addiction androgen receptor.
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spelling oxford-uuid:cae00a00-b460-40ed-8991-6a8ed637be862022-09-30T07:00:36ZInhibition of CDK9 activity compromises global splicing in prostate cancer cellsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:cae00a00-b460-40ed-8991-6a8ed637be86EnglishSymplectic ElementsTaylor and Francis2021Hu, QPoulose, NGirmay, SHelevä, ADoultsinos, DGondane, ASteele, RELiu, XLoda, MLiu, STang, DMills, IGItkonen, HMCyclin-dependent kinase 9 (CDK9) phosphorylates RNA polymerase II to promote productive transcription elongation. Here we show that short-term CDK9 inhibition affects the splicing of thousands of mRNAs. CDK9 inhibition impairs global splicing and there is no evidence for a coordinated response between the alternative splicing and the overall transcriptome. Alternative splicing is a feature of aggressive prostate cancer (CRPC) and enables the generation of the anti-androgen resistant version of the ligand-independent androgen receptor, AR-v7. We show that CDK9 inhibition results in the loss of AR and AR-v7 expression due to the defects in splicing, which sensitizes CRPC cells to androgen deprivation. Finally, we demonstrate that CDK9 expression increases as PC cells develop CRPC-phenotype both in vitro and also in patient samples. To conclude, here we show that CDK9 inhibition compromises splicing in PC cells, which can be capitalized on by targeting the PC-specific addiction androgen receptor.
spellingShingle Hu, Q
Poulose, N
Girmay, S
Helevä, A
Doultsinos, D
Gondane, A
Steele, RE
Liu, X
Loda, M
Liu, S
Tang, D
Mills, IG
Itkonen, HM
Inhibition of CDK9 activity compromises global splicing in prostate cancer cells
title Inhibition of CDK9 activity compromises global splicing in prostate cancer cells
title_full Inhibition of CDK9 activity compromises global splicing in prostate cancer cells
title_fullStr Inhibition of CDK9 activity compromises global splicing in prostate cancer cells
title_full_unstemmed Inhibition of CDK9 activity compromises global splicing in prostate cancer cells
title_short Inhibition of CDK9 activity compromises global splicing in prostate cancer cells
title_sort inhibition of cdk9 activity compromises global splicing in prostate cancer cells
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