4.5 Review

Advancements in chemical biology targeting the kinases and phosphatases of RNA polymerase II-mediated transcription

Journal

CURRENT OPINION IN CHEMICAL BIOLOGY
Volume 63, Issue -, Pages 68-77

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.cbpa.2021.02.002

Keywords

RNA polymerase II; CDK; PP1; PP2A; Transcription; Chemical biology; Chemical genetics; Targeted covalent; Ahatog-sensitive kinase

Funding

  1. National Institutes of Health [R01GM104896, R01GM125882, R01CA069202]
  2. Welch Foundation [F-1778]

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Phosphorylation of RNA polymerase II is crucial for the temporal progression of eukaryotic transcription, and chemical genetic methods have been used to investigate pathways regulated by kinases and phosphatases targeting RNAP II. Recent advancements in chemical biology have led to the discovery of inhibitors and activators for kinases/phosphatases, providing new avenues for studying RNA polymerase II-mediated transcription.
Phosphorylation of RNA polymerase II (RNAP II) coordinates the temporal progression of eukaryotic transcription. The development and application of chemical genetic methods have enhanced our ability to investigate the intricate and intertwined pathways regulated by the kinases and phosphatases targeting RNAP II to ensure transcription accuracy and efficiency. Although identifying small molecules that modulate these enzymes has been challenging due to their highly conserved structures, powerful new chemical biology strategies such as targeted covalent inhibitors and small molecule degraders have significantly improved chemical probe specificity. The recent success in discovering phosphatase holoenzyme activators and inhibitors, which demonstrates the feasibility of selective targeting of individual phosphatase complexes, opens up new avenues into the study of transcription. Herein, we summarize how chemical biology is used to delineate kinases' identities involved in RNAP II regulation and new concepts in inhibitor/activator design implemented for kinases/phosphatases involved in modulating RNAP II-mediated transcription.

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