| Literature DB >> 33714893 |
Wantae Kim1, Blase LeBlanc2, Wendy L Matthews2, Zhong-Yin Zhang3, Yan Zhang4.
Abstract
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.Entities:
Keywords: Analog-sensitive kinase; CDK; Chemical biology; Chemical genetics; PP1; PP2A; RNA polymerase II; Targeted covalent inhibitor; Transcription
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Year: 2021 PMID: 33714893 PMCID: PMC8384638 DOI: 10.1016/j.cbpa.2021.02.002
Source DB: PubMed Journal: Curr Opin Chem Biol ISSN: 1367-5931 Impact factor: 8.972