Transcriptional elongation control in developmental gene expression, aging, and disease
- PMID: 37922911
- DOI: 10.1016/j.molcel.2023.10.004
Transcriptional elongation control in developmental gene expression, aging, and disease
Abstract
The elongation stage of transcription by RNA polymerase II (RNA Pol II) is central to the regulation of gene expression in response to developmental and environmental cues in metazoan. Dysregulated transcriptional elongation has been associated with developmental defects as well as disease and aging processes. Decades of genetic and biochemical studies have painstakingly identified and characterized an ensemble of factors that regulate RNA Pol II elongation. This review summarizes recent findings taking advantage of genetic engineering techniques that probe functions of elongation factors in vivo. We propose a revised model of elongation control in this accelerating field by reconciling contradictory results from the earlier biochemical evidence and the recent in vivo studies. We discuss how elongation factors regulate promoter-proximal RNA Pol II pause release, transcriptional elongation rate and processivity, RNA Pol II stability and RNA processing, and how perturbation of these processes is associated with developmental disorders, neurodegenerative disease, cancer, and aging.
Keywords: BRD4; CDK9; Integrator; NELF; RNA polymerase II; SEC; SPT5; SPT6; aging; cancer; development; elongation; super elongation complex; transcription.
Copyright © 2023. Published by Elsevier Inc.
Conflict of interest statement
Declaration of interests The authors declare no competing interests.
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