{"title":"Transcription elongation mechanisms that control gene expression in erythropoiesis.","authors":"Kaustav Mukherjee, James J Bieker","doi":"10.1016/bs.ctdb.2026.06.004","DOIUrl":null,"url":null,"abstract":"<p><p>The regulation of RNA transcript abundance relies on the control of two key early steps in gene expression: transcription initiation and productive elongation. Although DNA-directed RNA polymerase provides the intrinsic catalytic activity required for RNA synthesis, its ability to effectively produce a transcript relies on accurate recruitment to specific DNA sites to initiate RNA polymerization, followed by release from promoter-proximal pausing into a productive elongation machine. These steps are governed by accessory factors that not only facilitate the assembly of a functional pre-initiation complex but also exert both negative and positive control over polymerase pause/elongation status. We describe experiments that have elucidated these mechanisms in the context of erythropoiesis.</p>","PeriodicalId":55191,"journal":{"name":"Current Topics in Developmental Biology","volume":"170 ","pages":"345-372"},"PeriodicalIF":0.0000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Topics in Developmental Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/bs.ctdb.2026.06.004","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/6/23 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
The regulation of RNA transcript abundance relies on the control of two key early steps in gene expression: transcription initiation and productive elongation. Although DNA-directed RNA polymerase provides the intrinsic catalytic activity required for RNA synthesis, its ability to effectively produce a transcript relies on accurate recruitment to specific DNA sites to initiate RNA polymerization, followed by release from promoter-proximal pausing into a productive elongation machine. These steps are governed by accessory factors that not only facilitate the assembly of a functional pre-initiation complex but also exert both negative and positive control over polymerase pause/elongation status. We describe experiments that have elucidated these mechanisms in the context of erythropoiesis.