| Literature DB >> 33388754 |
Anne V McNamara1, Raheela Awais2, Hiroshi Momiji3, Lee Dunham4, Karen Featherstone4, Claire V Harper5, Antony A Adamson6, Sabrina Semprini7, Nicholas A Jones1, David G Spiller1, John J Mullins7, Bärbel F Finkenstädt3, David Rand3, Michael R H White1, Julian R E Davis4.
Abstract
Gene transcription occurs in short bursts interspersed with silent periods, and these kinetics can be altered by promoter structure. The effect of alternate promoter architecture on transcription bursting is not known. We studied the human prolactin (hPRL) gene that contains 2 promoters, a pituitary-specific promoter that requires the transcription factor Pit-1 and displays dramatic transcriptional bursting activity and an alternate upstream promoter that is active in nonpituitary tissues. We studied large hPRL genomic fragments with luciferase reporters, and used bacterial artificial chromosome recombineering to manipulate critical promoter regions. Stochastic switch mathematical modelling of single-cell time-lapse luminescence image data revealed that the Pit-1-dependent promoter showed longer, higher-amplitude transcriptional bursts. Knockdown studies confirmed that the presence of Pit-1 stabilized and prolonged periods of active transcription. Pit-1 therefore plays an active role in establishing the timing of transcription cycles, in addition to its cell-specific functions.Entities:
Keywords: Pit-1; gene transcription; pituitary; prolactin gene; promoter; transcription timing
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Year: 2021 PMID: 33388754 PMCID: PMC7871365 DOI: 10.1210/endocr/bqaa249
Source DB: PubMed Journal: Endocrinology ISSN: 0013-7227 Impact factor: 5.051