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Transcription Factor Pit-1 Affects Transcriptional Timing in the Dual-Promoter Human Prolactin Gene
Author(s) -
A. McNamara,
Raheela Awais,
Hiroshi Momiji,
Lee Dunham,
Karen Featherstone,
Claire V. Harper,
Antony Adamson,
Sabrina Semprini,
Nicholas A. Jones,
David G. Spiller,
John J. Mullins,
Bärbel Finkenstädt,
D.A.J. Rand,
Michael White,
J.R. Davis
Publication year - 2021
Publication title -
endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.674
H-Index - 257
eISSN - 1945-7170
pISSN - 0013-7227
DOI - 10.1210/endocr/bqaa249
Subject(s) - transcription factor , promoter , prolactin , gene , endocrinology , medicine , biology , transcription (linguistics) , genetics , gene expression , hormone , linguistics , philosophy
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.

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