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Transcription Factor Pit-1 Affects Transcriptional Timing in the Dual-Promoter Human Prolactin Gene

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...

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Autores principales: McNamara, Anne V, Awais, Raheela, Momiji, Hiroshi, Dunham, Lee, Featherstone, Karen, Harper, Claire V, Adamson, Antony A, Semprini, Sabrina, Jones, Nicholas A, Spiller, David G, Mullins, John J, Finkenstädt, Bärbel F, Rand, David, White, Michael R H, Davis, Julian R E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871365/
https://www.ncbi.nlm.nih.gov/pubmed/33388754
http://dx.doi.org/10.1210/endocr/bqaa249
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author McNamara, Anne V
Awais, Raheela
Momiji, Hiroshi
Dunham, Lee
Featherstone, Karen
Harper, Claire V
Adamson, Antony A
Semprini, Sabrina
Jones, Nicholas A
Spiller, David G
Mullins, John J
Finkenstädt, Bärbel F
Rand, David
White, Michael R H
Davis, Julian R E
author_facet McNamara, Anne V
Awais, Raheela
Momiji, Hiroshi
Dunham, Lee
Featherstone, Karen
Harper, Claire V
Adamson, Antony A
Semprini, Sabrina
Jones, Nicholas A
Spiller, David G
Mullins, John J
Finkenstädt, Bärbel F
Rand, David
White, Michael R H
Davis, Julian R E
author_sort McNamara, Anne V
collection PubMed
description 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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spelling pubmed-78713652021-02-17 Transcription Factor Pit-1 Affects Transcriptional Timing in the Dual-Promoter Human Prolactin Gene McNamara, Anne V Awais, Raheela Momiji, Hiroshi Dunham, Lee Featherstone, Karen Harper, Claire V Adamson, Antony A Semprini, Sabrina Jones, Nicholas A Spiller, David G Mullins, John J Finkenstädt, Bärbel F Rand, David White, Michael R H Davis, Julian R E Endocrinology Research Articles 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. Oxford University Press 2021-01-03 /pmc/articles/PMC7871365/ /pubmed/33388754 http://dx.doi.org/10.1210/endocr/bqaa249 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
McNamara, Anne V
Awais, Raheela
Momiji, Hiroshi
Dunham, Lee
Featherstone, Karen
Harper, Claire V
Adamson, Antony A
Semprini, Sabrina
Jones, Nicholas A
Spiller, David G
Mullins, John J
Finkenstädt, Bärbel F
Rand, David
White, Michael R H
Davis, Julian R E
Transcription Factor Pit-1 Affects Transcriptional Timing in the Dual-Promoter Human Prolactin Gene
title Transcription Factor Pit-1 Affects Transcriptional Timing in the Dual-Promoter Human Prolactin Gene
title_full Transcription Factor Pit-1 Affects Transcriptional Timing in the Dual-Promoter Human Prolactin Gene
title_fullStr Transcription Factor Pit-1 Affects Transcriptional Timing in the Dual-Promoter Human Prolactin Gene
title_full_unstemmed Transcription Factor Pit-1 Affects Transcriptional Timing in the Dual-Promoter Human Prolactin Gene
title_short Transcription Factor Pit-1 Affects Transcriptional Timing in the Dual-Promoter Human Prolactin Gene
title_sort transcription factor pit-1 affects transcriptional timing in the dual-promoter human prolactin gene
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871365/
https://www.ncbi.nlm.nih.gov/pubmed/33388754
http://dx.doi.org/10.1210/endocr/bqaa249
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