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Functionally distinct promoter classes initiate transcription via different mechanisms reflected in focused versus dispersed initiation patterns

Recruitment of RNA polymerase II (Pol II) to promoters is essential for transcription. Despite conflicting evidence, the Pol II preinitiation complex (PIC) is often thought to have a uniform composition and to assemble at all promoters via an identical mechanism. Here, using Drosophila melanogaster...

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Autores principales: Serebreni, Leonid, Pleyer, Lisa‐Marie, Haberle, Vanja, Hendy, Oliver, Vlasova, Anna, Loubiere, Vincent, Nemčko, Filip, Bergauer, Katharina, Roitinger, Elisabeth, Mechtler, Karl, Stark, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183819/
https://www.ncbi.nlm.nih.gov/pubmed/37013908
http://dx.doi.org/10.15252/embj.2023113519
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author Serebreni, Leonid
Pleyer, Lisa‐Marie
Haberle, Vanja
Hendy, Oliver
Vlasova, Anna
Loubiere, Vincent
Nemčko, Filip
Bergauer, Katharina
Roitinger, Elisabeth
Mechtler, Karl
Stark, Alexander
author_facet Serebreni, Leonid
Pleyer, Lisa‐Marie
Haberle, Vanja
Hendy, Oliver
Vlasova, Anna
Loubiere, Vincent
Nemčko, Filip
Bergauer, Katharina
Roitinger, Elisabeth
Mechtler, Karl
Stark, Alexander
author_sort Serebreni, Leonid
collection PubMed
description Recruitment of RNA polymerase II (Pol II) to promoters is essential for transcription. Despite conflicting evidence, the Pol II preinitiation complex (PIC) is often thought to have a uniform composition and to assemble at all promoters via an identical mechanism. Here, using Drosophila melanogaster S2 cells as a model, we demonstrate that different promoter classes function via distinct PICs. Promoter DNA of developmentally regulated genes readily associates with the canonical Pol II PIC, whereas housekeeping promoters do not, and instead recruit other factors such as DREF. Consistently, TBP and DREF are differentially required by distinct promoter types. TBP and its paralog TRF2 also function at different promoter types in a partially redundant manner. In contrast, TFIIA is required at all promoters, and we identify factors that can recruit and/or stabilize TFIIA at housekeeping promoters and activate transcription. Promoter activation by tethering these factors is sufficient to induce the dispersed transcription initiation patterns characteristic of housekeeping promoters. Thus, different promoter classes utilize distinct mechanisms of transcription initiation, which translate into different focused versus dispersed initiation patterns.
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spelling pubmed-101838192023-05-16 Functionally distinct promoter classes initiate transcription via different mechanisms reflected in focused versus dispersed initiation patterns Serebreni, Leonid Pleyer, Lisa‐Marie Haberle, Vanja Hendy, Oliver Vlasova, Anna Loubiere, Vincent Nemčko, Filip Bergauer, Katharina Roitinger, Elisabeth Mechtler, Karl Stark, Alexander EMBO J Articles Recruitment of RNA polymerase II (Pol II) to promoters is essential for transcription. Despite conflicting evidence, the Pol II preinitiation complex (PIC) is often thought to have a uniform composition and to assemble at all promoters via an identical mechanism. Here, using Drosophila melanogaster S2 cells as a model, we demonstrate that different promoter classes function via distinct PICs. Promoter DNA of developmentally regulated genes readily associates with the canonical Pol II PIC, whereas housekeeping promoters do not, and instead recruit other factors such as DREF. Consistently, TBP and DREF are differentially required by distinct promoter types. TBP and its paralog TRF2 also function at different promoter types in a partially redundant manner. In contrast, TFIIA is required at all promoters, and we identify factors that can recruit and/or stabilize TFIIA at housekeeping promoters and activate transcription. Promoter activation by tethering these factors is sufficient to induce the dispersed transcription initiation patterns characteristic of housekeeping promoters. Thus, different promoter classes utilize distinct mechanisms of transcription initiation, which translate into different focused versus dispersed initiation patterns. John Wiley and Sons Inc. 2023-04-04 /pmc/articles/PMC10183819/ /pubmed/37013908 http://dx.doi.org/10.15252/embj.2023113519 Text en © 2023 The Authors. Published under the terms of the CC BY 4.0 license. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Serebreni, Leonid
Pleyer, Lisa‐Marie
Haberle, Vanja
Hendy, Oliver
Vlasova, Anna
Loubiere, Vincent
Nemčko, Filip
Bergauer, Katharina
Roitinger, Elisabeth
Mechtler, Karl
Stark, Alexander
Functionally distinct promoter classes initiate transcription via different mechanisms reflected in focused versus dispersed initiation patterns
title Functionally distinct promoter classes initiate transcription via different mechanisms reflected in focused versus dispersed initiation patterns
title_full Functionally distinct promoter classes initiate transcription via different mechanisms reflected in focused versus dispersed initiation patterns
title_fullStr Functionally distinct promoter classes initiate transcription via different mechanisms reflected in focused versus dispersed initiation patterns
title_full_unstemmed Functionally distinct promoter classes initiate transcription via different mechanisms reflected in focused versus dispersed initiation patterns
title_short Functionally distinct promoter classes initiate transcription via different mechanisms reflected in focused versus dispersed initiation patterns
title_sort functionally distinct promoter classes initiate transcription via different mechanisms reflected in focused versus dispersed initiation patterns
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183819/
https://www.ncbi.nlm.nih.gov/pubmed/37013908
http://dx.doi.org/10.15252/embj.2023113519
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