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Combinatorial transcription factor binding encodes cis-regulatory wiring of forebrain GABAergic neurogenesis

Transcription factors (TFs) bind combinatorially to genomic cis-regulatory elements (cREs), orchestrating transcription programs. While studies of chromatin state and chromosomal interactions have revealed dynamic neurodevelopmental cRE landscapes, parallel understanding of the underlying TF binding...

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Autores principales: Catta-Preta, Rinaldo, Lindtner, Susan, Ypsilanti, Athena, Price, James, Abnousi, Armen, Su-Feher, Linda, Wang, Yurong, Juric, Ivan, Jones, Ian R., Akiyama, Jennifer A., Hu, Ming, Shen, Yin, Visel, Axel, Pennacchio, Len A., Dickel, Diane, Rubenstein, John L R, Nord, Alex S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10327028/
https://www.ncbi.nlm.nih.gov/pubmed/37425940
http://dx.doi.org/10.1101/2023.06.28.546894
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author Catta-Preta, Rinaldo
Lindtner, Susan
Ypsilanti, Athena
Price, James
Abnousi, Armen
Su-Feher, Linda
Wang, Yurong
Juric, Ivan
Jones, Ian R.
Akiyama, Jennifer A.
Hu, Ming
Shen, Yin
Visel, Axel
Pennacchio, Len A.
Dickel, Diane
Rubenstein, John L R
Nord, Alex S
author_facet Catta-Preta, Rinaldo
Lindtner, Susan
Ypsilanti, Athena
Price, James
Abnousi, Armen
Su-Feher, Linda
Wang, Yurong
Juric, Ivan
Jones, Ian R.
Akiyama, Jennifer A.
Hu, Ming
Shen, Yin
Visel, Axel
Pennacchio, Len A.
Dickel, Diane
Rubenstein, John L R
Nord, Alex S
author_sort Catta-Preta, Rinaldo
collection PubMed
description Transcription factors (TFs) bind combinatorially to genomic cis-regulatory elements (cREs), orchestrating transcription programs. While studies of chromatin state and chromosomal interactions have revealed dynamic neurodevelopmental cRE landscapes, parallel understanding of the underlying TF binding lags. To elucidate the combinatorial TF-cRE interactions driving mouse basal ganglia development, we integrated ChIP-seq for twelve TFs, H3K4me3-associated enhancer-promoter interactions, chromatin and transcriptional state, and transgenic enhancer assays. We identified TF-cREs modules with distinct chromatin features and enhancer activity that have complementary roles driving GABAergic neurogenesis and suppressing other developmental fates. While the majority of distal cREs were bound by one or two TFs, a small proportion were extensively bound, and these enhancers also exhibited exceptional evolutionary conservation, motif density, and complex chromosomal interactions. Our results provide new insights into how modules of combinatorial TF-cRE interactions activate and repress developmental expression programs and demonstrate the value of TF binding data in modeling gene regulatory wiring.
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spelling pubmed-103270282023-07-08 Combinatorial transcription factor binding encodes cis-regulatory wiring of forebrain GABAergic neurogenesis Catta-Preta, Rinaldo Lindtner, Susan Ypsilanti, Athena Price, James Abnousi, Armen Su-Feher, Linda Wang, Yurong Juric, Ivan Jones, Ian R. Akiyama, Jennifer A. Hu, Ming Shen, Yin Visel, Axel Pennacchio, Len A. Dickel, Diane Rubenstein, John L R Nord, Alex S bioRxiv Article Transcription factors (TFs) bind combinatorially to genomic cis-regulatory elements (cREs), orchestrating transcription programs. While studies of chromatin state and chromosomal interactions have revealed dynamic neurodevelopmental cRE landscapes, parallel understanding of the underlying TF binding lags. To elucidate the combinatorial TF-cRE interactions driving mouse basal ganglia development, we integrated ChIP-seq for twelve TFs, H3K4me3-associated enhancer-promoter interactions, chromatin and transcriptional state, and transgenic enhancer assays. We identified TF-cREs modules with distinct chromatin features and enhancer activity that have complementary roles driving GABAergic neurogenesis and suppressing other developmental fates. While the majority of distal cREs were bound by one or two TFs, a small proportion were extensively bound, and these enhancers also exhibited exceptional evolutionary conservation, motif density, and complex chromosomal interactions. Our results provide new insights into how modules of combinatorial TF-cRE interactions activate and repress developmental expression programs and demonstrate the value of TF binding data in modeling gene regulatory wiring. Cold Spring Harbor Laboratory 2023-06-28 /pmc/articles/PMC10327028/ /pubmed/37425940 http://dx.doi.org/10.1101/2023.06.28.546894 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Catta-Preta, Rinaldo
Lindtner, Susan
Ypsilanti, Athena
Price, James
Abnousi, Armen
Su-Feher, Linda
Wang, Yurong
Juric, Ivan
Jones, Ian R.
Akiyama, Jennifer A.
Hu, Ming
Shen, Yin
Visel, Axel
Pennacchio, Len A.
Dickel, Diane
Rubenstein, John L R
Nord, Alex S
Combinatorial transcription factor binding encodes cis-regulatory wiring of forebrain GABAergic neurogenesis
title Combinatorial transcription factor binding encodes cis-regulatory wiring of forebrain GABAergic neurogenesis
title_full Combinatorial transcription factor binding encodes cis-regulatory wiring of forebrain GABAergic neurogenesis
title_fullStr Combinatorial transcription factor binding encodes cis-regulatory wiring of forebrain GABAergic neurogenesis
title_full_unstemmed Combinatorial transcription factor binding encodes cis-regulatory wiring of forebrain GABAergic neurogenesis
title_short Combinatorial transcription factor binding encodes cis-regulatory wiring of forebrain GABAergic neurogenesis
title_sort combinatorial transcription factor binding encodes cis-regulatory wiring of forebrain gabaergic neurogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10327028/
https://www.ncbi.nlm.nih.gov/pubmed/37425940
http://dx.doi.org/10.1101/2023.06.28.546894
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