Transcription factors (TFs) bind combinatorially to cis-regulatory elements, orchestrating transcriptional programs. Although studies of chromatin state and chromosomal interactions have demonstrated dynamic neurodevelopmental cis-regulatory landscapes, parallel understanding of TF interactions lags. To elucidate combinatorial TF binding driving mouse basal ganglia development, we integrated chromatin immunoprecipitation sequencing (ChIP-seq) for twelve TFs, H3K4me3-associated enhancer-promoter interactions, chromatin and gene expression data, and functional enhancer assays. We identified sets of putative regulatory elements with shared TF binding (TF-pRE modules) that orchestrate distinct processes of GABAergic neurogenesis and suppress other cell fates. The majority of pREs were bound by one or two TFs; however, a small proportion were extensively bound. These sequences had exceptional evolutionary conservation and motif density, complex chromosomal interactions, and activity as in vivo enhancers. Our results provide insights into the combinatorial TF-pRE interactions that activate and repress expression programs during telencephalon neurogenesis and demonstrate the value of TF binding toward modeling developmental transcriptional wiring.
Combinatorial transcription factor binding encodes cis-regulatory wiring of mouse forebrain GABAergic neurogenesis.
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作者:Catta-Preta Rinaldo, Lindtner Susan, Ypsilanti Athena, Seban Nicolas, Price James D, Abnousi Armen, Su-Feher Linda, Wang Yurong, Cichewicz Karol, Boerma Sally A, Juric Ivan, Jones Ian R, Akiyama Jennifer A, Hu Ming, Shen Yin, Visel Axel, Pennacchio Len A, Dickel Diane E, Rubenstein John L R, Nord Alex S
| 期刊: | Developmental Cell | 影响因子: | 8.700 |
| 时间: | 2025 | 起止号: | 2025 Jan 20; 60(2):288-304 |
| doi: | 10.1016/j.devcel.2024.10.004 | ||
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