Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina

Summary: Gene regulatory networks (GRNs), consisting of transcription factors and their target sites, control neurogenesis and cell-fate specification in the developing central nervous system. In this study, we use integrated single-cell RNA and single-cell ATAC sequencing (scATAC-seq) analysis in d...

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Autores principales: Pin Lyu, Thanh Hoang, Clayton P. Santiago, Eric D. Thomas, Andrew E. Timms, Haley Appel, Megan Gimmen, Nguyet Le, Lizhi Jiang, Dong Won Kim, Siqi Chen, David F. Espinoza, Ariel E. Telger, Kurt Weir, Brian S. Clark, Timothy J. Cherry, Jiang Qian, Seth Blackshaw
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/bb845b0091334d5fbe14f15fb9a4f379
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spelling oai:doaj.org-article:bb845b0091334d5fbe14f15fb9a4f3792021-11-18T04:47:49ZGene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina2211-124710.1016/j.celrep.2021.109994https://doaj.org/article/bb845b0091334d5fbe14f15fb9a4f3792021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S221112472101473Xhttps://doaj.org/toc/2211-1247Summary: Gene regulatory networks (GRNs), consisting of transcription factors and their target sites, control neurogenesis and cell-fate specification in the developing central nervous system. In this study, we use integrated single-cell RNA and single-cell ATAC sequencing (scATAC-seq) analysis in developing mouse and human retina to identify multiple interconnected, evolutionarily conserved GRNs composed of cell-type-specific transcription factors that both activate genes within their own network and inhibit genes in other networks. These GRNs control temporal patterning in primary progenitors, regulate transition from primary to neurogenic progenitors, and drive specification of each major retinal cell type. We confirm that NFI transcription factors selectively activate expression of genes promoting late-stage temporal identity in primary retinal progenitors and identify other transcription factors that regulate rod photoreceptor specification in postnatal retina. This study inventories cis- and trans-acting factors that control retinal development and can guide cell-based therapies aimed at replacing retinal neurons lost to disease.Pin LyuThanh HoangClayton P. SantiagoEric D. ThomasAndrew E. TimmsHaley AppelMegan GimmenNguyet LeLizhi JiangDong Won KimSiqi ChenDavid F. EspinozaAriel E. TelgerKurt WeirBrian S. ClarkTimothy J. CherryJiang QianSeth BlackshawElsevierarticleretinadevelopmenttranscription factorneurogenesissingle-cell ATAC-seqsingle-cell RNA-seqBiology (General)QH301-705.5ENCell Reports, Vol 37, Iss 7, Pp 109994- (2021)
institution DOAJ
collection DOAJ
language EN
topic retina
development
transcription factor
neurogenesis
single-cell ATAC-seq
single-cell RNA-seq
Biology (General)
QH301-705.5
spellingShingle retina
development
transcription factor
neurogenesis
single-cell ATAC-seq
single-cell RNA-seq
Biology (General)
QH301-705.5
Pin Lyu
Thanh Hoang
Clayton P. Santiago
Eric D. Thomas
Andrew E. Timms
Haley Appel
Megan Gimmen
Nguyet Le
Lizhi Jiang
Dong Won Kim
Siqi Chen
David F. Espinoza
Ariel E. Telger
Kurt Weir
Brian S. Clark
Timothy J. Cherry
Jiang Qian
Seth Blackshaw
Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina
description Summary: Gene regulatory networks (GRNs), consisting of transcription factors and their target sites, control neurogenesis and cell-fate specification in the developing central nervous system. In this study, we use integrated single-cell RNA and single-cell ATAC sequencing (scATAC-seq) analysis in developing mouse and human retina to identify multiple interconnected, evolutionarily conserved GRNs composed of cell-type-specific transcription factors that both activate genes within their own network and inhibit genes in other networks. These GRNs control temporal patterning in primary progenitors, regulate transition from primary to neurogenic progenitors, and drive specification of each major retinal cell type. We confirm that NFI transcription factors selectively activate expression of genes promoting late-stage temporal identity in primary retinal progenitors and identify other transcription factors that regulate rod photoreceptor specification in postnatal retina. This study inventories cis- and trans-acting factors that control retinal development and can guide cell-based therapies aimed at replacing retinal neurons lost to disease.
format article
author Pin Lyu
Thanh Hoang
Clayton P. Santiago
Eric D. Thomas
Andrew E. Timms
Haley Appel
Megan Gimmen
Nguyet Le
Lizhi Jiang
Dong Won Kim
Siqi Chen
David F. Espinoza
Ariel E. Telger
Kurt Weir
Brian S. Clark
Timothy J. Cherry
Jiang Qian
Seth Blackshaw
author_facet Pin Lyu
Thanh Hoang
Clayton P. Santiago
Eric D. Thomas
Andrew E. Timms
Haley Appel
Megan Gimmen
Nguyet Le
Lizhi Jiang
Dong Won Kim
Siqi Chen
David F. Espinoza
Ariel E. Telger
Kurt Weir
Brian S. Clark
Timothy J. Cherry
Jiang Qian
Seth Blackshaw
author_sort Pin Lyu
title Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina
title_short Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina
title_full Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina
title_fullStr Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina
title_full_unstemmed Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina
title_sort gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina
publisher Elsevier
publishDate 2021
url https://doaj.org/article/bb845b0091334d5fbe14f15fb9a4f379
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