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Nucleome Dynamics during Retinal Development

delete2019-11-01
delete60
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OA
AI
J
Jacqueline L. Norrie
M
Marybeth Lupo
B
Beisi Xu
I
Issam Aldiri
M
Marc Valentine
P
Putnam, Daniel
L
Lyra Griffiths
J
Jiakun Zhang
D
Dianna A. Johnson
J
John Easton
Y
Ying Shao
V
Victoria Honnell
S
Sharon Frase
S
Shondra Miller
V
Valerie Stewart
X
Xin Zhou
陈翔 封面图
陈翔 (Xiang Chen) *
M
Michael A. Dyer *
DOI:10.1016/j.neuron.2019.08.002delete
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摘要

摘要

En 中文
More than 8,000 genes are turned on or off as progenitor cells produce the 7 classes of retinal cell types during development. Thousands of enhancers are also active in the developing retinae, many having features of cell- and developmental stage-specific activity. We studied dynamic changes in the 3D chromatin landscape important for precisely orchestrated changes in gene expression during retinal development by ultra-deep in situ Hi-C analysis on murine retinae. We identified developmental-stage-specific changes in chromatin compartments and enhancer-promoter interactions. We developed a machine learning-based algorithm to map euchromatin and heterochromatin domains genome-wide and overlaid it with chromatin compartments identified by Hi-C. Single-cell ATAC-seq and RNA-seq were integrated with our Hi-C and previous ChIP-seq data to identify cell- and developmental-stage-specific super-enhancers (SEs). We identified a bipolar neuron-specific core regulatory circuit SE upstream of Vsx2, whose deletion in mice led to the loss of bipolar neurons.
Keyword:
NON-SYNDROMIC MICROPHTHALMIA/ANOPHTHALMIA
GENE-EXPRESSION
HOMEOBOX GENE
GENOME
MUTATIONS
CELLS
CHX10
ARCHITECTURE
TOOL
PRINCIPLES
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Neuron 封面图
Neuron
IF:
15
论文数:
1.4W
被引数:
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U
University of Tennessee Health Science Center
学者数:
7.0K
论文数: 5.4K
被引数: 1.0W
University of Tennessee System 封面图
University of Tennessee System
学者数:
2.9W
论文数: 2.7W
被引数: 115
引用论文

引用论文

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