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About:
Single cell resolution regulatory landscape of the mouse kidney highlights cellular differentiation programs and renal disease targets
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covidontheweb.inria.fr
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Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Single cell resolution regulatory landscape of the mouse kidney highlights cellular differentiation programs and renal disease targets
Creator
Liu, Hongbo
Li, Mingyao
Aranyi, Tamas
Balzer, Michael
Kaestner, Klaus
Kim, Junhyong
Kondo, Ayano
Kwan, Amy
Ma, Ziyuan
Miao, Zhen
Pontoglio, Marco
Susztak, Katalin
Wu, Junnan
Source
BioRxiv
abstract
Determining the epigenetic program that generates unique cell types in the kidney is critical for understanding cell-type heterogeneity during tissue homeostasis and injury response. Here, we profiled open chromatin and gene expression in developing and adult mouse kidneys at single cell resolution. We show critical reliance of gene expression on distal regulatory elements (enhancers). We define key cell type-specific transcription factors and major gene-regulatory circuits for kidney cells. Dynamic chromatin and expression changes during nephron progenitor differentiation demonstrated that podocyte commitment occurs early and is associated with sustained Foxl1 expression. Renal tubule cells followed a more complex differentiation, where Hfn4a was associated with proximal and Tfap2b with distal fate. Mapping single nucleotide variants associated with human kidney disease identified critical cell types, developmental stages, genes, and regulatory mechanisms. We provide a global single cell resolution view of chromatin accessibility of kidney development. The dataset is available via interactive public websites.
has issue date
2020-06-04
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bibo:doi
10.1101/2020.05.24.113910
has license
biorxiv
sha1sum (hex)
7abe757f8c153c9ceee6e4418759ec73e9d9cea1
schema:url
https://doi.org/10.1101/2020.05.24.113910
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Single cell resolution regulatory landscape of the mouse kidney highlights cellular differentiation programs and renal disease targets
schema:publication
bioRxiv
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covid:7abe757f8c153c9ceee6e4418759ec73e9d9cea1#body_text
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schema:about
of
named entity 'sustained'
named entity 'kidney disease'
named entity 'provide'
named entity 'expression'
named entity 'PROGRAM'
named entity 'EXPRESSION'
named entity 'HERE'
named entity 'CELL'
named entity 'WHERE'
named entity 'VIEW'
named entity 'mechanisms'
named entity 'enhancers'
named entity 'open'
named entity 'early'
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named entity 'tissue homeostasis'
named entity 'gene expression'
named entity 'regulatory elements'
named entity 'cell type'
named entity 'podocyte'
named entity 'kidney disease'
named entity 'regulatory mechanisms'
named entity 'single nucleotide'
named entity 'gene expression'
named entity 'Single cell'
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named entity 'kidney'
named entity 'GWAS'
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named entity 'target gene'
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named entity 'gene'
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named entity 'scRNA-seq'
named entity 'cell type'
named entity 'cell type'
named entity 'kidney'
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