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Automated minute scale RNA-seq of pluripotent stem cell differentiation reveals early divergence of human and mouse gene expression kinetics.
Barry, Christopher; Schmitz, Matthew T; Argus, Cara; Bolin, Jennifer M; Probasco, Mitchell D; Leng, Ning; Duffin, Bret M; Steill, John; Swanson, Scott; McIntosh, Brian E; Stewart, Ron; Kendziorski, Christina; Thomson, James A; Bacher, Rhonda.
Afiliação
  • Barry C; Morgridge Institute for Research, Madison, WI, United States of America.
  • Schmitz MT; Morgridge Institute for Research, Madison, WI, United States of America.
  • Argus C; Morgridge Institute for Research, Madison, WI, United States of America.
  • Bolin JM; Morgridge Institute for Research, Madison, WI, United States of America.
  • Probasco MD; Morgridge Institute for Research, Madison, WI, United States of America.
  • Leng N; Morgridge Institute for Research, Madison, WI, United States of America.
  • Duffin BM; Morgridge Institute for Research, Madison, WI, United States of America.
  • Steill J; Morgridge Institute for Research, Madison, WI, United States of America.
  • Swanson S; Morgridge Institute for Research, Madison, WI, United States of America.
  • McIntosh BE; Morgridge Institute for Research, Madison, WI, United States of America.
  • Stewart R; Morgridge Institute for Research, Madison, WI, United States of America.
  • Kendziorski C; Department of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, WI, United States of America.
  • Thomson JA; Morgridge Institute for Research, Madison, WI, United States of America.
  • Bacher R; Department of Cell and Regenerative Biology, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States of America.
PLoS Comput Biol ; 15(12): e1007543, 2019 12.
Article em En | MEDLINE | ID: mdl-31815944
ABSTRACT
Pluripotent stem cells retain the developmental timing of their species of origin in vitro, an observation that suggests the existence of a cell-intrinsic developmental clock, yet the nature and machinery of the clock remain a mystery. We hypothesize that one possible component may lie in species-specific differences in the kinetics of transcriptional responses to differentiation signals. Using a liquid-handling robot, mouse and human pluripotent stem cells were exposed to identical neural differentiation conditions and sampled for RNA-sequencing at high frequency, every 4 or 10 minutes, for the first 10 hours of differentiation to test for differences in transcriptomic response rates. The majority of initial transcriptional responses occurred within a rapid window in the first minutes of differentiation for both human and mouse stem cells. Despite similarly early onsets of gene expression changes, we observed shortened and condensed gene expression patterns in mouse pluripotent stem cells compared to protracted trends in human pluripotent stem cells. Moreover, the speed at which individual genes were upregulated, as measured by the slopes of gene expression changes over time, was significantly faster in mouse compared to human cells. These results suggest that downstream transcriptomic response kinetics to signaling cues are faster in mouse versus human cells, and may offer a partial account for the vast differences in developmental rates across species.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diferenciação Celular / Células-Tronco Pluripotentes / RNA-Seq Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diferenciação Celular / Células-Tronco Pluripotentes / RNA-Seq Idioma: En Ano de publicação: 2019 Tipo de documento: Article