TY - JOUR
T1 - Identification of novel long noncoding RNAs underlying vertebrate cardiovascular development
AU - Kurian, Leo
AU - Aguirre, Aitor
AU - Sancho-Martinez, Ignacio
AU - Benner, Christopher
AU - Hishida, Tomoaki
AU - Nguyen, Thai B.
AU - Reddy, Pradeep
AU - Nivet, Emmanuel
AU - Krause, Marie N.
AU - Nelles, David A.
AU - Esteban, Concepcion Rodriguez
AU - Campistol, Josep M.
AU - Yeo, Gene W.
AU - Belmonte, Juan Carlos Izpisua
N1 - Publisher Copyright:
© 2015 American Heart Association, Inc.
PY - 2015
Y1 - 2015
N2 - Background - Long noncoding RNAs (lncRNAs) have emerged as critical epigenetic regulators with important functions in development and disease. Here, we sought to identify and functionally characterize novel lncRNAs critical for vertebrate development. Methods and Results - By relying on human pluripotent stem cell differentiation models, we investigated lncRNAs differentially regulated at key steps during human cardiovascular development with a special focus on vascular endothelial cells. RNA sequencing led to the generation of large data sets that serve as a gene expression roadmap highlighting gene expression changes during human pluripotent cell differentiation. Stage-specific analyses led to the identification of 3 previously uncharacterized lncRNAs, TERMINATOR, ALIEN, and PUNISHER, specifically expressed in undifferentiated pluripotent stem cells, cardiovascular progenitors, and differentiated endothelial cells, respectively. Functional characterization, including localization studies, dynamic expression analyses, epigenetic modification monitoring, and knockdown experiments in lower vertebrates, as well as murine embryos and human cells, confirmed a critical role for each lncRNA specific for each analyzed developmental stage. Conclusions - We have identified and functionally characterized 3 novel lncRNAs involved in vertebrate and human cardiovascular development, and we provide a comprehensive transcriptomic roadmap that sheds new light on the molecular mechanisms underlying human embryonic development, mesodermal commitment, and cardiovascular specification.
AB - Background - Long noncoding RNAs (lncRNAs) have emerged as critical epigenetic regulators with important functions in development and disease. Here, we sought to identify and functionally characterize novel lncRNAs critical for vertebrate development. Methods and Results - By relying on human pluripotent stem cell differentiation models, we investigated lncRNAs differentially regulated at key steps during human cardiovascular development with a special focus on vascular endothelial cells. RNA sequencing led to the generation of large data sets that serve as a gene expression roadmap highlighting gene expression changes during human pluripotent cell differentiation. Stage-specific analyses led to the identification of 3 previously uncharacterized lncRNAs, TERMINATOR, ALIEN, and PUNISHER, specifically expressed in undifferentiated pluripotent stem cells, cardiovascular progenitors, and differentiated endothelial cells, respectively. Functional characterization, including localization studies, dynamic expression analyses, epigenetic modification monitoring, and knockdown experiments in lower vertebrates, as well as murine embryos and human cells, confirmed a critical role for each lncRNA specific for each analyzed developmental stage. Conclusions - We have identified and functionally characterized 3 novel lncRNAs involved in vertebrate and human cardiovascular development, and we provide a comprehensive transcriptomic roadmap that sheds new light on the molecular mechanisms underlying human embryonic development, mesodermal commitment, and cardiovascular specification.
KW - Cardiovascular system
KW - Growth and development
KW - RNA, long noncoding
KW - Transcriptome
KW - Vertebrates
UR - http://www.scopus.com/inward/record.url?scp=84929359342&partnerID=8YFLogxK
U2 - 10.1161/CIRCULATIONAHA.114.013303
DO - 10.1161/CIRCULATIONAHA.114.013303
M3 - Article
C2 - 25739401
AN - SCOPUS:84929359342
SN - 0009-7322
VL - 131
SP - 1278
EP - 1290
JO - Circulation
JF - Circulation
IS - 14
ER -