Identification of Novel Long Noncoding RNAs Underlying Vertebrate Cardiovascular Development
Identification of Novel Long Noncoding RNAs Underlying Vertebrate Cardiovascular Development
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.
- French National Centre for Scientific Research France
- National Research Institute for Agriculture, Food and Environment France
- Département Sciences sociales, agriculture et alimentation, espace et environnement France
- Sanford Consortium for Regenerative Medicine United States
- Salk Institute for Biological Studies United States
Pluripotent Stem Cells, 570, 571, Molecular Sequence Data, growth and development, 610, Embryonic Development, [SDV.BC.IC] Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB], Cardiovascular System, Morpholinos, Mice, Fetal Heart, [SDV.BC.IC]Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB], Human Umbilical Vein Endothelial Cells, Animals, Humans, Developmental, Cell Lineage, Myocytes, Cardiac, Zebrafish, Embryonic Stem Cells, Myocytes, Sequence Analysis, RNA, Chromosome Mapping, Endothelial Cells, Gene Expression Regulation, Developmental, Cell Differentiation, Gene Expression Regulation, Vertebrates, RNA, Long Noncoding, RNA, Long Noncoding, Transcriptome, Cardiac, Sequence Analysis
Pluripotent Stem Cells, 570, 571, Molecular Sequence Data, growth and development, 610, Embryonic Development, [SDV.BC.IC] Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB], Cardiovascular System, Morpholinos, Mice, Fetal Heart, [SDV.BC.IC]Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB], Human Umbilical Vein Endothelial Cells, Animals, Humans, Developmental, Cell Lineage, Myocytes, Cardiac, Zebrafish, Embryonic Stem Cells, Myocytes, Sequence Analysis, RNA, Chromosome Mapping, Endothelial Cells, Gene Expression Regulation, Developmental, Cell Differentiation, Gene Expression Regulation, Vertebrates, RNA, Long Noncoding, RNA, Long Noncoding, Transcriptome, Cardiac, Sequence Analysis
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