Integration of genome-wide approaches identifies lncRNAs of adult neural stem cells and their progeny in vivo.
Cell Stem Cell, 2013/5/02;12(5):616-28.
Ramos AD[1], Diaz A, Nellore A, Delgado RN, Park KY, Gonzales-Roybal G, Oldham MC, Song JS, Lim DA
Affiliations
PMID: 23583100
Impact factor: 25.269
Abstract
Long noncoding RNAs (lncRNAs) have been described in cell lines and various whole tissues, but lncRNA analysis of development in vivo is limited. Here, we comprehensively analyze lncRNA expression for the adult mouse subventricular zone neural stem cell lineage. We utilize complementary genome-wide techniques including RNA-seq, RNA CaptureSeq, and ChIP-seq to associate specific lncRNAs with neural cell types, developmental processes, and human disease states. By integrating data from chromatin state maps, custom microarrays, and FACS purification of the subventricular zone lineage, we stringently identify lncRNAs with potential roles in adult neurogenesis. shRNA-mediated knockdown of two such lncRNAs, Six3os and Dlx1as, indicate roles for lncRNAs in the glial-neuronal lineage specification of multipotent adult stem cells. Our data and workflow thus provide a uniquely coherent in vivo lncRNA analysis and form the foundation of a user-friendly online resource for the study of lncRNAs in development and disease.
MeSH terms
Adult Stem Cells; Alternative Splicing; Animals; Cell Differentiation; Cell Lineage; Cerebral Ventricles; Embryonic Stem Cells; Gene Expression Regulation, Developmental; Genome; Histones; Humans; Lysine; Male; Methylation; Mice; Mice, Inbred C57BL; Neural Stem Cells; Neurogenesis; Neurons; Protein Isoforms; Protein Processing, Post-Translational; RNA, Long Noncoding; RNA, Messenger; Reproducibility of Results; Time Factors
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