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Spatiotemporal expression and transcriptional perturbations by long noncoding RNAs in the mouse brain

Authors :
Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory
Goff, Loyal A.
Groff, Abigail F.
Sauvageau, Martin
Trayes-Gibson, Zachary
Sanchez-Gomez, Diana B.
Morse, Michael
Martin, Ryan D.
Elcavage, Lara E.
Liapis, Stephen C.
Gonzalez-Celeiro, Meryem
Plana, Olivia
Li, Eric
Gerhardinger, Chiara
Tomassy, Giulio S.
Arlotta, Paola
Rinn, John L.
Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory
Goff, Loyal A.
Groff, Abigail F.
Sauvageau, Martin
Trayes-Gibson, Zachary
Sanchez-Gomez, Diana B.
Morse, Michael
Martin, Ryan D.
Elcavage, Lara E.
Liapis, Stephen C.
Gonzalez-Celeiro, Meryem
Plana, Olivia
Li, Eric
Gerhardinger, Chiara
Tomassy, Giulio S.
Arlotta, Paola
Rinn, John L.
Source :
National Academy of Sciences (U.S.)
Publication Year :
2016

Abstract

Long noncoding RNAs (lncRNAs) have been implicated in numerous cellular processes including brain development. However, the in vivo expression dynamics and molecular pathways regulated by these loci are not well understood. Here, we leveraged a cohort of 13 lncRNA-null mutant mouse models to investigate the spatiotemporal expression of lncRNAs in the developing and adult brain and the transcriptome alterations resulting from the loss of these lncRNA loci. We show that several lncRNAs are differentially expressed both in time and space, with some presenting highly restricted expression in only selected brain regions. We further demonstrate altered regulation of genes for a large variety of cellular pathways and processes upon deletion of the lncRNA loci. Finally, we found that 4 of the 13 lncRNAs significantly affect the expression of several neighboring protein-coding genes in a cis-like manner. By providing insight into the endogenous expression patterns and the transcriptional perturbations caused by deletion of the lncRNA locus in the developing and postnatal mammalian brain, these data provide a resource to facilitate future examination of the specific functional relevance of these genes in neural development, brain function, and disease.<br />National Science Foundation (U.S.) (Postdoctoral Research Fellowship in Biology DBI-0905973)

Details

Database :
OAIster
Journal :
National Academy of Sciences (U.S.)
Notes :
application/pdf, en_US
Publication Type :
Electronic Resource
Accession number :
edsoai.on1141880225
Document Type :
Electronic Resource