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Profiles of Long Noncoding RNAs in Human Naive and Memory T Cells.


ABSTRACT: We employed whole-genome RNA-sequencing to profile mRNAs and both annotated and novel long noncoding RNAs (lncRNAs) in human naive, central memory, and effector memory CD4+ T cells. Loci transcribing both lineage-specific annotated and novel lncRNA are adjacent to lineage-specific protein-coding genes in the genome. Lineage-specific novel lncRNA loci are transcribed from lineage-specific typical- and supertranscriptional enhancers and are not multiexonic, thus are more similar to enhancer RNAs. Novel enhancer-associated lncRNAs transcribed from the IFNG locus bind the transcription factor NF-?B and enhance binding of NF-?B to the IFNG genomic locus. Depletion of the annotated lncRNA, IFNG-AS1, or one IFNG enhancer-associated lncRNA abrogates IFNG expression by memory T cells, indicating these lncRNAs have biologic function.

SUBMITTER: Spurlock CF 

PROVIDER: S-EPMC5508595 | biostudies-literature | 2017 Jul

REPOSITORIES: biostudies-literature

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Profiles of Long Noncoding RNAs in Human Naive and Memory T Cells.

Spurlock Charles F CF   Shaginurova Guzel G   Tossberg John T JT   Hester Jonathan D JD   Chapman Nathaniel N   Guo Yan Y   Crooke Philip S PS   Aune Thomas M TM  

Journal of immunology (Baltimore, Md. : 1950) 20170609 2


We employed whole-genome RNA-sequencing to profile mRNAs and both annotated and novel long noncoding RNAs (lncRNAs) in human naive, central memory, and effector memory CD4<sup>+</sup> T cells. Loci transcribing both lineage-specific annotated and novel lncRNA are adjacent to lineage-specific protein-coding genes in the genome. Lineage-specific novel lncRNA loci are transcribed from lineage-specific typical- and supertranscriptional enhancers and are not multiexonic, thus are more similar to enha  ...[more]

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