4.5 Review

Long noncoding RNAs in T lymphocytes

Journal

JOURNAL OF LEUKOCYTE BIOLOGY
Volume 99, Issue 1, Pages 31-44

Publisher

WILEY
DOI: 10.1189/jlb.1RI0815-389R

Keywords

epigenetics; lncRNA; adaptive immunity

Funding

  1. U.S. National Institutes of Health [R01 AI044924, R21 AR063846]
  2. National Science Foundation Graduate Research Fellowship Program [DGE0909667]
  3. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI044924] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [R21AR063846] Funding Source: NIH RePORTER

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Long noncoding RNAs are recently discovered regulatory RNA molecules that do not code for proteins but influence a vast array of biologic processes. In vertebrates, the number of long noncoding RNA genes is thought to greatly exceed the number of protein-coding genes. It is also thought that long noncoding RNAs drive the biologic complexity observed in vertebrates compared with that in invertebrates. Evidence of this complexity has been found in the T-lymphocyte compartment of the adaptive immune system. In the present review, we describe our current level of understanding of the expression of specific long or large intergenic or intervening long noncoding RNAs during T-lymphocyte development in the thymus and differentiation in the periphery and highlight the mechanisms of action that specific long noncoding RNAs employ to regulate T-lymphocyte function, both in vitro and in vivo.

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