Unknown

Dataset Information

0

The RAG recombinase dictates functional heterogeneity and cellular fitness in natural killer cells.


ABSTRACT: The emergence of recombination-activating genes (RAGs) in jawed vertebrates endowed adaptive immune cells with the ability to assemble a diverse set of antigen receptor genes. In contrast, innate lymphocytes, such as natural killer (NK) cells, are not believed to require RAGs. Here, we report that NK cells unable to express RAGs or RAG endonuclease activity during ontogeny exhibit a cell-intrinsic hyperresponsiveness but a diminished capacity to survive following virus-driven proliferation, a reduced expression of DNA damage response mediators, and defects in the repair of DNA breaks. Evidence for this novel function of RAG has also been observed in T cells and innate lymphoid cells (ILCs), revealing an unexpected role for RAG proteins beyond V(D)J recombination. We propose that DNA cleavage events mediated by RAG endow developing adaptive and innate lymphocytes with a cellular "fitness" that safeguards their persistence later in life during episodes of rapid proliferation or cellular stress.

SUBMITTER: Karo JM 

PROVIDER: S-EPMC4371485 | biostudies-literature | 2014 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications

The RAG recombinase dictates functional heterogeneity and cellular fitness in natural killer cells.

Karo Jenny M JM   Schatz David G DG   Sun Joseph C JC  

Cell 20140901 1


The emergence of recombination-activating genes (RAGs) in jawed vertebrates endowed adaptive immune cells with the ability to assemble a diverse set of antigen receptor genes. In contrast, innate lymphocytes, such as natural killer (NK) cells, are not believed to require RAGs. Here, we report that NK cells unable to express RAGs or RAG endonuclease activity during ontogeny exhibit a cell-intrinsic hyperresponsiveness but a diminished capacity to survive following virus-driven proliferation, a re  ...[more]

Similar Datasets

| S-EPMC6608018 | biostudies-literature
| S-EPMC9676120 | biostudies-literature
| S-EPMC6564036 | biostudies-literature
| S-EPMC8291384 | biostudies-literature
| S-EPMC5543290 | biostudies-literature
| S-EPMC9547868 | biostudies-literature
| S-EPMC9729827 | biostudies-literature
| S-EPMC3528503 | biostudies-literature
| S-EPMC5203794 | biostudies-literature
| S-EPMC6718415 | biostudies-literature