| First Author | Tian Y | Year | 2020 |
| Journal | Nucleic Acids Res | Volume | 48 |
| Issue | 15 | Pages | 8724-8739 |
| PubMed ID | 32735645 | Mgi Jnum | J:295976 |
| Mgi Id | MGI:6455099 | Doi | 10.1093/nar/gkaa643 |
| Citation | Tian Y, et al. (2020) Transcriptome-wide stability analysis uncovers LARP4-mediated NFkappaB1 mRNA stabilization during T cell activation. Nucleic Acids Res 48(15):8724-8739 |
| abstractText | T cell activation is a well-established model for studying cellular responses to exogenous stimulation. Motivated by our previous finding that intron retention (IR) could lead to transcript instability, in this study, we performed BruChase-Seq to experimentally monitor the expression dynamics of nascent transcripts in resting and activated CD4+ T cells. Computational modeling was then applied to quantify the stability of spliced and intron-retained transcripts on a genome-wide scale. Beyond substantiating that intron-retained transcripts were considerably less stable than spliced transcripts, we found a global stabilization of spliced mRNAs upon T cell activation, although the stability of intron-retained transcripts remained relatively constant. In addition, we identified that La-related protein 4 (LARP4), an RNA-binding protein (RBP) known to enhance mRNA stability, was involved in T cell activation-dependent mRNA stabilization. Knocking out Larp4 in mice destabilized Nfkappab1 mRNAs and reduced secretion of interleukin-2 (IL2) and interferon-gamma (IFNgamma), two factors critical for T cell proliferation and function. We propose that coordination between splicing regulation and mRNA stability may provide a novel paradigm to control spatiotemporal gene expression during T cell activation. |
