MiRNA post-transcriptional modification dynamics in T cell activation

被引:14
|
作者
Rodriguez-Galan, Ana [1 ,2 ]
Dosil, Sara G. [1 ,2 ]
Jose Gomez, Manuel [2 ]
Fernandez-Delgado, Irene [1 ,2 ]
Fernandez-Messina, Lola [1 ,2 ,3 ]
Sanchez-Cabo, Fatima [2 ]
Sanchez-Madrid, Francisco [1 ,2 ,3 ]
机构
[1] Univ Autonoma Madrid UAM, Inst Invest Sanitaria Princesa IIS IP, Serv Inmunol Hosp Univ La Princesa, Madrid 28006, Spain
[2] Ctr Nacl Invest Cardiovasc CNIC, Vasc Pathophysiol Area, Madrid 28029, Spain
[3] Inst Salud Carlos III, CIBER Enfermedades Cardiovasc, Madrid 28029, Spain
关键词
3' ADENYLATION; MICRORNA EXPRESSION; MESSENGER-RNAS; PRE-MICRORNA; URIDYLATION; STABILIZATION; DEGRADATION; REPERTOIRE; BIOGENESIS; MODULATION;
D O I
10.1016/j.isci.2021.102530
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
T cell activation leads to extensive changes in the miRNA repertoire. Although overall miRNA expression decreases within a few hours of T cell activation, some individual miRNAs are specifically upregulated. Using next-generation sequencing, we assessed miRNA expression and post-transcriptional modification kinetics in human primary CD4+ T cells upon T cell receptor (TCR) or type I interferon stimulation. This analysis identified differential expression of multiple miRNAs not previously linked to T cell activation. Remarkably, upregulated miRNAs showed a higher frequency of 30 adenylation. TCR stimulation was followed by increased expression of RNA modifying enzymes and the RNA degrading enzymes Dis3L2 and Eri1. In the midst of this adverse environment, 30 adenylationmay serve a protective function that could be exploited to improve miRNA stability for T cell-targeted therapy.
引用
收藏
页数:20
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