3′ Uridylation controls mature microRNA turnover during CD4 T-cell activation

Author:

Gutiérrez-Vázquez CristinaORCID,Enright Anton J.,Rodríguez-Galán Ana,Pérez-García Arantxa,Collier Paul,Jones Matthew R.,Benes Vladimir,Mizgerd Joseph P.,Mittelbrunn María,Ramiro Almudena R.,Sánchez-Madrid Francisco

Abstract

Activation of T lymphocytes requires a tight regulation of microRNA (miRNA) expression. Terminal uridyltransferases (TUTases) catalyze 3′ nontemplated nucleotide addition (3′NTA) to miRNAs, which may influence miRNA stability and function. Here, we investigated 3′NTA to mature miRNA in CD4 T lymphocytes by deep sequencing. Upon T-cell activation, miRNA sequences bearing terminal uridines are specifically decreased, concomitantly with down-regulation of TUT4 and TUT7 enzymes. Analyzing TUT4-deficient T lymphocytes, we proved that this terminal uridyltransferase is essential for the maintenance of miRNA uridylation in the steady state of T lymphocytes. Analysis of synthetic uridylated miRNAs shows that 3′ addition of uridine promotes degradation of these uridylated miRNAs after T-cell activation. Our data underline post-transcriptional uridylation as a mechanism to fine-tune miRNA levels during T-cell activation.

Funder

Ministerio de Economía y Competitividad-Spain

FEDER

The Centro Nacional de Investigaciones Cardiovasculares

Ministerio de Economía y Competitividad-Spain and the Pro-CNIC Foundation

Instituto de Salud Carlos III

FPU program

Publisher

Cold Spring Harbor Laboratory

Subject

Molecular Biology

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