Identification of a terminal uridylyl transferase implicated in the protection of deadenylated messager RNAs 3' end in Arabidopsis thaliana

The work presented in this manuscript defines a new role of mRNA uridylation, using Arabidopsis as a model organism. RNA uridylation is catalyzed by RNA nucleotidyltransferases belonging to the non canonical poly(A) polymerase (ncPAP) family. Among the 14 genes encoding ncPAPs in Arabidopsis, we identified a terminal uridylyl transferase, TUT1, responsible for mRNA uridylation. Our results show that mRNAs are uridylated by TUT1 after a deadenylation step. Uridylation doesn’t modify mRNA degradation rates but is essential for deadenylated mRNA 3’ end protection against 3’- 5’ exoribonucleolytic attacks and to prevent 3’ truncated aberrant mRNA formation. Interestingly, this protection by uridylation is detected in polysomes. One biological function of mRNA uridylation is to establish a 5’-3’ mRNA degradation polarity that could be essential in the case of cotranslational mRNA decay.

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Source https://theses.hal.science/tel-00881163
Author Sement, François
Maintainer CCSD
Last Updated May 9, 2026, 02:46 (UTC)
Created May 9, 2026, 02:46 (UTC)
Identifier NNT: 2012STRAJ132
Language fr
Rights https://about.hal.science/hal-authorisation-v1/
contributor Institut de Biologie Moléculaire des Plantes (IBMP) ; Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)
creator Sement, François
date 2012-09-27T00:00:00
harvest_object_id 1f59babb-a240-4136-af14-b409a5dc734f
harvest_source_id 3374d638-d20b-4672-ba96-a23232d55657
harvest_source_title test moissonnage SELUNE
metadata_modified 2026-03-30T00:00:00
set_spec type:THESE