Unknown

Dataset Information

0

A role for the universal Kae1/Qri7/YgjD (COG0533) family in tRNA modification.


ABSTRACT: The YgjD/Kae1 family (COG0533) has been on the top-10 list of universally conserved proteins of unknown function for over 5 years. It has been linked to DNA maintenance in bacteria and mitochondria and transcription regulation and telomere homeostasis in eukaryotes, but its actual function has never been found. Based on a comparative genomic and structural analysis, we predicted this family was involved in the biosynthesis of N(6)-threonylcarbamoyl adenosine, a universal modification found at position 37 of tRNAs decoding ANN codons. This was confirmed as a yeast mutant lacking Kae1 is devoid of t(6)A. t(6)A(-) strains were also used to reveal that t(6)A has a critical role in initiation codon restriction to AUG and in restricting frameshifting at tandem ANN codons. We also showed that YaeZ, a YgjD paralog, is required for YgjD function in vivo in bacteria. This work lays the foundation for understanding the pleiotropic role of this universal protein family.

SUBMITTER: El Yacoubi B 

PROVIDER: S-EPMC3049207 | biostudies-literature | 2011 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

A role for the universal Kae1/Qri7/YgjD (COG0533) family in tRNA modification.

El Yacoubi Basma B   Hatin Isabelle I   Deutsch Christopher C   Kahveci Tamer T   Rousset Jean-Pierre JP   Iwata-Reuyl Dirk D   Murzin Alexey G AG   de Crécy-Lagard Valérie V  

The EMBO journal 20110201 5


The YgjD/Kae1 family (COG0533) has been on the top-10 list of universally conserved proteins of unknown function for over 5 years. It has been linked to DNA maintenance in bacteria and mitochondria and transcription regulation and telomere homeostasis in eukaryotes, but its actual function has never been found. Based on a comparative genomic and structural analysis, we predicted this family was involved in the biosynthesis of N(6)-threonylcarbamoyl adenosine, a universal modification found at po  ...[more]

Similar Datasets

| S-EPMC3194906 | biostudies-literature
| S-EPMC2760799 | biostudies-other
| S-EPMC10321239 | biostudies-literature
| S-EPMC4963248 | biostudies-literature
| S-EPMC3561968 | biostudies-literature
| S-EPMC3049205 | biostudies-literature
| S-EPMC7099136 | biostudies-literature
| S-EPMC3814370 | biostudies-literature
| S-EPMC5437908 | biostudies-literature
| S-EPMC1855720 | biostudies-literature