Yeast m6A methylated mRNAs are enriched on translating ribosomes during meiosis, and under Rapamycin treatment
Ontology highlight
ABSTRACT: Interest in mRNA methylation has exploded in recent years. The sudden interest in a 40 year old discovery was due in part to the recent finding of FTO?s (Fat Mass Obesity) N6-methyl-adenosine (m6A) deaminase activity, thus suggested a link between obesity-associated diseases and the presence of m6A in mRNA. Another catalyst of the sudden rise in mRNA methylation research was the release of mRNA methylomes for human, mouse and Saccharomyces cerevisiae. However, the molecular function, or functions of this mRNA ?epimark? remain to be discovered. There is supportive evidence that m6A could be a mark for mRNA degradation due to its binding to YTH domain proteins, and consequently being chaperoned to P bodies. Nonetheless, only a subpopulation of the methylome was found binding to YTHDF2 in He
ORGANISM(S): Saccharomyces cerevisiae SK1
SUBMITTER: Eva Haeffner
PROVIDER: E-GEOD-68435 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
ACCESS DATA