Decapping of stabilized, polyadenylated mRNA in yeast pab1 mutants

Citation
Jp. Morrissey et al., Decapping of stabilized, polyadenylated mRNA in yeast pab1 mutants, YEAST, 15(8), 1999, pp. 687-702
Citations number
48
Categorie Soggetti
Biotecnology & Applied Microbiology",Microbiology
Journal title
YEAST
ISSN journal
0749503X → ACNP
Volume
15
Issue
8
Year of publication
1999
Pages
687 - 702
Database
ISI
SICI code
0749-503X(19990615)15:8<687:DOSPMI>2.0.ZU;2-M
Abstract
Interaction of the poly(A) binding protein, Pab1p, with mRNA plays an impor tant role in gene expression. This work describes an analysis of pab1 mutan ts in Saccharomyces cerevisiae. Yeast pab1 mutants were found to be sensiti ve to elevated concentrations of copper (Cu) and 3-aminotriazole (3-AT) in the growth medium. This phenotype arises because these pab1 mutants underac cumulate mRNA, including the CUP1 and HIS3 mRNAs, the products of which are required for Cu and 3-AT resistance, respectively. To determine the cause of the mRNA underaccumulation, mRNA turnover and production were examined i n the pab1-53 mutant. It was found that although the pattern of mRNA decay was altered, and substantial decapping of polyadenylated mRNA could be dete cted, mRNA was not destabilized in this strain. It was also found that the pab1 mutant was impaired in the production of mRNA. These data show that th e decreased level of mRNA in the pab1-53 mutant arises from poor production , and they suggest that yeast Pab1p is involved in an aspect of nuclear mRN A metabolism. They also indicate that deadenylation can be uncoupled from d ecapping without significant changes in an mRNA's stability, and that this uncoupling can be tolerated by yeast. Copyright (C) 1999 John Wiley & Sons, Ltd.