Analysis of an essential requirement for the poly(A) binding protein function using cross-species complementation

被引:23
作者
Chekanova, JA
Shaw, RJ
Belostotsky, DA [1 ]
机构
[1] SUNY Albany, Dept Biol Sci, Albany, NY 12222 USA
[2] SUNY Albany, Ctr Mol Genet, Albany, NY 12222 USA
关键词
D O I
10.1016/S0960-9822(01)00371-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Poly(A) binding protein (PABP) is an essential, well-conserved, multifunctional protein involved in translational initiation, mRNA biogenesis, and degradation [1-5]. We have used a cross-species complementation approach to address the nature of the essential requirement for PABP in yeast. The expression of Pab3p, a member of the Arabidopsis thaliana PABP multigene family, rescues the lethal phenotype associated with the loss of the yeast Pab1p. However, Pab3p neither protects the mRNA 5' cap from premature removal, nor does it support poly(A)-dependent translational initiation or the synergistic enhancement of translation by the poly(A) tail and 5' cap in yeast. However, Pab3p corrects the temporal lag prior to the entry of the mRNA into the degradation pathway characteristic of pab1 Delta yeast strains. Furthermore, this lag correction by Pab3p requires Pan3p, a subunit of poly(A) nuclease, an enzyme involved in the mRNA 3'-end processing. Importantly, the substitution of! Pab3p for the yeast Pab1p is synthetically lethal with the PAN3 gene deletion. These results show that the function of PABP in mRNA biogenesis alone could be sufficient to support cell viability in yeast.
引用
收藏
页码:1207 / 1214
页数:8
相关论文
共 24 条
[1]   Yeast Pab1 interacts with Rna15 and participates in the control of the poly(A) tail length in vitro [J].
Amrani, N ;
Minet, M ;
LeGouar, M ;
Lacroute, F ;
Wyers, F .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (07) :3694-3701
[2]   The 3′ to 5′ degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3′ to 5′ exonucleases of the exosome complex [J].
Anderson, JSJ ;
Parker, R .
EMBO JOURNAL, 1998, 17 (05) :1497-1506
[3]   A pollen-, ovule-, and early embryo-specific poly(A) binding protein from Arabidopsis complements essential functions in yeast [J].
Belostotsky, DA ;
Meagher, RB .
PLANT CELL, 1996, 8 (08) :1261-1275
[4]   Poly(A) tail length control in Saccharomyces cerevisiae occurs by message-specific deadenylation [J].
Brown, CE ;
Sachs, AB .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6548-6559
[5]   Mechanisms and control of mRNA turnover in Saccharomyces cerevisiae [J].
Caponigro, G ;
Parker, R .
MICROBIOLOGICAL REVIEWS, 1996, 60 (01) :233-+
[6]   MULTIPLE FUNCTIONS FOR POLY(A)-BINDING PROTEIN IN MESSENGER-RNA DECAPPING AND DEADENYLATION IN YEAST [J].
CAPONIGRO, G ;
PARKER, R .
GENES & DEVELOPMENT, 1995, 9 (19) :2421-2432
[7]   A TURNOVER PATHWAY FOR BOTH STABLE AND UNSTABLE MESSENGER-RNAS IN YEAST - EVIDENCE FOR A REQUIREMENT FOR DEADENYLATION [J].
DECKER, CJ ;
PARKER, R .
GENES & DEVELOPMENT, 1993, 7 (08) :1632-1643
[9]   Translational control of dosage compensation in Drosophila by sex-lethal:: cooperative silencing via the 5′ and 3′ UTRs of msl-2 mRNA is independent of the poly(A) tail [J].
Gebauer, F ;
Corona, DFV ;
Preiss, T ;
Becker, PB ;
Hentze, MW .
EMBO JOURNAL, 1999, 18 (21) :6146-6154
[10]   Multiple portions of poly(A)-binding protein stimulate translation in vivo [J].
Gray, NK ;
Coller, JM ;
Dickson, KS ;
Wickens, M .
EMBO JOURNAL, 2000, 19 (17) :4723-4733