Saccharomyces cerevisiae homologs of mammalian B and B' subunits of protein phosphatase 2A direct the enzyme to distinct cellular functions

被引:89
作者
Zhao, Y
Boguslawski, G
Zitomer, RS
DePaoliRoach, AA
机构
[1] INDIANA UNIV, SCH MED, DEPT BIOCHEM & MOL BIOL, INDIANAPOLIS, IN 46202 USA
[2] SUNY ALBANY, DEPT BIOL SCI, ALBANY, NY 12222 USA
关键词
D O I
10.1074/jbc.272.13.8256
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
Protein phosphatase 2A (PP2A) is a major cellular serine/threonine protein phosphatase, present in the cell in a variety of heterotrimeric forms that differ in their associated regulatory B-subunit. Cloning of the mammalian B' subunit has allowed the identification of a highly homologous Saccharomyces cerevisiae gene, RTS1. Disruption of the gene results in a temperature-sensitive growth defect that can be suppressed by expression of rabbit B'alpha or B'gamma isoforms. The B'alpha subunit is much more effective in restoring normal growth at 37 degrees C than B'gamma. Immunoprecipitated Rts1p was found associated with type 2A-specific protein phosphatase activity that is sensitive to 2 nM okadaic acid, but not to 100 nM phosphatase inhibitor-2, and to be phosphorylated in vivo. However, overexpression of RTS1 was unable to suppress the cold sensitivity, defective cytokinesis, and abnormal cell morphology resulting from defects in the CDC55 gene, which encodes the yeast homolog of a different B subunit of another form of 2A phosphatase, PP2A(1). These results indicate that Rts1p is a yeast homolog of the mammalian B' subunit and that the various regulatory B-subunits of PP2A are not functionally redundant but direct the enzyme to distinct cellular functions.
引用
收藏
页码:8256 / 8262
页数:7
相关论文
共 57 条
[1]  
AMMERER G, 1983, METHOD ENZYMOL, V101, P192
[2]  
Ausubel FM, 1995, CURRENT PROTOCOLS MO
[3]   PBS2, A YEAST GENE ENCODING A PUTATIVE PROTEIN-KINASE, INTERACTS WITH THE RAS2 PATHWAY AND AFFECTS OSMOTIC SENSITIVITY OF SACCHAROMYCES-CEREVISIAE [J].
BOGUSLAWSKI, G .
JOURNAL OF GENERAL MICROBIOLOGY, 1992, 138 :2425-2432
[4]   THE STRUCTURE, ROLE, AND REGULATION OF TYPE-1 PROTEIN PHOSPHATASES [J].
BOLLEN, M ;
STALMANS, W .
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 27 (03) :227-281
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   AN OSMOSENSING SIGNAL TRANSDUCTION PATHWAY IN YEAST [J].
BREWSTER, JL ;
DEVALOIR, T ;
DWYER, ND ;
WINTER, E ;
GUSTIN, MC .
SCIENCE, 1993, 259 (5102) :1760-1763
[7]   REGULATION OF PROTEIN SERINE-THREONINE PHOSPHATASE TYPE-2A BY TYROSINE PHOSPHORYLATION [J].
CHEN, J ;
MARTIN, BL ;
BRAUTIGAN, DL .
SCIENCE, 1992, 257 (5074) :1261-1264
[8]  
CLOTET J, 1995, EUR J BIOCHEM, V229, P207, DOI 10.1111/j.1432-1033.1995.0207l.x
[9]   THE STRUCTURE AND REGULATION OF PROTEIN PHOSPHATASES [J].
COHEN, P .
ANNUAL REVIEW OF BIOCHEMISTRY, 1989, 58 :453-508
[10]   High complexity in the expression of the B' subunit of protein phosphatase 2A(0) - Evidence for the existence of at least seven novel isoforms [J].
Csortos, C ;
Zolnierowicz, S ;
Bako, E ;
Durbin, SD ;
DePaoliRoach, AA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (05) :2578-2588