MSI3, A MULTICOPY SUPPRESSOR OF MUTANTS HYPERACTIVATED IN THE RAS-CAMP PATHWAY, ENCODES A NOVEL HSP70 PROTEIN OF SACCHAROMYCES-CEREVISIAE

被引:43
作者
SHIRAYAMA, M [1 ]
KAWAKAMI, K [1 ]
MATSUI, Y [1 ]
TANAKA, K [1 ]
TOHE, A [1 ]
机构
[1] UNIV TOKYO, INST MED SCI, DEPT TUMOR BIOL, MINATO KU, TOKYO 108, JAPAN
来源
MOLECULAR AND GENERAL GENETICS | 1993年 / 240卷 / 03期
关键词
HEAT SHOCK RESPONSE; HSP70; SACCHAROMYCES-CEREVISIAE; RAS-CAMP PATHWAY; MULTICOPY SUPPRESSOR OF IRA1;
D O I
10.1007/BF00280382
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
The MSI3 gene was isolated as a multicopy suppressor of the heat shock-sensitive phenotype of the ira1 mutation, which causes hyperactivation of the RAS-cAMP pathway. Overexpression of MSI3 also suppresses the heat shock-sensitive phenotype of the bcy1 mutant. Determination of the DNA sequence of MSI3 revealed that MSI3 can encode a 77.4 kDa protein related to the HSP70 family. The amino acid sequence of Msi3p is about 30% identical to that of the Ssa1p of Saccharomyces cerevisiae. This contrasts with the finding that members of the HSP70 family generally show at least 50% amino acid identity. The consensus nucleotide sequence of the heat shock element (HSE) was found in the upstream region of MSI3. Moreover, the steady-state levels of the MSI3 mRNA and protein were increased upon heat shock. These results indicate that the MSI3 gene encodes a novel HSP70-like heat shock protein. Disruption of the MSI3 gene was associated with a temperature sensitive growth phenotype but unexpectedly, thermotolerance was enhanced in the disruptant.
引用
收藏
页码:323 / 332
页数:10
相关论文
共 45 条
[11]   PURIFICATION OF A RAS-RESPONSIVE ADENYLYL CYCLASE COMPLEX FROM SACCHAROMYCES-CEREVISIAE BY USE OF AN EPITOPE ADDITION METHOD [J].
FIELD, J ;
NIKAWA, J ;
BROEK, D ;
MACDONALD, B ;
RODGERS, L ;
WILSON, IA ;
LERNER, RA ;
WIGLER, M .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2159-2165
[12]   3-DIMENSIONAL STRUCTURE OF THE ATPASE FRAGMENT OF A 70K HEAT-SHOCK COGNATE PROTEIN [J].
FLAHERTY, KM ;
DELUCAFLAHERTY, C ;
MCKAY, DB .
NATURE, 1990, 346 (6285) :623-628
[13]   THE RAS ONCOGENE - AN IMPORTANT REGULATORY ELEMENT IN LOWER EUKARYOTIC ORGANISMS [J].
GIBBS, JB ;
MARSHALL, MS .
MICROBIOLOGICAL REVIEWS, 1989, 53 (02) :171-185
[14]   NEW YEAST-ESCHERICHIA-COLI SHUTTLE VECTORS CONSTRUCTED WITH INVITRO MUTAGENIZED YEAST GENES LACKING 6-BASE PAIR RESTRICTION SITES [J].
GIETZ, RD ;
SUGINO, A .
GENE, 1988, 74 (02) :527-534
[15]   STUDIES ON TRANSFORMATION OF ESCHERICHIA-COLI WITH PLASMIDS [J].
HANAHAN, D .
JOURNAL OF MOLECULAR BIOLOGY, 1983, 166 (04) :557-580
[16]   UNIDIRECTIONAL DIGESTION WITH EXONUCLEASE-III CREATES TARGETED BREAKPOINTS FOR DNA SEQUENCING [J].
HENIKOFF, S .
GENE, 1984, 28 (03) :351-359
[17]   DURABLE SYNTHESIS OF HIGH MOLECULAR-WEIGHT HEAT-SHOCK PROTEINS IN G0-CELLS OF THE YEAST AND OTHER EUKARYOTES [J].
IIDA, H ;
YAHARA, I .
JOURNAL OF CELL BIOLOGY, 1984, 99 (01) :199-207
[18]   TRANSFORMATION OF INTACT YEAST-CELLS TREATED WITH ALKALI CATIONS [J].
ITO, H ;
FUKUDA, Y ;
MURATA, K ;
KIMURA, A .
JOURNAL OF BACTERIOLOGY, 1983, 153 (01) :163-168
[19]  
KAWAKAMI K, 1992, GENETICS, V131, P821
[20]   SUCCESSIVE ACTION OF DNAK, DNAJ AND GROEL ALONG THE PATHWAY OF CHAPERONE-MEDIATED PROTEIN FOLDING [J].
LANGER, T ;
LU, C ;
ECHOLS, H ;
FLANAGAN, J ;
HAYER, MK ;
HARTL, FU .
NATURE, 1992, 356 (6371) :683-689