Physiological effects of unassembled chaperonin Cct subunits in the yeast Saccharomyces cerevisiae

被引:38
作者
Kabir, MA
Kaminska, J
Segel, GB
Bethlendy, G
Lin, P
Della Seta, F
Blegen, C
Swiderek, KM
Zoladek, T
Arndt, KT
Sherman, F
机构
[1] Univ Rochester, Med Ctr, Dept Biochem & Biophys, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, Dept Pediat, Rochester, NY 14642 USA
[3] Polish Acad Sci, Inst Biochem & Biophys, Dept Genet, Warsaw, Poland
[4] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[5] ZymoGenet Inc, Seattle, WA 98102 USA
关键词
chaperonins; Cct; TOR2; LST8; RSP5; SIT4; SAP155;
D O I
10.1002/yea.1210
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
Eukaryotic chaperonins, the Cct complexes, are assembled into two rings, each of which is composed of a stoichiometric array of eight different subunits, which are denoted Cct1p-Cct8p. Overexpression of a single CCT gene in Saccharomyces cerevisiae causes an increase of the corresponding Cct subunit, but not of the Cct complex. Nevertheless, overexpression of certain Cct subunits, especially CCT6, suppresses a wide range of abnormal phenotypes, including those caused by the diverse types of conditional mutations tor2-21, lst8-2 and rsp5-9 and those caused by the concomitant overexpression of Sit4p and Sap155p. The examination of 73 altered forms of Cct6p revealed that the cct6-24 mutation, containing GDGTT --> AAAAA replacements of the conserved ATP-binding motif, was unable to suppress any of these traits, although the cct6-24 allele was completely functional for growth. These results provide evidence for functional differences among Cct subunits and for physiological properties of unassembled subunits. We suggest that the suppression is due to the competition of specific Cct subunits for activities that normally modify various cellular components. Furthermore, we also suggest that the Cct subunits can act as suppressors only in certain states, such as when associated with ATP. Copyright (C) 2005 John Wiley Sons, Ltd.
引用
收藏
页码:219 / 239
页数:21
相关论文
共 80 条
  • [1] TOR controls translation initiation and early G1 progression in yeast
    Barbet, NC
    Schneider, U
    Helliwell, SB
    Stansfield, I
    Tuite, MF
    Hall, MN
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (01) : 25 - 42
  • [2] Starvation induces vacuolar targeting and degradation of the tryptophan permease in yeast
    Beck, T
    Schmidt, A
    Hall, MN
    [J]. JOURNAL OF CELL BIOLOGY, 1999, 146 (06) : 1227 - 1237
  • [3] The TOR (target of rapamycin) signal transduction pathway regulates the stability of translation initiation factor eIF4G in the yeast Saccharomyces cerevisiae
    Berset, C
    Trachsel, H
    Altmann, M
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (08) : 4264 - 4269
  • [4] LST8 negatively regulates amino acid biosynthesis as a component of the TOR pathway
    Chen, EJ
    Kaiser, CA
    [J]. JOURNAL OF CELL BIOLOGY, 2003, 161 (02) : 333 - 347
  • [5] NONCHROMOSOMAL ANTIBIOTIC RESISTANCE IN BACTERIA - GENETIC TRANSFORMATION OF ESCHERICHIA-COLI BY R-FACTOR DNA
    COHEN, SN
    CHANG, ACY
    HSU, L
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (08) : 2110 - &
  • [6] NPR1 kinase and RSP5-BUL1/2 ubiquitin ligase control GLN3-dependent transcription in Saccharomyces cerevisiae
    Crespo, JL
    Helliwell, SB
    Wiederkehr, C
    Demougin, P
    Fowler, B
    Primig, M
    Hall, MN
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (36) : 37512 - 37517
  • [7] Rapid protein identification using a microscale electrospray LC/MS system on an ion trap mass spectrometer
    Davis, MT
    Lee, TD
    [J]. JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1998, 9 (03) : 194 - 201
  • [8] Prions affect the appearance of other prions:: The story of [PIN+]
    Derkatch, IL
    Bradley, ME
    Hong, JY
    Liebman, SW
    [J]. CELL, 2001, 106 (02) : 171 - 182
  • [9] Crystal structure of the thermosome, the archaeal chaperonin and homolog of CCT
    Ditzel, L
    Löwe, J
    Stock, D
    Stetter, KO
    Huber, H
    Huber, R
    Steinbacher, S
    [J]. CELL, 1998, 93 (01) : 125 - 138
  • [10] Dunn CD, 2003, GENETICS, V165, P35