GroES/GroEL and DnaK/DnaJ have distinct roles in stress responses and during cell cycle progression in Caulobacter crescentus

被引:117
作者
Susin, Michelle F. [1 ]
Baldini, Regina L. [1 ]
Gueiros-Filho, Frederico [1 ]
Gomes, Suely L. [1 ]
机构
[1] Univ Sao Paulo, Inst Quim, Dept Bioquim, BR-05508000 Sao Paulo, Brazil
关键词
D O I
10.1128/JB.00824-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Misfolding and aggregation of protein molecules are major threats to all living organisms. Therefore, cells have evolved quality control systems for proteins consisting of molecular chaperones and proteases, which prevent protein aggregation by either refolding or degrading misfolded proteins. DnaK/DnaJ and GroES/GroEL are the best-characterized molecular chaperone systems in bacteria. In Caulobacter crescentus these chaperone machines are the products of essential genes, which are both induced by heat shock and cell cycle regulated. In this work, we characterized the viabilities of conditional dnaKJ and groESL mutants under different types of environmental stress, as well as under normal physiological conditions. We observed that C crescentus cells with GroES/EL depleted are quite resistant to heat shock, ethanol, and freezing but are sensitive to oxidative, saline, and osmotic stresses. In contrast, cells with DnaK/J depleted are not affected by the presence of high concentrations of hydrogen peroxide, NaCl, and sucrose but have a lower survival rate after heat shock, exposure to ethanol, and freezing and are unable to acquire thermotolerance. Cells lacking these chaperones also have morphological defects under normal growth conditions. The absence of GroE proteins results in long, pinched filamentous cells with several Z-rings, whereas cells lacking DnaK/J are only somewhat more elongated than normal predivisional cells, and most of them do not have Z-rings. These findings indicate that there is cell division arrest, which occurs at different stages depending on the chaperone machine affected. Thus, the two chaperone systems have distinct roles in stress responses and during cell cycle progression in C. crescentus.
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页码:8044 / 8053
页数:10
相关论文
共 82 条
[31]   Regulated degradation of chromosome replication proteins DnaA and CtrA in Caulobacter crescentus [J].
Gorbatyuk, B ;
Marczynski, GT .
MOLECULAR MICROBIOLOGY, 2005, 55 (04) :1233-1245
[32]   LISTERIA-MONOCYTOGENES CAN GROW IN MACROPHAGES WITHOUT THE AID OF PROTEINS INDUCED BY ENVIRONMENTAL STRESSES [J].
HANAWA, T ;
YAMAMOTO, T ;
KAMIYA, S .
INFECTION AND IMMUNITY, 1995, 63 (12) :4595-4599
[33]   Protein folding - Molecular chaperones in the cytosol: from nascent chain to folded protein [J].
Hartl, FU ;
Hayer-Hartl, M .
SCIENCE, 2002, 295 (5561) :1852-1858
[34]   Cell cycle-dependent duplication and bidirectional migration of SeqA-associated DNA-protein complexes in E-coli [J].
Hiraga, S ;
Ichinose, C ;
Niki, H ;
Yamazoe, M .
MOLECULAR CELL, 1998, 1 (03) :381-387
[35]   Oscillating global regulators control the genetic circuit driving a bacterial cell cycle [J].
Holtzendorff, J ;
Hung, D ;
Brende, P ;
Reisenauer, A ;
Viollier, PH ;
McAdams, HH ;
Shapiro, L .
SCIENCE, 2004, 304 (5673) :983-987
[36]   PROTEIN FOLDING IN THE CELL - FUNCTIONS OF 2 FAMILIES OF MOLECULAR CHAPERONE, HSP 60 AND TF55-TCP1 [J].
HORWICH, AL ;
WILLISON, KR .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1993, 339 (1289) :313-326
[37]   DnaA coordinates replication initiation and cell cycle transcription in Caulobacter crescentus [J].
Hottes, AK ;
Shapiro, L ;
McAdams, HH .
MOLECULAR MICROBIOLOGY, 2005, 58 (05) :1340-1353
[38]   Identification of in vivo substrates of the chaperonin GroEL [J].
Houry, WA ;
Frishman, D ;
Eckerskorn, C ;
Lottspeich, F ;
Hartl, FU .
NATURE, 1999, 402 (6758) :147-154
[39]   Mechanism of substrate recognition by the chaperonin GroEL [J].
Houry, WA .
BIOCHEMISTRY AND CELL BIOLOGY, 2001, 79 (05) :569-577
[40]  
HUPP TR, 1993, J BIOL CHEM, V268, P13128