Molecular and evolutionary basis of the cellular stress response

被引:1075
作者
Kültz, D [1 ]
机构
[1] Univ Calif Davis, Dept Anim Sci, Physiol Genom Grp, Davis, CA 95616 USA
关键词
molecular evolution; macromolecular damage; molecular chaperones; redox-regulation; DNA repair;
D O I
10.1146/annurev.physiol.67.040403.103635
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The cellular stress response is a universal mechanism of extraordinary physiological/pathophysiological significance. It represents a defense reaction of cells to damage that environmental forces inflict on macromolecules. Many aspects of the cellular stress response are not stressor specific because cells monitor stress based on macromolecular damage without regard to the type of stress that causes such damage. Cellular mechanisms activated by DNA damage and protein damage are interconnected and share common elements. Other cellular responses directed at re-establishing homeostasis are stressor specific and often activated in parallel to the cellular stress response. All organisms have stress proteins, and universally conserved stress proteins can be regarded as the minimal stress proteome. Functional analysis of the minimal stress proteome yields information about key aspects of the cellular stress response, including physiological mechanisms of sensing membrane lipid, protein, and DNA damage; redox sensing and regulation; cell cycle control; macromolecular stabilization/repair; and control of energy metabolism. In addition, cells can quantify stress and activate a death program (apoptosis) when tolerance limits are exceeded.
引用
收藏
页码:225 / 257
页数:33
相关论文
共 207 条
[1]   Chloroplast proteases: Possible regulators of gene expression? [J].
Adam, Z .
BIOCHIMIE, 2000, 82 (6-7) :647-654
[2]   Role of redox potential and reactive oxygen species in stress signaling [J].
Adler, V ;
Yin, ZM ;
Tew, KD ;
Ronai, Z .
ONCOGENE, 1999, 18 (45) :6104-6111
[3]   Double-strand break repair: are Rad51/RecA-DNA joints barriers to DNA replication? [J].
Aguilera, A .
TRENDS IN GENETICS, 2001, 17 (06) :318-321
[4]   FTSH, A MEMBRANE-BOUND ATPASE, FORMS A COMPLEX IN THE CYTOPLASMIC MEMBRANE OF ESCHERICHIA-COLI [J].
AKIYAMA, Y ;
YOSHIHISA, T ;
ITO, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (40) :23485-23490
[5]   FtsH (HflB) is an ATP-dependent protease selectively acting on SecY and some other membrane proteins [J].
Akiyama, Y ;
Kihara, A ;
Tokuda, H ;
Ito, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (49) :31196-31201
[6]   Bacterial suicide through stress [J].
Aldsworth, TG ;
Sharman, RL ;
Dodd, CER .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1999, 56 (5-6) :378-383
[7]   The effect of drought and ultraviolet radiation on growth and stress markers in pea and wheat [J].
Alexieva, V ;
Sergiev, I ;
Mapelli, S ;
Karanov, E .
PLANT CELL AND ENVIRONMENT, 2001, 24 (12) :1337-1344
[8]   Heat shock proteins can protect aged human and rodent cells from different stressful stimuli [J].
Alsbury, S ;
Papageorgiou, K ;
Latchman, DS .
MECHANISMS OF AGEING AND DEVELOPMENT, 2004, 125 (03) :201-209
[9]   Functional genomics as a window on radiation stress signaling [J].
Amundson, SA ;
Bittner, M ;
Fornace, AJ .
ONCOGENE, 2003, 22 (37) :5828-5833
[10]   Cyclophilins and their possible role in the stress response [J].
Andreeva, L ;
Heads, R ;
Green, CJ .
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 1999, 80 (06) :305-315