Control and regulation of the cellular responses to cold shock: the responses in yeast and mammalian systems

被引:195
作者
Al-Fageeh, Mohamed B. [1 ]
Smales, C. Mark [1 ]
机构
[1] Univ Kent, Dept Biosci, Prot Sci Grp, Canterbury CT2 7NJ, Kent, England
基金
英国生物技术与生命科学研究理事会;
关键词
cellular response; cold-shock protein; cold-shock response; control of gene expression; sub-physiological temperature; yeast;
D O I
10.1042/BJ20060166
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
Although the cold-shock response has now been studied in a number of different organisms for several decades, it is only in the last few years that we have begun to understand the molecular mechanisms that govern adaptation to cold stress. Notably, all organisms from prokaryotes to plants and higher eukaryotes respond to cold shock in a comparatively similar manner. The general response of cells to cold stress is the elite and rapid overexpression of a small group of proteins, the so-called CSPs (cold-shock proteins). The most well characterized CSP is CspA, the major CSP expressed in Escherichia coli upon temperature downshift. More recently, a number of reports have shown that exposing yeast or mammalian cells to sub-physiological temperatures (< 30 or < 37 degrees C respectively) invokes a co-ordinated cellular response involving modulation of transcription, translation, metabolism, the cell cycle and the cell cytoskeleton. In the present review, we summarize the regulation and role of coldshock genes and proteins in the adaptive response upon decreased temperature with particular reference to yeast and in vitro cultured mammalian cells. Finally, we present an integrated model for the co-ordinated responses required to maintain the viability and integrity of mammalian cells upon mild hypothermic cold shock.
引用
收藏
页码:247 / 259
页数:13
相关论文
共 129 条
[81]   Deletion analysis of cspA of Escherichia coli: requirement of the AT-rich UP element for cspA transcription and the downstream box in the coding region for its cold shock induction [J].
Mitta, M ;
Fang, L ;
Inouye, M .
MOLECULAR MICROBIOLOGY, 1997, 26 (02) :321-335
[82]   Effects of temperature shift on cell cycle, apoptosis and nucleotide pools in CHO cell batch cultures [J].
Moore, A ;
Mercer, J ;
Dutina, G ;
Donahue, CJ ;
Bauer, KD ;
Mather, JP ;
Etcheverry, T ;
Ryll, T .
CYTOTECHNOLOGY, 1997, 23 (1-3) :47-54
[83]   Genome-wide expression analysis of yeast response during exposure to 4°C [J].
Murata, Y ;
Homma, T ;
Kitagawa, E ;
Momose, Y ;
Sato, MS ;
Odani, M ;
Shimizu, H ;
Hasegawa-Mizusawa, M ;
Matsumoto, R ;
Mizukami, S ;
Fujita, K ;
Parveen, M ;
Komatsu, Y ;
Iwahashi, H .
EXTREMOPHILES, 2006, 10 (02) :117-128
[84]   On the integral closures of certain ideals generated by regular sequences [J].
Nishida, K .
JOURNAL OF PURE AND APPLIED ALGEBRA, 2000, 152 (1-3) :289-292
[85]   Diurnal change of the cold-inducible RNA-binding protein (Cirp) expression in mouse brain [J].
Nishiyama, H ;
Xue, JH ;
Sato, T ;
Fukuyama, H ;
Mizuno, N ;
Houtani, T ;
Sugimoto, T ;
Fujita, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 245 (02) :534-538
[86]   Cloning and characterization of human CIRP (cold-inducible RNA-binding protein) cDNA and chromosomal assignment of the gene [J].
Nishiyama, H ;
Higashitsuji, H ;
Yokoi, H ;
Itoh, K ;
Danno, S ;
Matsuda, T ;
Fujita, J .
GENE, 1997, 204 (1-2) :115-120
[87]   A glycine-rich RNA-binding protein mediating cold-inducible suppression of mammalian cell growth [J].
Nishiyama, H ;
Itoh, K ;
Kaneko, Y ;
Kishishita, M ;
Yoshida, O ;
Fujita, J .
JOURNAL OF CELL BIOLOGY, 1997, 137 (04) :899-908
[88]   Screening of genes that respond to cryopreservation stress using yeast DNA microarray [J].
Odani, M ;
Komatsu, Y ;
Oka, S ;
Iwahashi, H .
CRYOBIOLOGY, 2003, 47 (02) :155-164
[89]   Phosphorylation of c-Jun N-terminal kinase in human hepatoblastoma cells is transiently increased by cold exposure and further enhanced by subsequent warm incubation of the cells [J].
Ohsaka, Y ;
Ohgiya, S ;
Hoshino, T ;
Ishizaki, K .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2002, 12 (2-3) :111-118
[90]   A downshift in temperature activates the high osmolarity glycerol (HOG) pathway, which determines freeze tolerance in Saccharomyces cerevisiae [J].
Panadero, J ;
Pallotti, C ;
Rodríguez-Vargas, S ;
Randez-Gil, F ;
Prieto, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (08) :4638-4645