Cellular stress and RNA splicing

被引:152
作者
Biamonti, Giuseppe [1 ]
Caceres, Javier F. [2 ]
机构
[1] CNR, Ist Genet Mol, I-27100 Pavia, Italy
[2] Western Gen Hosp, MRC, Human Genet Unit, Inst Genet & Mol Med, Edinburgh EH4 2XU, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
HEAT-SHOCK PROTEINS; INDUCED NUCLEAR-BODIES; MESSENGER-RNA; SR PROTEINS; SUBCELLULAR-DISTRIBUTION; REGULATORY PROTEIN; BINDING PROTEIN; HELA-CELLS; HNRNP A1; SRP38;
D O I
10.1016/j.tibs.2008.11.004
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
In response to physical and chemical stresses that affect protein folding and, thus, the execution of normal metabolic processes, cells activate gene-expression strategies aimed at increasing their chance of survival. One target of several stressing agents is pre-mRNA splicing, which is inhibited upon heat shock. Recently, the molecular basis of this splicing inhibition has begun to emerge. Interestingly, different mechanisms seem to be in place to block constitutive pre-mRNA splicing and to affect alternative splicing regulation. This could be important to modulate gene expression during recovery from stress. Thus, pre-mRNA splicing emerges as a central mechanism to integrate cellular and metabolic stresses into gene-expression profiles.
引用
收藏
页码:146 / 153
页数:8
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