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Embracing the void-how much do we really know about targeting and translocation to the endoplasmic reticulum?
被引:32
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Schuldiner, Maya
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Weizmann Inst Sci, Dept Mol Genet, IL-7610001 Rehovot, Israel Weizmann Inst Sci, Dept Mol Genet, IL-7610001 Rehovot, Israel
机构:
[1] Weizmann Inst Sci, Dept Mol Genet, IL-7610001 Rehovot, Israel
关键词:
SIGNAL RECOGNITION PARTICLE;
TAIL-ANCHORED PROTEINS;
SYNTHESIZING SECRETORY PROTEIN;
ER MEMBRANE;
SACCHAROMYCES-CEREVISIAE;
CONDUCTING CHANNEL;
BETA-SUBUNIT;
POSTTRANSLATIONAL TRANSLOCATION;
FUNCTIONAL-CHARACTERIZATION;
MICROSOMAL-MEMBRANES;
D O I:
10.1016/j.ceb.2014.02.004
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
In order for a protein to enter the secretory pathway, two crucial steps must occur: it first needs to be targeted to the cytosolic surface of the endoplasmic reticulum (ER), and then be translocated across the ER membrane. Although for many years studies of targeting focused on the signal recognition particle, recent findings reveal that several alternative targeting pathways exist, some still undescribed, and some only recently elucidated. In addition, many genes implicated in the translocation step have not been assigned a specific function. Here, we will focus on the open questions regarding ER targeting and translocation, and discuss how combining classical biochemistry with systematic approaches can promote our understanding of these essential cellular steps.
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页码:8 / 17
页数:10
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