Mechanisms Determining the Morphology of the Peripheral ER

被引:409
作者
Shibata, Yoko [2 ,3 ]
Shemesh, Tom [1 ]
Prinz, William A. [4 ]
Palazzo, Alexander F. [2 ,5 ]
Kozlov, Michael M. [1 ]
Rapoport, Tom A. [2 ]
机构
[1] Tel Aviv Univ, Sackler Fac Med, Dept Physiol & Pharmacol, IL-69978 Tel Aviv, Israel
[2] Harvard Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[4] NIDDK, Lab Cell Biochem & Biol, NIH, Bethesda, MD 20892 USA
[5] Univ Toronto, Dept Biochem, Toronto, ON M5S 1A8, Canada
基金
以色列科学基金会;
关键词
ENDOPLASMIC-RETICULUM; MEMBRANE-PROTEINS; RIBOSOME RECEPTOR; ROUGH; BINDING; IDENTIFICATION; BIOSYNTHESIS; MICROTUBULES; ORGANIZATION; GTPASES;
D O I
10.1016/j.cell.2010.11.007
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
The endoplasmic reticulum (ER) consists of the nuclear envelope and a peripheral network of tubules and membrane sheets. The tubules are shaped by the curvature-stabilizing proteins reticulons and DP1/Yop1p, but how the sheets are formed is unclear. Here, we identify several sheet-enriched membrane proteins in the mammalian ER, including proteins that translocate and modify newly synthesized polypeptides, as well as coiled-coil membrane proteins that are highly upregulated in cells with proliferated ER sheets, all of which are localized by membrane-bound polysomes. These results indicate that sheets and tubules correspond to rough and smooth ER, respectively. One of the coiled-coil proteins, Climp63, serves as a "luminal ER spacer'' and forms sheets when overexpressed. More universally, however, sheet formation appears to involve the reticulons and DP1/Yop1p, which localize to sheet edges and whose abundance determines the ratio of sheets to tubules. These proteins may generate sheets by stabilizing the high curvature of edges.
引用
收藏
页码:774 / 788
页数:15
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