Embracing the void-how much do we really know about targeting and translocation to the endoplasmic reticulum?

被引:32
作者
Aviram, Naama [1 ]
Schuldiner, Maya [1 ]
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.
引用
收藏
页码:8 / 17
页数:10
相关论文
共 106 条
[1]   Novel Role of Calmodulin in Regulating Protein Transport to Mitochondria in a Unicellular Eukaryote [J].
Aich, Abhishek ;
Shaha, Chandrima .
MOLECULAR AND CELLULAR BIOLOGY, 2013, 33 (22) :4579-4593
[2]   All roads lead to Rome (but some may be harder to travel): SRP-independent translocation into the endoplasmic reticulum [J].
Ast, Tslil ;
Schuldiner, Maya .
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2013, 48 (03) :273-288
[3]   A Network of Cytosolic Factors Targets SRP-Independent Proteins to the Endoplasmic Reticulum [J].
Ast, Tslil ;
Cohen, Galit ;
Schuldiner, Maya .
CELL, 2013, 152 (05) :1134-1145
[4]   Structure of Monomeric Yeast and Mammalian Sec61 Complexes Interacting with the Translating Ribosome [J].
Becker, Thomas ;
Bhushan, Shashi ;
Jarasch, Alexander ;
Armache, Jean-Paul ;
Funes, Soledad ;
Jossinet, Fabrice ;
Gumbart, James ;
Mielke, Thorsten ;
Berninghausen, Otto ;
Schulten, Klaus ;
Westhof, Eric ;
Gilmore, Reid ;
Mandon, Elisabet C. ;
Beckmann, Roland .
SCIENCE, 2009, 326 (5958) :1369-1373
[5]   Architecture of the protein-conducting channel associated with the translating 80S ribosome [J].
Beckmann, R ;
Spahn, CMT ;
Eswar, N ;
Helmers, J ;
Penczek, PA ;
Sali, A ;
Frank, J ;
Blobel, G .
CELL, 2001, 107 (03) :361-372
[6]   BiP Modulates the Affinity of Its Co-chaperone ERj1 for Ribosomes [J].
Benedix, Julia ;
Lajoie, Patrick ;
Jaiswal, Himjyot ;
Burgard, Carsten ;
Greiner, Markus ;
Zimmermann, Richard ;
Rospert, Sabine ;
Snapp, Erik L. ;
Dudek, Johanna .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (47) :36427-36433
[8]   ERj1p uses a universal ribosomal adaptor site to coordinate the 80S ribosome at the membrane [J].
Blau, M ;
Mullapudi, S ;
Becker, T ;
Dudek, J ;
Zimmermann, R ;
Penczek, PA ;
Beckmann, R .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2005, 12 (11) :1015-1016
[9]   A SEC63P-BIP COMPLEX FROM YEAST IS REQUIRED FOR PROTEIN TRANSLOCATION IN A RECONSTITUTED PROTEOLIPOSOME [J].
BRODSKY, JL ;
SCHEKMAN, R .
JOURNAL OF CELL BIOLOGY, 1993, 123 (06) :1355-1363
[10]   BIP AND SEC63P ARE REQUIRED FOR BOTH CO- AND POSTTRANSLATIONAL PROTEIN TRANSLOCATION INTO THE YEAST ENDOPLASMIC-RETICULUM [J].
BRODSKY, JL ;
GOECKELER, J ;
SCHEKMAN, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (21) :9643-9646