Targeting and translocation of proteins to the endoplasmic reticulum at a glance

被引:89
|
作者
Aviram, Naama [1 ,2 ]
Schuldiner, Maya [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Genet, IL-7610001 Rehovot, Israel
[2] Rockefeller Univ, Lab Bacteriol, 1230 York Ave, New York, NY 10065 USA
基金
以色列科学基金会;
关键词
GET; Organelles; SND; SRP; Protein targeting; Endoplasmic reticulum; SIGNAL RECOGNITION PARTICLE; TAIL-ANCHORED PROTEINS; YEAST SACCHAROMYCES-CEREVISIAE; SYNTHESIZING SECRETORY PROTEIN; PEROXISOMAL MATRIX PROTEINS; INNER NUCLEAR-MEMBRANE; SRP RECEPTOR; ER MEMBRANE; DEPENDENT TRANSLOCATION; MICROSOMAL-MEMBRANES;
D O I
10.1242/jcs.204396
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The evolutionary emergence of organelles was a defining process in diversifying biochemical reactions within the cell and enabling multicellularity. However, compartmentalization also imposed a great challenge-the need to import proteins synthesized in the cytosol into their respective sites of function. For example, one-third of all genes encode for proteins that must be targeted and translocated into the endoplasmic reticulum (ER), which serves as the entry site to the majority of endomembrane compartments. Decades of research have set down the fundamental principles of how proteins get from the cytosol into the ER, and recent studies have brought forward new pathways and additional regulators enabling better definition of the rules governing substrate recognition. In this Cell Science at a Glance article and the accompanying poster, we give an overview of our current understanding of the multifaceted and regulated processes of protein targeting and translocation to the ER.
引用
下载
收藏
页码:4079 / 4085
页数:7
相关论文
共 50 条
  • [31] The environment of nascent secretory and membrane proteins at the endoplasmic reticulum membrane during translocation and integration
    Johnson, AE
    Liao, S
    Lin, J
    Hamman, B
    Do, H
    Cowie, A
    Andrews, DW
    COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1995, 60 : 71 - 82
  • [32] Targeting expression of expanded polyglutamine proteins to the endoplasmic reticulum or mitochondria prevents their aggregation
    Rousseau, E
    Dehay, B
    Ben-Haïem, A
    Trottier, Y
    Morange, M
    Bertolotti, A
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (26) : 9648 - 9653
  • [33] Identification of the endoplasmic reticulum targeting signal in vesicle-associated membrane proteins
    Kim, PK
    Hollerbach, C
    Trimble, WS
    Leber, B
    Andrews, DW
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (52) : 36876 - 36882
  • [34] TARGETING PROTEINS TO DIATOM PLASTIDS INVOLVES TRANSPORT THROUGH AN ENDOPLASMIC-RETICULUM
    BHAYA, D
    GROSSMAN, A
    MOLECULAR & GENERAL GENETICS, 1991, 229 (03): : 400 - 404
  • [35] Targeting expression of expanded polyglutamine proteins to the endoplasmic reticulum or mitochondria prevents their aggregation
    Erwann Rousseau
    Benjamin Dehay
    Léa Ben-Haïem
    Yvon Trottier
    Michel Morange
    Anne Bertolotti
    Microbial Cell Factories, 5 (Suppl 1)
  • [36] The host targeting motif in exported Plasmodium proteins is cleaved in the parasite endoplasmic reticulum
    Osborne, Andrew R.
    Speicher, Kaye D.
    Tamez, Pamela A.
    Bhattacharjee, Souvik
    Speicher, David W.
    Haldar, Kasturi
    MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2010, 171 (01) : 25 - 31
  • [37] Targeting endoplasmic reticulum-resident proteins for the treatment of B cell cancer
    Tang, Chih-Hang Anthony
    Del Valle, Juan R.
    Hu, Chih-Chi Andrew
    CANCER RESEARCH, 2019, 79 (13)
  • [38] Polypeptide translocation machinery of the yeast endoplasmic reticulum
    Lyman, SK
    Schekman, R
    EXPERIENTIA, 1996, 52 (12): : 1042 - 1049
  • [39] PROTEIN TRANSLOCATION ACROSS THE ENDOPLASMIC-RETICULUM
    NG, DTW
    WALTER, P
    CURRENT OPINION IN CELL BIOLOGY, 1994, 6 (04) : 510 - 516
  • [40] THE PROTEIN TRANSLOCATION MACHINERY OF THE ENDOPLASMIC-RETICULUM
    WALTER, P
    GILMORE, R
    MULLER, M
    BLOBEL, G
    PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1982, 300 (1099) : 225 - 228