Homologs of the yeast Sec complex subunits Sec62p and Sec63p are abundant proteins in dog pancreas microsomes

被引:129
作者
Tyedmers, J
Lerner, M
Bies, C
Dudek, J
Skowronek, MH
Haas, IG
Heim, N
Nastainczyk, W
Volkmer, J
Zimmermann, R [1 ]
机构
[1] Univ Saarland, D-66421 Homburg, Germany
[2] Biochem Zentrum Heidelberg, D-69120 Heidelberg, Germany
关键词
D O I
10.1073/pnas.97.13.7214
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cotranslational protein transport into dog pancreas microsomes involves the Sec61p complex plus a luminal heat shock protein 70, Posttranslational protein transport into the yeast endoplasmic reticulum (ER) involves the so-called Sec complex in the membrane, comprising a similar Sec61p subcomplex, the putative signal peptide receptor subcomplex, and the heat shock protein 40-type subunit, Sec63p, plus a luminal heat shock protein 70, Recently, human homologs of yeast proteins Sec62p and Sec63p were discovered. Here we determined the concentrations of these two membrane proteins in dog pancreas microsomes and observed that the canine homologs of yeast proteins Sec62p and Sec63p are abundant proteins, present in almost equimolar concentrations as compared with Sec61 alpha p monomers, Furthermore, we detected fractions of these two proteins in association with each other as well as with the Sec61p complex, The J domain of the human Sec63p was shown to interact with immunoglobulin heavy chain binding protein. Thus, the membrane of the mammalian ER contains components, known from the posttranslationally operating protein translocase in yeast. We suggest that these components are required for efficient cotranslational protein transport into the mammalian ER as well as for other transport processes.
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页码:7214 / 7219
页数:6
相关论文
共 40 条
[1]  
Baxter BK, 1996, MOL CELL BIOL, V16, P6444
[2]   A Scj1p homolog and folding catalysts present in dog pancreas microsomes [J].
Bies, C ;
Guth, S ;
Janoschek, K ;
Nastainczyk, W ;
Volkmer, J ;
Zimmermann, R .
BIOLOGICAL CHEMISTRY, 1999, 380 (10) :1175-1182
[3]   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
[4]   The lumenal domain of Sec63p stimulates the ATPase activity of BiP and mediates BiP recruitment to the translocon in Saccharomyces cerevisiae [J].
Corsi, AK ;
Schekman, R .
JOURNAL OF CELL BIOLOGY, 1997, 137 (07) :1483-1493
[5]   A novel Hsp7O of the yeast ER lumen is required for the efficient translocation of a number of protein precursors [J].
Craven, RA ;
Egerton, M ;
Stirling, CJ .
EMBO JOURNAL, 1996, 15 (11) :2640-2650
[6]   Identification of a human cDNA homologue to the Drosophila translocation protein 1 (Dtrp1) [J].
Daimon, M ;
Susa, S ;
Suzuki, K ;
Kato, T ;
Yamatani, K ;
Sasaki, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 230 (01) :100-104
[7]   SEC62 ENCODES A PUTATIVE MEMBRANE-PROTEIN REQUIRED FOR PROTEIN TRANSLOCATION INTO THE YEAST ENDOPLASMIC-RETICULUM [J].
DESHAIES, RJ ;
SCHEKMAN, R .
JOURNAL OF CELL BIOLOGY, 1989, 109 (06) :2653-2664
[8]   ASSEMBLY OF YEAST SEC PROTEINS INVOLVED IN TRANSLOCATION INTO THE ENDOPLASMIC-RETICULUM INTO A MEMBRANE-BOUND MULTISUBUNIT COMPLEX [J].
DESHAIES, RJ ;
SANDERS, SL ;
FELDHEIM, DA ;
SCHEKMAN, R .
NATURE, 1991, 349 (6312) :806-808
[9]   A YEAST MUTANT DEFECTIVE AT AN EARLY STAGE IN IMPORT OF SECRETORY PROTEIN PRECURSORS INTO THE ENDOPLASMIC-RETICULUM [J].
DESHAIES, RJ ;
SCHEKMAN, R .
JOURNAL OF CELL BIOLOGY, 1987, 105 (02) :633-645
[10]   A microsomal ATP-binding protein involved in efficient protein transport into the mammalian endoplasmic reticulum [J].
Dierks, T ;
Volkmer, J ;
Schlenstedt, G ;
Jung, C ;
Sandholzer, U ;
Zachmann, K ;
Schlotterhose, P ;
Neifer, K ;
Schmidt, B ;
Zimmermann, R .
EMBO JOURNAL, 1996, 15 (24) :6931-6942