A conserved function of YidC in the biogenesis of respiratory chain complexes

被引:126
作者
van der Laan, M
Urbanus, ML
ten Hagen-Jongman, CM
Nouwen, N
Oudega, B
Harms, N
Driessen, AJM
Luirink, J
机构
[1] Vrije Univ Amsterdam, Fac Earth & Life Sci, Dept Mol Microbiol, NL-1081 HV Amsterdam, Netherlands
[2] Univ Groningen, Groningen Biomol Sci & Biotechnol Inst, Dept Microbiol, NL-9751 NN Haren, Netherlands
关键词
D O I
10.1073/pnas.0636761100
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
The Escherichia coli inner membrane protein (IMP) YidC is involved in the membrane integration of IMPS both in concert with and independently from the Sec translocase. YidC seems to be dispensable for the assembly of Sec-dependent IMPS, and so far it has been shown to be essential only for the proper Sec-independent integration of some phage coat proteins. Here, we studied the physiological consequences of YidC depletion in an effort to understand the essential function of YidC. The loss of YidC rapidly and specifically induced the Psp stress response, which is accompanied by a reduction of the proton-motive force. This reduction is due to defects in the functional assembly of cytochrome o oxidase and the F1Fo ATPase complex, which is reminiscent of the effects of mutations in the yidC homologue OXA1 in the yeast mitochondrial inner membrane. The integration of CyoA (subunit II of the cytochrome o oxidase) and F(o)c (membrane subunit of the F1Fo ATPase) appeared exceptionally sensitive to depletion of YidC, suggesting that these IMPS are natural substrates of a membrane integration and assembly pathway in which YidC plays an exclusive or at least a pivotal role.
引用
收藏
页码:5801 / 5806
页数:6
相关论文
共 40 条
[1]   YidC, an assembly site for polytopic Escherichia coli membrane proteins located in immediate proximity to the SecYE translocon and lipids [J].
Beck, K ;
Eisner, G ;
Trescher, D ;
Dalbey, RE ;
Brunner, J ;
Müller, M .
EMBO REPORTS, 2001, 2 (08) :709-714
[2]   OXA1, A SACCHAROMYCES-CEREVISIAE NUCLEAR GENE WHOSE SEQUENCE IS CONSERVED FROM PROKARYOTES TO EUKARYOTES CONTROLS CYTOCHROME-OXIDASE BIOGENESIS [J].
BONNEFOY, N ;
CHALVET, F ;
HAMEL, P ;
SLONIMSKI, PP ;
DUJARDIN, G .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 239 (02) :201-212
[3]   THE TRANSLOCATION OF NEGATIVELY CHARGED RESIDUES ACROSS THE MEMBRANE IS DRIVEN BY THE ELECTROCHEMICAL POTENTIAL - EVIDENCE FOR AN ELECTROPHORESIS-LIKE MEMBRANE TRANSFER MECHANISM [J].
CAO, GQ ;
KUHN, A ;
DALBEY, RE .
EMBO JOURNAL, 1995, 14 (05) :866-875
[4]   Differential use of the signal recognition particle translocase targeting pathway for inner membrane protein assembly in Escherichia coli [J].
de Gier, JWL ;
Scotti, PA ;
Sääf, A ;
Valent, QA ;
Kuhn, A ;
Luirink, J ;
von Heijne, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14646-14651
[5]   OPTIMAL POSTTRANSLATIONAL TRANSLOCATION OF THE PRECURSOR OF PHOE PROTEIN ACROSS ESCHERICHIA-COLI MEMBRANE-VESICLES REQUIRES BOTH ATP AND THE PROTONMOTIVE FORCE [J].
DEVRIJE, T ;
TOMMASSEN, J ;
DEKRUIJFF, B .
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 900 (01) :63-72
[6]   DIRECT INTERACTION BETWEEN LINEAR ELECTRON-TRANSFER CHAINS AND SOLUTE TRANSPORT-SYSTEMS IN BACTERIA [J].
ELFERINK, MGL ;
HELLINGWERF, KJ ;
VANBELKUM, MJ ;
POOLMAN, B ;
KONINGS, WN .
FEMS MICROBIOLOGY LETTERS, 1984, 21 (03) :293-298
[7]  
ERECHAGA I, 2002, FEBS LETT, V515, P189
[8]  
Gennis R., 1996, ESCHERICHIA COLI SAL, V1, P217
[9]   Oxa1p acts as a general membrane insertion machinery for proteins encoded by mitochondrial DNA [J].
Hell, K ;
Neupert, W ;
Stuart, RA .
EMBO JOURNAL, 2001, 20 (06) :1281-1288
[10]   New prospects in studying the bacterial signal recognition particle pathway [J].
Herskovits, AA ;
Bochkareva, ES ;
Bibi, E .
MOLECULAR MICROBIOLOGY, 2000, 38 (05) :927-939