Saccharomyces cerevisiae Pex14p contains two independent Pex5p binding sites, which are both essential for PTS1 protein import

被引:27
作者
Williams, C [1 ]
van den Berg, M [1 ]
Distel, B [1 ]
机构
[1] Acad Med Ctr, Dept Med Biochem, NL-1105 AZ Amsterdam, Netherlands
来源
FEBS LETTERS | 2005年 / 579卷 / 16期
关键词
peroxisome; Pex14p; Pex5p; WxxxF/Y motif; protein import;
D O I
10.1016/j.febslet.2005.05.011
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
Pex14p is a peroxisomal membrane-associated protein involved in docking of both Pex5p and Pex7p to the peroxisomal membrane. Previous studies have shown that, in humans, the N-terminal region of Pex14p interacts with WxxxF/Y motifs in Pex5p. Here, we report that Saccharomyces cerevisiae Pex14p contains two independent Pex5p binding sites, one in the N- and one in the C-terminus. Using deletion analysis we show that, in vivo, both of these interactions are needed for PTS1 import. Furthermore, we show that the characterized WxxxF/Y motifs of Pex5p are not essential for binding to the N-terminus of Pex14p but do play a role in the interaction with the Pex14 C-terminus. Thus, the data suggest that the mechanism of the Pex14p-Pex5p interaction in yeast is different from that previously reported for humans. (c) 2005 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3416 / 3420
页数:5
相关论文
共 26 条
[1]   Pex8p:: An intraperioxisomal organizer of the peroxisomal import machinery [J].
Agne, B ;
Meindl, NM ;
Niederhoff, K ;
Einwächter, H ;
Rehling, P ;
Sickmann, A ;
Meyer, HE ;
Girzalsky, W ;
Kunau, WH .
MOLECULAR CELL, 2003, 11 (03) :635-646
[2]   Pex14p, a peroxisomal membrane protein binding both receptors of the two PTS-dependent import pathways [J].
Albertini, M ;
Rehling, P ;
Erdmann, R ;
Girzalsky, W ;
Kiel, JAKW ;
Veenhuis, M ;
Kunau, WH .
CELL, 1997, 89 (01) :83-92
[3]   Saccharomyces cerevisiae PTS1 receptor Pex5p interacts with the SH3 domain of the peroxisomal membrane protein Pex13p in an unconventional, non-PXXP-related manner [J].
Bottger, G ;
Barnett, P ;
Klein, ATJ ;
Kragt, A ;
Tabak, HF ;
Distel, B .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (11) :3963-3976
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   PROTEIN-INTERACTION CLONING IN YEAST - IDENTIFICATION OF MAMMALIAN PROTEINS THAT REACT WITH THE LEUCINE ZIPPER OF JUN [J].
CHEVRAY, PM ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (13) :5789-5793
[6]   Analysis of the sequence motifs responsible for the interactions of peroxins 14 and 5, which are involved in glycosome biogenesis in Trypanosoma brucei [J].
Choe, J ;
Moyersoen, J ;
Roach, C ;
Carter, TL ;
Fan, E ;
Michels, PAM ;
Hol, WGJ .
BIOCHEMISTRY, 2003, 42 (37) :10915-10922
[7]   Multiple PEX genes are required for proper subcellular distribution and stability of Pex5p, the PTS1 receptor: Evidence that PTS1 protein import is mediated by a cycling receptor [J].
Dodt, G ;
Gould, SJ .
JOURNAL OF CELL BIOLOGY, 1996, 135 (06) :1763-1774
[8]  
ELGERSMA Y, 1993, GENETICS, V135, P731
[9]  
Gatto GJ, 2000, NAT STRUCT BIOL, V7, P1091
[10]   MUTATIONAL ANALYSIS OF THE N-TERMINAL TOPOGENIC SIGNAL OF WATERMELON GLYOXYSOMAL MALATE-DEHYDROGENASE USING THE HETEROLOGOUS HOST HANSENULA-POLYMORPHA [J].
GIETL, C ;
FABER, KN ;
VANDERKLEI, IJ ;
VEENHUIS, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (08) :3151-3155