Yeast Vps55p, a functional homolog of human obesity receptor gene-related protein, is involved in late endosome to vacuole trafficking

被引:33
作者
Belgareh-Touzé, N
Avaro, S
Rouillé, Y
Hoflack, B
Haguenauer-Tsapis, R [1 ]
机构
[1] Univ Paris 06, Ctr Natl Rech Sci, Unite Mixte Rech, Jacques Monod Inst, F-7592 Paris 05, France
[2] Univ Paris 07, Ctr Natl Rech Sci, Unite Mixte Rech, Jacques Monod Inst, F-7592 Paris 05, France
[3] Ctr Natl Rech Sci, Pasteur Inst, F-59021 Lille, France
关键词
D O I
10.1091/mbc.01-12-0597
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Saccharomyces cerevisiae VPS55 (YJR044c) gene encodes a small protein of 140 amino acids with four potential transmembrane domains. VPS55 belongs to a family of genes of unknown function, including the human gene encoding the obesity receptor gene-related protein (OB-RGRP). Yeast cells with a disrupted VPS55 present normal vacuolar morphology, but exhibit an abnormal secretion of the Golgi form of the soluble vacuolar carboxypeptidase Y. However, trafficking of the membrane-bound vacuolar alkaline phosphatase remains normal. The endocytosis of uracil permease, used as an endocytic marker, is normal in vps55Delta cells, but its degradation is delayed and this marker transiently accumulates in late endosomal compartments. We also found that Vps55p is mainly localized in the late endosomes. Collectively, these results indicate that Vps55p is involved in late endosome to vacuole trafficking. Finally, we show that human OB-RGRP displays the same distribution as Vps55p and corrects the phenotypic defects of the vps55Delta strain. Therefore, the function of Vps55p has been conserved throughout evolution. This study highlights the importance of the multispanning Vps55p and OB-RGRP in membrane trafficking to the vacuole/lysosome of eukaryotic cells.
引用
收藏
页码:1694 / 1708
页数:15
相关论文
共 79 条
[1]   PEP4 GENE OF SACCHAROMYCES-CEREVISIAE ENCODES PROTEINASE-A, A VACUOLAR ENZYME REQUIRED FOR PROCESSING OF VACUOLAR PRECURSORS [J].
AMMERER, G ;
HUNTER, CP ;
ROTHMAN, JH ;
SAARI, GC ;
VALLS, LA ;
STEVENS, TH .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (07) :2490-2499
[2]   STRUCTURE AND FUNCTION OF THE YEAST VACUOLAR MEMBRANE PROTON ATPASE [J].
ANRAKU, Y ;
UMEMOTO, N ;
HIRATA, R ;
WADA, Y .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1989, 21 (05) :589-603
[3]   Mutants defective in secretory/vacuolar pathways in the EUROFAN collection of yeast disruptants [J].
Avaro, S ;
Belgareh-Touzé, N ;
Sibella-Argüelles, C ;
Volland, C ;
Haguenauer-Tsapis, R .
YEAST, 2002, 19 (04) :351-371
[4]   The leptin receptor promoter controls expression of a second distinct protein [J].
Bailleul, B ;
Akerblom, I ;
Strosberg, AD .
NUCLEIC ACIDS RESEARCH, 1997, 25 (14) :2752-2758
[5]   ISOLATION OF YEAST MUTANTS DEFECTIVE IN PROTEIN TARGETING TO THE VACUOLE [J].
BANKAITIS, VA ;
JOHNSON, LM ;
EMR, SD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (23) :9075-9079
[6]   Novel syntaxin homologue, Pep12p, required for the sorting of lumenal hydrolases to the lysosome-like vacuole in yeast [J].
Becherer, KA ;
Rieder, SE ;
Emr, SD ;
Jones, EW .
MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (04) :579-594
[7]   The sodium/proton exchanger Nhx1p is required for endosomal protein trafficking in the yeast Saccharomyces cerevisiae [J].
Bowers, K ;
Levi, BP ;
Patel, FI ;
Stevens, TH .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (12) :4277-4294
[8]   Vacuole biogenesis in Saccharomyces cerevisiae:: Protein transport pathways to the yeast vacuole [J].
Bryant, NJ ;
Stevens, TH .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1998, 62 (01) :230-+
[9]   THE CYTOPLASMIC TAIL DOMAIN OF THE VACUOLAR PROTEIN SORTING RECEPTOR VPS1OP AND A SUBSET OF VPS GENE-PRODUCTS REGULATE RECEPTOR STABILITY, FUNCTION, AND LOCALIZATION [J].
CEREGHINO, JL ;
MARCUSSON, EG ;
EMR, SD .
MOLECULAR BIOLOGY OF THE CELL, 1995, 6 (09) :1089-1102
[10]   VIP17/MAL, a lipid raft-associated protein, is involved in apical transport in MDCK cells [J].
Cheong, KH ;
Zacchetti, D ;
Schneeberger, EE ;
Simons, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (11) :6241-6248