PEX3 functions as a PEX19 docking factor in the import of class I peroxisomal membrane proteins

被引:175
作者
Fang, Y [1 ]
Morrell, JC [1 ]
Jones, JM [1 ]
Gould, SJ [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA
关键词
PMP import; temperature-sensitive mutants; Zellweger syndrome; organelle biogenesis; protein import;
D O I
10.1083/jcb.200311131
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
PEX19 is a chaperone and import receptor for newly synthesized, class I peroxisomal membrane proteins (PMPs). PEX19 binds these PMPs in the cytoplasm and delivers them to the peroxisome for subsequent insertion into the peroxisome membrane, indicating that there may be a PEX19 docking factor in the peroxisome membrane. Here we show that PEX3 is required for PEX19 to dock at peroxisomes, interacts specifically with the docking domain of PEX19, and is required for recruitment of the PEX19 docking domain to peroxisomes. PEX3 is also sufficient to dock PEX19 at heterologous organelles and binds PEX19 via a conserved motif that is essential for this docking activity and for PEX3 function in general. Not surprisingly, transient inhibition of PEX3 abrogates class I PMP import but has no effect on class II PMP import or peroxisomal matrix protein import. Taken together, these results suggest that PEX3 plays a selective, essential, and direct role in PMP import as a docking factor for PEX19.
引用
收藏
页码:863 / 875
页数:13
相关论文
共 55 条
[1]   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
[2]  
BAKERBRACHMANN C, 1998, YEAST, V14, P115
[3]   Two different targeting signals direct human peroxisomal membrane protein 22 to peroxisomes [J].
Brosius, U ;
Dehmel, T ;
Gärtner, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (01) :774-784
[4]   PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import [J].
Chang, CC ;
Warren, DS ;
Sacksteder, KA ;
Gould, SJ .
JOURNAL OF CELL BIOLOGY, 1999, 147 (04) :761-773
[5]  
Chang CC, 1999, J CELL SCI, V112, P1579
[6]   Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders [J].
Chang, CC ;
Lee, WH ;
Moser, H ;
Valle, D ;
Gould, SJ .
NATURE GENETICS, 1997, 15 (04) :385-388
[7]   Rab8b and its interacting partner TRIP8b are involved in regulated secretion in AtT20 cells [J].
Chen, S ;
Liang, MC ;
Chia, JN ;
Ngsee, JK ;
Ting, AE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (16) :13209-13216
[8]   IN-VITRO INSERTION OF THE 22-KD PEROXISOMAL MEMBRANE-PROTEIN INTO ISOLATED RAT-LIVER PEROXISOMES [J].
DIESTELKOTTER, P ;
JUST, WW .
JOURNAL OF CELL BIOLOGY, 1993, 123 (06) :1717-1725
[9]   Unified nomenclature for peroxisome biogenesis factors [J].
Distel, B ;
Erdmann, R ;
Gould, SJ ;
Blobel, G ;
Crane, DI ;
Cregg, JM ;
Dodt, G ;
Fujiki, Y ;
Goodman, JM ;
Just, WW ;
Kiel, JAKW ;
Kunau, WH ;
Lazarow, PB ;
Mannaerts, GP ;
Moser, HW ;
Osumi, T ;
Rachubinski, RA ;
Roscher, A ;
Subramani, S ;
Tabak, HF ;
Tsukamoto, T ;
Valle, D ;
vanderKlei, I ;
vanVeldhoven, PP ;
Veenhuis, M .
JOURNAL OF CELL BIOLOGY, 1996, 135 (01) :1-3
[10]   MUTATIONS IN THE PTS1 RECEPTOR GENE, PXR1, DEFINE COMPLEMENTATION GROUP-2 OF THE PEROXISOME BIOGENESIS DISORDERS [J].
DODT, G ;
BRAVERMAN, N ;
WONG, C ;
MOSER, A ;
MOSER, HW ;
WATKINS, P ;
VALLE, D ;
GOULD, SJ .
NATURE GENETICS, 1995, 9 (02) :115-125