Deciphering endocytosis in Caenorhabditis elegans

被引:61
作者
Fares, H
Grant, B
机构
[1] Rutgers State Univ, Dept Mol Biol & Biochem, Nelson Biol Labs, Piscataway, NJ 08854 USA
[2] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85721 USA
关键词
C; elegans; coelomocyte; cup-5; endocytosis; mucolipins; oocyte; recycling; Rme-1; Rme-2; Rme-8;
D O I
10.1034/j.1600-0854.2002.30103.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We discuss in this review recent studies using the worm Caenorhabditis elegans to decipher endocytic trafficking in a multicellular organism. Recent advances, including in vivo assay systems, new genetic screens, comparative functional analysis of conserved proteins, and RNA-mediated interference (RNAi) in C. elegans, are being used to study the functions of known membrane trafficking factors and to identify new ones. The ability to monitor endocytosis in vivo in worms allows one to test current endocytosis models and to demonstrate the physiological significance of factors identified by genetic and biochemical methods. The available human genome sequence facilitates comparative studies where human homologs of new factors identified in C. elegans can be quickly assayed for similar function using traditional cell biological methods in mammalian cell systems. New studies in C. elegans have used a combination of these techniques to reveal novel metazoan-specific trafficking factors required for endocytosis. Many more metazoan-specific trafficking factors and insights into the mechanisms of endocytosis are likely to be uncovered by analysis in C elegans.
引用
收藏
页码:11 / 19
页数:9
相关论文
共 59 条
  • [1] Mucolipidosis type IV
    Bach, G
    [J]. MOLECULAR GENETICS AND METABOLISM, 2001, 73 (03) : 197 - 203
  • [3] Identification of the gene causing mucolipidosis type IV
    Bargal, R
    Avidan, N
    Ben-Asher, E
    Olender, Z
    Zeigler, M
    Frumkin, A
    Raas-Rothschild, A
    Glusman, G
    Lancet, D
    Bach, G
    [J]. NATURE GENETICS, 2000, 26 (01) : 118 - 121
  • [4] Cloning of the gene encoding a novel integral membrane protein, mucolipidin - and identification of the two major founder mutations causing mucolipidosis type IV
    Bassi, MT
    Manzoni, M
    Monti, E
    Pizzo, MT
    Ballabio, A
    Borsani, G
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (05) : 1110 - 1120
  • [5] FINE-STRUCTURE OF CELOMOCYTE OF ADULT ASCARIS-SUUM
    BOLLA, RI
    WEINSTEIN, PP
    CAIN, GD
    [J]. JOURNAL OF PARASITOLOGY, 1972, 58 (06) : 1025 - 1036
  • [6] Bossinger O, 1996, INT J DEV BIOL, V40, P431
  • [7] CELL CELL COMMUNICATION IN THE EMBRYO OF CAENORHABDITIS-ELEGANS
    BOSSINGER, O
    SCHIERENBERG, E
    [J]. DEVELOPMENTAL BIOLOGY, 1992, 151 (02) : 401 - 409
  • [8] Fluoxetine-resistant mutants in C-elegans define a novel family of transmembrane proteins
    Choy, RKM
    Thomas, JH
    [J]. MOLECULAR CELL, 1999, 4 (02) : 143 - 152
  • [9] CHRISTENSEN MT, 2001, IN PRESS J BIOL CHEM
  • [10] A common set of engulfment genes mediates removal of both apoptotic and necrotic cell corpses in C-elegans
    Chung, SB
    Gumienny, TL
    Hengartner, MO
    Driscoll, M
    [J]. NATURE CELL BIOLOGY, 2000, 2 (12) : 931 - 937