Transducing touch in Caenorhabditis elegans

被引:114
作者
Goodman, MB [1 ]
Schwarz, EM
机构
[1] Stanford Univ, Sch Med, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
[2] CALTECH, Div Biol, Pasadena, CA 91125 USA
关键词
mechanosensation; ion channels; amiloride; DEG/ENaC channels; TRP channels;
D O I
10.1146/annurev.physiol.65.092101.142659
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Mechanosensation has been studied for decades, but understanding of its molecular mechanism is only now emerging from studies in Caenorhabditis elegans and Drosophila melanogaster. In both cases, the entry point proved to be genetic screens that allowed molecules needed for mechanosensation to be identified without any prior understanding of the likely components. In C. elegans, genetic screens revealed molecules needed for touch sensation along the body wall and other regions of force sensitivity. Members of two extensive membrane protein families have emerged as candidate sensory mechanotransduction channels: mec-4 and mec-10, which encode amiloride-sensitive channels (ASCs or DEG/ENaCs), and osm-9, which encodes a TRP ion channel. There are roughly 50 other members of these families whose functions in C. elegans are unknown. This article classifies these channels in C. elegans, with an emphasis on insights into their function derived from mutation. We also review the neuronal cell types in which these channels might be expressed and mediate mechanotransduction.
引用
收藏
页码:429 / 452
页数:26
相关论文
共 108 条
  • [1] Ripped pocket and pickpocket, novel Drosophila DEG/ENaC subunits expressed in early development and in mechanosensory neurons
    Adams, CM
    Anderson, MG
    Motto, DG
    Price, MP
    Johnson, WA
    Welsh, MJ
    [J]. JOURNAL OF CELL BIOLOGY, 1998, 140 (01) : 143 - 152
  • [2] The impulses produced by sensory nerve endings. Part I.
    Adrian, ED
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1926, 61 (01): : 49 - 72
  • [3] The impulses produced by sensory nerve-endings. Part 2. The response of a single end-organ.
    Adrian, ED
    Zotterman, Y
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1926, 61 (02): : 151 - 171
  • [4] The InterPro database, an integrated documentation resource for protein families, domains and functional sites
    Apweiler, R
    Attwood, TK
    Bairoch, A
    Bateman, A
    Birney, E
    Biswas, M
    Bucher, P
    Cerutti, T
    Corpet, F
    Croning, MDR
    Durbin, R
    Falquet, L
    Fleischmann, W
    Gouzy, J
    Hermjakob, H
    Hulo, N
    Jonassen, I
    Kahn, D
    Kanapin, A
    Karavidopoulou, Y
    Lopez, R
    Marx, B
    Mulder, NJ
    Oinn, TM
    Pagni, M
    Servant, F
    Sigrist, CJA
    Zdobnov, EM
    [J]. NUCLEIC ACIDS RESEARCH, 2001, 29 (01) : 37 - 40
  • [5] BARGMANN CI, 1990, COLD SPRING HARB SYM, V55, P529
  • [6] Barr MM, 1999, NATURE, V401, P386, DOI 10.1038/43913
  • [7] The Caenorhabditis elegans autosomal dominant polycystic kidney disease gene homologs lov-1 and pkd-2 act in the same pathway
    Barr, MM
    DeModena, J
    Braun, D
    Nguyen, CQ
    Hall, DH
    Sternberg, PW
    [J]. CURRENT BIOLOGY, 2001, 11 (17) : 1341 - 1346
  • [8] Bateman A, 2004, NUCLEIC ACIDS RES, V32, pD138, DOI [10.1093/nar/gkp985, 10.1093/nar/gkh121, 10.1093/nar/gkr1065]
  • [9] Brinkmann M, 1996, J COMP PHYSIOL A, V178, P125
  • [10] AMILORIDE-SENSITIVE EPITHELIAL NA+ CHANNEL IS MADE OF 3 HOMOLOGOUS SUBUNITS
    CANESSA, CM
    SCHILD, L
    BUELL, G
    THORENS, B
    GAUTSCHI, I
    HORISBERGER, JD
    ROSSIER, BC
    [J]. NATURE, 1994, 367 (6462) : 463 - 467