Inositol 1,4,5-trisphosphate signaling regulates mating behavior in Caenorhabditis elegans males

被引:26
|
作者
Gower, NJD
Walker, DS
Baylis, HA [1 ]
机构
[1] Univ Cambridge, Dept Zool, Cambridge CB2 3EJ, England
[2] Babraham Inst, Lab Receptor Signaling, Cambridge CB2 4AT, England
关键词
D O I
10.1091/mbc.E05-02-0096
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Complex behavior requires the coordinated action of the nervous system and nonneuronal targets. Male mating in Caenorhabditis elegans consists of a series of defined behavioral steps that lead to the physiological outcomes required for successful impregnation. We demonstrate that signaling mediated by inositol 1,4,5-trisphosphate (IP3) is required at several points during mating. Disruption of IP3 receptor (itr-1) function results in dramatic loss of male fertility, due to defects in turning behavior (during vulva location), spicule insertion and sperm transfer. To elucidate the signaling pathways responsible, we knocked down the six C. elegans genes encoding phospholipase C (PLC) family members. egl-8, which encodes PLC-beta, functions in spicule insertion and sperm transfer. itr-1 and egl-8 are widely expressed in the male reproductive system. An itr-1 gain-of-function mutation rescues infertility caused by egl-8 RNA interference, indicating that egl-8 and itr-1 function together as central components of the signaling events controlling sperm transfer.
引用
收藏
页码:3978 / 3986
页数:9
相关论文
共 50 条
  • [1] The inositol 1,4,5-trisphosphate receptor regulates epidermal cell migration in Caenorhabditis elegans
    Thomas-Virnig, CL
    Sims, PA
    Simske, JS
    Hardin, J
    CURRENT BIOLOGY, 2004, 14 (20) : 1882 - 1887
  • [2] Inositol 1,4,5-trisphosphate signaling regulates rhythmic contractile activity of myoepithelial sheath cells in Caenorhabditis elegans
    Yin, XY
    Gower, NJD
    Baylis, HA
    Strange, K
    MOLECULAR BIOLOGY OF THE CELL, 2004, 15 (08) : 3938 - 3949
  • [3] Inositol 1,4,5-Trisphosphate Signalling Regulates the Avoidance Response to Nose Touch in Caenorhabditis elegans
    Walker, Denise S.
    Vazquez-Manrique, Rafael P.
    Gower, Nicholas J. D.
    Gregory, Elizabeth
    Schafer, William R.
    Baylis, Howard A.
    PLOS GENETICS, 2009, 5 (09):
  • [4] Regulated disruption of inositol 1,4,5-trisphosphate signaling in Caenorhabditis elegans reveals new functions in feeding and embryogenesis
    Walker, DS
    Gower, NJD
    Ly, S
    Bradley, GL
    Baylis, HA
    MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (04) : 1329 - 1337
  • [5] Inositol 1,4,5-trisphosphate receptors and calcium signaling
    Michikawa, T
    Miyawaki, A
    Furuichi, T
    Mikoshiba, K
    CRITICAL REVIEWS IN NEUROBIOLOGY, 1996, 10 (01): : 39 - 55
  • [6] The inositol 1,4,5-trisphosphate receptors
    Bezprozvanny, I
    CELL CALCIUM, 2005, 38 (3-4) : 261 - 272
  • [7] INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR
    MIKOSHIBA, K
    TRENDS IN PHARMACOLOGICAL SCIENCES, 1993, 14 (03) : 86 - 89
  • [8] THE INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR
    MIKOSHIBA, K
    FURUICHI, T
    MIYAWAKI, A
    YOSHIKAWA, S
    MAEDA, N
    NIINOBE, M
    NAKADE, S
    NAKAGAWA, T
    OKANO, H
    ARUGA, J
    CIBA FOUNDATION SYMPOSIA, 1992, 164 : 17 - 35
  • [9] Activating calcium release through inositol 1,4,5-trisphosphate receptors without inositol 1,4,5-trisphosphate
    Bootman, MD
    Berridge, MJ
    Roderick, HL
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (11) : 7320 - 7322
  • [10] Selective determinants of inositol 1,4,5-trisphosphate and adenophostin A interactions with type 1 inositol 1,4,5-trisphosphate receptors
    Rossi, Ana M.
    Sureshan, Kana M.
    Riley, Andrew M.
    Potter, Barry V. L.
    Taylor, Colin W.
    BRITISH JOURNAL OF PHARMACOLOGY, 2010, 161 (05) : 1070 - 1085