Inositol 1,4,5-Trisphosphate Signalling Regulates the Avoidance Response to Nose Touch in Caenorhabditis elegans

被引:23
作者
Walker, Denise S. [1 ,2 ]
Vazquez-Manrique, Rafael P. [1 ]
Gower, Nicholas J. D. [1 ]
Gregory, Elizabeth [1 ]
Schafer, William R. [2 ]
Baylis, Howard A. [1 ]
机构
[1] Univ Cambridge, Dept Zool, Cambridge, England
[2] MRC Lab Mol Biol, Cambridge, England
来源
PLOS GENETICS | 2009年 / 5卷 / 09期
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
C-ELEGANS; NERVOUS-SYSTEM; CHEMICAL REPELLENTS; GLUTAMATE-RECEPTOR; PHOSPHOLIPASE-C; ASH NEURONS; IN-VIVO; CHANNELS; PROTEINS; GENE;
D O I
10.1371/journal.pgen.1000636
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
When Caenorhabditis elegans encounters an unfavourable stimulus at its anterior, it responds by initiating an avoidance response, namely reversal of locomotion. The amphid neurons, ASHL and ASHR, are polymodal in function, with roles in the avoidance responses to high osmolarity, nose touch, and both volatile and non-volatile repellents. The mechanisms that underlie the ability of the ASH neurons to respond to such a wide range of stimuli are still unclear. We demonstrate that the inositol 1,4,5-trisphosphate receptor (IP3R), encoded by itr-1, functions in the reversal responses to nose touch and benzaldehyde, but not in other known ASH-mediated responses. We show that phospholipase C beta (EGL-8) and phospholipase C gamma (PLC-3), which catalyse the production of IP3, both function upstream of ITR-1 in the response to nose touch. We use neuron-specific gene rescue and neuron-specific disruption of protein function to show that the site of ITR-1 function is the ASH neurons. By rescuing plc-3 and egl-8 in a neuron-specific manner, we show that both are acting in ASH. Imaging of nose touch-induced Ca2+ transients in ASH confirms these conclusions. In contrast, the response to benzaldehyde is independent of PLC function. Thus, we have identified distinct roles for the IP3R in two specific responses mediated by ASH.
引用
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页数:10
相关论文
共 47 条
[1]  
BARGMANN CI, 1990, COLD SH Q B, V55, P529
[2]   Inositol 1,4,5-trisphosphate receptors are strongly expressed in the nervous system, pharynx, intestine, gonad and excretory cell of Caenorhabditis elegans and are encoded by a single gene (itr-1) [J].
Baylis, HA ;
Furuichi, T ;
Yoshikawa, F ;
Mikoshiba, K ;
Sattelle, DB .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 294 (02) :467-476
[3]  
CHALFIE M, 1985, J NEUROSCI, V5, P956
[4]   Feeding status and serotonin rapidly and reversibly modulate a Caenorhabditis elegans chemosensory circuit [J].
Chao, MY ;
Komatsu, H ;
Fukuto, HS ;
Dionne, HM ;
Hart, AC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (43) :15512-15517
[5]   Inositol trisphosphate mediates a RAS-independent response to LET-23 receptor tyrosine kinase activation in C-elegans [J].
Clandinin, TR ;
DeModena, JA ;
Sternberg, PW .
CELL, 1998, 92 (04) :523-533
[6]  
Colbert HA, 1997, J NEUROSCI, V17, P8259
[7]   Eph and NMDA receptors control Ca2+/calmodulin-dependent protein kinase II activation during C-elegans oocyte meiotic maturation [J].
Corrigan, C ;
Subramanian, R ;
Miller, MA .
DEVELOPMENT, 2005, 132 (23) :5225-5237
[8]  
CULOTTI JG, 1978, GENETICS, V90, P243
[9]   The inositol trisphosphate receptor regulates a 50-second behavioral rhythm in C-elegans [J].
Dal Santo, P ;
Logan, MA ;
Chisholm, AD ;
Jorgensen, EM .
CELL, 1999, 98 (06) :757-767
[10]   Neuronal substrates of complex behaviors in C-elegans [J].
de Bono, M ;
Maricq, AV .
ANNUAL REVIEW OF NEUROSCIENCE, 2005, 28 :451-501