Chemical sensitivity in Caenorhabditis elegans

被引:18
作者
Bergarnasco, C. [1 ]
Bazzicalupo, P. [1 ]
机构
[1] CNR, Inst Genet & Biofis A Buzzatti Traverso, I-80131 Naples, Italy
关键词
taste; smell; chemoreceptor genes; G protein signalling; RGS proteins; chemical coding; chemical discrimination;
D O I
10.1007/s00018-006-6114-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The small nematode Caenorhabditis elegans lives in the soil, where mechanical, thermal and most of all chemical stimuli strongly influence its behavior. Here we briefly review how chemical sensitivity is organized at the cellular and molecular level in this organism. C. elegans has less than 40 chemosensory neurons. With few exceptions each neuron senses more than one substance and each substance is sensed by more than one neuron. At the molecular level, as in other organisms, also in C elegans, seven transmembrane G-protein-coupled receptors (GPCRs), heterotrimeric G proteins, cyclic nucleotidegated ion channels, TRP channels and Call play crucial roles in chemical sensitivity. An unusual feature, possibly due to C. elegans strong dependence on chemical cues, is the very large number of GPCR chemoreceptor genes (1300-1700) coded in its genome. Genetic approaches have also allowed the identification of new molecules involved in chemical sensitivity that would not have been discovered otherwise. In addition to the basic factors involved in primary signalling, the studies in C. elegans have revealed a network of regulatory pathways and molecules suggesting that fine modulation of the responsiveness of neurons is important, possibly to allow worms to negotiate a continuously changing environment. The experimental versatility of C. elegans has made it possible, in many cases, to determine precisely in which neuron a given molecule or pathway is required and for which biological response. This type of information can contribute to the general field of sensory signalling because it provides correlations between the biochemical properties of molecules and their cellular functions and between these and the in vivo behavioral responses of the animal.
引用
收藏
页码:1510 / 1522
页数:13
相关论文
共 63 条
[11]  
Colbert HA, 1997, J NEUROSCI, V17, P8259
[12]   Proteins interacting with Caenorhabditis elegans Gα subunits [J].
Cuppen, E ;
van der Linden, AM ;
Jansen, G ;
Plasterk, RHA .
COMPARATIVE AND FUNCTIONAL GENOMICS, 2003, 4 (05) :479-491
[13]   Neuronal substrates of complex behaviors in C-elegans [J].
de Bono, M ;
Maricq, AV .
ANNUAL REVIEW OF NEUROSCIENCE, 2005, 28 :451-501
[14]   Odorant receptor localization to olfactory cilia is mediated by ODR-4, a novel membrane-associated protein [J].
Dwyer, ND ;
Troemel, ER ;
Sengupta, P ;
Bargmann, CI .
CELL, 1998, 93 (03) :455-466
[15]  
Fujiwara M, 1999, DEVELOPMENT, V126, P4839
[16]   G protein-coupled receptor kinase function is essential for chemosensation in C-elegans [J].
Fukuto, HS ;
Ferkey, DM ;
Apicella, AJ ;
Lans, H ;
Sharmeen, T ;
Chen, W ;
Lefkowitz, RJ ;
Jansen, G ;
Schafer, WR ;
Hart, AC .
NEURON, 2004, 42 (04) :581-593
[17]   Dopaminergic supersensitivity in G protein-coupled receptor kinase 6-deficient mice [J].
Gainetdinov, RR ;
Bohn, LM ;
Sotnikova, TD ;
Cyr, M ;
Laakso, A ;
Macrae, AD ;
Torres, GE ;
Kim, KM ;
Lefkowitz, RJ ;
Caron, MG ;
Premont, RT .
NEURON, 2003, 38 (02) :291-303
[18]   Oxygen sensation and social feeding mediated by a C-elegans guanylate cyclase homologue [J].
Gray, JM ;
Karow, DS ;
Lu, H ;
Chang, AJ ;
Chang, JS ;
Ellis, RE ;
Marletta, MA ;
Bargmann, CI .
NATURE, 2004, 430 (6997) :317-322
[19]  
Hart AC, 1999, J NEUROSCI, V19, P1952
[20]   In vivo imaging of C-elegans ASH neurons:: cellular response and adaptation to chemical repellents [J].
Hilliard, MA ;
Apicella, AJ ;
Kerr, R ;
Suzuki, H ;
Bazzicalupo, P ;
Schafer, WR .
EMBO JOURNAL, 2005, 24 (01) :63-72