Coevolution of neuropeptidergic signaling systems: from worm to man

被引:46
作者
Janssen, Tom [1 ]
Lindemans, Marleen [1 ]
Meelkop, Ellen [1 ]
Temmerman, Liesbet [1 ]
Schoofs, Liliane [1 ]
机构
[1] KULeuven, Dept Biol, Funct Genom & Prote Unit, Louvain, Belgium
来源
PHYLOGENETIC ASPECTS OF NEUROPEPTIDES: FROM INVERTEBRATES TO HUMANS | 2010年 / 1200卷
关键词
coevolution; GPCR; neuropeptide; C; elegans; PROTEIN-COUPLED RECEPTORS; CAENORHABDITIS-ELEGANS; FUNCTIONAL-CHARACTERIZATION; GENE FAMILIES; DROSOPHILA; PEPTIDE; IDENTIFICATION; EXPRESSION; CHOLECYSTOKININ; ACTIVATION;
D O I
10.1111/j.1749-6632.2010.05506.x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Despite the general knowledge and repeated predictions of peptide G protein-coupled receptors following the elucidation of the Caenorhabditis elegans genome in 1998, only a few have been deorphanized so far. This was attributed to the apparent lack of coevolution between (neuro)peptides and their cognate receptors. To resolve this issue, we have used an in silico genomic data mining tool to identify the real putative peptide GPCRs in the C. elegans genome and then made a well-considered selection of orphan peptide GPCRs. To maximize our chances of a successful deorphanization, we adopted a combined reverse pharmacology approach. At this moment, we have successfully uncovered four C. elegans neuropeptide signaling systems that support the theory of receptor-ligand coevolution. All four systems are extremely well conserved within nematodes and show a high degree of similarity with their vertebrate and arthropod counterparts. Our data indicate that these four neuropeptide signaling systems have been well conserved during the course of evolution and that they were already well established prior to the divergence of protostomes and deuterostomes.
引用
收藏
页码:1 / 14
页数:14
相关论文
共 58 条
[1]   Tyramine functions independently of octopamine in the Caenorhabditis elegans nervous system [J].
Alkema, MJ ;
Hunter-Ensor, M ;
Ringstad, N ;
Horvitz, HR .
NEURON, 2005, 46 (02) :247-260
[2]   Vasoactive intestinal polypeptide mediates circadian rhythmicity and synchrony in mammalian clock neurons [J].
Aton, SJ ;
Colwell, CS ;
Harmar, AJ ;
Waschek, J ;
Herzog, ED .
NATURE NEUROSCIENCE, 2005, 8 (04) :476-483
[3]   Combining evidence using p-values: application to sequence homology searches [J].
Bailey, TL ;
Gribskov, M .
BIOINFORMATICS, 1998, 14 (01) :48-54
[4]   Neurobiology of the Caenorhabditis elegans genome [J].
Bargmann, CI .
SCIENCE, 1998, 282 (5396) :2028-2033
[5]   Neuromedin U and its receptors: Structure, function, and physiological roles [J].
Brighton, PJ ;
Szekeres, PG ;
Willars, GB .
PHARMACOLOGICAL REVIEWS, 2004, 56 (02) :231-248
[6]   Insect G protein-coupled receptors and signal transduction [J].
Broeck, JV .
ARCHIVES OF INSECT BIOCHEMISTRY AND PHYSIOLOGY, 2001, 48 (01) :1-12
[7]   Exploring the neurotransmitter labyrinth in nematodes [J].
Brownlee, DJA ;
Fairweather, I .
TRENDS IN NEUROSCIENCES, 1999, 22 (01) :16-24
[8]   The Drosophila gene CG9918 codes for a pyrokinin-1 receptor [J].
Cazzamali, G ;
Torp, M ;
Hauser, F ;
Williamson, M ;
Grimmelikhuijzen, CJP .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 335 (01) :14-19
[9]   VPAC receptor modulation of neuroexcitability in intracardiac neurons - Dependence on intracellular calcium mobilization and synergistic enhancement by PAC1 receptor activation [J].
DeHaven, W ;
Cuevas, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (39) :40609-40621
[10]   Cholecystokinin and gastrin receptors [J].
Dufresne, Marlene ;
Seva, Catherine ;
Fourmy, Daniel .
PHYSIOLOGICAL REVIEWS, 2006, 86 (03) :805-847