Functional and Nonfunctional Forms of CquiOR91, an Odorant Selectivity Subunit of Culex quinquefasciatus

被引:7
作者
Hughes, David T. [1 ,3 ]
Pelletier, Julien [2 ,4 ]
Rahman, Suhaila [1 ]
Chen, Sisi [1 ,5 ]
Leal, Walter S. [2 ]
Luetje, Charles W. [1 ]
机构
[1] Univ Miami, Dept Mol & Cellular Pharmacol, Miller Sch Med, R-189,POB 016189, Miami, FL 33101 USA
[2] Univ Calif Davis, Dept Mol & Cellular Biol, 1 Shields Ave, Davis, CA 95616 USA
[3] Ohio State Univ, Dept Internal Med, Wexner Med Ctr, Columbus, OH 43210 USA
[4] Keele Univ, Sch Life Sci, Keele ST5 5BG, Staffs, England
[5] Leidos Biomed Res Inc, Rockville, MD 20892 USA
基金
美国国家卫生研究院;
关键词
electrophysiology; insect; olfaction; polymorphism; receptor; Xenopus oocytes; MOSQUITO ANOPHELES-GAMBIAE; SOUTHERN HOUSE MOSQUITO; RECEPTOR GENE; CARBON-DIOXIDE; DROSOPHILA; CALIFORNIA; OLFACTION; DIPTERA; HUMANS; DEET;
D O I
10.1093/chemse/bjx011
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
In Culex quinquefasciatus, CquiOR91 is the ortholog of 2 larvae-specific odorant receptors (ORs) from Anopheles gambiae (Agam\Or40, previously shown to respond to several odorant ligands including the broad-spectrum repellent N,N-diethyl-3-methylbenzamide, DEET) and Aedes aegypti (Aaeg\Or40). When we cloned full-length CquiOR91 from a Culex quinquefasciatus larval head RNA sample, we found 2 alleles of this OR, differing at 9 residues. Functional analysis using the Xenopus oocyte expression system and 2-electrode voltage clamp electrophysiology revealed one allele (CquiOR91.1) to be nonfunctional, whereas the other allele (CquiOR91.2) was functional. Receptors formed by CquiOR91.2 and Cqui\Orco responded to (-)-fenchone, (+)-fenchone, and DEET, similar to what has been reported for Agam\Or40. We also identified 5 novel odorant ligands for the CquiOR91.2 + Cqui\Orco receptor: 2-isobutylthiazole, veratrole, eucalyptol, d-camphor, and safranal, with safranal being the most potent. To explore possible reasons for the lack of function for CquiOR91.1, we generated a series of mutant CquiOR91.2 subunits, in which the residue at each of the 9 polymorphic residue positions was changed from what occurs in CquiOR91.2 to what occurs in CquiOR91.1. Eight of the 9 mutant versions of CquiOR91.2 formed functional receptors, responding to (-)-fenchone. Only the CquiOR91.2 Y183C mutant was nonfunctional. The reverse mutation (C183Y) conferred function on CquiOR91.1 , which became responsive to (-)-fenchone and safranal. These results indicate that the "defect" in CquiOR91.1 that prevents function is the cysteine at position 183.
引用
收藏
页码:333 / 341
页数:9
相关论文
共 32 条
[1]   Atypical membrane topology and heteromeric function of Drosophila odorant receptors in vivo [J].
Benton, R ;
Sachse, S ;
Michnick, SW ;
Vosshall, LB .
PLOS BIOLOGY, 2006, 4 (02) :240-257
[2]   Variant Ionotropic Glutamate Receptors as Chemosensory Receptors in Drosophila [J].
Benton, Richard ;
Vannice, Kirsten S. ;
Gomez-Diaz, Carolina ;
Vosshall, Leslie B. .
CELL, 2009, 136 (01) :149-162
[3]   Molecular characterization of the Aedes aegypti odorant receptor gene family [J].
Bohbot, J. ;
Pitts, R. J. ;
Kwon, H.-W. ;
Ruetzler, M. ;
Robertson, H. M. ;
Zwiebel, L. J. .
INSECT MOLECULAR BIOLOGY, 2007, 16 (05) :525-537
[4]   Odorant reception in the malaria mosquito Anopheles gambiae [J].
Carey, Allison F. ;
Wang, Guirong ;
Su, Chih-Ying ;
Zwiebel, Laurence J. ;
Carlson, John R. .
NATURE, 2010, 464 (7285) :66-U77
[5]   Phenylthiophenecarboxamide Antagonists of the Olfactory Receptor Co-Receptor Subunit from a Mosquito [J].
Chen, Sisi ;
Luetje, Charles W. .
PLOS ONE, 2013, 8 (12)
[6]  
Chen Sisi, 2014, F1000Res, V3, P84, DOI 10.12688/f1000research.3825.1
[7]  
Chen SS, 2012, PLOS ONE, V7, DOI [10.1371/journal.pone.0036784, 10.1371/journal.pone.0050456, 10.1371/journal.pone.0049275, 10.1371/journal.pone.0045763]
[8]   NPS@:: Network Protein Sequence Analysis [J].
Combet, C ;
Blanchet, C ;
Geourjon, C ;
Deléage, G .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (03) :147-150
[9]   orco mutant mosquitoes lose strong preference for humans and are not repelled by volatile DEET [J].
DeGennaro, Matthew ;
McBride, Carolyn S. ;
Seeholzer, Laura ;
Nakagawa, Takao ;
Dennis, Emily J. ;
Goldman, Chloe ;
Jasinskiene, Nijole ;
James, Anthony A. ;
Vosshall, Leslie B. .
NATURE, 2013, 498 (7455) :487-491
[10]   Insect odorant receptors are molecular targets of the insect repellent DEET [J].
Ditzen, Mathias ;
Pellegrino, Maurizio ;
Vosshall, Leslie B. .
SCIENCE, 2008, 319 (5871) :1838-1842