Complex genetic architecture of Drosophila aggressive behavior

被引:52
作者
Zwarts, Liesbeth [2 ,3 ]
Magwire, Michael M. [1 ,4 ]
Carbone, Mary Anna [1 ,4 ]
Versteven, Marijke [2 ,3 ]
Herteleer, Liesbet [2 ,3 ]
Anholt, Robert R. H. [4 ,5 ]
Callaerts, Patrick [2 ,3 ]
Mackay, Trudy F. C. [1 ,4 ]
机构
[1] N Carolina State Univ, Dept Genet, Raleigh, NC 27695 USA
[2] Catholic Univ Louvain, Ctr Human Genet, Lab Dev Genet, B-3000 Louvain, Belgium
[3] VIB, B-3000 Louvain, Belgium
[4] N Carolina State Univ, WM Keck Ctr Behav Biol, Raleigh, NC 27695 USA
[5] N Carolina State Univ, Dept Biol, Raleigh, NC 27695 USA
基金
美国国家卫生研究院;
关键词
ODOR-GUIDED BEHAVIOR; MICE LACKING; SEROTONIN; EPISTASIS; NEURONS; PHARMACOGENETICS; DEPRESSION; GENOTYPE; LOCI;
D O I
10.1073/pnas.1113877108
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
Epistasis and pleiotropy feature prominently in the genetic architecture of quantitative traits but are difficult to assess in outbred populations. We performed a diallel cross among coisogenic Drosophila P-element mutations associated with hyperaggressive behavior and showed extensive epistatic and pleiotropic effects on aggression, brain morphology, and genome-wide transcript abundance in head tissues. Epistatic interactions were often of greater magnitude than homozygous effects, and the topology of epistatic networks varied among these phenotypes. The transcriptional signatures of homozygous and double heterozygous genotypes derived from the six mutations imply a large mutational target for aggressive behavior and point to evolutionarily conserved genetic mechanisms and neural signaling pathways affecting this universal fitness trait.
引用
收藏
页码:17070 / 17075
页数:6
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