Genetic architecture of natural variation in cuticular hydrocarbon composition in Drosophila melanogaster
Lauren M Dembeck,
Katalin Böröczky,
Wen Huang,
Coby Schal,
Robert R H Anholt,
Trudy F C Mackay
Affiliations
Lauren M Dembeck
Department of Biological Sciences, North Carolina State University, Raleigh, United States; Genetics Program, North Carolina State University, Raleigh, United States; W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, United States
Katalin Böröczky
Genetics Program, North Carolina State University, Raleigh, United States; W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, United States; Department of Entomology, North Carolina State University, Raleigh, United States
Wen Huang
Department of Biological Sciences, North Carolina State University, Raleigh, United States; Genetics Program, North Carolina State University, Raleigh, United States; W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, United States
Coby Schal
Genetics Program, North Carolina State University, Raleigh, United States; W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, United States; Department of Entomology, North Carolina State University, Raleigh, United States
Robert R H Anholt
Department of Biological Sciences, North Carolina State University, Raleigh, United States; Genetics Program, North Carolina State University, Raleigh, United States; W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, United States
Trudy F C Mackay
Department of Biological Sciences, North Carolina State University, Raleigh, United States; Genetics Program, North Carolina State University, Raleigh, United States; W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, United States
Insect cuticular hydrocarbons (CHCs) prevent desiccation and serve as chemical signals that mediate social interactions. Drosophila melanogaster CHCs have been studied extensively, but the genetic basis for individual variation in CHC composition is largely unknown. We quantified variation in CHC profiles in the D. melanogaster Genetic Reference Panel (DGRP) and identified novel CHCs. We used principal component (PC) analysis to extract PCs that explain the majority of CHC variation and identified polymorphisms in or near 305 and 173 genes in females and males, respectively, associated with variation in these PCs. In addition, 17 DGRP lines contain the functional Desat2 allele characteristic of African and Caribbean D. melanogaster females (more 5,9-C27:2 and less 7,11-C27:2, female sex pheromone isomers). Disruption of expression of 24 candidate genes affected CHC composition in at least one sex. These genes are associated with fatty acid metabolism and represent mechanistic targets for individual variation in CHC composition.