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No Boundaries: Genomes, Organisms, and Ecological Interactions Responsible for Divergence and Reproductive Isolation

Overview
Journal J Hered
Specialty Genetics
Date 2014 Aug 24
PMID 25149252
Citations 5
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Abstract

Revealing the genetic basis of traits that cause reproductive isolation, particularly premating or sexual isolation, usually involves the same challenges as most attempts at genotype-phenotype mapping and so requires knowledge of how these traits are expressed in different individuals, populations, and environments, particularly under natural conditions. Genetic dissection of speciation phenotypes thus requires understanding of the internal and external contexts in which underlying genetic elements are expressed. Gene expression is a product of complex interacting factors internal and external to the organism including developmental programs, the genetic background including nuclear-cytotype interactions, epistatic relationships, interactions among individuals or social effects, stochasticity, and prevailing variation in ecological conditions. Understanding of genomic divergence associated with reproductive isolation will be facilitated by functional expression analysis of annotated genomes in organisms with well-studied evolutionary histories, phylogenetic affinities, and known patterns of ecological variation throughout their life cycles. I review progress and prospects for understanding the pervasive role of host plant use on genetic and phenotypic expression of reproductive isolating mechanisms in cactophilic Drosophila mojavensis and suggest how this system can be used as a model for revealing the genetic basis for species formation in organisms where speciation phenotypes are under the joint influences of genetic and environmental factors.

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References
1.
Frentiu F, Adamski M, McGraw E, Blows M, Chenoweth S . An expressed sequence tag (EST) library for Drosophila serrata, a model system for sexual selection and climatic adaptation studies. BMC Genomics. 2009; 10:40. PMC: 2653539. DOI: 10.1186/1471-2164-10-40. View

2.
Kang E, Han B, Furlotte N, Joo J, Shih D, Davis R . Meta-analysis identifies gene-by-environment interactions as demonstrated in a study of 4,965 mice. PLoS Genet. 2014; 10(1):e1004022. PMC: 3886926. DOI: 10.1371/journal.pgen.1004022. View

3.
Etges W, de Oliveira C, Gragg E, Ortiz-Barrientos D, Noor M, Ritchie M . Genetics of incipient speciation in Drosophila mojavensis. I. Male courtship song, mating success, and genotype x environment interactions. Evolution. 2007; 61(5):1106-19. DOI: 10.1111/j.1558-5646.2007.00104.x. View

4.
Oshlack A, Robinson M, Young M . From RNA-seq reads to differential expression results. Genome Biol. 2010; 11(12):220. PMC: 3046478. DOI: 10.1186/gb-2010-11-12-220. View

5.
Shaw K, Parsons Y . Divergence of mate recognition behavior and its consequences for genetic architectures of speciation. Am Nat. 2008; 159 Suppl 3:S61-75. DOI: 10.1086/338373. View