Genetic Mapping of Sexual Isolation Between E and Z Pheromone Strains of the European Corn Borer (Ostrinia nubilalis)

• Published in: Genetics (Austin) Vol. 167; no. 1; pp. 301 - 309
• Main Authors: Dopman, Erik B, Bogdanowicz, Steven M, Harrison, Richard G
• Format: Journal Article
• Language: English
• Published: United States Genetics Soc America 01.05.2004; Genetics Society of America
• Subjects: Alleles; Animal reproduction; Animals; Chromosome Mapping - methods; Corn; Female; Gene Frequency; Gene mapping; Genetic diversity; Genetic Linkage; Genetic Markers; Genotype; Hormones; Insects; Lepidoptera - genetics; Male; Microsatellite Repeats; Models, Genetic; Ostrinia nubilalis; Pheromones - genetics; Pheromones - metabolism; Protein Isoforms; Pyralidae; Recombination, Genetic; Sex Attractants - genetics; Sex Factors; Speciation
• ISSN: 0016-6731; 1943-2631; 1943-2631
• DOI: 10.1534/genetics.167.1.301

The E and Z pheromone strains of the European corn borer (ECB) provide an exceptional model system for examining the genetic basis of sexual isolation. Differences at two major genes account for variation in female pheromone production and male behavioral response, components of the pheromone communication system known to be important for mate recognition and mate choice. Strains of ECB are morphologically indistinguishable, and surveys of allozyme and DNA sequence variation have revealed significant allele frequency differences at only a single sex-linked locus, Tpi. Here we present a detailed genetic linkage map of ECB using AFLP and microsatellite markers and map the factors responsible for pheromone production (Pher) and male response (Resp). Our map covers 1697 cM and identifies all 31 linkage groups in ECB. Both Resp and Tpi map to the Z (sex) chromosome, but the distance between these markers (>20 cM) argues against the hypothesis that patterns of variation at Tpi are explained by tight linkage to this “speciation gene.” However, we show, through analysis of marker density, that Tpi is located in a region of low recombination and suggest that a second Z-linked reproductive barrier could be responsible for the origin and/or persistence of differentiation at Tpi.