Development, characterisation, inheritance, and cross-species utility of American lobster ( Homarus americanus) microsatellite and mtDNA PCR-RFLP markers

• Published in: Genome
• Main Authors: Jones, Matthew W, O'Reilly, Patrick T, McPherson, Arran A, McParland, Tara L, Armstrong, Dawn E, Cox, Andrea J, Spence, Koren R, Kenchington, Ellen L, Taggart, Chris T, Bentzen, Paul
• Format: Article in Journal/Newspaper
• Language: English
• Published: Canadian Science Publishing 2003
• Subjects: Genetics; Molecular Biology; General Medicine; Biotechnology; European lobster; Homarus gammarus
• Online Access: http://dx.doi.org/10.1139/g02-105; http://www.nrcresearchpress.com/doi/pdf/10.1139/g02-105

Effective management of exploited species demands contemporary knowledge of population structure and mating patterns. Genetic markers can prove useful in providing this knowledge. Despite its commercial importance, genetic markers for American lobster (Homarus americanus) are limited. We developed 12 tetra- and 1 trinucleotide microsatellite loci for American lobster that exhibit little stuttering after PCR amplification. Gene diversity of these loci ranged from 0.516 to 0.929. A four-locus multiplex permits rapid genotyping of progeny in parentage experiments with a paternity exclusion probability over the four loci of 97.8%. We examined the loci for conformity to Hardy-Weinberg expectations (HWE) and linkage using individuals from one location and found that four loci deviated from HWE. We also tested inheritance and pairwise linkage using 48 embryos from each of two females. With the exception of two loci that were derived from the same clone and separated by 72 bp, no evidence of linkage was found. We, for the first time, demonstrate the occurrence of multiple paternity in American lobster. We also observed an apparent occurrence of dispermic androgenesis, possibly the first documentation of such an event within a species. Ten of the loci amplified in European lobster (Homarus gammarus), although two were monomorphic and one deviated significantly from HWE. We quantified mitochondrial DNA (mtDNA) sequence variation through the use of PCR amplification of two DNA fragments, followed by digestion with restriction enzymes; eight haplotypes were detected. One of the two fragments amplified in European lobster. Both sets of markers should prove useful for population discrimination purposes, and the microsatellites, in particular the four-locus multiplex, should prove highly amenable to rapidly addressing questions about mating patterns.Key Words: low-stutter microsatellites, mtDNA PCR–RFLP, multiple paternity, dispermic androgenesis, American lobster.