Factors affecting avian cross‐species microsatellite amplification

Compilation and analysis of information from the literature regarding cross‐species microsatellite amplification and polymorphism success, and relating this to source‐target species genetic distance as estimated by pairwise cytochrome b ( cytb ) divergence, enabled an in‐depth investigation of factors affecting avian cross‐species microsatellite amplification. Source‐target species cytb distances provided accurate estimates of cross‐species microsatellite amplification/polymorphism success rates not only in birds, but also in taxa where microsatellites cross‐amplify across contrasting levels of taxonomic classification (frogs and cetaceans). As cytb is one of the most commonly sequenced DNA regions, pairwise cytb genetic distances should therefore be useful for predicting cross‐species microsatellite success across a range of taxonomic groups. While the most important factor affecting cross‐species microsatellite amplification/polymorphism success was a negative association with source‐target species genetic distance, associations with additional features affecting cross‐species amplification/polymorphism success included: decreasing PCR annealing temperature significantly increasing the chance of successful cross‐species amplification, and a significant positive association between source species polymorphism and the proportion of target species in which a locus revealed polymorphism. No association between cross‐species amplification and repeat motif (di‐, tri‐, or tetranucelotide) or repeat structure (perfect, imperfect, or compound) was observed. A set of nine loci which cross‐amplified across an unusually broad range of passerine bird species were also identified, and could serve as a good starting point for cross‐species amplification testing in passerine species for which insufficient loci are available.