Abstract
Selection on coevolving sperm‐ and egg‐recognition molecules is a potent engine of population divergence leading to reproductive isolation and speciation. The study of receptor–ligand pairs can reveal co‐evolution of male‐ and female‐expressed genes or differences between their evolution in response to selective factors such as sperm competition and sexual conflict. Phylogeographical studies of these patterns have been limited by targeted gene methods that favour short protein‐coding sequences amplifiable by PCR . Here, I use high‐throughput transcriptomic methods to characterize the structure and divergence of full‐length coding sequences for the gene encoding the protein component of a large complex egg surface glycopeptide receptor for the sperm acrosomal protein bindin from the sea star Patiria miniata . I used a simple but effective method for resolving nucleotide polymorphisms into haplotypes for phylogeny‐based analyses of selection. The protein domain organization of sea star egg bindin receptor ( EBR 1) was similar to sea urchins and included a pair of protein‐recognition domains plus a series of tandem repeat domains of two types. Two populations separated by a well‐characterized phylogeographical break included lineages of EBR 1 alleles under positive selection at several codons (similar to selection on sperm bindin in the same populations). However, these populations shared the same alleles that were under selection for amino acid differences at multiple codons (unlike the pattern of selection for population divergence in sperm bindin). The significance of positively selected EBR 1 domains and alleles could be tested in functional analyses of fertilization rates associated with EBR 1 (and bindin) polymorphisms.