Gene Turnover in the Avian Globin Gene Families and Evolutionary Changes in Hemoglobin Isoform Expression

The apparent stasis in the evolution of avian chromosomes suggests that birds may have experienced relatively low rates of gene gain and loss in multigene families. To investigate this possibility and to explore the phenotypic consequences of variation in gene copy number, we examined evolutionary changes in the families of genes that encode the alpha- and beta-type subunits of hemoglobin (Hb), the tetrameric alpha(2)beta(2) protein responsible for blood-O-2 transport. A comparative genomic analysis of 52 bird species revealed that the size and membership composition of the alpha- and beta-globin gene families have remained remarkably constant during approximately 100 My of avian evolution. Most interspecific variation in gene content is attributable to multiple independent inactivations of the alpha(D)-globin gene, which encodes the alpha-chain subunit of a functionally distinct Hb isoform (HbD) that is expressed in both embryonic and definitive erythrocytes. Due to consistent differences in O-2-binding properties between HbD and the major adult-expressed Hb isoform, HbA (which incorporates products of the alpha(A)-globin gene), recurrent losses of alpha(D)-globin contribute to among-species variation in blood-O-2 affinity. Analysis of HbA/HbD expression levels in the red blood cells of 122 bird species revealed high variability among lineages and strong phylogenetic signal. In comparison with the homologous gene clusters in mammals, the low retention rate for lineage-specific gene duplicates in the avian globin gene clusters suggests that the developmental regulation of Hb synthesis in birds may be more highly conserved, with orthologous genes having similar stage-specific expression profiles and similar functional properties in disparate taxa.