The molecular background of the aspartate aminotransferase polymorphism in Littorina snails maintained by strong selection on small spatial scales

• Published in: Gene Vol. 876; p. 147517
• Main Authors: Mittermayer, Felix, Helmerson, Cecilia, Duvetorp, Mårten, Johannesson, Kerstin, Panova, Marina
• Format: Journal Article
• Language: English; Norwegian
• Published: Netherlands Elsevier B.V 05.08.2023
• Subjects: Allozyme; Animals; Aspartate Aminotransferases; Evolutionary Biology; Evolutionsbiologi; Gene duplication; Gene structure; Genetic clines; Genetics; Genetik; Isoenzymes - genetics; Littorina saxatilis; Marine snail; Phylogeny; Polymorphism, Genetic; Selection; Snails - genetics; Selection; Littorina saxatilis; Gene structure; Genetic clines; EPIC primer; Allozyme; cds; AAT; mya; IEP; Gene duplication; cDNA; Marine snail
• ISSN: 0378-1119; 1879-0038; 1879-0038
• DOI: 10.1016/j.gene.2023.147517

•DNA variation is characterized for aspartate aminotransferase allozymes in snails.•Allozyme alleles differ by 2–4 substitutions.•Aspartate aminotransferase is expressed in the snail at the constant level.•Aspartate aminotransferase gene is present in the snail genome in multiple copies. Allozymes present several classical examples of divergent selection, including the variation in the cytosolic aspartate aminotransferase (AAT) in the intertidal snails Littorina saxatilis. AAT is a part of the asparate-malate shuttle, in the interidal molluscs involved in the anaerobic respiration during desiccation. Previous allozyme studies reported the sharp gradient in the frequencies of the AAT100and the AAT120 alleles between the low and high shores in the Northern Europe and the differences in their enzymatic activity, supporting the role of AAT in adaptation to desiccation. However, the populations in the Iberian Peninsula showed the opposite allele cline. Using the mRNA sequencing and the genome pool-seq analyses we characterize DNA sequences of the different AAT alleles, report the amino acid replacements behind the allozyme variation and show that same allozyme alleles in Northern and Southern populations have different protein sequences. Gene phylogeny reveals that the AAT100 and the northern AAT120 alleles represent the old polymorphism, shared among the closely related species of Littorina, while the southern AAT120 allele is more recently derived from AAT100. Further, we show that the Aat gene is expressed at constitutive level in different genotypes and conditions, supporting the role of structural variation in regulation of enzyme activity. Finally, we report the location and the structure of the gene in the L. saxatilis genome and the presence of two additional non-functional gene copies. Altogether, we provide a missing link between the classical allozyme studies and the genome scans and bring together the results produced over decades of the genetic research.