Epistatic Effects Between Amino Acid Insertions and Substitutions Mediate Toxin resistance of Vertebrate Na+, K+-ATPases. (6th December 2022)

• Record Type: Journal Article
• Authors: Mohammadi, Shabnam; Özdemir, Halil İbrahim; Ozbek, Pemra; Sumbul, Fidan; Stiller, Josefin; Deng, Yuan; Crawford, Andrew J; Rowland, Hannah M; Storz, Jay F; Andolfatto, Peter; Dobler, Susanne
• Editors: Malik, Harmit
• Is Part Of: Molecular biology and evolution. Volume 39:Number 12(2022)
• Publication Date: 2022-12-06
• Subjects: Na+K+-ATPase -- cardiotonic steroids -- chinchilla -- sandgrouse -- indel evolution; Molecular biology -- Periodicals; Molecular evolution -- Periodicals; Evolution, Molecular -- Periodicals; Molecular Biology -- Periodicals; 572.8
• DOI: 10.1093/molbev/msac258
• Languages: English
• ISSNs: 0737-4038

Abstract

Abstract: The recurrent evolution of resistance to cardiotonic steroids (CTS) across diverse animals most frequently involves convergent amino acid substitutions in the H1-H2 extracellular loop of Na +, K + -ATPase (NKA). Previous work revealed that hystricognath rodents (e.g., chinchilla) and pterocliform birds (sandgrouse) have convergently evolved amino acid insertions in the H1-H2 loop, but their functional significance was not known. Using protein engineering, we show that these insertions have distinct effects on CTS resistance in homologs of each of the two species that strongly depend on intramolecular interactions with other residues. Removing the insertion in the chinchilla NKA unexpectedly increases CTS resistance and decreases NKA activity. In the sandgrouse NKA, the amino acid insertion and substitution Q111R both contribute to an augmented CTS resistance without compromising ATPase activity levels. Molecular docking simulations provide additional insight into the biophysical mechanisms responsible for the context-specific mutational effects on CTS insensitivity of the enzyme. Our results highlight the diversity of genetic substrates that underlie CTS insensitivity in vertebrate NKA and reveal how amino acid insertions can alter the phenotypic effects of point mutations at key sites in the same protein domain.