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Interpreting the Evolutionary Echoes of a Protein Complex Essential for Inner-Ear Mechanosensation.
Nisler, Collin R; Narui, Yoshie; Scheib, Emily; Choudhary, Deepanshu; Bowman, Jacob D; Mandayam Bharathi, Harsha; Lynch, Vincent J; Sotomayor, Marcos.
Afiliação
  • Nisler CR; Department of Chemistry and Biochemistry, The Ohio State University, 484 W 12th Avenue, Columbus, OH.
  • Narui Y; Biophysics Graduate Program, The Ohio State University, 484 W 12th Avenue, Columbus, OH.
  • Scheib E; Center for Electron Microscopy and Analysis, The Ohio State University, 1275-1305 Kinnear Road, Columbus, OH.
  • Choudhary D; Department of Chemistry and Biochemistry, The Ohio State University, 484 W 12th Avenue, Columbus, OH.
  • Bowman JD; Department of Chemistry and Biochemistry, The Ohio State University, 484 W 12th Avenue, Columbus, OH.
  • Mandayam Bharathi H; Department of Biological Sciences, University at Buffalo, SUNY, 551 Cooke Hall, Buffalo, NY, USA.
  • Lynch VJ; Department of Chemistry and Biochemistry, The Ohio State University, 484 W 12th Avenue, Columbus, OH.
  • Sotomayor M; Department of Biological Sciences, University at Buffalo, SUNY, 551 Cooke Hall, Buffalo, NY, USA.
Mol Biol Evol ; 40(4)2023 04 04.
Article em En | MEDLINE | ID: mdl-36911992
ABSTRACT
The sensory epithelium of the inner ear, found in all extant lineages of vertebrates, has been subjected to over 500 million years of evolution, resulting in the complex inner ear of modern vertebrates. Inner-ear adaptations are as diverse as the species in which they are found, and such unique anatomical variations have been well studied. However, the evolutionary details of the molecular machinery that is required for hearing are less well known. Two molecules that are essential for hearing in vertebrates are cadherin-23 and protocadherin-15, proteins whose interaction with one another acts as the focal point of force transmission when converting sound waves into electrical signals that the brain can interpret. This "tip-link" interaction exists in every lineage of vertebrates, but little is known about the structure or mechanical properties of these proteins in most non-mammalian lineages. Here, we use various techniques to characterize the evolution of this protein interaction. Results show how evolutionary sequence changes in this complex affect its biophysical properties both in simulations and experiments, with variations in interaction strength and dynamics among extant vertebrate lineages. Evolutionary simulations also characterize how the biophysical properties of the complex in turn constrain its evolution and provide a possible explanation for the increase in deafness-causing mutants observed in cadherin-23 relative to protocadherin-15. Together, these results suggest a general picture of tip-link evolution in which selection acted to modify the tip-link interface, although subsequent neutral evolution combined with varying degrees of purifying selection drove additional diversification in modern tetrapods.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocaderinas / Orelha Interna Limite: Animals Idioma: En Revista: Mol Biol Evol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocaderinas / Orelha Interna Limite: Animals Idioma: En Revista: Mol Biol Evol Ano de publicação: 2023 Tipo de documento: Article