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Molecular parallelism in fast-twitch muscle proteins in echolocating mammals

Detecting associations between genomic changes and phenotypic differences is fundamental to understanding how phenotypes evolved. By systematically screening for parallel amino acid substitutions, we detected known as well as novel cases (Strc, Tecta, and Cabp2) of parallelism between echolocating b...

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Published in:Science advances 2018-09, Vol.4 (9), p.eaat9660-eaat9660
Main Authors: Lee, Jun-Hoe, Lewis, Kevin M, Moural, Timothy W, Kirilenko, Bogdan, Borgonovo, Barbara, Prange, Gisa, Koessl, Manfred, Huggenberger, Stefan, Kang, ChulHee, Hiller, Michael
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cited_by cdi_FETCH-LOGICAL-c427t-cfce7a0d4e67ad2b0d63d23b8d21963e71e7a820ee4ac3e7aec0e57cba380f943
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container_end_page eaat9660
container_issue 9
container_start_page eaat9660
container_title Science advances
container_volume 4
creator Lee, Jun-Hoe
Lewis, Kevin M
Moural, Timothy W
Kirilenko, Bogdan
Borgonovo, Barbara
Prange, Gisa
Koessl, Manfred
Huggenberger, Stefan
Kang, ChulHee
Hiller, Michael
description Detecting associations between genomic changes and phenotypic differences is fundamental to understanding how phenotypes evolved. By systematically screening for parallel amino acid substitutions, we detected known as well as novel cases (Strc, Tecta, and Cabp2) of parallelism between echolocating bats and toothed whales in proteins that could contribute to high-frequency hearing adaptations. Our screen also showed that echolocating mammals exhibit an unusually high number of parallel substitutions in fast-twitch muscle fiber proteins. Both echolocating bats and toothed whales produce an extremely rapid call rate when homing in on their prey, which was shown in bats to be powered by specialized superfast muscles. We show that these genes with parallel substitutions ( , , , and ) are expressed in the superfast sound-producing muscle of bats. Furthermore, we found that the calcium storage protein calsequestrin 1 of the little brown bat and the bottlenose dolphin functionally converged in its ability to form calcium-sequestering polymers at lower calcium concentrations, which may contribute to rapid calcium transients required for superfast muscle physiology. The proteins that our genomic screen detected could be involved in the convergent evolution of vocalization in echolocating mammals by potentially contributing to both rapid Ca transients and increased shortening velocities in superfast muscles.
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SciAdv r-articles
title Molecular parallelism in fast-twitch muscle proteins in echolocating mammals
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