Evolutionary novelty in gravity sensing through horizontal gene transfer and high-order protein assembly.

Horizontal gene transfer (HGT) can promote evolutionary adaptation by transforming a species' relationship to the environment. In most well-understood cases of HGT, acquired and donor functions appear to remain closely related. Thus, the degree to which HGT can lead to evolutionary novelties re...

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Main Authors: Tu Anh Nguyen, Jamie Greig, Asif Khan, Cara Goh, Gregory Jedd
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-04-01
Series:PLoS Biology
Online Access:http://europepmc.org/articles/PMC5915273?pdf=render
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spelling doaj-1eeab932109d469dabd5cdea16b57bdd2021-07-02T04:00:01ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852018-04-01164e200492010.1371/journal.pbio.2004920Evolutionary novelty in gravity sensing through horizontal gene transfer and high-order protein assembly.Tu Anh NguyenJamie GreigAsif KhanCara GohGregory JeddHorizontal gene transfer (HGT) can promote evolutionary adaptation by transforming a species' relationship to the environment. In most well-understood cases of HGT, acquired and donor functions appear to remain closely related. Thus, the degree to which HGT can lead to evolutionary novelties remains unclear. Mucorales fungi sense gravity through the sedimentation of vacuolar protein crystals. Here, we identify the octahedral crystal matrix protein (OCTIN). Phylogenetic analysis strongly supports acquisition of octin by HGT from bacteria. A bacterial OCTIN forms high-order periplasmic oligomers, and inter-molecular disulphide bonds are formed by both fungal and bacterial OCTINs, suggesting that they share elements of a conserved assembly mechanism. However, estimated sedimentation velocities preclude a gravity-sensing function for the bacterial structures. Together, our data suggest that HGT from bacteria into the Mucorales allowed a dramatic increase in assembly scale and emergence of the gravity-sensing function. We conclude that HGT can lead to evolutionary novelties that emerge depending on the physiological and cellular context of protein assembly.http://europepmc.org/articles/PMC5915273?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Tu Anh Nguyen
Jamie Greig
Asif Khan
Cara Goh
Gregory Jedd
spellingShingle Tu Anh Nguyen
Jamie Greig
Asif Khan
Cara Goh
Gregory Jedd
Evolutionary novelty in gravity sensing through horizontal gene transfer and high-order protein assembly.
PLoS Biology
author_facet Tu Anh Nguyen
Jamie Greig
Asif Khan
Cara Goh
Gregory Jedd
author_sort Tu Anh Nguyen
title Evolutionary novelty in gravity sensing through horizontal gene transfer and high-order protein assembly.
title_short Evolutionary novelty in gravity sensing through horizontal gene transfer and high-order protein assembly.
title_full Evolutionary novelty in gravity sensing through horizontal gene transfer and high-order protein assembly.
title_fullStr Evolutionary novelty in gravity sensing through horizontal gene transfer and high-order protein assembly.
title_full_unstemmed Evolutionary novelty in gravity sensing through horizontal gene transfer and high-order protein assembly.
title_sort evolutionary novelty in gravity sensing through horizontal gene transfer and high-order protein assembly.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2018-04-01
description Horizontal gene transfer (HGT) can promote evolutionary adaptation by transforming a species' relationship to the environment. In most well-understood cases of HGT, acquired and donor functions appear to remain closely related. Thus, the degree to which HGT can lead to evolutionary novelties remains unclear. Mucorales fungi sense gravity through the sedimentation of vacuolar protein crystals. Here, we identify the octahedral crystal matrix protein (OCTIN). Phylogenetic analysis strongly supports acquisition of octin by HGT from bacteria. A bacterial OCTIN forms high-order periplasmic oligomers, and inter-molecular disulphide bonds are formed by both fungal and bacterial OCTINs, suggesting that they share elements of a conserved assembly mechanism. However, estimated sedimentation velocities preclude a gravity-sensing function for the bacterial structures. Together, our data suggest that HGT from bacteria into the Mucorales allowed a dramatic increase in assembly scale and emergence of the gravity-sensing function. We conclude that HGT can lead to evolutionary novelties that emerge depending on the physiological and cellular context of protein assembly.
url http://europepmc.org/articles/PMC5915273?pdf=render
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