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...
Main Authors: | , , , , |
---|---|
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 |
id |
doaj-1eeab932109d469dabd5cdea16b57bdd |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT tuanhnguyen evolutionarynoveltyingravitysensingthroughhorizontalgenetransferandhighorderproteinassembly AT jamiegreig evolutionarynoveltyingravitysensingthroughhorizontalgenetransferandhighorderproteinassembly AT asifkhan evolutionarynoveltyingravitysensingthroughhorizontalgenetransferandhighorderproteinassembly AT caragoh evolutionarynoveltyingravitysensingthroughhorizontalgenetransferandhighorderproteinassembly AT gregoryjedd evolutionarynoveltyingravitysensingthroughhorizontalgenetransferandhighorderproteinassembly |
_version_ |
1721340762414645248 |