Please use this identifier to cite or link to this item:
https://doi.org/10.1371/journal.pbio.2004920
DC Field | Value | |
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dc.title | Evolutionary novelty in gravity sensing through horizontal gene transfer and high-order protein assembly | |
dc.contributor.author | Nguyen T.A. | |
dc.contributor.author | Greig J. | |
dc.contributor.author | Khan A. | |
dc.contributor.author | Goh C. | |
dc.contributor.author | Jedd G. | |
dc.date.accessioned | 2020-03-18T05:54:43Z | |
dc.date.available | 2020-03-18T05:54:43Z | |
dc.date.issued | 2018 | |
dc.identifier.citation | Nguyen T.A., Greig J., Khan A., Goh C., Jedd G. (2018). Evolutionary novelty in gravity sensing through horizontal gene transfer and high-order protein assembly. PLoS Biology 16 (4) : e2004920. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pbio.2004920 | |
dc.identifier.issn | 15449173 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/165619 | |
dc.description.abstract | 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. © 2018 Nguyen et al. | |
dc.publisher | Public Library of Science | |
dc.source | Unpaywall 20200320 | |
dc.subject | bacterial protein | |
dc.subject | octahedral crystal matrix protein | |
dc.subject | oligomer | |
dc.subject | unclassified drug | |
dc.subject | bacterial protein | |
dc.subject | green fluorescent protein | |
dc.subject | photoprotein | |
dc.subject | recombinant protein | |
dc.subject | red fluorescent protein | |
dc.subject | amino terminal sequence | |
dc.subject | Article | |
dc.subject | bacterial structures | |
dc.subject | carboxy terminal sequence | |
dc.subject | controlled study | |
dc.subject | gene | |
dc.subject | gravity sensing | |
dc.subject | horizontal gene transfer | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | mass spectrometry | |
dc.subject | molecular evolution | |
dc.subject | molecular imaging | |
dc.subject | nonhuman | |
dc.subject | octin gene | |
dc.subject | Phycomyces blakesleeanus | |
dc.subject | phylogeny | |
dc.subject | protein analysis | |
dc.subject | protein assembly | |
dc.subject | protein expression | |
dc.subject | protein localization | |
dc.subject | protein structure | |
dc.subject | cell vacuole | |
dc.subject | chemistry | |
dc.subject | classification | |
dc.subject | Escherichia coli | |
dc.subject | evolution | |
dc.subject | gene expression | |
dc.subject | gene vector | |
dc.subject | genetics | |
dc.subject | gravity | |
dc.subject | HeLa cell line | |
dc.subject | metabolism | |
dc.subject | molecular cloning | |
dc.subject | Mucorales | |
dc.subject | periplasm | |
dc.subject | protein multimerization | |
dc.subject | reporter gene | |
dc.subject | Bacterial Proteins | |
dc.subject | Biological Evolution | |
dc.subject | Cloning, Molecular | |
dc.subject | Escherichia coli | |
dc.subject | Gene Expression | |
dc.subject | Gene Transfer, Horizontal | |
dc.subject | Genes, Reporter | |
dc.subject | Genetic Vectors | |
dc.subject | Gravitation | |
dc.subject | Green Fluorescent Proteins | |
dc.subject | HeLa Cells | |
dc.subject | Humans | |
dc.subject | Luminescent Proteins | |
dc.subject | Mucorales | |
dc.subject | Periplasm | |
dc.subject | Phylogeny | |
dc.subject | Protein Multimerization | |
dc.subject | Recombinant Proteins | |
dc.subject | Vacuoles | |
dc.type | Article | |
dc.contributor.department | BIOLOGY (NU) | |
dc.contributor.department | BIOCHEMISTRY | |
dc.description.doi | 10.1371/journal.pbio.2004920 | |
dc.description.sourcetitle | PLoS Biology | |
dc.description.volume | 16 | |
dc.description.issue | 4 | |
dc.description.page | e2004920 | |
dc.published.state | Published | |
Appears in Collections: | Elements Staff Publications |
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