Cargando…

Transmembrane Domain Lengths Serve as Signatures of Organismal Complexity and Viral Transport Mechanisms

It is known that membrane proteins are important in various secretory pathways, with a possible role of their transmembrane domains (TMDs) as sorting determinant factors. One key aspect of TMDs associated with various “checkposts” (i.e. organelles) of intracellular trafficking is their length. To ex...

Descripción completa

Detalles Bibliográficos
Autores principales: Singh, Snigdha, Mittal, Aditya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772119/
https://www.ncbi.nlm.nih.gov/pubmed/26925972
http://dx.doi.org/10.1038/srep22352
_version_ 1782418509688471552
author Singh, Snigdha
Mittal, Aditya
author_facet Singh, Snigdha
Mittal, Aditya
author_sort Singh, Snigdha
collection PubMed
description It is known that membrane proteins are important in various secretory pathways, with a possible role of their transmembrane domains (TMDs) as sorting determinant factors. One key aspect of TMDs associated with various “checkposts” (i.e. organelles) of intracellular trafficking is their length. To explore possible linkages in organisms with varying “complexity” and differences in TMD lengths of membrane proteins associated with different organelles (such as Endoplasmic Reticulum, Golgi, Endosomes, Nucleus, Plasma Membrane), we analyzed ~70000 membrane protein sequences in over 300 genomes of fungi, plants, non-mammalian vertebrates and mammals. We report that as we move from simpler to complex organisms, variation in organellar TMD lengths decreases, especially compared to their respective plasma membranes, with increasing organismal complexity. This suggests an evolutionary pressure in modulating length of TMDs of membrane proteins with increasing complexity of communication between sub-cellular compartments. We also report functional applications of our findings by discovering remarkable distinctions in TMD lengths of membrane proteins associated with different intracellular transport pathways. Finally, we show that TMD lengths extracted from viral proteins can serve as somewhat weak indicators of viral replication sites in plant cells but very strong indicators of different entry pathways employed by animal viruses.
format Online
Article
Text
id pubmed-4772119
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-47721192016-03-07 Transmembrane Domain Lengths Serve as Signatures of Organismal Complexity and Viral Transport Mechanisms Singh, Snigdha Mittal, Aditya Sci Rep Article It is known that membrane proteins are important in various secretory pathways, with a possible role of their transmembrane domains (TMDs) as sorting determinant factors. One key aspect of TMDs associated with various “checkposts” (i.e. organelles) of intracellular trafficking is their length. To explore possible linkages in organisms with varying “complexity” and differences in TMD lengths of membrane proteins associated with different organelles (such as Endoplasmic Reticulum, Golgi, Endosomes, Nucleus, Plasma Membrane), we analyzed ~70000 membrane protein sequences in over 300 genomes of fungi, plants, non-mammalian vertebrates and mammals. We report that as we move from simpler to complex organisms, variation in organellar TMD lengths decreases, especially compared to their respective plasma membranes, with increasing organismal complexity. This suggests an evolutionary pressure in modulating length of TMDs of membrane proteins with increasing complexity of communication between sub-cellular compartments. We also report functional applications of our findings by discovering remarkable distinctions in TMD lengths of membrane proteins associated with different intracellular transport pathways. Finally, we show that TMD lengths extracted from viral proteins can serve as somewhat weak indicators of viral replication sites in plant cells but very strong indicators of different entry pathways employed by animal viruses. Nature Publishing Group 2016-03-01 /pmc/articles/PMC4772119/ /pubmed/26925972 http://dx.doi.org/10.1038/srep22352 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Singh, Snigdha
Mittal, Aditya
Transmembrane Domain Lengths Serve as Signatures of Organismal Complexity and Viral Transport Mechanisms
title Transmembrane Domain Lengths Serve as Signatures of Organismal Complexity and Viral Transport Mechanisms
title_full Transmembrane Domain Lengths Serve as Signatures of Organismal Complexity and Viral Transport Mechanisms
title_fullStr Transmembrane Domain Lengths Serve as Signatures of Organismal Complexity and Viral Transport Mechanisms
title_full_unstemmed Transmembrane Domain Lengths Serve as Signatures of Organismal Complexity and Viral Transport Mechanisms
title_short Transmembrane Domain Lengths Serve as Signatures of Organismal Complexity and Viral Transport Mechanisms
title_sort transmembrane domain lengths serve as signatures of organismal complexity and viral transport mechanisms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772119/
https://www.ncbi.nlm.nih.gov/pubmed/26925972
http://dx.doi.org/10.1038/srep22352
work_keys_str_mv AT singhsnigdha transmembranedomainlengthsserveassignaturesoforganismalcomplexityandviraltransportmechanisms
AT mittaladitya transmembranedomainlengthsserveassignaturesoforganismalcomplexityandviraltransportmechanisms