Shared protein complex subunits contribute to explaining disrupted co-occurrence
The gene composition of present-day genomes has been shaped by a complicated evolutionary history, resulting in diverse distributions of genes across genomes. The pattern of presence and absence of a gene in different genomes is called its phylogenetic profile. It has been shown that proteins whose...
Gespeichert in:
Veröffentlicht in: | PLoS computational biology 2013-07, Vol.9 (7), p.e1003124-e1003124 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | e1003124 |
---|---|
container_issue | 7 |
container_start_page | e1003124 |
container_title | PLoS computational biology |
container_volume | 9 |
creator | Schneider, Adrian Seidl, Michael F Snel, Berend |
description | The gene composition of present-day genomes has been shaped by a complicated evolutionary history, resulting in diverse distributions of genes across genomes. The pattern of presence and absence of a gene in different genomes is called its phylogenetic profile. It has been shown that proteins whose encoding genes have highly similar profiles tend to be functionally related: As these genes were gained and lost together, their encoded proteins can probably only perform their full function if both are present. However, a large proportion of genes encoding interacting proteins do not have matching profiles. In this study, we analysed one possible reason for this, namely that phylogenetic profiles can be affected by multi-functional proteins such as shared subunits of two or more protein complexes. We found that by considering triplets of proteins, of which one protein is multi-functional, a large fraction of disturbed co-occurrence patterns can be explained. |
doi_str_mv | 10.1371/journal.pcbi.1003124 |
format | Article |
fullrecord | <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_1430786455</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A341456426</galeid><doaj_id>oai_doaj_org_article_08125a6195a84cd6a6edce282a2d8278</doaj_id><sourcerecordid>A341456426</sourcerecordid><originalsourceid>FETCH-LOGICAL-c656t-50d3e2e1e74f768fb67bcc9b149e94d5f39b42435635f11e2f826a83944606693</originalsourceid><addsrcrecordid>eNqVUk1v1DAUjBCItgv_AEGOcNgl_ozDAamq-FipAkThbDnOS-qV1w52TLf_Hqe7rbpH5IOt55nRmzevKF6haoVIjd5vfApO2dWoW7NCVUUQpk-KU8QYWdaEiaeP3ifFWYybjGGi4c-LE0xETVGNT4sfV9cqQFeOwU9gXKn9drSwK2NqkzNTzAU3BdOmCcrJl7AbrTLOuKHsTAxpnDJX-6XXOoUATsOL4lmvbISXh3tR_P786dfF1-Xl9y_ri_PLpeaMT0tWdQQwIKhpX3PRt7xutW5aRBtoaMd60rQUU8I4YT1CgHuBuRKkoZRXnDdkUbzZ647WR3kYRpSIkqoWnGbni2K9R3RebeQYzFaFW-mVkXcFHwapwmS0BVkJhJniqGFKUN1xxaHTgAVWuBO4Flnrw17rRg0w2wcnnQraxDtBa9owi9-kIJ2drzG1UVKKMeWZ_PHQamq3s3CeqLJHHR3_OHMtB_9X5pgZRbOTtweB4P8kiJPcmqjBWuXAp9k0QpzQqqYZutpDB5V9Gdf7rKjz6WBrcpbQm1w_JxRRximem3t3RJjzht00qBSjXF_9_A_st2Ms3WN18DEG6B_8okrOC3yfmZwXWB4WONNeP57VA-l-Y8k_oofu2Q</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1411634074</pqid></control><display><type>article</type><title>Shared protein complex subunits contribute to explaining disrupted co-occurrence</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Public Library of Science (PLoS)</source><creator>Schneider, Adrian ; Seidl, Michael F ; Snel, Berend</creator><creatorcontrib>Schneider, Adrian ; Seidl, Michael F ; Snel, Berend</creatorcontrib><description>The gene composition of present-day genomes has been shaped by a complicated evolutionary history, resulting in diverse distributions of genes across genomes. The pattern of presence and absence of a gene in different genomes is called its phylogenetic profile. It has been shown that proteins whose encoding genes have highly similar profiles tend to be functionally related: As these genes were gained and lost together, their encoded proteins can probably only perform their full function if both are present. However, a large proportion of genes encoding interacting proteins do not have matching profiles. In this study, we analysed one possible reason for this, namely that phylogenetic profiles can be affected by multi-functional proteins such as shared subunits of two or more protein complexes. We found that by considering triplets of proteins, of which one protein is multi-functional, a large fraction of disturbed co-occurrence patterns can be explained.</description><identifier>ISSN: 1553-7358</identifier><identifier>ISSN: 1553-734X</identifier><identifier>EISSN: 1553-7358</identifier><identifier>DOI: 10.1371/journal.pcbi.1003124</identifier><identifier>PMID: 23874172</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Algorithms ; Biology ; Cell cycle ; duplication ; eukaryotes ; evolution ; functional modules ; Gene expression ; Genome ; Genomes ; Genomics ; identification ; network ; Phylogenetics ; Phylogeny ; Proteins ; Proteins - chemistry ; Proteins - genetics ; Proteins - metabolism ; Studies ; Yeast</subject><ispartof>PLoS computational biology, 2013-07, Vol.9 (7), p.e1003124-e1003124</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Schneider et al 2013 Schneider et al</rights><rights>Wageningen University & Research</rights><rights>2013 Schneider et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Schneider A, Seidl MF, Snel B (2013) Shared Protein Complex Subunits Contribute to Explaining Disrupted Co-occurrence. PLoS Comput Biol 9(7): e1003124. doi:10.1371/journal.pcbi.1003124</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c656t-50d3e2e1e74f768fb67bcc9b149e94d5f39b42435635f11e2f826a83944606693</citedby><cites>FETCH-LOGICAL-c656t-50d3e2e1e74f768fb67bcc9b149e94d5f39b42435635f11e2f826a83944606693</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715415/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715415/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79343,79344</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23874172$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schneider, Adrian</creatorcontrib><creatorcontrib>Seidl, Michael F</creatorcontrib><creatorcontrib>Snel, Berend</creatorcontrib><title>Shared protein complex subunits contribute to explaining disrupted co-occurrence</title><title>PLoS computational biology</title><addtitle>PLoS Comput Biol</addtitle><description>The gene composition of present-day genomes has been shaped by a complicated evolutionary history, resulting in diverse distributions of genes across genomes. The pattern of presence and absence of a gene in different genomes is called its phylogenetic profile. It has been shown that proteins whose encoding genes have highly similar profiles tend to be functionally related: As these genes were gained and lost together, their encoded proteins can probably only perform their full function if both are present. However, a large proportion of genes encoding interacting proteins do not have matching profiles. In this study, we analysed one possible reason for this, namely that phylogenetic profiles can be affected by multi-functional proteins such as shared subunits of two or more protein complexes. We found that by considering triplets of proteins, of which one protein is multi-functional, a large fraction of disturbed co-occurrence patterns can be explained.</description><subject>Algorithms</subject><subject>Biology</subject><subject>Cell cycle</subject><subject>duplication</subject><subject>eukaryotes</subject><subject>evolution</subject><subject>functional modules</subject><subject>Gene expression</subject><subject>Genome</subject><subject>Genomes</subject><subject>Genomics</subject><subject>identification</subject><subject>network</subject><subject>Phylogenetics</subject><subject>Phylogeny</subject><subject>Proteins</subject><subject>Proteins - chemistry</subject><subject>Proteins - genetics</subject><subject>Proteins - metabolism</subject><subject>Studies</subject><subject>Yeast</subject><issn>1553-7358</issn><issn>1553-734X</issn><issn>1553-7358</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNqVUk1v1DAUjBCItgv_AEGOcNgl_ozDAamq-FipAkThbDnOS-qV1w52TLf_Hqe7rbpH5IOt55nRmzevKF6haoVIjd5vfApO2dWoW7NCVUUQpk-KU8QYWdaEiaeP3ifFWYybjGGi4c-LE0xETVGNT4sfV9cqQFeOwU9gXKn9drSwK2NqkzNTzAU3BdOmCcrJl7AbrTLOuKHsTAxpnDJX-6XXOoUATsOL4lmvbISXh3tR_P786dfF1-Xl9y_ri_PLpeaMT0tWdQQwIKhpX3PRt7xutW5aRBtoaMd60rQUU8I4YT1CgHuBuRKkoZRXnDdkUbzZ647WR3kYRpSIkqoWnGbni2K9R3RebeQYzFaFW-mVkXcFHwapwmS0BVkJhJniqGFKUN1xxaHTgAVWuBO4Flnrw17rRg0w2wcnnQraxDtBa9owi9-kIJ2drzG1UVKKMeWZ_PHQamq3s3CeqLJHHR3_OHMtB_9X5pgZRbOTtweB4P8kiJPcmqjBWuXAp9k0QpzQqqYZutpDB5V9Gdf7rKjz6WBrcpbQm1w_JxRRximem3t3RJjzht00qBSjXF_9_A_st2Ms3WN18DEG6B_8okrOC3yfmZwXWB4WONNeP57VA-l-Y8k_oofu2Q</recordid><startdate>20130701</startdate><enddate>20130701</enddate><creator>Schneider, Adrian</creator><creator>Seidl, Michael F</creator><creator>Snel, Berend</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISN</scope><scope>ISR</scope><scope>7X8</scope><scope>5PM</scope><scope>QVL</scope><scope>DOA</scope></search><sort><creationdate>20130701</creationdate><title>Shared protein complex subunits contribute to explaining disrupted co-occurrence</title><author>Schneider, Adrian ; Seidl, Michael F ; Snel, Berend</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c656t-50d3e2e1e74f768fb67bcc9b149e94d5f39b42435635f11e2f826a83944606693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Algorithms</topic><topic>Biology</topic><topic>Cell cycle</topic><topic>duplication</topic><topic>eukaryotes</topic><topic>evolution</topic><topic>functional modules</topic><topic>Gene expression</topic><topic>Genome</topic><topic>Genomes</topic><topic>Genomics</topic><topic>identification</topic><topic>network</topic><topic>Phylogenetics</topic><topic>Phylogeny</topic><topic>Proteins</topic><topic>Proteins - chemistry</topic><topic>Proteins - genetics</topic><topic>Proteins - metabolism</topic><topic>Studies</topic><topic>Yeast</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schneider, Adrian</creatorcontrib><creatorcontrib>Seidl, Michael F</creatorcontrib><creatorcontrib>Snel, Berend</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>NARCIS:Publications</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS computational biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schneider, Adrian</au><au>Seidl, Michael F</au><au>Snel, Berend</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Shared protein complex subunits contribute to explaining disrupted co-occurrence</atitle><jtitle>PLoS computational biology</jtitle><addtitle>PLoS Comput Biol</addtitle><date>2013-07-01</date><risdate>2013</risdate><volume>9</volume><issue>7</issue><spage>e1003124</spage><epage>e1003124</epage><pages>e1003124-e1003124</pages><issn>1553-7358</issn><issn>1553-734X</issn><eissn>1553-7358</eissn><abstract>The gene composition of present-day genomes has been shaped by a complicated evolutionary history, resulting in diverse distributions of genes across genomes. The pattern of presence and absence of a gene in different genomes is called its phylogenetic profile. It has been shown that proteins whose encoding genes have highly similar profiles tend to be functionally related: As these genes were gained and lost together, their encoded proteins can probably only perform their full function if both are present. However, a large proportion of genes encoding interacting proteins do not have matching profiles. In this study, we analysed one possible reason for this, namely that phylogenetic profiles can be affected by multi-functional proteins such as shared subunits of two or more protein complexes. We found that by considering triplets of proteins, of which one protein is multi-functional, a large fraction of disturbed co-occurrence patterns can be explained.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23874172</pmid><doi>10.1371/journal.pcbi.1003124</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1553-7358 |
ispartof | PLoS computational biology, 2013-07, Vol.9 (7), p.e1003124-e1003124 |
issn | 1553-7358 1553-734X 1553-7358 |
language | eng |
recordid | cdi_plos_journals_1430786455 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Public Library of Science (PLoS) |
subjects | Algorithms Biology Cell cycle duplication eukaryotes evolution functional modules Gene expression Genome Genomes Genomics identification network Phylogenetics Phylogeny Proteins Proteins - chemistry Proteins - genetics Proteins - metabolism Studies Yeast |
title | Shared protein complex subunits contribute to explaining disrupted co-occurrence |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T07%3A17%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Shared%20protein%20complex%20subunits%20contribute%20to%20explaining%20disrupted%20co-occurrence&rft.jtitle=PLoS%20computational%20biology&rft.au=Schneider,%20Adrian&rft.date=2013-07-01&rft.volume=9&rft.issue=7&rft.spage=e1003124&rft.epage=e1003124&rft.pages=e1003124-e1003124&rft.issn=1553-7358&rft.eissn=1553-7358&rft_id=info:doi/10.1371/journal.pcbi.1003124&rft_dat=%3Cgale_plos_%3EA341456426%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1411634074&rft_id=info:pmid/23874172&rft_galeid=A341456426&rft_doaj_id=oai_doaj_org_article_08125a6195a84cd6a6edce282a2d8278&rfr_iscdi=true |