Sub-grouping and sub-functionalization of the RIFIN multi-copy protein family

<p>Abstract</p> <p>Background</p> <p>Parasitic protozoans possess many multicopy gene families which have central roles in parasite survival and virulence. The number and variability of members of these gene families often make it difficult to predict possible functions...

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Main Authors: Sonnhammer Erik L, Abhiman Saraswathi, Joannin Nicolas, Wahlgren Mats
Format: Article
Language:English
Published: BMC 2008-01-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/9/19
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spelling doaj-041dd52f32eb4812b59fb7375ec852412020-11-25T01:03:37ZengBMCBMC Genomics1471-21642008-01-01911910.1186/1471-2164-9-19Sub-grouping and sub-functionalization of the RIFIN multi-copy protein familySonnhammer Erik LAbhiman SaraswathiJoannin NicolasWahlgren Mats<p>Abstract</p> <p>Background</p> <p>Parasitic protozoans possess many multicopy gene families which have central roles in parasite survival and virulence. The number and variability of members of these gene families often make it difficult to predict possible functions of the encoded proteins. The families of extra-cellular proteins that are exposed to a host immune response have been driven via immune selection to become antigenically variant, and thereby avoid immune recognition while maintaining protein function to establish a chronic infection.</p> <p>Results</p> <p>We have combined phylogenetic and function shift analyses to study the evolution of the RIFIN proteins, which are antigenically variant and are encoded by the largest multicopy gene family in <it>Plasmodium falciparum</it>. We show that this family can be subdivided into two major groups that we named A- and B-RIFIN proteins. This suggested sub-grouping is supported by a recently published study that showed that, despite the presence of the <it>Plasmodium </it>export (PEXEL) motif in all RIFIN variants, proteins from each group have different cellular localizations during the intraerythrocytic life cycle of the parasite. In the present study we show that function shift analysis, a novel technique to predict functional divergence between sub-groups of a protein family, indicates that RIFINs have undergone neo- or sub-functionalization.</p> <p>Conclusion</p> <p>These results question the general trend of clustering large antigenically variant protein groups into homogenous families. Assigning functions to protein families requires their subdivision into meaningful groups such as we have shown for the RIFIN protein family. Using phylogenetic and function shift analysis methods, we identify new directions for the investigation of this broad and complex group of proteins.</p> http://www.biomedcentral.com/1471-2164/9/19
collection DOAJ
language English
format Article
sources DOAJ
author Sonnhammer Erik L
Abhiman Saraswathi
Joannin Nicolas
Wahlgren Mats
spellingShingle Sonnhammer Erik L
Abhiman Saraswathi
Joannin Nicolas
Wahlgren Mats
Sub-grouping and sub-functionalization of the RIFIN multi-copy protein family
BMC Genomics
author_facet Sonnhammer Erik L
Abhiman Saraswathi
Joannin Nicolas
Wahlgren Mats
author_sort Sonnhammer Erik L
title Sub-grouping and sub-functionalization of the RIFIN multi-copy protein family
title_short Sub-grouping and sub-functionalization of the RIFIN multi-copy protein family
title_full Sub-grouping and sub-functionalization of the RIFIN multi-copy protein family
title_fullStr Sub-grouping and sub-functionalization of the RIFIN multi-copy protein family
title_full_unstemmed Sub-grouping and sub-functionalization of the RIFIN multi-copy protein family
title_sort sub-grouping and sub-functionalization of the rifin multi-copy protein family
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2008-01-01
description <p>Abstract</p> <p>Background</p> <p>Parasitic protozoans possess many multicopy gene families which have central roles in parasite survival and virulence. The number and variability of members of these gene families often make it difficult to predict possible functions of the encoded proteins. The families of extra-cellular proteins that are exposed to a host immune response have been driven via immune selection to become antigenically variant, and thereby avoid immune recognition while maintaining protein function to establish a chronic infection.</p> <p>Results</p> <p>We have combined phylogenetic and function shift analyses to study the evolution of the RIFIN proteins, which are antigenically variant and are encoded by the largest multicopy gene family in <it>Plasmodium falciparum</it>. We show that this family can be subdivided into two major groups that we named A- and B-RIFIN proteins. This suggested sub-grouping is supported by a recently published study that showed that, despite the presence of the <it>Plasmodium </it>export (PEXEL) motif in all RIFIN variants, proteins from each group have different cellular localizations during the intraerythrocytic life cycle of the parasite. In the present study we show that function shift analysis, a novel technique to predict functional divergence between sub-groups of a protein family, indicates that RIFINs have undergone neo- or sub-functionalization.</p> <p>Conclusion</p> <p>These results question the general trend of clustering large antigenically variant protein groups into homogenous families. Assigning functions to protein families requires their subdivision into meaningful groups such as we have shown for the RIFIN protein family. Using phylogenetic and function shift analysis methods, we identify new directions for the investigation of this broad and complex group of proteins.</p>
url http://www.biomedcentral.com/1471-2164/9/19
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