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Stable Allele Frequency Distribution of the Plasmodium falciparum clag Genes Encoding Components of the High Molecular Weight Rhoptry Protein Complex
Plasmodium falciparum Clag protein is a candidate component of the plasmodial surface anion channel located on the parasite-infected erythrocyte. This protein is encoded by 5 separated clag genes and forms a RhopH complex with the other components. Previously, a signature of positive diversifying se...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Tropical Medicine
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521051/ https://www.ncbi.nlm.nih.gov/pubmed/23264726 http://dx.doi.org/10.2149/tmh.2012-13 |
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author | Alexandre, Jean Semé Fils Xangsayarath, Phonepadith Kaewthamasorn, Morakot Yahata, Kazuhide Sattabongkot, Jetsumon Udomsangpetch, Rachanee Kaneko, Osamu |
author_facet | Alexandre, Jean Semé Fils Xangsayarath, Phonepadith Kaewthamasorn, Morakot Yahata, Kazuhide Sattabongkot, Jetsumon Udomsangpetch, Rachanee Kaneko, Osamu |
author_sort | Alexandre, Jean Semé Fils |
collection | PubMed |
description | Plasmodium falciparum Clag protein is a candidate component of the plasmodial surface anion channel located on the parasite-infected erythrocyte. This protein is encoded by 5 separated clag genes and forms a RhopH complex with the other components. Previously, a signature of positive diversifying selection was detected on the hypervariable region of clag2 and clag8 by population-based analyses using P. falciparum originating from Thailand in 1988–1989. In this study, we obtained the sequence of this region of 3 clag genes (clag2, clag8, and clag9) in 2005 and evaluated the changes over time in the frequency distribution of the polymorphism of these gene products by comparison with the sequences obtained in 1988–1989. We found no difference in the frequency distribution of 18 putatively neutral loci between the 2 groups, evidence that the background of the parasite population structure has remained stable over 14 years. Although the frequency distribution of most of the polymorphic sites in the hypervariable region of Clag2, Clag8, and Clag9 was stable over 14 years, we found that a proportion of the major Clag2 group and one amino acid position of Clag8 changed significantly. This may be a response to a certain type of pressure. |
format | Online Article Text |
id | pubmed-3521051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Japanese Society of Tropical Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-35210512012-12-21 Stable Allele Frequency Distribution of the Plasmodium falciparum clag Genes Encoding Components of the High Molecular Weight Rhoptry Protein Complex Alexandre, Jean Semé Fils Xangsayarath, Phonepadith Kaewthamasorn, Morakot Yahata, Kazuhide Sattabongkot, Jetsumon Udomsangpetch, Rachanee Kaneko, Osamu Trop Med Health Original Article Plasmodium falciparum Clag protein is a candidate component of the plasmodial surface anion channel located on the parasite-infected erythrocyte. This protein is encoded by 5 separated clag genes and forms a RhopH complex with the other components. Previously, a signature of positive diversifying selection was detected on the hypervariable region of clag2 and clag8 by population-based analyses using P. falciparum originating from Thailand in 1988–1989. In this study, we obtained the sequence of this region of 3 clag genes (clag2, clag8, and clag9) in 2005 and evaluated the changes over time in the frequency distribution of the polymorphism of these gene products by comparison with the sequences obtained in 1988–1989. We found no difference in the frequency distribution of 18 putatively neutral loci between the 2 groups, evidence that the background of the parasite population structure has remained stable over 14 years. Although the frequency distribution of most of the polymorphic sites in the hypervariable region of Clag2, Clag8, and Clag9 was stable over 14 years, we found that a proportion of the major Clag2 group and one amino acid position of Clag8 changed significantly. This may be a response to a certain type of pressure. The Japanese Society of Tropical Medicine 2012-09 2012-08-11 /pmc/articles/PMC3521051/ /pubmed/23264726 http://dx.doi.org/10.2149/tmh.2012-13 Text en © 2012 Japanese Society of Tropical Medicine 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 work is properly cited. |
spellingShingle | Original Article Alexandre, Jean Semé Fils Xangsayarath, Phonepadith Kaewthamasorn, Morakot Yahata, Kazuhide Sattabongkot, Jetsumon Udomsangpetch, Rachanee Kaneko, Osamu Stable Allele Frequency Distribution of the Plasmodium falciparum clag Genes Encoding Components of the High Molecular Weight Rhoptry Protein Complex |
title | Stable Allele Frequency Distribution of the Plasmodium falciparum clag Genes Encoding Components of the High Molecular Weight Rhoptry Protein Complex |
title_full | Stable Allele Frequency Distribution of the Plasmodium falciparum clag Genes Encoding Components of the High Molecular Weight Rhoptry Protein Complex |
title_fullStr | Stable Allele Frequency Distribution of the Plasmodium falciparum clag Genes Encoding Components of the High Molecular Weight Rhoptry Protein Complex |
title_full_unstemmed | Stable Allele Frequency Distribution of the Plasmodium falciparum clag Genes Encoding Components of the High Molecular Weight Rhoptry Protein Complex |
title_short | Stable Allele Frequency Distribution of the Plasmodium falciparum clag Genes Encoding Components of the High Molecular Weight Rhoptry Protein Complex |
title_sort | stable allele frequency distribution of the plasmodium falciparum clag genes encoding components of the high molecular weight rhoptry protein complex |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521051/ https://www.ncbi.nlm.nih.gov/pubmed/23264726 http://dx.doi.org/10.2149/tmh.2012-13 |
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