| Literature DB >> 21292901 |
Yue Wang1, Osamu Kaneko, Jetsumon Sattabongkot, Jun-Hu Chen, Feng Lu, Jong-Yil Chai, Satoru Takeo, Takafumi Tsuboi, Francisco J Ayala, Yong Chen, Chae Seung Lim, Eun-Taek Han.
Abstract
Plasmodium vivax msp1p, a paralog of the candidate vaccine antigen P. vivax merozoite surface protein 1, possesses a signal peptide at its N-terminus and two epidermal growth factor-like domains at its C-terminus with a glycosylphosphatidylinositol attachment site. The msp1p gene locus may have originated by a duplication of the msp1 gene locus in a common ancestor of the analyzed Plasmodium species and lost from P. yoelii, P. berghei, and P. falciparum during their evolutionary history. Full-length sequences of the msp1p gene were generally highly conserved; they had a few amino acid substitutions, one highly polymorphic E/Q-rich region, and a single-to-triple hepta-peptide repeat motif. Twenty-one distinguishable allelic types (A1-A21) of the E/Q-rich region were identified from worldwide isolates. Among them, four types were detected in isolates from South Korea. The length polymorphism of the E/Q-rich region might be useful as a genetic marker for population structure studies in malaria-endemic areas.Entities:
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Year: 2011 PMID: 21292901 PMCID: PMC3029184 DOI: 10.4269/ajtmh.2011.10-0432
Source DB: PubMed Journal: Am J Trop Med Hyg ISSN: 0002-9637 Impact factor: 2.345