Plasmodium falciparum myosins:: Transcription and translation during asexual parasite development

被引:17
作者
Chaparro-Olaya, J
Margos, A
Coles, DJ
Dluzewski, AR
Mitchell, GH
Wasserman, MM
Pinder, JC
机构
[1] Kings Coll London, Randall Div Cell & Mol Biophys, London SE1 1UL, England
[2] Lab Biochem, Inst Nacl Salud, Bogota, Colombia
[3] Kings Coll London, Guys Hosp, Guys Kings Coll & St Thomas Hosp, Sch Med,Dept Immunobiol, London, England
[4] Univ Nacl Colombia, Fac Sci, Dept Chem, Bogota, Colombia
来源
CELL MOTILITY AND THE CYTOSKELETON | 2005年 / 60卷 / 04期
关键词
apicomplexa; Plasmodium; malaria; sequence; asexual stages; invasion; motility; myosin; Pfmyo-D;
D O I
10.1002/cm.20055
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Six myosins genes are now annotated in the Plasmodium falciparum Genome Project. Malaria myosins have been named alphabetically; accordingly, we refer to the two latest additions as Pfmyo-E and Pfmyo-F. Both new myosins contain regions characteristic of the functional motor domain of "true" myosins and, unusually for P. falciparum myosins, Pfmyo-F encodes two consensus IQ light chain-binding motifs. Phylogenetic analysis of the 17 currently known apicomplexan myosins together with one representative of each myosin class clusters all but one of the apicomplexan sequences together in Class XIV. This refines the earlier definition of the Class XIV Subclasses XIVa and XIVb. RT-PCR on blood stage parasite mRNA amplifies a specific product for all six myosins and each shows developmentally regulated transcription. Thus: Pfmyo-A and Pfmyo-B genes are transcribed throughout development; Pfmyo-C is predominant in trophozoites; Pfmyo-D occurs in trophozoites and schizonts; Pfmyo-E though barely present in earlier stages is abundant in schizonts; Pfmyo-F increases steadily throughout development and maturation. It is known that Pfmyo-A and Pfmyo-B are synthesised during late schizogony and we now show that Pfmyo-D expression is also temporally regulated to late trophozoites and schizonts where it distributes close to segregating nuclei. Thus, in asexual stages myosin synthesis does not always parallel transcript accumulation, showing that translation is also regulated. The implication is that the mRNAs are either subjected to turnover, synthesised and degraded, or that they are sequestered in an inactivate form until required for protein synthesis. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:200 / 213
页数:14
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