Bringaud Frédéric, Ghedin Elodie, Blandin Gaëlle, Bartholomeu Daniella C, Caler Elisabet, Levin Mariano J, Baltz Théo, El-Sayed Najib M
Laboratoire de Génomique Fonctionnelle Des Trypanosomatides, Université Victor Segalen Bordeaux 2, UMR-5162 CNRS, 146 Rue Léo Saignat, 33076 Bordeaux Cedex, France.
Mol Biochem Parasitol. 2006 Feb;145(2):158-70. doi: 10.1016/j.molbiopara.2005.09.017. Epub 2005 Oct 10.
The ingi and L1Tc non-LTR retrotransposons--which constitute the ingi clade--are abundant in the genome of the trypanosomatid species Trypanosoma brucei and Trypanosoma cruzi, respectively. The corresponding retroelements, however, are not present in the genome of a closely related trypanosomatid, Leishmania major. To study the evolution of non-LTR retrotransposons in trypanosomatids, we have analyzed all ingi/L1Tc elements and highly degenerate ingi/L1Tc-related sequences identified in the recently completed T. brucei, T. cruzi and L. major genomes. The coding sequences of 242 degenerate ingi/L1Tc-related elements (DIREs) in all three genomes were reconstituted by removing the numerous frame shifts. Three independent phylogenetic analyses conducted on the conserved domains encoded by these elements show that all DIREs, including the 52 L. major DIREs, form a monophyletic group belonging to the ingi clade. This indicates that the trypanosomatid ancestor contained active mobile elements that have been retained in the Trypanosoma species, but were lost from L. major genome, where only remnants (DIRE) are detectable. All 242 DIREs analyzed group together according to their species origin with the exception of 11 T. cruzi DIREs which are close to the T. brucei ingi/DIRE families. Considering the absence of known horizontal transfer between the African T. brucei and the South-American T. cruzi, this suggests that this group of elements evolved at a lower rate when compared to the other trypanosomatid elements. Interestingly, the only nucleotide sequence conserved between ingi and L1Tc (the first 79 residues) is also present at the 5'-extremity of all the full length DIREs and suggests a possible role for this conserved motif, as well as for DIREs.
ingi和L1Tc非长末端重复逆转座子(它们构成了ingi进化枝)分别在锥虫物种布氏锥虫和克氏锥虫的基因组中大量存在。然而,在亲缘关系密切的锥虫利什曼原虫的基因组中却不存在相应的逆转元件。为了研究锥虫中非长末端重复逆转座子的进化,我们分析了在最近完成测序的布氏锥虫、克氏锥虫和利什曼原虫基因组中鉴定出的所有ingi/L1Tc元件以及高度退化的ingi/L1Tc相关序列。通过去除众多移码突变,对这三个基因组中242个退化的ingi/L1Tc相关元件(DIREs)的编码序列进行了重构。对这些元件编码的保守结构域进行的三次独立系统发育分析表明,所有DIREs,包括52个利什曼原虫DIREs,形成了一个属于ingi进化枝的单系类群。这表明锥虫的祖先含有活跃的可移动元件,这些元件在锥虫物种中得以保留,但在利什曼原虫基因组中丢失了,在利什曼原虫基因组中只能检测到残余物(DIRE)。除了11个与布氏锥虫ingi/DIRE家族接近的克氏锥虫DIREs外,所有分析的242个DIREs都根据其物种来源归为一组。考虑到非洲的布氏锥虫和南美洲的克氏锥虫之间不存在已知的水平转移,这表明与其他锥虫元件相比,这一组元件的进化速度较慢。有趣的是,ingi和L1Tc之间唯一保守的核苷酸序列(前79个残基)也存在于所有全长DIREs的5'末端,这表明这个保守基序以及DIREs可能具有某种作用。