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dc.contributor.authorBringaud, Frédéric
dc.contributor.authorGarcı́a-Pérez, José Luis
dc.contributor.authorRodríguez Heras, Sara 
dc.contributor.authorLópez, Manuel C
dc.date.accessioned2024-02-06T12:26:48Z
dc.date.available2024-02-06T12:26:48Z
dc.date.issued2002
dc.identifier.citationBringaud F, García-Pérez JL, Heras SR, Ghedin E, El-Sayed NM, Andersson B, Baltz T, Lopez MC. Identification of non-autonomous non-LTR retrotransposons in the genome of Trypanosoma cruzi. Mol Biochem Parasitol. 2002 Sep-Oct;124(1-2):73-8. doi: 10.1016/s0166-6851(02)00167-6es_ES
dc.identifier.urihttps://hdl.handle.net/10481/88440
dc.description.abstractAs observed for most eukaryotic cells, trypanosomatids contains non-LTR retrotransposons randomly inserted in the nuclear genome. Autonomous retroelements which, code for their own transposition, have been characterized in Trypanosoma brucei (ingi) and Trypanosoma cruzi (L1Tc), whereas non-autonomous retroelements have only been characterized in T. brucei (RIME). Here, we have characterized in the genome of Trypanosoma cruzi four complete copies of a non-autonomous non-LTR retrotransposon, called NARTc. This 0.26 kb NARTc element has the characteristics of non-LTR retrotransposons: the presence a poly(dA) tail and of a short flanking duplicated motif. Analysis of the Genome Survey Sequence databases indicated that the Trypanosoma cruzi haploid genome contains about 140 NARTc copies and about twice as many L1Tc copies. Interestingly, the NARTc and L1Tc retroelements share, with the Trypanosoma brucei ingi and RIME retrotransposons, a common sequence (the first 45 bp with 91% identity), whereas the remaining sequences are very divergent. This suggests that these four trypanosome non-LTR retrotransposons were derived from the same common ancester and the sequence of their 5’-extremity may have a functional role. In addition, the genome of Leishmania major contains the same conserved motif present in the trypanosome retroelements, whicle no transposable elements have been detected so far in Leishmania spes_ES
dc.description.sponsorshipWe are extremely grateful to the Instituto de Investigaciones Biotecnolo´ gicas, Buenos Aires, Argentina (IIB INTECH*/http://cruzi.unsam.edu.ar/gss.html*/ cfrasch@iib.unsam.edu.ar) and the Instituto de Parasitologia y Biomedicina, Granada, Spain (IPBLN), for all the GSS and EST sequences released on the T. cruzi database (http://www.ebi.ac.uk/blast2/parasites.html), and the Wellcome Trust Sanger Institute (http:// www.sanger.ac.uk/Projects/L_major) for the DNA genomic sequences released on the L. major database. We also would like to thank M. Levin for useful discussion all along this analysis. This work was supported by the CNRS, the Conseil Re´gional d’Aquitaine, the GDR Parasitologie (CNRS), the Ministe`re de l’Education Nationale de la Recherche et de la Technologie (Action Microbiologie). S.R. Heras, J.L. Garcı´a- Pe´rez, M.C. Lo´pez were supported by BFM2000-1381 from MCyT, Spain. N.M. El-Sayed and E. Ghedin were supported by NIH grant U01-AI45038 (NES).es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleIdentification of non-autonomous non-LTR retrotransposons in the genome of Trypanosoma cruzies_ES
dc.typejournal articlees_ES
dc.rights.accessRightsembargoed accesses_ES
dc.identifier.doi10.1016/s0166-6851(02)00167-6
dc.type.hasVersionVoRes_ES


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