dc.contributorUniversidade Estadual de Campinas (UNICAMP)
dc.contributorLNLS
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:25:51Z
dc.date.accessioned2022-10-05T16:35:23Z
dc.date.available2014-05-20T15:25:51Z
dc.date.available2022-10-05T16:35:23Z
dc.date.created2014-05-20T15:25:51Z
dc.date.issued2006-04-01
dc.identifierParasitology Research. New York: Springer, v. 98, n. 5, p. 447-454, 2006.
dc.identifier0932-0113
dc.identifierhttp://hdl.handle.net/11449/36180
dc.identifier10.1007/s00436-005-0036-4
dc.identifierWOS:000236207300009
dc.identifier7449821021440644
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3907960
dc.description.abstractThe Leishmania amazonensis telomerase gene was cloned by a polymerase chain reaction-based strategy using primers designed from a Leishmania major sequence that shared similarities with conserved telomerase motifs. The genes from three other species were cloned for comparative purposes. A ClustalW multiple-sequence alignment demonstrated that the Leishmania telomerases show greater homology with each other than with the proteins of other kinetoplastids and eukaryotes. Characterization experiments indicated that the putative Leishmania telomerase gene was probably in single copy and located in the largest chromosomes. A single messenger ribonucleic acid transcript was found in promastigotes. Phylogenetic analysis suggested that Leishmania telomerase might represent a liaison between the oldest and the newest branches of telomerases.
dc.languageeng
dc.publisherSpringer
dc.relationParasitology Research
dc.relation2.558
dc.relation0,991
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.titleThe putative telomerase reverse transcriptase component of Leishmania amazonensis: gene cloning and characterization
dc.typeArtigo


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