Cloning leishmania telomeres in yeast by complementation

Descripción del Articulo

Leishmania telemores were cloned in yeast by complementation using a half arm of the yeast artificial chromosome vector pJS97. A single copy marker associated to the telomere (YT2) located 6 kb away from one end of a megabase size chromosome of 1116c8 was cloned by end rescue and DNA sequenced. The...

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Detalles Bibliográficos
Autor: Espinoza, José
Formato: artículo
Fecha de Publicación:2003
Institución:Instituto Peruano de Energía Nuclear
Repositorio:IPEN-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorio.ipen.gob.pe:20.500.13054/363
Enlace del recurso:https://hdl.handle.net/20.500.13054/363
Nivel de acceso:acceso abierto
Materia:Leishmania telemores
Parásitos
Enfermedad de leishmaniasis
Secuencia de cromosomas
Descripción
Sumario:Leishmania telemores were cloned in yeast by complementation using a half arm of the yeast artificial chromosome vector pJS97. A single copy marker associated to the telomere (YT2) located 6 kb away from one end of a megabase size chromosome of 1116c8 was cloned by end rescue and DNA sequenced. The sequence of 1479 bp did not show a significant homology with any sequence stored in GenBank. Leishmania telomeres are amenable to be cloned and maintained in yeast, this approach will facilitate the analysis of telomere and subtelomere regions which are usually underrepresented in genomic libraries.
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