English   español  
Por favor, use este identificador para citar o enlazar a este item: http://hdl.handle.net/10261/8432
Compartir / Impacto:
Estadísticas
Add this article to your Mendeley library MendeleyBASE
Ver citas en Google académico
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar otros formatos: Exportar EndNote (RIS)Exportar EndNote (RIS)Exportar EndNote (RIS)
Título

Mispair extension fidelity of human immunodeficiency virus type 1 reverse transcriptases with amino acid substitutions affecting Tyr115

Autor Martín-Hernández, Ana M.; Gutiérrez-Rivas, Mónica; Domingo, Esteban; Menéndez-Arias, Luis
Palabras clave HIV-1 RT
Fecha de publicación 1997
EditorOxford University Press
Citación Nucleic Acids Res., 1997; 25: 1383 - 1389.
ResumenThe role of Tyr115 of human immunodeficiency virus type 1 reverse transcriptase (HIV-1 RT) in the mispair extension fidelity of DNA dependent DNA synthesis was analysed by using a series of 15 mutant enzymes with substitutions at Tyr115. Their kinetic parameters for elongation using homopolymeric RNA-DNA and heteropolymeric DNA-DNA complexes showed major effects of the amino acid substitutions on the K m value for dNTP. Enzymes with large hydrophobic residues at position 115 displayed lower K m values than enzymes with small and charged amino acids at this position. The influence of all these amino acid replacements in mispair extension fidelity assays was analyzed using three different mismatches (A:C, A:G and A:A) at the 3 ' -terminal position of the primer DNA. For the A:C mispair, a 2.6-33.4-fold increase in mispair extension efficiency ( f ext) was observed as compared with the wild-type enzyme. Unexpectedly, all the mutants tested as well as the wild-type RT were very efficient in extending the A:G and A:A transversion mispairs. This effect was due to the template-primer sequence context and not to the buffer conditions of the assay. The data support a role of Tyr115 in accommodating the complementary nucleotide into the nascent DNA while polymerization takes place.
Versión del editorhttp://nar.oxfordjournals.org/cgi/content/full/25/7/1383
URI http://hdl.handle.net/10261/8432
ISSN0305-1048 (print)
1362-4962 (online)
Aparece en las colecciones: (CBM) Artículos
Ficheros en este ítem:
Fichero Descripción Tamaño Formato  
AMMartín-Hernández_NAR_1383.pdf93,75 kBAdobe PDFVista previa
Visualizar/Abrir
Mostrar el registro completo
 


NOTA: Los ítems de Digital.CSIC están protegidos por copyright, con todos los derechos reservados, a menos que se indique lo contrario.