English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/8432
logo share SHARE   Add this article to your Mendeley library MendeleyBASE
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:

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

AuthorsMartín-Hernández, Ana M.; Gutiérrez-Rivas, Mónica; Domingo, Esteban ; Menéndez-Arias, Luis
KeywordsHIV-1 RT
Issue Date1997
PublisherOxford University Press
CitationNucleic Acids Res., 1997; 25: 1383 - 1389.
AbstractThe 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.
Publisher version (URL)http://nar.oxfordjournals.org/cgi/content/full/25/7/1383
Appears in Collections:(CBM) Artículos
Files in This Item:
File Description SizeFormat 
AMMartín-Hernández_NAR_1383.pdf93,75 kBAdobe PDFThumbnail
Show full item record
Review this work

WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.