Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/57713
Type: Artigo de periódico
Title: Molecular analysis of chronic granulomatous disease caused by defects in gp91-phox
Author: Patino, PJ
Perez, JE
Lopez, JA
Condino-Neto, A
Grumach, AS
Botero, JH
Curnutte, JT
de Olarte, DG
Abstract: Chronic granulomatous disease (CGD) is an uncommon inherited disorder of phagocytic cells in which a defective respiratory burst leads to severe recurrent bacterial and fungal infections. The disease is a consequence of mutations in one of the four molecules that constitute the NADPH oxidase system of electron transport, whose most critical component is an unusual flavocytochrome b localized in the plasma and specific granule membranes. Mutations in the CYBB gene (localized in the short arm of the X chromosome) encoding the beta-subunit of this flavocytochrome (gp91-phox), which is are responsible for 60-65% of all cases of CGD. In this paper, we report the molecular characterization of seven unrelated kindreds native from Colombia and Brazil with CGD caused by gp91-phox deficiency. The exons with the possible mutation were identified by single-strand conformational polymorphism (SSCP) of genomic DNA and then confirmed by DNA sequencing. In one patient we found a substitution of A to G in the penultimate nucleotide of intron 12 (IVS12-2A-->G). In four other cases, four different nonsense mutations were detected: R91X, W106X, R157X, and R290X and the other two patients showed missense substitutions: E225V and C244Y. In six of these kindreds, all mothers were carriers but one that did not present any change in the gp91-phox gene, which indicates a de novo mutation in this kindred. Then, these family-specific mutations in gp91-phox produce different structural defects that alter the expression or function of an essential component of phagocyte oxidase, Hum Mutat 13:29-37, 1999. (C) 1999 Wiley-Liss, Inc.
Subject: neutrophils
chronic granulomatous disease
mutations in gp91-phox
SSCP-PCR
DNA sequencing
Country: EUA
Editor: Wiley-liss
Rights: fechado
Identifier DOI: 10.1002/(SICI)1098-1004(1999)13:1<29
Date Issue: 1999
Appears in Collections:Unicamp - Artigos e Outros Documentos

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