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A novel point mutation in the CYBB gene promoter leading to a rare X minus chronic granulomatous disease variant--impact on the microbicidal activity of neutrophils.

Defendi F.
•
DECLEVA, EVA
•
Martel C.
altro
Stasia M.J.
2009
  • journal article

Periodico
BIOCHIMICA ET BIOPHYSICA ACTA
Abstract
This article reports an atypical and extremely rare case of X-linked CGD in an Italian family characterized by a low expression of gp91phox (X91- CGD). A novel point mutation in the CYBB gene's promoter (insertion of a T at position -54T to -56T) appeared to prevent the full expression of this gene in the patient's neutrophils and correlated with a residual oxidase activity in the whole cells population. The expression and functional activity of the oxidase in eosinophils appeared to be almost normal. Gel shift assays indicated that the mutation led to decreased interactions with DNA-binding proteins. The total O2- production in the patient's granulocytes (5-7% of normal) supported no microbicidal power after 45 min and 60 min of contact with S. aureus and C. albicans, respectively. Despite this residual oxidase activity, the patients suffered from severe and life-threatening infections. It was concluded that in these X91- CGD neutrophils, the O2- production per se was not sufficient to protect the patient against severe infections.
DOI
10.1016/j.bbadis.2009.01.005
Archivio
http://hdl.handle.net/11368/2742698
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-61549137180
http://www.sciencedirect.com/science/article/pii/S0925443909000064
Diritti
metadata only access
Soggetti
  • Chronic granulomatous...

  • CYBB gene promoter

  • Point mutation

  • Cytochrome b558

  • NADPH oxidase

  • Microbicidal activity...

Scopus© citazioni
13
Data di acquisizione
Jun 14, 2022
Vedi dettagli
Web of Science© citazioni
16
Data di acquisizione
Mar 24, 2024
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