Different unequal cross-over events between NCF1 and its pseudogenes in autosomal p47(Phox)-deficient chronic granulomatous disease

作者：Hayrapetyan Astghik; Dencher Paula C D; van Leeuwen Karin; de Boer Martin; Roos Dirk^*

来源：Biochimica et Biophysica Acta-Molecular Basis of Disease, 2013, 1832(10): 1662-1672.

DOI：10.1016/j.bbadis.2013.05.001

• Chronic granulomatous disease
• NCF1
• NCF1 pseudogene
• Genetic cross-over
• Partial NCF1 deletion
• Fusion gene

Chronic granulomatous disease (CGD) is a rare congenital disorder in which phagocytes cannot generate superoxide (O-2(-)) and other microbicidal oxidants due to mutations in one of the five components of the O-2(-)-generating NADPH oxidase complex. The most common autosomal subtype of CGD is caused by mutations in NCF1, encoding the NADPH subunit p47(Phox). Usually, these mutations are the result of unequal exchange of chromatid between NCF1 and one of its two pseudogenes. We have now investigated in detail the breakpoints within or between these (pseudo) NCF1 genes in 43 families with p47(Phox)-deficient CGD by means of multiplex ligase-dependent probe amplification (MLPA). In 24 families the patients totally lacked NCF1 sequences, indicating that in these families the cross-over points are located between NCF1 and its pseudogenes. Six other families were compound heterozygous for a total NCF1 deletion and another mutation in NCF1 on the other allele. In 8 families, the patients lacked NCF1 exons 1-4 but had retained NCF1 exons 6-10, indicating that a cross-over point is located within NCF1 between exons 4 and 6. Similarly, in 4 families a cross-over point was located within NCF1 between exons 2 and 4. Similar cross-avers, in heterozygous form, were observed in family members of the patients. Several patients were compound heterozygous for total and partial NCF1 deletions. Thus, at least three different cross-over points exist within the NCF1 gene cluster, indicating that autosomal p47(Phox)-deficient CGD is genetically heterogeneous but can be dissected in detail by MLPA.

• 出版日期2013-10