Next-generation sequencing is a straightforward tool for the identification of disease genes in extended genomic regions. Autozygosity mapping was performed on a five-generation inbred Italian family with three siblings affected with Clericuzio-type poikiloderma with neutropenia (PN [MIM `4173]), a rare autosomal-recessive genodermatosis characterised by poikiloderma, pachyonychia, and chronic neutropenia. The siblings were initially diagnosed as affected with Rothmund-Thomson syndrome (RTS [MIM #268400]), with which PN shows phenotypic overlap. Linkage analysis on all living subjects of the family identified a large 16q region inherited identically by descent (IBD) in all affected family members. Deep sequencing of this 3.4 Mb region previously enriched with array capture revealed a homozygous c.504-2 A>C mismatch in all affected siblings. The mutation destroys the invariant AG acceptor site of intron 4 of the evolutionarily conserved C16orf57 gene. Two distinct deleterious mutations (c.502A>G and c.666_676+1del12) identified in an unrelated PN patient confirmed that the C16orf57 gene is responsible for PN. The function of the predicted C16orf57 gene is unknown, but its product has been shown to be interconnected to RECQL4 protein via SMAD4 proteins. The unravelled clinical and genetic identity of PN allows patients to undergo genetic testing and follow-up.

Volpi, L., Roversi, G., Colombo, E., Leijsten, N., Concolino, D., Calabria, A., et al. (2010). Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene. AMERICAN JOURNAL OF HUMAN GENETICS, 86(1), 72-76 [10.1016/j.ajhg.2009.11.014].

Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene

ROVERSI, GAIA;
2010

Abstract

Next-generation sequencing is a straightforward tool for the identification of disease genes in extended genomic regions. Autozygosity mapping was performed on a five-generation inbred Italian family with three siblings affected with Clericuzio-type poikiloderma with neutropenia (PN [MIM `4173]), a rare autosomal-recessive genodermatosis characterised by poikiloderma, pachyonychia, and chronic neutropenia. The siblings were initially diagnosed as affected with Rothmund-Thomson syndrome (RTS [MIM #268400]), with which PN shows phenotypic overlap. Linkage analysis on all living subjects of the family identified a large 16q region inherited identically by descent (IBD) in all affected family members. Deep sequencing of this 3.4 Mb region previously enriched with array capture revealed a homozygous c.504-2 A>C mismatch in all affected siblings. The mutation destroys the invariant AG acceptor site of intron 4 of the evolutionarily conserved C16orf57 gene. Two distinct deleterious mutations (c.502A>G and c.666_676+1del12) identified in an unrelated PN patient confirmed that the C16orf57 gene is responsible for PN. The function of the predicted C16orf57 gene is unknown, but its product has been shown to be interconnected to RECQL4 protein via SMAD4 proteins. The unravelled clinical and genetic identity of PN allows patients to undergo genetic testing and follow-up.
Articolo in rivista - Articolo scientifico
Genomics; Male; Evolution, Molecular; Rothmund-Thomson Syndrome; Skin Diseases; Open Reading Frames; Female; Genotype; Heterozygote; Neutropenia; Abnormalities, Multiple; Homozygote; Humans; Sequence Analysis, DNA; DNA Mutational Analysis; Pedigree; Diagnosis, Differential
English
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Volpi, L., Roversi, G., Colombo, E., Leijsten, N., Concolino, D., Calabria, A., et al. (2010). Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene. AMERICAN JOURNAL OF HUMAN GENETICS, 86(1), 72-76 [10.1016/j.ajhg.2009.11.014].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/28437
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