http://www.cnr.it/ontology/cnr/individuo/prodotto/ID26936
Microdeletion/duplication at the Xq28 IP locus causes a de novo IKBKG/NEMO/IKKgamma exon4_10 deletion in families with Incontinentia Pigmenti (Articolo in rivista)
- Type
- Label
- Microdeletion/duplication at the Xq28 IP locus causes a de novo IKBKG/NEMO/IKKgamma exon4_10 deletion in families with Incontinentia Pigmenti (Articolo in rivista) (literal)
- Anno
- 2009-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/humu.21069 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Fusco F.; Paciolla M.; Pescatore A.; Lioi M.B.; Ayuso C.; Faravelli F.; Gentile M.; Zollino M.; D'Urso M.; Miano M.G.; Ursini M.V. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#note
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Institute of Genetics and Biophysics ''Adriano Buzzati-Traverso'' (IGB-CNR), Naples, Italy; University of Basilicata, Potenza, Italy; Department
of Genetics Foundation Jimenez Diaz, Madrid, Spain; Department of Genetic Sciences, Galliera Hospital, Genoa, Italy; IRCCS '' Saverio De
Bellis'' Medical Genetics Unit, Bari, Italy; Catholic University, Institute of Medical Genetics, Rome, Italy (literal)
- Titolo
- Microdeletion/duplication at the Xq28 IP locus causes a de novo IKBKG/NEMO/IKKgamma exon4_10 deletion in families with Incontinentia Pigmenti (literal)
- Abstract
- The Incontinentia Pigmenti (IP) locus contains
the IKBKG/NEMO/IKKgamma gene and its truncated
pseudogene copy, IKBKGP/deltaNEMO. The major
genetic defect in IP is a heterozygous exon4_10 IKBKG
deletion (IKBKGdel) caused by a recombination between
two consecutive MER67B repeats. We analyzed 91 IP
females carrying the IKBKGdel, 59 of whom carrying de
novo mutations (65%). In eight parents, we found two
recurrent nonpathological variants of IP locus, which were
also present as rare polymorphism in control population:
the IKBKGPdel, corresponding to the exon4_10 deletion
in the pseudogene, and the MER67Bdup, that replicates
the exon4_10 region downstream of the normal IKBKG
gene. Using quantitative DNA analysis and microsatellite
mapping, we established that both variants might promote
the generation of the pathological IKBKGdel. Indeed, in
family IP-516, the exon4_10 deletion was repositioned in
the same allele from the pseudogene to the gene, whereas
in family IP-688, the MER67Bdup generated the pathological
IKBKGdel by recombination between two direct
nonadjacent MER67Bs. Moreover, we found an instance
of somatic recombination in a MER67Bdup variant,
creating the IKBKGdel in an IP male. Our data suggest
that the IP locus undergoes recombination producing
recurrent variants that might be ''at risk'' of generating de
novo IKBKGdel by NAHR during either meiotic or
mitotic division. (literal)
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