Premium
Common structural features characterize interstitial intrachromosomal Xp and 18q triplications
Author(s) -
Giorda Roberto,
Beri Silvana,
Bonaglia M. Clara,
Spaccini Luigina,
Scelsa Barbara,
Manolakos Emmanouil,
Mina Erika Della,
Ciccone Roberto,
Zuffardi Orsetta
Publication year - 2011
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.34248
Subject(s) - biology , breakpoint , genetics , chromosome , tetrasomy , homologous chromosome , gene , clinical phenotype , phenotype , cytogenetics
Rare intrachromosomal triplications producing partial tetrasomies have been reported for a number of chromosomes. A detailed molecular characterization, necessary to define the mechanism of their formation, has so far been lacking. We report on the detailed clinical, cytogenetic, and molecular characterization of two triplications, one de novo involving chromosome 18q, the other familial on chromosome Xp. The clinical phenotype of the patient with 18q triplication, very likely due to overexpression of one or more of the genes in the region, consists mainly of facial dysmorphisms and developmental delay. The familial Xp triplication does not cause an increase in the number of copies of any gene and is almost certainly a polymorphism. The rearrangements are actually complex duplications/triplications. In both patients, their proximal breakpoints are located within complex segmental duplications, one containing the VCX gene cluster on chromosome Xp, the other the TCEB3 genes on chromosome 18q. A proximal duplicated region is also present in both patients. All junctions we analyzed were formed by non‐homologous end joining (NHEJ). The structural features shared between our patients suggest the involvement of a common mechanism in the genesis of interstitial intrachromosomal triplications. © 2011 Wiley Periodicals, Inc.