Cytogenetic molecular delineation of a terminal 18q deletion suggesting neo-telomere formation
| Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
|---|---|
| Data(s) |
19/10/2012
19/10/2012
2010
|
| Resumo |
Deletion of the long arm of chromosome 18 is one of the most common segmental aneusomies compatible with life and usually involves a deletion of the terminal chromosomal region. However, the mechanisms implicated in the stabilization of terminal deletions are not well understood. In this study, we analyzed a girl with moderate mental retardation who had a cytogenetically visible terminal 18q deletion. In order to characterize the breakpoint in the terminal 18q region, we used fluorescence In situ hybridization (FISH) with bacterial artificial chromosomes (BACs) and pan-telomeric probes and also the array technique based on comparative genomic hybridization (array-CGH). FISH with pan-telomeric probes revealed no signal in the terminal region of the deleted chromosome, indicating the absence of normal telomere repeat (TTAGGG)n sequences in 18q. We suggest that neo-telomere formation by chromosome healing was involved in the repair and stabilization of this terminal deletion. (C) 2010 Elsevier Masson SAS. All rights reserved. CAPES FAPESP (Brazil) |
| Identificador |
EUROPEAN JOURNAL OF MEDICAL GENETICS, v.53, n.6, p.404-407, 2010 1769-7212 http://producao.usp.br/handle/BDPI/22932 10.1016/j.ejmg.2010.08.007 |
| Idioma(s) |
eng |
| Publicador |
ELSEVIER SCIENCE BV |
| Relação |
European Journal of Medical Genetics |
| Direitos |
restrictedAccess Copyright ELSEVIER SCIENCE BV |
| Palavras-Chave | #18q Deletion #Terminal deletion #Telomere healing #Neo-telomere #HUMAN-CHROMOSOMES #INTERSTITIAL DELETIONS #MONOSOMY 1P36 #REPEATS #REARRANGEMENTS #HYBRIDIZATION #MECHANISMS #BREAKAGE #FUSION #DNA #Genetics & Heredity |
| Tipo |
article original article publishedVersion |