Large intragenic deletions within the DMD locus account for about 60% of Duchenne and Becker muscular dystrophy patients. Two deletion hot-spots have been described in the dystrophin gene, but the mechanisms that determine chromosome breaks in these regions are unknown, and the huge dimensions of the gene have hampered the description of a consistent number of breakpoint sequences. A long-distance polymerase chain reaction strategy was used to amplify 20 deletion junctions involving the major hot-spot and to describe breakpoint position at the sequence level. These junctions were analyzed together with previously reported breakpoint locations so as to increase the sample number and possibly provide a comprehensive study. Minisatellite core sequences, chi elements, translin-binding sites, Pur elements, and matrix attachment regions were sought over the whole gene. Sequence-dependent DNA curvature and duplex stability were also calculated throughout the gene, and their cumulative frequency distribution was evaluated. No association with either sequence or structure elements involved in known illegitimate recombination mechanisms was identified. This study highlights the importance of a whole gene approach to rule out the presumptive role of specific features that, when locally analyzed, might suggest involvement in gene rearrangements.

Sironi, M., Pozzoli, U., Cagliani, R., Giorda, R., Comi, G., Bardoni, A., et al. (2003). Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot. HUMAN GENETICS, 112(3), 272-288 [10.1007/s00439-002-0881-5].

Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot

Sironi M
;
2003

Abstract

Large intragenic deletions within the DMD locus account for about 60% of Duchenne and Becker muscular dystrophy patients. Two deletion hot-spots have been described in the dystrophin gene, but the mechanisms that determine chromosome breaks in these regions are unknown, and the huge dimensions of the gene have hampered the description of a consistent number of breakpoint sequences. A long-distance polymerase chain reaction strategy was used to amplify 20 deletion junctions involving the major hot-spot and to describe breakpoint position at the sequence level. These junctions were analyzed together with previously reported breakpoint locations so as to increase the sample number and possibly provide a comprehensive study. Minisatellite core sequences, chi elements, translin-binding sites, Pur elements, and matrix attachment regions were sought over the whole gene. Sequence-dependent DNA curvature and duplex stability were also calculated throughout the gene, and their cumulative frequency distribution was evaluated. No association with either sequence or structure elements involved in known illegitimate recombination mechanisms was identified. This study highlights the importance of a whole gene approach to rule out the presumptive role of specific features that, when locally analyzed, might suggest involvement in gene rearrangements.
Articolo in rivista - Articolo scientifico
Base Sequence; DNA Primers; Dystrophin; Gene Deletion; Heat; Humans; Introns; Sequence Analysis, DNA
English
2003
112
3
272
288
reserved
Sironi, M., Pozzoli, U., Cagliani, R., Giorda, R., Comi, G., Bardoni, A., et al. (2003). Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot. HUMAN GENETICS, 112(3), 272-288 [10.1007/s00439-002-0881-5].
File in questo prodotto:
File Dimensione Formato  
Sironi-2003-Human Genetics-VoR.pdf

Solo gestori archivio

Tipologia di allegato: Publisher’s Version (Version of Record, VoR)
Licenza: Tutti i diritti riservati
Dimensione 446.73 kB
Formato Adobe PDF
446.73 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/516141
Citazioni
  • Scopus 27
  • ???jsp.display-item.citation.isi??? 20
Social impact