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Complex genomic rea...
Complex genomic rearrangements in the dystrophin gene due to replication-based mechanisms
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Baskin, Berivan (författare)
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Stavropoulos, Dimitri J. (författare)
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Rebeiro, Paige A. (författare)
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visa fler...
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Orr, Jennifer (författare)
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Li, Martin (författare)
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Steele, Leslie (författare)
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Marshall, Christian R. (författare)
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Lemire, Edmond G. (författare)
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Boycott, Kym M. (författare)
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Gibson, William (författare)
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Ray, Peter N. (författare)
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visa färre...
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(utgivare)
- Wiley-Blackwell 2014
- 2014
- Engelska.
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Ingår i: Molecular Genetics & Genomic Medicine. - 2324-9269. ; 2:6, 539-547
Abstract
Ämnesord
Stäng
- Genomic rearrangements such as intragenic deletions and duplications are the most prevalent type of mutations in the dystrophin gene resulting in Duchenne and Becker muscular dystrophy (D/BMD). These copy number variations (CNVs) are nonrecurrent and can result from either nonhomologous end joining (NHEJ) or microhomology-mediated replication-dependent recombination (MMRDR). We characterized five DMD patients with complex genomic rearrangements using a combination of MLPA/mRNA transcript analysis/custom array comparative hybridization arrays (CGH) and breakpoint sequence analysis to investigate the mechanisms for these rearrangements. Two patients had complex rearrangements that involved microhomologies at breakpoints. One patient had a noncontiguous insertion of 89.7 kb chromosome 4 into intron 43 of DMD involving three breakpoints with 2–5 bp microhomology at the junctions. A second patient had an inversion of exon 44 flanked by intronic deletions with two breakpoint junctions each showing 2 bp microhomology. The third patient was a female with an inherited deletion of exon 47 in DMD on the maternal allele and a de novo noncontiguous duplication of exons 45–49 in DMD and MID1 on the paternal allele. The other two patients harbored complex noncontiguous duplications within the dystrophin gene. We propose a replication-based mechanisms for all five complex DMD rearrangements. This study identifies additional underlying mechanisms in DMD, and provides insight into the molecular bases of these genomic rearrangements.
Ämnesord
- Medical and Health Sciences (hsv)
- Basic Medicine (hsv)
- Medical Genetics (hsv)
- Medicin och hälsovetenskap (hsv)
- Medicinska grundvetenskaper (hsv)
- Medicinsk genetik (hsv)
Nyckelord
- Duchenne muscular dystrophy
- dystrophin
- MMRDR
- mRNA
- rearrangement
- replication
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Till lärosätets databas
- Av författaren/redakt...
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Baskin, Berivan
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Stavropoulos, Di ...
-
Rebeiro, Paige A ...
-
Orr, Jennifer
-
Li, Martin
-
Steele, Leslie
-
visa fler...
-
Marshall, Christ ...
-
Lemire, Edmond G ...
-
Boycott, Kym M.
-
Gibson, William
-
Ray, Peter N.
-
visa färre...
- Av lärosätet
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