Non-B DNA conformations, genomic rearrangements, and human disease (Q35869768)

10 August 2017

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title

Non-B DNA conformations, genomic rearrangements, and human disease (English)

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10 August 2017

1

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10 August 2017

Robert D Wells

2

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10 August 2017

language of work or name

English

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publication date

23 August 2004

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Journal of Biological Chemistry

10 August 2017

published in

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10 August 2017

volume

279

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10 August 2017

issue

46

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10 August 2017

page(s)

47411-47414

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The Role of DNA Structure in Genetic Regulatio

10 August 2017

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Unusual DNA duplex and hairpin motifs.

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Dimeric DNA quadruplex containing major groove-aligned A-T-A-T and G-C-G-C tetrads stabilized by inter-subunit Watson-Crick A-T and G-C pairs

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Breakpoints of gross deletions coincide with non-B DNA conformations

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A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2

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Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure

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The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats

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The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.

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Genome architecture catalyzes nonrecurrent chromosomal rearrangements

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Reciprocal crossovers and a positional preference for strand exchange in recombination events resulting in deletion or duplication of chromosome 17p11.2.

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Palindromic but not G-rich sequences are targets of class switch recombination

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AID enzyme-induced hypermutation in an actively transcribed gene in fibroblasts

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Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

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Mechanism and timing of mitotic rearrangements in the subtelomeric D4Z4 repeat involved in facioscapulohumeral muscular dystrophy

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21 January 2018

Identifiers

DOI

10.1074/JBC.R400028200

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10 August 2017

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