Literature DB >> 21925314

Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements.

Pengfei Liu1, Ayelet Erez, Sandesh C Sreenath Nagamani, Shweta U Dhar, Katarzyna E Kołodziejska, Avinash V Dharmadhikari, M Lance Cooper, Joanna Wiszniewska, Feng Zhang, Marjorie A Withers, Carlos A Bacino, Luis Daniel Campos-Acevedo, Mauricio R Delgado, Debra Freedenberg, Adolfo Garnica, Theresa A Grebe, Dolores Hernández-Almaguer, LaDonna Immken, Seema R Lalani, Scott D McLean, Hope Northrup, Fernando Scaglia, Lane Strathearn, Pamela Trapane, Sung-Hae L Kang, Ankita Patel, Sau Wai Cheung, P J Hastings, Paweł Stankiewicz, James R Lupski, Weimin Bi.   

Abstract

Complex genomic rearrangements (CGRs) consisting of two or more breakpoint junctions have been observed in genomic disorders. Recently, a chromosome catastrophe phenomenon termed chromothripsis, in which numerous genomic rearrangements are apparently acquired in one single catastrophic event, was described in multiple cancers. Here, we show that constitutionally acquired CGRs share similarities with cancer chromothripsis. In the 17 CGR cases investigated, we observed localization and multiple copy number changes including deletions, duplications, and/or triplications, as well as extensive translocations and inversions. Genomic rearrangements involved varied in size and complexities; in one case, array comparative genomic hybridization revealed 18 copy number changes. Breakpoint sequencing identified characteristic features, including small templated insertions at breakpoints and microhomology at breakpoint junctions, which have been attributed to replicative processes. The resemblance between CGR and chromothripsis suggests similar mechanistic underpinnings. Such chromosome catastrophic events appear to reflect basic DNA metabolism operative throughout an organism's life cycle.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21925314      PMCID: PMC3242451          DOI: 10.1016/j.cell.2011.07.042

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  37 in total

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  194 in total

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3.  RAD51 mutants cause replication defects and chromosomal instability.

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7.  The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV alleles.

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10.  Clinical genomics and contextualizing genome variation in the diagnostic laboratory.

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