Title of article :
Chromosome Catastrophes Involve Replication Mechanisms Generating Complex Genomic Rearrangements
Author/Authors :
Pengfei Liu، نويسنده , , Ayelet Erez، نويسنده , , Sandesh C. Sreenath Nagamani، نويسنده , , Shweta U. Dhar، نويسنده , , Katarzyna E. Ko?odziejska، نويسنده , , Avinash V. Dharmadhikari، نويسنده , , M. Lance Cooper، نويسنده , , Joanna Wiszniewska، نويسنده , , Feng Zhang، نويسنده , , Marjorie A. Withers، نويسنده , , Carlos A. Bacino، نويسنده , , Luis Daniel Campos-Acevedo، نويسنده , , Mauricio R. Delgado، نويسنده , , Debra Freedenberg، نويسنده , , Adolfo Garnica، نويسنده , , Theresa A. Grebe، نويسنده , , Dolores Hern?ndez-Almaguer، نويسنده , , LaDonna Immken، نويسنده , , Seema R. Lalani، نويسنده , , Scott D. McLean، نويسنده , , et al.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2011
Pages :
15
From page :
889
To page :
903
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 organismʹs life cycle.
Journal title :
CELL
Serial Year :
2011
Journal title :
CELL
Record number :
1020828
Link To Document :
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