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Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors
Author(s) -
Nathaniel D. Anderson,
Richard de Borja,
Matthew D. Young,
Fabio Fuligni,
Andrej Rosic,
Nicola D. Roberts,
Simon Hajjar,
Mehdi Layeghifard,
Aovokmet,
Paul E. Kowalski,
Matthew Anaka,
Scott Davidson,
Mehdi Zarrei,
Badr Id Said,
Laura Schreiner,
Remi Marchand,
Joseph Sitter,
Nalan Gökgöz,
Ledia Brunga,
Garrett T. Graham,
Anthony Fullam,
Nischalan Pillay,
Jeffrey A. Toretsky,
Akihiko Yoshida,
Tatsuhiro Shibata,
Markus Metzler,
Gino R. Somers,
Stephen W. Scherer,
Adrienne M. Flanagan,
Peter J. Campbell,
Joshua D. Schiffman,
Mary Shago,
Ludmil B. Alexandrov,
Jay S. Wunder,
Irene L. Andrulis,
David Malkin,
Sam Behjati,
Adam Shlien
Publication year - 2018
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aam8419
Subject(s) - soft tissue , gene , gene duplication , non canonical , biology , genetics , computational biology , microbiology and biotechnology , pathology , medicine
Sarcomas are cancers of the bone and soft tissue often defined by gene fusions. Ewing sarcoma involves fusions between EWSR1 , a gene encoding an RNA binding protein, and E26 transformation-specific (ETS) transcription factors. We explored how and when EWSR1-ETS fusions arise by studying the whole genomes of Ewing sarcomas. In 52 of 124 (42%) of tumors, the fusion gene arises by a sudden burst of complex, loop-like rearrangements, a process called chromoplexy, rather than by simple reciprocal translocations. These loops always contained the disease-defining fusion at the center, but they disrupted multiple additional genes. The loops occurred preferentially in early replicating and transcriptionally active genomic regions. Similar loops forming canonical fusions were found in three other sarcoma types. Chromoplexy-generated fusions appear to be associated with an aggressive form of Ewing sarcoma. These loops arise early, giving rise to both primary and relapse Ewing sarcoma tumors, which can continue to evolve in parallel.

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