Oncogenes create a unique landscape of fragile sites

被引：65

作者：

Miron, Karin ^{[1
]}

Golan-Lev, Tamar ^{[1
]}

Dvir, Raz ^{[1
]}

Ben-David, Eyal ^{[1
]}

Kerem, Batsheva ^{[1
]}

机构：

[1] Hebrew Univ Jerusalem, Inst Life Sci, Dept Genet, IL-91904 Jerusalem, Israel

来源：

NATURE COMMUNICATIONS | 2015年 / 6卷

基金：

以色列科学基金会;

关键词：

DNA-DAMAGE RESPONSE; CYCLIN-E; GENOMIC INSTABILITY; COMMON; CANCER; REPLICATION; CELLS; TARGETS;

D O I：

10.1038/ncomms8094

中图分类号：

O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

Recurrent genomic instability in cancer is attributed to positive selection and/or the sensitivity of specific genomic regions to breakage. Among these regions are fragile sites (FSs), genomic regions sensitive to replication stress conditions induced by the DNA polymerase inhibitor aphidicolin. However, the basis for the majority of cancer genomic instability hotspots remains unclear. Aberrant oncogene expression induces replication stress, leading to DNA breaks and genomic instability. Here we map the cytogenetic locations of oncogene-induced FSs and show that in the same cells, each oncogene creates a unique fragility landscape that only partially overlaps with aphidicolin-induced FSs. Oncogene-induced FSs colocalize with cancer breakpoints and large genes, similar to aphidicolin-induced FSs. The observed plasticity in the fragility landscape of the same cell type following oncogene expression highlights an additional level of complexity in the molecular basis for recurrent fragility in cancer.

引用

页数：7

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