Neotelomeres and telomere-spanning chromosomal arm fusions in cancer genomes revealed by long-read sequencing

被引:2
|
作者
Tan, Kar-Tong [1 ,2 ,3 ]
Slevin, Michael K. [1 ]
Leibowitz, Mitchell L. [1 ,2 ,3 ]
Garrity-Janger, Max [1 ,2 ,3 ]
Shan, Jidong [4 ]
Li, Heng [1 ,3 ]
Meyerson, Matthew [1 ,2 ,3 ]
机构
[1] Dana Farber Canc Inst, Boston, MA 02215 USA
[2] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[3] Harvard Med Sch, Boston, MA 02215 USA
[4] Albert Einstein Coll Med, Dept Genet, Bronx, NY 10461 USA
来源
CELL GENOMICS | 2024年 / 4卷 / 07期
关键词
TERT PROMOTER MUTATIONS; CELL-LINES; VARIANT REPEATS; DNA; EVOLUTION; MECHANISMS; HALLMARKS; SUBSET; GENES; SITE;
D O I
10.1016/j.xgen.2024.100588
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Alterations in the structure and location of telomeres are pivotal in cancer genome evolution. Here, we applied both long-read and short-read genome sequencing to assess telomere repeat-containing structures in cancers and cancer cell lines. Using long-read genome sequences that span telomeric repeats, we defined four types of telomere repeat variations in cancer cells: neotelomeres where telomere addition heals chromosome breaks, chromosomal arm fusions spanning telomere repeats, fusions of neotelomeres, and peri-centromeric fusions with adjoined telomere and centromere repeats. These results provide a framework for the systematic study of telomeric repeats in cancer genomes, which could serve as a model for understanding the somatic evolution of other repetitive genomic elements.
引用
收藏
页数:24
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