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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:
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.
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页数:24
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