Unknown

Dataset Information

0

Homologous recombination-dependent repair of telomeric DSBs in proliferating human cells.


ABSTRACT: Telomeres prevent chromosome ends from being recognized as double-stranded breaks (DSBs). Meanwhile, G/C-rich repetitive telomeric DNA is susceptible to attack by DNA-damaging agents. How cells balance the need to protect DNA ends and the need to repair DNA lesions in telomeres is unknown. Here we show that telomeric DSBs are efficiently repaired in proliferating cells, but are irreparable in stress-induced and replicatively senescent cells. Using the CRISPR-Cas9 technique, we specifically induce DSBs at telomeric or subtelomeric regions. We find that DSB repair (DSBR) at subtelomeres occurs in an error-prone manner resulting in small deletions, suggestive of NHEJ. However, DSBR in telomeres involves 'telomere-clustering', 3'-protruding C-rich telomeric ssDNA, and HR between sister-chromatid or interchromosomal telomeres. DSBR in telomeres is suppressed by deletion or inhibition of Rad51. These findings reveal proliferation-dependent DSBR in telomeres and suggest that telomeric HR, which is normally constitutively suppressed, is activated in the context of DSBR.

SUBMITTER: Mao P 

PROVIDER: S-EPMC4942568 | biostudies-literature | 2016 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

Homologous recombination-dependent repair of telomeric DSBs in proliferating human cells.

Mao Pingsu P   Liu Jingfan J   Zhang Zepeng Z   Zhang Hong H   Liu Haiying H   Gao Song S   Rong Yikang S YS   Zhao Yong Y  

Nature communications 20160711


Telomeres prevent chromosome ends from being recognized as double-stranded breaks (DSBs). Meanwhile, G/C-rich repetitive telomeric DNA is susceptible to attack by DNA-damaging agents. How cells balance the need to protect DNA ends and the need to repair DNA lesions in telomeres is unknown. Here we show that telomeric DSBs are efficiently repaired in proliferating cells, but are irreparable in stress-induced and replicatively senescent cells. Using the CRISPR-Cas9 technique, we specifically induc  ...[more]

Similar Datasets

| S-EPMC8289408 | biostudies-literature
| S-EPMC6959610 | biostudies-literature
2020-04-14 | GSE148573 | GEO
| S-EPMC4741384 | biostudies-literature
| S-EPMC4415602 | biostudies-literature
| S-EPMC5601504 | biostudies-literature
2020-04-14 | GSE148571 | GEO
2020-04-13 | GSE148572 | GEO
| S-EPMC2909591 | biostudies-literature
| S-EPMC4846143 | biostudies-literature