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bioRxiv · 10.1101/295220

Timely double-strand break repair and pathway choice in pericentromeric heterochromatin depend on the histone demethylase dKDM4A

Janssen, A.·Colmenares, S. U.·Lee, T.·Karpen, G. H.
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Abstract

Introduction Introduction Results Discussion Materials Methods References One of the most harmful DNA lesions is a double-strand break (DSB), whose improper repair can lead to formation of aberrant chromosomes linked to cancer and developmental diseases 1. At DSBs, the severed strands of the DNA helix are repaired by a variety of mechanisms. The two major DSB repair pathways are Non-Homologous End Joining (NHEJ) and Homologous Recombination (HR). NHEJ repairs DNA by ligating both ends of the DSB together, often resulting in small insertions and deletions at the break site. HR repair involves more extensive processing of the DSB site, in which 5 to 3 end-resection of the DSB ends results in a single-stranded DNA sequence that invades and perfectly copies homologous sequences to repair the DS ...

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Janssen, A., Colmenares, S. U., Lee, T., Karpen, G. H.. 2018-04-05. Timely double-strand break repair and pathway choice in pericentromeric heterochromatin depend on the histone demethylase dKDM4A. https://doi.org/10.1101/295220

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