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  2. Double-strand break repair model - Wikipedia

    en.wikipedia.org/wiki/Double-strand_break_repair...

    A double-strand break repair model refers to the various models of pathways that cells undertake to repair double strand-breaks (DSB). DSB repair is an important cellular process, as the accumulation of unrepaired DSB could lead to chromosomal rearrangements, tumorigenesis or even cell death. [ 1 ]

  3. DNA repair - Wikipedia

    en.wikipedia.org/wiki/DNA_repair

    The main double-strand break repair pathways. Double-strand breaks, in which both strands in the double helix are severed, are particularly hazardous to the cell because they can lead to genome rearrangements. In fact, when a double-strand break is accompanied by a cross-linkage joining the two strands at the same point, neither strand can be ...

  4. Microhomology-mediated end joining - Wikipedia

    en.wikipedia.org/wiki/Microhomology-mediated_end...

    Microhomology-mediated end joining (MMEJ), also known as alternative nonhomologous end-joining (Alt-NHEJ) is one of the pathways for repairing double-strand breaks in DNA. As reviewed by McVey and Lee, [1] the foremost distinguishing property of MMEJ is the use of microhomologous sequences during the alignment of broken ends before joining, thereby resulting in deletions flanking the original ...

  5. DNA damage (naturally occurring) - Wikipedia

    en.wikipedia.org/wiki/DNA_damage_(naturally...

    However, rad strains, which are deficient in DNA repair, exhibit a markedly different response. For instance, rad52 cells, which cannot repair double-stranded DNA breaks, tend to permanently arrest in G2 when exposed to even very low levels of x-irradiation, and rarely end up progressing through the later stages of the cell cycle.

  6. DNA repair-deficiency disorder - Wikipedia

    en.wikipedia.org/wiki/DNA_repair-deficiency_disorder

    But elimination of any gene essential for base excision repair kills the embryo—it is too lethal to display symptoms (much less symptoms of cancer or "accelerated aging"). [38] Rothmund-Thomson syndrome and xeroderma pigmentosum display symptoms dominated by vulnerability to cancer, whereas progeria and Werner syndrome show the most features ...

  7. Nijmegen breakage syndrome - Wikipedia

    en.wikipedia.org/wiki/Nijmegen_breakage_syndrome

    Nijmegen breakage syndrome (NBS) is a rare autosomal recessive [2] congenital disorder causing chromosomal instability, probably as a result of a defect in the double Holliday junction DNA repair mechanism and/or the synthesis dependent strand annealing mechanism for repairing double strand breaks in DNA (see Homologous recombination).

  8. Non-homologous end joining - Wikipedia

    en.wikipedia.org/wiki/Non-homologous_end_joining

    Non-homologous end joining (NHEJ) is a pathway that repairs double-strand breaks in DNA. It is called "non-homologous" because the break ends are directly ligated without the need for a homologous template, in contrast to homology directed repair (HDR), which requires a homologous sequence to guide repair.

  9. BRCA2 - Wikipedia

    en.wikipedia.org/wiki/BRCA2

    Recombinational repair of DNA double-strand damage - some key steps. ATM (ATM) is a protein kinase that is recruited and activated by DNA double-strand breaks. DNA double-strand damages also activate the Fanconi anemia core complex (FANCA/B/C/E/F/G/L/M). [20] The FA core complex monoubiquitinates the downstream targets FANCD2 and FANCI. [21]