Searching journal content for articles similar to Egli et al. 14 (7): 1382.

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  1. ..., and A3The histone locus in Drosophila melanogaster is present at the 39DE region of Chromosome 2L, bordering the pericentromeric heterochromatin. The highly homogeneous nature of this locus has impeded its resolution to the base pair level. The current reference iso-1 Rel6 has only ∼69 kb (12 units...
  2. ...et al. 2016). Tetrahymena possesses a unique nuclear architecture containing a transcriptionally active macronucleus (MAC), and a transcriptionally silent micronucleus (MIC). During sexual reproduction, the new MAC chromosomes undergo ∼200 regulated double-stranded DNA breaks and endoreplication...
  3. .... The subtelomeric elements, including rDNA, were massively rearranged and involved in breakage–fusion–bridge cycles, translocations, recombinations, and chromosome circularization. These events were established progressively over time and displayed heterogeneity at the subpopulation level. New telomere...
  4. ...of the sgRNA/Cas9 complex to scan the DNA for target sites.When we analyzed the cleavage efficiencies of sgRNAs used in Drosophila (Ren et al. 2014), we observed a good overlap with the ability of those sgRNAs to adopt the correct structure and having a high cleavage efficiency. Further refinement...
  5. ...in Drosophila melanogaster and human, and the chromosomes under selective pressure at the lactase locus in humans. We then applied recombClust to the complex human 1q21.1 region, where nonallelic homologous recombination produces deleterious phenotypes. We discovered and validated the presence of two different...
  6. ...-element related array in Drosophila guanche is comprised of elements missing ∼100 nt of terminal sequence (Miller et al. 1992), and all elements in the fixed Bari1 tandem array have incomplete TIRs (Marsano et al. 2003). The terminal inverted repeats at the ends of DNA transposons are endonuclease cut sites...
  7. ...repeats (Fig. 5) can also be seen in Drosophila melanogaster Blm mutants (Garcia et al. 2011), suggesting the existence of a common mechanism for DEL formation in a Blm-deficient background. BLM helicase acts to unwind secondary DNA structures at the telomere (Sfeir et al. 2009). The loss of BLM may...
  8. ...regions.Meiotic crossovers form via inter-homolog repair of DNA double-strand breaks (DSBs) that are generated by SPO11 topoisomerase-related complexes (Szostak et al. 1983; Keeney et al. 1997; Robert et al. 2016; Vrielynck et al. 2016). Diverse eukaryotes have evidence for recombination hotspots, which...
  9. ...crossover could contribute to centromere evolution (Smith 1976). In this influential model, meiotic DNA double-strand breaks (DSBs) are repaired using a nonallelic location on a homolog, with the potential to cause gain and loss of intervening tandem repeats (Smith 1976). However, it is widely documented...
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  10. ...%). In CC-2931, a Crypton and a previously undescribed type of DNA element have caused 71% of chromosomal rearrangements, whereas in CC-1952, a Dualen LINE is associated with 87% of duplications. Other SMs, notably large duplications in CC-2931, are likely products of various double-strand break repair...
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