Searching journal content for articles similar to Chrast et al. 7 (6): 615.

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  1. ...and Amon 2011). Disorders like Down syndrome, caused by the triplication of Chromosome 21, and Cri du chat syndrome, caused by the deletion of a region of Chromosome 5p, affect the expression of hundreds of genes and perturb normal development. 8p syndrome, caused by rearrangements affecting the p arm...
  2. ...enrichment despite lacking well-positioned nucleosomes (Fig. 3E). This noncanonical H3K27me3 enrichment resembles the pattern observed in female Drosophila GSCs, in which H3K27me3 is detectable at both inactive and active gene loci (DeLuca et al. 2020).In contrast, in CySC-like cells, H3K27me3 is most...
  3. ...to Muller element F in Drosophila melanogaster (the ancestral fly X Chromosome; 55.6% of fly Muller F genes, chi-squared test, 1 d.f., P = 3.84 × 10−31) (Vicoso and Bachtrog 2013) despite 400 million years of divergence. Through functional enrichment analysis, we show that these conserved X-linked genes...
  4. ...and derepression of enhancer activity under stress-associated conditions. These results point to chromatin-level changes that may prime these cells for altered transcriptional programs with age.Polycomb repression of barrier membrane genes in aging enterocytesA major defect of the aging Drosophila gut is breakdown...
  5. ...Transposable elements contribute to the evolution of host shift–related genes in cactophilic Drosophila species Daniel Siqueira de Oliveira1,2,3, Anaïs Larue2, William Vilas Boas Nunes2, Francois Sabot4, Alejandra Bodelón5, María Pilar García Guerreiro5, Cristina Vieira2 and Claudia Marcia...
  6. ...regulation. By critically examining both established tools and emerging techniques such as editing, synthetic chromosomes, and high-resolution imaging, we provide a practical framework for investigators seeking to uncover direct regulators of specific genes. Our goal is to guide the design of experiments...
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  7. ...and maintaining the alleles in heterozygous sites in one or two of the four chromosome copies.Gene expression from Leish Chr 31 is controlled by down-regulation of all chromosomal copies to a similar extentPrevious works from Prieto Barja et al. (2017) and Dumetz et al. (2017) have demonstrated that having extra...
  8. ..., the clearest one against GA-rich repeats in the human . However, our study reveals a systematic failure of both technologies to sequence and assemble specific exons of Drosophila melanogaster genes, indicating an overlooked limitation. Namely, multiple Y-linked exons are nearly or completely absent from raw...
  9. ...”) number and subsequent divergence of function (Hahn 2009).Approximately 75% of lung cancers have WGD events during their evolutionary history (Jamal-Hanjani et al. 2017). Furthermore, changes in gene copy number owing to aneuploidy, in which chromosomes or chromosomal regions are gained or lost, represent...
  10. ...and 5 kb (Colby and Williams 1993). The 5-kb repeat unit has a 242-bp insert between H1 and H3 genes. These variants are present in a number of Drosophila species, indicating that their origin predates the speciation event (Strausbaugh and Weinberg 1982). Figure 3B shows the distribution of 5- and 4...
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