Searching journal content for articles similar to Jamieson et al. 26 (1): 97.

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  1. ...insertions and lineage-specific duplicated genes. Our findings suggest independent evolution of subterminal caps converging on a common genetic and epigenetic structure that promoted ectopic exchange as well as the emergence of novel genes at transition regions between euchromatin and heterochromatin...
  2. ...armigera, Polycomb group (PcG) proteins regulate PTTH production and prevent diapause entry through the control of H3K27me3 (Lu et al. 2013). By ovary-specific knockdown of histone mark writers and erasers, DiVito Evans et al. (2023) showed that H3K4me3 and H3K36me1 depletion promotes reproductive diapause...
  3. ...of the wheat are marked by constitutive heterochromatin (IWGSC 2018; Li et al. 2019; Concia et al. 2020). Additionally, H3K27me2 associates with crossover suppression in wheat, despite distal enrichment (Liu et al. 2021). However, fine-scale relationships between chromatin, meiotic recombination, axis...
  4. ...into sharp peaks again during ZGA. By simultaneous depletion of H3K4me3 demethylase KDM5B and KDM5C, we determined that broad H3K4me3 domain maintenance impaired ZGA gene expression, suggesting its function to prevent premature ZGA entry. In contrast, broad H3K27me3 domains underwent global removal upon...
  5. ...-rich and gene-poor regions, corresponding to euchromatin and heterochromatin, respectively. Heterochromatin can be further divided into two classes: facultative, which is dynamic and marked by H3K27me3, and constitutive, which is largely stable and marked by H3K9me2/3 (Grewal and Jia 2007). Constitutive...
  6. ...by DNA damage harboring the “loss of heterochromatin” phenotype, we observed progressive 3D reorganization of heterochromatin during senescence. Facultative and constitutive heterochromatin marked by H3K27me3 and H3K9me3, respectively, show different alterations. Facultative heterochromatin tends...
  7. ...heterochromatin formation is often associated with histone H3 trimethylated at lysine 27 (H3K27me3), a mark that is absent in constitutive heterochromatin (Peters et al. 2003). H3K27me3, which is catalyzed in mammals by Polycomb 5Corresponding authors. E-mail chantalat@cng.fr. E-mail matthieu...
  8. ...,b; Adhvaryu et al. 2014). Neurospora dim-5mutants lack detectable H3K9me3 and cytosine DNAmethylation (Tamaru and Selker 2001; Tamaru et al. 2003; Lewis et al. 2008), HP1 is mislocalized but retained within the nucleus (Freitag et al. 2004), and H3K27me2/3 is redistributed to former H3K9me3 regions (Basenko...
  9. ...of the depleted samples over the whole range considered (from ∼3.5- to ∼13-fold), with the highest gains at the lowest amounts of sequencing data (6 to 25 million fragments) (Fig. 4A). Because a genotyped position does not necessarily allow the variant to be identified (this also depends on allele coverage), we...
  10. ...inaccessible to transcription factors, and H3K27me3, a hallmark of facultative heterochromatin that is frequently regulated in a tissue-specific manner and is accessible to transcription factors and associated with paused RNA polymerase (Becker et al. 2016). We observed that almost half of the NAD regions...
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