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  1. ...MHC in newts illuminates the evolutionary dynamics of complex regions in giant s Wiesław Babik1, Katarzyna Dudek1, Gemma Palomar1,2, Marzena Marszałek1,3, Grzegorz Dubin4, Maximina H. Yun5,6 and Magdalena Migalska1 1Institute of Environmental Sciences, Faculty of Biology, Jagiellonian University...
  2. ...is driven in part by recognition of DNA sequence, genetic variation can influence TF–DNA associations and gene regulation. To identify variants that impact TF binding in human brain tissues, we assessed allele-specific binding (ASB) at heterozygous variants for 94 TFs in nine brain regions from two donors...
  3. ...Genetic variation in recalcitrant repetitive regions of the Drosophila melanogaster Harsh G. Shukla1,2, Mahul Chakraborty3 and J.J. Emerson1,4 1Department of Ecology and Evolutionary Biology, University of California Irvine, Irvine, California 92697, USA; 2Graduate Program in Mathematical...
  4. ...equally to this work. Corresponding author: sgillett@cornellcollege.eduAbstractGenome-wide association studies (GWASs) and expression analyses implicate noncoding regulatory regions as harboring risk factors for psychiatric disease, but functional characterization of these regions remains limited. Here...
  5. ...expression. We find that enhancers showing tissue-specific activity are highly enriched in intronic regions and regulate the expression of genes involved in tissue-specific functions, whereas housekeeping genes are more often controlled by intergenic enhancers, common to many tissues. Notably, an intergenic...
  6. ...preferentially in the promoter of nonexpressed alleles of imprinted genes. Furthermore, we found that most of the paternal specifically positioned nucleosomes (pat-nucleosomes) were associated with parent-of-origin-dependent differential methylated regions, suggesting a functional link between the maternal...
  7. ...in KS1 and KS2 = 60.01 and 1508.9, respectively.Aging-related regions show preferentially disrupted chromatin accessibility in KS1 and KS2 neurons but not in B or T cellsOur findings yield insights into (1) the genomic distribution of the chromatin defects in KS1 and KS2 and (2) the cell type...
  8. ...betweenmaternal and paternal imprinting and differential expression between males and females (Supplemental Fig. S22). Allele-specific methylation of differentially methylated regions (DMRs) is the primary epigenetic mechanism of imprinting, controlling monoallelic expression (Supplemental Fig. S6; Skaar et al...
  9. ...Long-read assembly of the insect model organism Tribolium castaneum reveals spread of satellite DNA in gene-rich regions by recurrent burst events Marin Volarić1,2, Evelin Despot-Slade1,2, Damira Veseljak1, Brankica Mravinac1 and Nevenka Meštrović1 1Ruđer Bošković Institute, 10000 Zagreb, Croatia...
  10. ...The aberrant epi of DNMT3B-mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory Varsha Poondi Krishnan1, Barbara Morone1, Shir Toubiana2, Monika Krzak3,6, Salvatore Fioriniello1, Floriana Della Ragione1...
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