Searching journal content for articles similar to Sin et al. 22 (5): 827.

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  1. ...in the early embryo. Scores of -wide surveys in sperm have reported patterns of chromatin accessibility, nucleosome localization, histone modification, and chromosome folding. Here, we revisit these studies in light of recent reports that sperm obtained from the mouse epididymis are contaminated with low...
  2. ...to postmeiotic silencing, with a subset of genes associated with spermiogenesis escaping postmeiotic silencing (Namekawa et al. 2006; Mueller et al. 2008). Of note is that MSCI impacts sex chromosome evolution (Potrzebowski et al. 2008). For example, the X Chromosome is enriched with genes expressed before...
  3. ...(Rodríguez Delgado et al. 2009). X-Chromosome inactivation (XCI) in placental mammals involves the spread of the XIST RNA in a proximity-dependent manner governed by three-dimensional chromatin architecture (Wang et al. 2018). The resulting inactive X Chromosome (Xi) also forms a unique bipartite structure...
  4. ..., and chromatin interactions for AGO2 in the nucleus compared with the cytoplasmic compartment during spermatogenic development. We then investigated how conditional loss of AGO2 in male germ cells impacts expression of genes targeted by its nuclear activity. Finally, we examined the phenotypic effects...
  5. ...identity elsewhere on the X Chromosome, which may reduce the impact of their loss. Gene families from palindromes shared by human, chimpanzee, and macaque also have conserved expression patterns: 20 of 21 such gene families have the same expression pattern in chimpanzee and human (Supplemental Fig. S7...
  6. ...drivers in males (e.g., Larracuente and Presgraves 2012), which may drive the rapid evolution of these repeats to escape the driver (e.g., Cabot et al. 1993; Larracuente 2014). The lack of recombination and male-limited transmission of Y Chromosomes also create opportunities for conflicts involving...
  7. ...Origins, evolution, and phenotypic impact of new genes Henrik Kaessmann 1 Center for Integrative Genomics, University of Lausanne, CH-1015 Lausanne, Switzerland Abstract Ever since the pre-molecular era, the birth of new genes with novel functions has been...
  8. ...been co-opted as retrocopy promoters during evolution. To test our hypothesis, we analyzed ChIP-seq data from matched mouse tissues for two enhancer-associated chromatin marks, monomethylation of histone H3 at lysine K4 (H3K4me1) (Heintzman et al. 2007) and acetylation of histone H3 at lysine 27 (H3K27...
  9. ...at the bottom of the panel. (B) Sequence evolution of miRNA families on the X chromosome and autosomes. To limit biases due to age variations, only eutherian-specific miRNA families predating the human-mouse split were considered. Meunier et al. 40 Genome Research www..org protein-coding genes counteracts MSCI...
  10. ...; Case et al. 2012; Charchar et al. 2012). Like autosomal chromosomes, ChrX and ChrYare thought to have once been identical pairs that were free to recombine and exchange genetic material. Over the course of evolution, ChrY became unique from all other chromosomes due to the acquisition of a dominant sex...
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