Searching journal content for articles similar to Krylov et al. 13 (10): 2229.

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  1. ..., specifically, how adaptive evolution and divergence precipitate HI and ultimately establish reproductive barriers, remains largely unknown. Despite decades of research into the genetic basis of speciation, only a very limited number of genes responsible for HI have been cloned (Maheshwari and Barbash 2011...
  2. ...). The piRNA pathway presents features of an adaptive defense system against TE invasion (Aravin et al. 2007; Brennecke et al. 2008; Khurana et al. 2011; Yu et al. 2019), but little is known about the processes driving its evolution. Many piRNA pathway genes encoding the proteins involved in TE silencing...
  3. ...sexual recombination, and indicates that aneuploidy is a relevant process in Leishmania’s survival and evolution. Chromosomal duplications were also shown to directly impact gene expression, in which chromosomes with extra copies were highly expressed compared with disomic counterparts, with the sole...
  4. ...in contrast to the 178 NLRs that are known in Arabidopsis and 387 in Brachypodium (Michael et al. 2017). In the wa7733 and wa8730 s, we found only a single canonical NLR gene. Although it has conserved homologs in the Spirodela s, it is very divergent from NLR genes of other species. Additionally, two NLR...
  5. ...correlations have taught us little about evolutionary dynamics governing gene duplication and divergence. Gene duplication followed by divergence is one of the primary driving forces behind functional innovation during evolution ( Ohno 1970 ; Lynch and Katju 2004 ). Currently, the divergence of two paralogs...
  6. ...environmental conditions. The lack of sexual reproduction, and consequently meiotic recombination, is thought to greatly affect the potential to generate novel genetic combinations. Especially, pathogenic microbes involved in an intimate interaction with a host need to continuously adapt their effector gene...
  7. ...to representing physical interactions, GRN edges can also represent regulatory relationships that can, for instance, be inferred by correlating gene expression profiles between genes and potential regulators. Initially this approach was developed for the yeast Saccharomyces cerevisiae (Segal et al. 2003). More...
  8. ...occupancy by key TFs during hematopoietic differentiation, correlate this dynamic binding with changes in gene expression, and search for determinants of differential occupancy. Here we focused on TAL1 (previously known as SCL), a TF that is indispensable atmultiple stages of hematopoiesis. This basic...
  9. ..., the active state of a GRNmodule is drawn. The nodes represent the genes with detectable transcripts; the edges represent the predicted interactions of the connecting nodes. Interactions were predicted by the MATISSE program, using correlation of expression changes in a window of three time points centered...
  10. .... ↵ Kunin, V. and Ouzounis, C.A. 2003 . The balance of driving forces during evolution in prokaryotes. Genome Res. 13 : 1589 -1594. ↵ Krylov, D.M., Wolf, Y.I., Rogozin, I.B., and Koonin, E.V. 2003 . Gene loss, protein sequence divergence, gene dispensability, expression level, and interactivity...
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