Searching journal content for articles similar to Keane et al. 24 (11): 1830.

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  1. ..., is currently lacking. In a systems biology approach, we classify here back-up, regulatory, and gene dosage functions for the 105 duplicate gene families of Saccharomyces cerevisiae metabolism. The key tool was the reconciled -scale metabolic model iLL672, which was based on the older iFF708. Computational...
  2. .... , Scharfe, C. , Davis, R.W. , Li, W.H. ( 2003 ) Role of duplicate genes in genetic robustness against mutations . Nature 421 : 63 – 66 . ↵ Guan, Y. , Dunham, M.J. , Troyanskaya, O.G. ( 2007 ) Functional analysis of gene duplications in Saccharomyces cerevisiae . Genetics 175 : 933 – 943 . ↵ Hakes, L...
  3. ...to the conclusion that duplication rarely results in adaptation. Here we contend that the above comparison is unfair because of a known duplication bias among genes with different fitness contributions. To rectify this problem, we compare homologous genes from the budding yeast Saccharomyces cerevisiae...
  4. ...(TEs) and other repetitive sequences are known to be one of the major causes of structural variations within individuals and species, promoting expansion, gene duplication, gene loss, genomic rearrangements, and reshaping of the overall genomic regulatory network (Bourque et al. 2018). Among fungi...
  5. ...values (Ks = 3 to 4) in the gymnolaemate bryozoans, which could indicate ancient WGD in this lineage, but the signal is very weak (Supplemental Fig. S7).Given this uncertainty, we then used MCScanX (Wang et al. 2012) to identify and align collinear blocks of genes within each . The presence of duplicated...
  6. ...dosage effects has engendered a robustgene balance hypothesis,” with a theoretical base that makes specific predictions as to gene content changes following different types of gene duplication. Genomic data from both chordate and angiosperm s fit these predictions: Each type of duplication provides...
  7. ...expression of neighboring genes, and conversely, gene silencing associated with aging ( Issa 2000 ) could activate neighboring genes. Transcriptional interference might also partially explain the recent finding that in Saccharomyces cerevisiae , adjacent pairs of genes tend to be coregulated ( Cohen et al...
  8. ...asymmetric rates of evolution, even the slower members of pairs show evidence of a burst of protein sequence evolution immediately after duplication. We discuss the contribution of neofunctionalization to duplicate gene preservation and propose that a form of subfunctionalization mediated by coding region...
  9. ...evolution using only branch length information. This offers two key advantages: (1) it allows us to leverage precompiled libraries of gene trees such as PANTHER, eliminating the need to construct a custom data set; and (2) it enables the analysis of ancient gene duplication events, where nucleotide...
  10. ...by expressing in S. cerevisiae 668 ribosomal protein (RP) gene promoters taken from nine yeast species and by further examining several pairs of orthologous promoters through a library of 91 chimeric promoters. Our results shed new light on how yeast promoters can evolve in sequencewhile preserving...
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