The evolution of gene duplications: classifying and distinguishing between models
By Hideki Innan, Fyodor A. Kondrashov. Nature reviews genetics, 2010
1,280 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/9ecb88ccdc4fe8059ef00d9f7c0bb8bbd05b12d0
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In Molecular Biology
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Citations in the corpus
- Origins, evolution, and phenotypic impact of new genes. (2010, positive): “This process was dubbed ‘‘subfunctionalization’’ and may be shaped by natural selection or involve purely neutral processes (Force et al. 1999; Conant and Wolfe 2008; Innan and Kondrashov 2010).”
- Adaptive laboratory evolution – principles and applications for biotechnology (2013, background): “Whereas there is an ongoing debate about the long-term fixation of gene duplications, either by their selective advantage under selection pressure, or by selective neutrality and fixation by random drift, they are a prerequisite for the development of novel molecular functions [129-131].”
- PANTHER version 14: more genomes, a new PANTHER GO-slim and improvements in enrichment analysis tools (2018, background): “Because of the importance of gene duplication in creating functional diversity within a family (6,7), PANTHER defines subfamilies in terms of gene duplication events.”
- Evolution of Gene Duplication in Plants1[OPEN] (2016, background): “Models for duplicate gene retention in general have been reviewed elsewhere (Innan and Kondrashov, 2010; Maere and Van de Peer, 2010); here, we will focus on examples of duplicate retention in plants (Fig.”
- Whole-genome duplication in teleost fishes and its evolutionary consequences (2014, background): “Whether this model is able to explain a substantial fraction of retained paralogues depends on two factors: The abundance of multifunctional genes and the abundance of situation where optimization of one function impairs another one (Innan and Kondrashov 2010).”
- Network analysis of the MVA and MEP pathways for isoprenoid synthesis. (2013, background): “Such paralogs may retain different subsets of the ancestral gene function, for example, activity during specific stages of development, in particular tissues, and/or under certain conditions (58).”