2015
DOI: 10.1186/s12862-015-0345-x
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Identification and analysis of unitary loss of long-established protein-coding genes in Poaceae shows evidences for biased gene loss and putatively functional transcription of relics

Abstract: BackgroundLong-established protein-coding genes may lose their coding potential during evolution (“unitary gene loss”). Members of the Poaceae family are a major food source and represent an ideal model clade for plant evolution research. However, the global pattern of unitary gene loss in Poaceae genomes as well as the evolutionary fate of lost genes are still less-investigated and remain largely elusive.ResultsUsing a locally developed pipeline, we identified 129 unitary gene loss events for long-established… Show more

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Cited by 14 publications
(15 citation statements)
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“…Orphan genes are sometimes considered as de novo genes originating from ancestral non‐coding sequences (Chen et al, 1997; Knowles & McLysaght, 2009; Li et al, 2010; Murphy & McLysaght, 2012; Xie et al, 2012). In fact, de novo formation is just one way by which orphan genes can form, as many orphan genes are derived from other distinct evolutionary processes, such as the duplication‐divergence mechanism (Schlotterer, 2015; Moyers & Zhang, 2016), TE exaptation (Toll‐Riera et al, 2009), loss of homologous genes in related species (Zhao et al, 2015), repetition of low‐complexity short peptides (Chen et al, 1997; Cheng & Chen, 1999), and horizontal gene transfer from fast‐evolving donors (Keeling & Palmer, 2008; Husnik & McCutcheon, 2018). An orphan gene can also originate through a combination of several origin mechanisms, such as the mixed origin mechanism in nematodes (Prabh & Rödelsperger, 2019).…”
Section: Discussionmentioning
confidence: 99%
“…Orphan genes are sometimes considered as de novo genes originating from ancestral non‐coding sequences (Chen et al, 1997; Knowles & McLysaght, 2009; Li et al, 2010; Murphy & McLysaght, 2012; Xie et al, 2012). In fact, de novo formation is just one way by which orphan genes can form, as many orphan genes are derived from other distinct evolutionary processes, such as the duplication‐divergence mechanism (Schlotterer, 2015; Moyers & Zhang, 2016), TE exaptation (Toll‐Riera et al, 2009), loss of homologous genes in related species (Zhao et al, 2015), repetition of low‐complexity short peptides (Chen et al, 1997; Cheng & Chen, 1999), and horizontal gene transfer from fast‐evolving donors (Keeling & Palmer, 2008; Husnik & McCutcheon, 2018). An orphan gene can also originate through a combination of several origin mechanisms, such as the mixed origin mechanism in nematodes (Prabh & Rödelsperger, 2019).…”
Section: Discussionmentioning
confidence: 99%
“…If the contemporary gene sequence resembles the coding sequence of the ancestor, the gene is likely to be annotated as an “unprocessed pseudogene” [ 14 ], and if there are no significant traces of the peptide sequence, as a lncRNA, and so those scenarios correspond to two regions in a continuum of coding sequence erosion. Previous studies have looked in detail at the potential noncoding functions of annotated transcribed pseudogenes in rodent [ 15 ], primate [ 16 ], and Poaceae lineages [ 17 ], but it has been difficult to estimate how many mammalian lncRNAs have protein-coding ancestry due to erosion of sequence similarity at large evolutionary distances. Three of the lncRNAs in the eutherian X-inactivation center—XIST, JPX, and FTX—are the only currently known examples of lncRNA genes born through this mechanism and retained across mammals [ 18 , 19 ].…”
Section: Introductionmentioning
confidence: 99%
“…A evolução das espécies de Poaceae seguiu uma sequência de eventos de aumento e redução do genoma Soreng et al 2015;Wang et al 2015). Enquanto o aumento do genoma ocorreu relacionado à poliploidia, a redução do genoma processou-se paralela à diploidização Kellog & Benetzen 2004;Parteson et al 2004;Zhao et al 2015;Wang et al 2015;.…”
Section: Aos Meus Queridos Pais Adail Pereiraunclassified