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Origin and Length Distribution of Unidirectional Prokaryotic Overlapping Genes

机译:单向原核重叠基因的起源和长度分布

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摘要

Prokaryotic unidirectional overlapping genes can be originated by disrupting and replacing of the start or stop codon of one protein-coding gene with another start or stop codon within the adjacent gene. However, the probability of disruption and replacement of a start or stop codon may differ significantly depending on the number and redundancy of the start and stop codons sets. Here, we performed a simulation study of the formation of unidirectional overlapping genes using a simple model of nucleotide change and contrasted it with empirical data. Our results suggest that overlaps originated by an elongation of the 3′-end of the upstream gene are significantly more frequent than those originated by an elongation of the 5′-end of the downstream gene. According to this, we propose a model for the creation of unidirectional overlaps that is based on the disruption probabilities of start codon and stop codon sets and on the different probabilities of phase 1 and phase 2 overlaps. Additionally, our results suggest that phase 2 overlaps are formed at higher rates than phase 1 overlaps, given the same evolutionary time. Finally, we propose that there is no need to invoke selection to explain the prevalence of long phase 1 unidirectional overlaps. Rather, the overrepresentation of long phase 1 relative to long phase 2 overlaps might occur because it is highly probable that phase 2 overlaps are retained as short overlaps by chance. Such a pattern is stronger if selection against very long overlaps is included in the model. Our model as a whole is able to explain to a large extent the empirical length distribution of unidirectional overlaps in prokaryotic genomes.
机译:原核单向重叠基因可以通过用相邻基因内的另一个起始或终止密码子破坏和替换一个蛋白质编码基因的起始或终止密码子而产生。但是,取决于起始密码子和终止密码子集的数量和冗余性,起始密码子或终止密码子的破坏和替换的可能性可能会显着不同。在这里,我们使用核苷酸变化的简单模型进行了单向重叠基因形成的模拟研究,并将其与经验数据进行了对比。我们的结果表明,上游基因3'端延伸引起的重叠比下游基因5'端延伸引起的重叠更为频繁。据此,我们提出了一个用于创建单向重叠的模型,该模型基于起始密码子和终止密码子集的破坏概率以及第一阶段和第二阶段重叠的不同概率。此外,我们的结果表明,在相同的进化时间下,第2阶段重叠的形成速率高于第1阶段重叠的速率。最后,我们建议无需调用选择来解释长相1单向重叠的普遍性。而是,可能会出现长相1相对于长相2重叠的过量表示,因为很可能将时相2重叠保留为偶然的短重叠。如果模型中包含针对非常长的重叠的选择,则这种模式会更强。我们的模型整体上可以在很大程度上解释原核基因组中单向重叠的经验长度分布。

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