A Class of Allopolyploidy Showing High Duplicate Retention and Continued Homoeologous Exchanges.

IF 3.2 2区 生物学 Q2 EVOLUTIONARY BIOLOGY
Abbey Coppage, Esha Bhatnagar, Mitali Joshi, Mustafa Siddiqui, Logan McRae, Gavin C Conant
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引用次数: 0

Abstract

We describe four ancient polyploidy events where the descendant taxa retain many more duplicated gene copies than has been seen in other paleopolyploidies of similar ages. Using POInT (the Polyploidy Orthology Inference Tool), we modeled the evolution of these four events, showing that they do not represent recent independent polyploidies despite the rarity of shared gene losses. We find that these events have elevated rates of interlocus gene conversion and that these gene conversion events are spatially clustered in the genomes. Regions of gene conversion also show very low synonymous divergence between the corresponding paralogous genes. We suggest that these genomes have experienced a delay in the return to a diploid state after their polyploidies. Under this hypothesis, homoeologous exchanges between the duplicated regions created by the polyploidy persist to this day, explaining the high rates of duplicate retention. Genomes with these characteristics arguably represent a new class of paleopolyploid taxa because they possess evolutionary patterns distinct from the more common and well-known paradigm of the rapid loss of many of the duplicated pairs created by polyploidy.

具有高度重复保留和持续同源交换的一类异源多倍体。
我们描述了四个古代多倍体事件,其中后代分类群保留了比其他类似年龄的古多倍体中所见的更多的重复基因拷贝。使用POInT (Polyploid Ortholog Inference Tool),我们对这四个事件的进化进行了建模,结果表明,尽管共享基因丢失很罕见,但它们并不代表最近独立的多倍体。我们发现这些事件提高了基因座间的基因转换率,并且这些基因转换事件在空间上聚集在基因组中。基因转换区域在相应的同源基因之间也显示出非常低的同义分化。我们认为,这些基因组在多倍体后回到二倍体状态时经历了延迟。根据这一假说,由多倍体产生的重复区域之间的同源交换一直持续到今天,解释了重复保留率高的原因。具有这些特征的基因组可能代表了一类新的古多倍体分类群,因为它们具有与多倍体产生的许多复制对快速丢失的更常见和众所周知的范式不同的进化模式。
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来源期刊
Genome Biology and Evolution
Genome Biology and Evolution EVOLUTIONARY BIOLOGY-GENETICS & HEREDITY
CiteScore
5.80
自引率
6.10%
发文量
169
审稿时长
1 months
期刊介绍: About the journal Genome Biology and Evolution (GBE) publishes leading original research at the interface between evolutionary biology and genomics. Papers considered for publication report novel evolutionary findings that concern natural genome diversity, population genomics, the structure, function, organisation and expression of genomes, comparative genomics, proteomics, and environmental genomic interactions. Major evolutionary insights from the fields of computational biology, structural biology, developmental biology, and cell biology are also considered, as are theoretical advances in the field of genome evolution. GBE’s scope embraces genome-wide evolutionary investigations at all taxonomic levels and for all forms of life — within populations or across domains. Its aims are to further the understanding of genomes in their evolutionary context and further the understanding of evolution from a genome-wide perspective.
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