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Genome Size Versus Genome Assemblies: Are the Genomes Truly Expanded in Polyploid Fungal Symbionts?

机译:基因组大小与基因组组装:基因组是真正扩增的多倍体真菌共生吗?

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摘要

Each day, as the amount of genomic data and bioinformatics resources grows, researchers are increasingly challenged with selecting the most appropriate approach to analyze their data. In addition, the opportunity to undertake comparative genomic analyses is growing rapidly. This is especially true for fungi due to their small genome sizes (i.e., mean 1C = 44.2 Mb). Given these opportunities and aiming to gain novel insights into the evolution of mutualisms, we focus on comparing the quality of whole genome assemblies for fungus-growing ants cultivars (Hymenoptera: Formicidae: Attini) and a free-living relative. Our analyses reveal that currently available methodologies and pipelines for analyzing whole-genome sequence data need refining. By using different genome assemblers, we show that the genome assembly size depends on what software is used. This, in turn, impacts gene number predictions, with higher gene numbers correlating positively with genome assembly size. Furthermore, the majority of fungal genome size data currently available are based on estimates derived from whole-genome assemblies generated from short-read genome data, rather than from the more accurate technique of flow cytometry. Here, we estimated the haploid genome sizes of three ant fungal symbionts by flow cytometry using the fungus Pleurotus ostreatus (Jacq.) P. Kumm. (1871) as a calibration standard. We found that published genome sizes based on genome assemblies are 2.5- to 3-fold larger than our estimates based on flow cytometry. We, therefore, recommend that flow cytometry is used to precalibrate genome assembly pipelines, to avoid incorrect estimates of genome sizes and ensure robust assemblies.
机译:每天,随着基因组数据和生物信息学资源的增加,研究人员越来越挑战,选择最适合分析其数据的方法。此外,承接比较基因组分析的机会正在迅速增长。由于它们的小基因组尺寸(即平均值1c = 44.2mb),这对真菌尤其如此。鉴于这些机会和旨在获得新的洞察力对共生主义的演变,我们专注于比较真菌生长蚂蚁品种的全基因组组装的质量(Hymenoptera:Formicidae:Attini)和自由生活相对。我们的分析显示,目前可用的方法和管道用于分析全基因组序列数据需要精炼。通过使用不同的基因组汇编器,我们表明基因组组装大小取决于所使用的软件。反过来,这会影响基因数预测,具有较高的基因数与基因组组装大小正相关。此外,目前可用的大多数真菌基因组大小数据基于从短读取基因组数据产生的全基因组组件中衍生的估计,而不是从流式细胞术的更准确的技术。在这里,我们通过使用真菌胸膜斑(JACQ.)P. Kumm,估计流式细胞仪估计三个蚂蚁真菌共生的单倍体基因组大小。 (1871)作为校准标准。我们发现,基于基因组组件的出版的基因组大小比基于流式细胞术的估计大2.5至3倍。因此,我们推荐流式细胞术用于预纤维突触基因组组件管道,以避免基因组尺寸的不正确估计,并确保鲁棒组件。

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