Next-generation sequencing provides important insights into the biology and evolution of the Botryosphaeriaceae

IF 5.7 2区 生物学 Q1 MYCOLOGY Fungal Biology Reviews Pub Date : 2021-12-01 DOI:10.1016/j.fbr.2021.09.002
Jan H. Nagel, Michael J. Wingfield, Bernard Slippers
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引用次数: 2

Abstract

Next-generation sequencing (NGS) has revolutionized research on fungi including Botryosphaeriaceae, a family of important plant and particularly tree pathogens. This review highlights the impact that NGS-generated genomes and transcriptomes have had on our understanding of the biology and evolution of these fungi. In less than a decade, 49 genomes representing 31 species in eight genera have been published for the Botryosphaeriaceae. These genomes have been used to show that species in this family are capable of sexual reproduction and that the evolution of their mating strategy is highly dynamic, due to multiple independent transitions from a heterothallic ancestral state to homothallism. Comparative genomics has further revealed an abundance of genes involved in infection and aggressiveness. These include plant cell wall-degrading enzymes and secondary metabolite biosynthetic genes as well as genes related to detoxification and cellular transport. Transcriptomics studies have shown that gene expression is tightly regulated and that there are often significant changes in gene expression occurring between early and late infection and as a response to environmental stress. Furthermore, the genomes of species in the Botryosphaeriaceae do not present genomic architecture compartmentalization based on gene and repeat density. Rather, gene organization patterns are influenced by gene co-expression patterns. NGS data have also made possible the development of molecular markers for some species and these can now also be used for species lacking genomic data. The growth of NGS platforms and their integration with other emerging technologies promises an even deeper understanding of the biology and evolution of the Botryosphaeriaceae and other plant pathogens. This will continue to promote and will also revolutionize the field of plant pathology.

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下一代测序提供了重要的见解,以生物学和进化的botryosphereriaceae
新一代测序(NGS)已经彻底改变了真菌的研究,包括Botryosphaeriaceae,这是一个重要的植物,特别是树木病原体家族。这篇综述强调了ngs生成的基因组和转录组对我们对这些真菌的生物学和进化的理解的影响。在不到十年的时间里,已经发表了Botryosphaeriaceae 8属31个物种的49个基因组。这些基因组已经被用来证明这个科中的物种能够有性繁殖,并且它们的交配策略的进化是高度动态的,因为它们从异源祖先状态到同源状态有多次独立的转变。比较基因组学进一步揭示了大量与感染和侵袭性有关的基因。这些基因包括植物细胞壁降解酶和次生代谢物生物合成基因以及与解毒和细胞运输相关的基因。转录组学研究表明,基因表达受到严格调控,在感染早期和晚期以及对环境应激的反应中,基因表达经常发生显著变化。此外,植物的基因组不存在基于基因和重复密度的基因组结构划分。相反,基因组织模式受到基因共表达模式的影响。NGS数据还使某些物种的分子标记的开发成为可能,这些标记现在也可用于缺乏基因组数据的物种。随着NGS平台的发展及其与其他新兴技术的整合,人们有望更深入地了解植物学和其他植物病原体的生物学和进化。这将继续促进并将彻底改变植物病理学领域。
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来源期刊
CiteScore
10.60
自引率
0.00%
发文量
36
期刊介绍: Fungal Biology Reviews is an international reviews journal, owned by the British Mycological Society. Its objective is to provide a forum for high quality review articles within fungal biology. It covers all fields of fungal biology, whether fundamental or applied, including fungal diversity, ecology, evolution, physiology and ecophysiology, biochemistry, genetics and molecular biology, cell biology, interactions (symbiosis, pathogenesis etc), environmental aspects, biotechnology and taxonomy. It considers aspects of all organisms historically or recently recognized as fungi, including lichen-fungi, microsporidia, oomycetes, slime moulds, stramenopiles, and yeasts.
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