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亚麻上不同毒力菌株的比较基因组分析

Comparative Genomic Analysis of Strains with Different Virulence on Flax.

作者信息

Dvorianinova Ekaterina M, Sigova Elizaveta A, Mollaev Timur D, Rozhmina Tatiana A, Kudryavtseva Ludmila P, Novakovskiy Roman O, Turba Anastasia A, Zhernova Daiana A, Borkhert Elena V, Pushkova Elena N, Melnikova Nataliya V, Dmitriev Alexey A

机构信息

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russia.

Moscow Institute of Physics and Technology, Moscow 141701, Russia.

出版信息

J Fungi (Basel). 2023 Dec 31;10(1):32. doi: 10.3390/jof10010032.

Abstract

is a flax fungal pathogen. The genus comprises differently virulent strains, leading to significant yield losses. However, there were no attempts to investigate the molecular mechanisms of pathogenicity from high-quality genome assemblies until this study. In this work, we sequenced the genomes of three strains of high (#390-1), medium (#757), and low (#771) virulence. We obtained more than 100× genome coverage with Oxford Nanopore Technologies reads (N50 = 12.1, 6.1, 5.0 kb) and more than 50× genome coverage with Illumina data (150 + 150 bp). Several assembly strategies were tested. The final assemblies were obtained using the Canu-Racon ×2-Medaka-Polca scheme. The assembled genomes had a size of 54.0-55.3 Mb, 26-32 contigs, N50 values > 5 Mb, and BUSCO completeness > 96%. A comparative genomic analysis showed high similarity among mitochondrial and nuclear genomes. However, a rearrangement event and the loss of a 0.7 Mb contig were revealed. After genome annotation with Funannotate, secreting proteins were selected using SignalP, and candidate effectors were predicted among them using EffectorP. The analysis of the InterPro annotations of predicted effectors revealed unique protein categories in each strain. The assembled genomes and the conducted comparative analysis extend the knowledge of the genetic diversity of and form the basis for establishing the molecular mechanisms of its pathogenicity.

摘要

是一种亚麻真菌病原体。该属包含不同毒力的菌株,会导致显著的产量损失。然而,在本研究之前,尚未有人尝试从高质量的基因组组装中研究其致病的分子机制。在这项工作中,我们对三株高毒力(#390 - 1)、中毒力(#757)和低毒力(#771)的菌株进行了基因组测序。我们通过牛津纳米孔技术读数获得了超过100倍的基因组覆盖度(N50分别为12.1、6.1、5.0 kb),并通过Illumina数据(150 + 150 bp)获得了超过50倍的基因组覆盖度。测试了几种组装策略。最终的组装是使用Canu - Racon×2 - Medaka - Polca方案获得的。组装后的基因组大小为54.0 - 55.3 Mb,有26 - 32个重叠群,N50值> 5 Mb,且BUSCO完整性> 96%。比较基因组分析表明线粒体和核基因组之间具有高度相似性。然而,发现了一个重排事件和一个0.7 Mb重叠群的丢失。在用Funannotate进行基因组注释后,使用SignalP选择分泌蛋白,并使用EffectorP在其中预测候选效应子。对预测效应子的InterPro注释分析揭示了每个菌株中独特的蛋白质类别。组装后的基因组和进行的比较分析扩展了对该病原体遗传多样性的认识,并为建立其致病的分子机制奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6853/10817032/f0659892bea6/jof-10-00032-g001.jpg

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