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蒺藜苜蓿炭疽菌全基因组揭示核心染色体内部的一个微型染色体样区域。

Complete genome of the Medicago anthracnose fungus, , reveals a mini-chromosome-like region within a core chromosome.

机构信息

Université Paris-Saclay, INRAE, UR BIOGER, 91120 Palaiseau, France.

Division of Biochemistry, Department of Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany.

出版信息

Microb Genom. 2024 Aug;10(8). doi: 10.1099/mgen.0.001283.

DOI:10.1099/mgen.0.001283
PMID:39166978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11338638/
Abstract

() is a phytopathogenic fungus causing significant economic losses on forage legume crops ( and species) worldwide. To gain insights into the genetic basis of fungal virulence and host specificity, we sequenced the genome of an isolate from using long-read (PacBio) technology. The resulting genome assembly has a total length of 51.7 Mb and comprises ten core chromosomes and two accessory chromosomes, all of which were sequenced from telomere to telomere. A total of 15, 631 gene models were predicted, including genes encoding potentially pathogenicity-related proteins such as candidate-secreted effectors (484), secondary metabolism key enzymes (110) and carbohydrate-active enzymes (619). Synteny analysis revealed extensive structural rearrangements in the genome of relative to the closely related Brassicaceae pathogen, . In addition, a 1.2 Mb species-specific region was detected within the largest core chromosome of that has all the characteristics of fungal accessory chromosomes (transposon-rich, gene-poor, distinct codon usage), providing evidence for exchange between these two genomic compartments. This region was also unique in having undergone extensive intra-chromosomal segmental duplications. Our findings provide insights into the evolution of accessory regions and possible mechanisms for generating genetic diversity in this asexual fungal pathogen.

摘要

()是一种植物病原真菌,可导致全球饲料豆科作物(和 种)造成重大经济损失。为了深入了解真菌毒力和宿主特异性的遗传基础,我们使用长读(PacBio)技术对来自 的分离株进行了基因组测序。得到的基因组组装总长为 51.7Mb,包含十个核心染色体和两个附加染色体,它们都是从端粒到端粒测序的。总共预测了 15631 个基因模型,包括编码潜在致病性相关蛋白的基因,如候选分泌效应物(484 个)、次级代谢关键酶(110 个)和碳水化合物活性酶(619 个)。共线性分析显示,与密切相关的芸薹科病原菌 相比, 中的基因组发生了广泛的结构重排。此外,在 的最大核心染色体中检测到一个 1.2Mb 的种特异性区域,该区域具有真菌附加染色体的所有特征(转座子丰富、基因贫乏、独特的密码子使用),为这两个基因组区室之间的交换提供了证据。该区域还在经历广泛的染色体内部片段重复中是独特的。我们的研究结果为辅助区域的进化以及这种无性真菌病原体产生遗传多样性的可能机制提供了线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/87fa8e0fa81a/mgen-10-01283-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/08b6a84d27b1/mgen-10-01283-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/89f80601a383/mgen-10-01283-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/6f31e10acfd6/mgen-10-01283-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/4d099c8df58d/mgen-10-01283-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/bbc085c2a334/mgen-10-01283-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/9e3e57d47768/mgen-10-01283-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/87fa8e0fa81a/mgen-10-01283-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/08b6a84d27b1/mgen-10-01283-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/89f80601a383/mgen-10-01283-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/6f31e10acfd6/mgen-10-01283-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/4d099c8df58d/mgen-10-01283-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/bbc085c2a334/mgen-10-01283-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/9e3e57d47768/mgen-10-01283-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d7b/11338638/87fa8e0fa81a/mgen-10-01283-g007.jpg

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