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基于核糖体DNA IGS2序列的用于野生松树根际外生菌根真菌的有用PCR引物组。

A useful PCR primer set for the ectomycorrhizal fungus in wild pine rhizosphere based on the nuclear ribosomal DNA IGS2 sequence.

作者信息

Misawa Hiroki, Tateishi Yu, Horimai Yuka, Mizuno Aira, Hida Fuuma, Furukawa Hitoshi, Kobayashi Hisayasu, Kawai Masataka, Yamanaka Takashi, Fukuda Masaki, Yamada Akiyoshi

机构信息

Graduate School of Science and Technology, Shinshu University.

Faculty of Agriculture, Shinshu University.

出版信息

Mycoscience. 2024 Jun 5;65(4):191-198. doi: 10.47371/mycosci.2024.05.001. eCollection 2024.

DOI:10.47371/mycosci.2024.05.001
PMID:39493650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11527769/
Abstract

is an edible ectomycorrhizal mushroom that forms a symbiotic association with Pinaceae trees by constructing a large extraradical mycelial area (called a shiro) in the soil. The detection of this fungal mycelium in the soil is crucial for estimating the success of outplanted mycorrhizal seedlings inoculated with under experimental conditions. Although several -specific DNA markers have been reported for efficient detection in the field, no comparative study has been conducted to assess their effectiveness. In the present study, we targeted the nuclear ribosomal DNA intergenic spacer 2 (IGS2) region for the detection of . The newly designed TmSP-I-2F/TmSP-I-2R primer pair, which targets a partial IGS2 sequence (543 bp), effectively detected from pine root and soil samples via PCR assay, outperforming other -specific primers. In combination with a PCR system targeting LTR DNA markers that were previously developed, a PCR system with the TmSP-I-2F/TmSP-I-2R primer pair set can expedite investigations of the dynamics of genets in mycorrhizas and shiro.

摘要

是一种可食用的外生菌根真菌,通过在土壤中构建一个大型的根外菌丝区域(称为菌索)与松科树木形成共生关系。在实验条件下,检测土壤中的这种真菌菌丝体对于评估接种了该真菌的外植菌根幼苗的成功情况至关重要。尽管已经报道了几种用于田间高效检测的该真菌特异性DNA标记,但尚未进行比较研究来评估它们的有效性。在本研究中,我们针对核糖体DNA基因间隔区2(IGS2)区域进行该真菌的检测。新设计的TmSP-I-2F/TmSP-I-2R引物对靶向部分IGS2序列(543 bp),通过PCR检测有效地从松树根和土壤样本中检测到了该真菌,其性能优于其他该真菌特异性引物。与先前开发的靶向LTR DNA标记的PCR系统相结合,具有TmSP-I-2F/TmSP-I-2R引物对的PCR系统可以加快对菌根和菌索中该真菌基因动态的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1833/11527769/78dfca545dad/MYC-65-191-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1833/11527769/612fbb9d5fd2/MYC-65-191-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1833/11527769/78dfca545dad/MYC-65-191-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1833/11527769/612fbb9d5fd2/MYC-65-191-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1833/11527769/78dfca545dad/MYC-65-191-g02.jpg

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本文引用的文献

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Near-complete de novo assembly of Tricholoma bakamatsutake chromosomes revealed the structural divergence and differentiation of Tricholoma genomes.近完整从头组装的松茸染色体揭示了松茸基因组的结构差异和分化。
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Spore germination and ectomycorrhizae formation of Tricholoma matsutake on pine root systems with previously established ectomycorrhizae from a dikaryotic mycelial isolate of T. matsutake.松露菌根真菌的担子菌双核菌丝体在已建立的外生菌根的松树根系上的孢子萌发和外生菌根形成。
Mycorrhiza. 2021 May;31(3):335-347. doi: 10.1007/s00572-021-01028-3. Epub 2021 Mar 24.
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A qPCR assay that specifically quantifies Tricholoma matsutake biomass in natural soil.一种特异性定量天然土壤中松口蘑生物量的qPCR检测方法。
Mycorrhiza. 2016 Nov;26(8):847-861. doi: 10.1007/s00572-016-0718-z. Epub 2016 Jul 1.
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MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets.MEGA7:适用于更大数据集的分子进化遗传学分析版本7.0
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Forest age correlates with fine-scale spatial structure of Matsutake mycorrhizas.林龄与松口蘑菌根的精细尺度空间结构相关。
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