Whole genome sequencing and analysis of the symbiotic Armillaria gallica M3 with Gastrodia elata

被引:0
|
作者
Luo, Cheng-Ying [1 ,2 ]
Lu, Yao [1 ,3 ]
Su, Lei [1 ,3 ]
Liu, Jia-Jia [1 ,3 ]
Miao, Jia-Yun [4 ]
Lin, Yi-Cen [1 ,3 ]
Lin, Lian-Bing [1 ,3 ]
机构
[1] Kunming Univ Sci & Technol, Fac Life Sci & Technol, Kunming 650500, Peoples R China
[2] Gastrodia Ind Dev Ctr Yiliang Cty, Zhaotong 657000, Peoples R China
[3] Yunnan Coll, Engn Res Ctr Replacement Technol Feed Antibiot, Kunming 650500, Peoples R China
[4] Yunnan Senhao Fungi Ind Co Ltd, Zhaotong 657600, Peoples R China
来源
BMC GENOMICS | 2025年 / 26卷 / 01期
关键词
Armillaria; Gastrodia elata; Symbiosis; Genome; Mechanism analysis; ANTIFUNGAL PROTEIN; ALIGNMENT; MELLEA; GENE; TOOL; PURIFICATION; GROWTH;
D O I
10.1186/s12864-024-10897-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background On the one hand, Armillaria is regarded as a plant disease that causes serious root rot of forest trees, on the other hand, Armillaria is also an important symbiotic fungi of the valuable Chinese herb Gastrodiaelata. Currently, the whole genome database of Armillaria is relatively limited, and it is expected that a more comprehensive understanding of the symbiotic interactions between Armillaria and G. elata can be achieved through genome-wide comparisons and functional annotations. Whole genome sequencing of Armillaria gallica M3 strain was performed using Oxford Nanopore Technologies sequencing platform, and the sequencing data were used to perform genome assembly, gene prediction and functional annotation, carbohydrate-active enzymes, and host-pathogen interactions using bioinformatics methods. Results In this study, we obtained an 83.33 M genome of A. gallica M3 strain, which consisted of 38 overlapping clusters with an N50 of 6,065,498 bp and a GC content of 47.43%. A total of 12,557 genes were identified in the genome of A. gallica M3, and the repetitive sequences accounted for about 44.36% of the genome. 42.26% of the genome was composed of glycoside hydrolases (GHs), 16.15% of the genome was composed of glycosyltransferases (GTs). In addition, 3412 genes in A. gallica M3 were involved in the host-pathogen interaction mechanism. results have elucidated the characteristics of A. gallica M3 from a genomic perspective to a certain extent. They help to analyze the inner mechanism of A. gallica M3 being able to symbiosis with G. elata at the genomic level, which is of great significance to the next related research of A. gallica M3.
引用
收藏
页数:12
相关论文
共 50 条
  • [41] Cloning and sequencing analysis of whole Spiroplasma genome in yeast
    Mizutani, Masaki
    Omori, Sawako
    Yamane, Noriko
    Suzuki, Yo
    Glass, John I.
    Chuang, Ray-Yuan
    Fukatsu, Takema
    Kakizawa, Shigeyuki
    FRONTIERS IN MICROBIOLOGY, 2024, 15
  • [42] Whole-genome sequencing analysis of the cardiometabolic proteome
    Gilly, Arthur
    Park, Young-Chan
    Png, Grace
    Barysenka, Andrei
    Fischer, Iris
    Bjornland, Thea
    Southam, Lorraine
    Suveges, Daniel
    Neumeyer, Sonja
    Rayner, N. William
    Tsafantakis, Emmanouil
    Karaleftheri, Maria
    Dedoussis, George
    Zeggini, Eleftheria
    NATURE COMMUNICATIONS, 2020, 11 (01)
  • [43] Whole-genome sequencing analysis of the cardiometabolic proteome
    Arthur Gilly
    Young-Chan Park
    Grace Png
    Andrei Barysenka
    Iris Fischer
    Thea Bjørnland
    Lorraine Southam
    Daniel Suveges
    Sonja Neumeyer
    N. William Rayner
    Emmanouil Tsafantakis
    Maria Karaleftheri
    George Dedoussis
    Eleftheria Zeggini
    Nature Communications, 11
  • [44] Whole-genome sequencing analysis of brain tumors
    Suzuki, Hiromichi
    Nakashima, Takuma
    Funakoshi, Yusuke
    Kanamori, Masayuki
    Shibahara, Ichiyo
    Suzuki, Tomonari
    Kinoshita, Manabu
    Sonoda, Yukihiko
    Arakawa, Yoshiki
    Nagane, Motoo
    Tanaka, Shota
    Ishida, Joji
    Saito, Ryuta
    Hanaya, Ryosuke
    Yoshimoto, Koji
    Narita, Yoshitaka
    CANCER SCIENCE, 2025, 116 : 626 - 626
  • [45] Whole genome sequencing for M/XDR tuberculosis surveillance and for resistance testing
    Walker, T. M.
    Merker, M.
    Kohl, T. A.
    Crook, D. W.
    Niemann, S.
    Peto, T. E. A.
    CLINICAL MICROBIOLOGY AND INFECTION, 2017, 23 (03) : 161 - 166
  • [46] Evaluation of whole exome sequencing as an alternative to BeadChip and whole genome sequencing in human population genetic analysis
    Zoltán Maróti
    Zsolt Boldogkői
    Dóra Tombácz
    Michael Snyder
    Tibor Kalmár
    BMC Genomics, 19
  • [47] Evaluation of whole exome sequencing as an alternative to BeadChip and whole genome sequencing in human population genetic analysis
    Maroti, Zoltan
    Boldogkoi, Zsolt
    Tombacz, Dora
    Snyder, Michael
    Kalmar, Tibor
    BMC GENOMICS, 2018, 19
  • [48] Genome-Wide Identification and Expression Analysis of the Basic Helix-Loop-Helix (bHLH) Transcription Factor Family in Gastrodia elata
    Lan, Shanshan
    Lin, Xin
    Wei, Maoqiong
    Feng, Guangheng
    Liu, Hongcheng
    Shao, Jinliang
    Li, Xinyu
    Chen, Zeli
    Liu, Zhenhuan
    PLANT MOLECULAR BIOLOGY REPORTER, 2025,
  • [49] Analysis of the bread wheat genome using whole-genome shotgun sequencing
    Rachel Brenchley
    Manuel Spannagl
    Matthias Pfeifer
    Gary L. A. Barker
    Rosalinda D’Amore
    Alexandra M. Allen
    Neil McKenzie
    Melissa Kramer
    Arnaud Kerhornou
    Dan Bolser
    Suzanne Kay
    Darren Waite
    Martin Trick
    Ian Bancroft
    Yong Gu
    Naxin Huo
    Ming-Cheng Luo
    Sunish Sehgal
    Bikram Gill
    Sharyar Kianian
    Olin Anderson
    Paul Kersey
    Jan Dvorak
    W. Richard McCombie
    Anthony Hall
    Klaus F. X. Mayer
    Keith J. Edwards
    Michael W. Bevan
    Neil Hall
    Nature, 2012, 491 : 705 - 710
  • [50] Genome sequencing guide: An introductory toolbox to whole-genome analysis methods
    Burian, Alexis N.
    Zhao, Wufan
    Lo, Te-Wen
    Thurtle-Schmidt, Deborah M.
    BIOCHEMISTRY AND MOLECULAR BIOLOGY EDUCATION, 2021, 49 (05) : 815 - 825