• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

重新发现一个老对手:优化的分子方法用于提取和测序粉霉(白粉菌目)真菌标本的 DNA 序列。

Rediscovering an old foe: Optimised molecular methods for DNA extraction and sequencing applications for fungarium specimens of powdery mildew (Erysiphales).

机构信息

Department of Jobs, Agriculture Victoria Research, Regions and Precincts, Bundoora, Australia.

School of Applied Systems Biology, La Trobe University, Bundoora, Australia.

出版信息

PLoS One. 2020 May 13;15(5):e0232535. doi: 10.1371/journal.pone.0232535. eCollection 2020.

DOI:10.1371/journal.pone.0232535
PMID:32401807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7219758/
Abstract

The purpose of this study was to identify a reliable DNA extraction protocol to use on 25-year-old powdery mildew specimens from the reference collection VPRI in order to produce high quality sequences suitable to address taxonomic phylogenetic questions. We tested 13 extraction protocols and two library preparation kits and found the combination of the E.Z.N.A.® Forensic DNA kit for DNA extraction and the NuGen Ovation® Ultralow System library preparation kit was the most suitable for this purpose.

摘要

本研究旨在确定一种可靠的 DNA 提取方案,用于从 VPRI 参考收藏中的 25 年陈 powder 样 mildew 标本中提取 DNA,以生成高质量的序列,从而解决分类系统发育问题。我们测试了 13 种提取方案和两种文库制备试剂盒,发现 E.Z.N.A.®法医 DNA 试剂盒用于 DNA 提取和 NuGen Ovation® Ultralow 系统文库制备试剂盒的组合最适合于这一目的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/e7d484debb21/pone.0232535.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/d8a5a95e92b0/pone.0232535.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/6ce42804caca/pone.0232535.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/c1025d8714e5/pone.0232535.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/e139d42e3c6f/pone.0232535.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/cebcc77ac522/pone.0232535.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/116916550e7f/pone.0232535.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/e7d484debb21/pone.0232535.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/d8a5a95e92b0/pone.0232535.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/6ce42804caca/pone.0232535.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/c1025d8714e5/pone.0232535.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/e139d42e3c6f/pone.0232535.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/cebcc77ac522/pone.0232535.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/116916550e7f/pone.0232535.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5363/7219758/e7d484debb21/pone.0232535.g007.jpg

相似文献

1
Rediscovering an old foe: Optimised molecular methods for DNA extraction and sequencing applications for fungarium specimens of powdery mildew (Erysiphales).重新发现一个老对手:优化的分子方法用于提取和测序粉霉(白粉菌目)真菌标本的 DNA 序列。
PLoS One. 2020 May 13;15(5):e0232535. doi: 10.1371/journal.pone.0232535. eCollection 2020.
2
Purification of High Molecular Weight Genomic DNA from Powdery Mildew for Long-Read Sequencing.从白粉病中纯化用于长读长测序的高分子量基因组DNA
J Vis Exp. 2017 Mar 31(121):55463. doi: 10.3791/55463.
3
Enhancing identification accuracy for powdery mildews using previously underexploited DNA loci.利用以前未充分利用的 DNA 位点提高白粉病的鉴定准确性。
Mycologia. 2019 Sep-Oct;111(5):798-812. doi: 10.1080/00275514.2019.1643644. Epub 2019 Aug 26.
4
Sequencing Herbarium Specimens of a Common Detrimental Plant Disease (Powdery Mildew).对常见有害植物病害(白粉病)的标本进行测序。
Phytopathology. 2020 Jul;110(7):1248-1254. doi: 10.1094/PHYTO-04-20-0139-PER. Epub 2020 Jun 3.
5
Comparison of various RNA extraction methods, cDNA preparation and isolation of calmodulin gene from a highly melanized isolate of apple leaf blotch fungus Marssonina coronaria.从高度黑化的苹果叶斑病菌(Marssonina coronaria)分离物中比较各种RNA提取方法、cDNA制备及钙调蛋白基因的分离
J Microbiol Methods. 2018 Aug;151:7-15. doi: 10.1016/j.mimet.2018.05.023. Epub 2018 May 29.
6
Ampelomyces mycoparasites from apple powdery mildew identified as a distinct group based on single-stranded conformation polymorphism analysis of the rDNA ITS region.基于核糖体DNA内转录间隔区(rDNA ITS)区域的单链构象多态性分析,从苹果白粉病中鉴定出的被孢霉属真菌寄生物为一个独特的类群。
Mycol Res. 2005 Apr;109(Pt 4):429-38. doi: 10.1017/s0953756204001820.
7
Neoerysiphe kerribeeensis sp. nov. (Ascomycota: Erysiphales), a new species of Neoerysiphe on native and introduced species of Senecio (Asteraceae) in Australia.新种 Neoerysiphe kerribeeensis sp. nov.(子囊菌门:白粉菌目),澳大利亚原产及引入的千里光属(菊科)植物上的 Neoerysiphe 新种。
Fungal Biol. 2010 Apr;114(4):340-4. doi: 10.1016/j.funbio.2010.02.002. Epub 2010 Feb 11.
8
Comparison of ITS sequences from UK and North American sugar-beet powdery mildews and the designation of Erysiphe betae.英国和北美甜菜白粉菌ITS序列的比较及甜菜白粉菌的命名
Mycol Res. 2007 Feb;111(Pt 2):204-12. doi: 10.1016/j.mycres.2006.10.010.
9
Powdery mildew of Chrysanthemum × morifolium: phylogeny and taxonomy in the context of Golovinomyces species on Asteraceae hosts.菊花白粉病:菊科寄主上球针壳属物种背景下的系统发育与分类
Mycologia. 2017 May-Jun;109(3):508-519. doi: 10.1080/00275514.2017.1358136. Epub 2017 Jul 27.
10
Multiple displacement amplification, a powerful tool for molecular genetic analysis of powdery mildew fungi.多重置换扩增,一种用于白粉病真菌分子遗传分析的强大工具。
Curr Genet. 2007 Mar;51(3):209-19. doi: 10.1007/s00294-006-0117-7.

引用本文的文献

1
What are the 100 most cited fungal genera?被引用次数最多的100个真菌属有哪些?
Stud Mycol. 2024 Jul;108:1-411. doi: 10.3114/sim.2024.108.01. Epub 2024 Jul 15.
2
Deciphering the Genomic Landscape and Virulence Mechanisms of the Wheat Powdery Mildew Pathogen f. sp. Wtn1: Insights from Integrated Genome Assembly and Conidial Transcriptomics.解析小麦白粉病菌f. sp. Wtn1的基因组图谱和致病机制:来自基因组组装和分生孢子转录组学的见解
J Fungi (Basel). 2024 Apr 3;10(4):267. doi: 10.3390/jof10040267.
3
Genetic Diversity Analysis based on the Virulence, Physiology and Regional Variability in Different Isolates of Powdery Mildew in Pea.

本文引用的文献

1
Enhancing identification accuracy for powdery mildews using previously underexploited DNA loci.利用以前未充分利用的 DNA 位点提高白粉病的鉴定准确性。
Mycologia. 2019 Sep-Oct;111(5):798-812. doi: 10.1080/00275514.2019.1643644. Epub 2019 Aug 26.
2
Low-cost cross-taxon enrichment of mitochondrial DNA using in-house synthesised RNA probes.使用内部合成的 RNA 探针进行低成本的跨分类群线粒体 DNA 富集。
PLoS One. 2019 Feb 4;14(2):e0209499. doi: 10.1371/journal.pone.0209499. eCollection 2019.
3
Genome skimming herbarium specimens for DNA barcoding and phylogenomics.
基于豌豆白粉病不同分离株的毒力、生理特性和区域变异性的遗传多样性分析
J Fungi (Basel). 2022 Jul 29;8(8):798. doi: 10.3390/jof8080798.
4
Current Insight into Culture-Dependent and Culture-Independent Methods in Discovering Ascomycetous Taxa.关于发现子囊菌分类群的依赖培养和不依赖培养方法的当前见解
J Fungi (Basel). 2021 Aug 28;7(9):703. doi: 10.3390/jof7090703.
5
Comparative evaluation of different molecular methods for DNA extraction from individual Teladorsagia circumcincta nematodes.比较不同分子方法从单个细颈袋形线虫中提取 DNA 的效果。
BMC Biotechnol. 2021 May 17;21(1):35. doi: 10.1186/s12896-021-00695-6.
6
Re-Evaluation of the Species Complex in Australia.澳大利亚物种复合体的重新评估。
J Fungi (Basel). 2021 Feb 26;7(3):171. doi: 10.3390/jof7030171.
7
Australia: A Continent Without Native Powdery Mildews? The First Comprehensive Catalog Indicates Recent Introductions and Multiple Host Range Expansion Events, and Leads to the Re-discovery of as a New Lineage of the Erysiphales.澳大利亚:一个没有本土白粉菌的大陆?首份综合名录显示了近期的引入情况和多次寄主范围扩展事件,并促成了作为白粉菌目新谱系的重新发现。
Front Microbiol. 2020 Jul 16;11:1571. doi: 10.3389/fmicb.2020.01571. eCollection 2020.
利用基因组浅层测序法研究植物标本馆标本进行DNA条形码分析和系统发育基因组学研究
Plant Methods. 2018 Jun 5;14:43. doi: 10.1186/s13007-018-0300-0. eCollection 2018.
4
Sequencing historical specimens: successful preparation of small specimens with low amounts of degraded DNA.测序历史标本:成功制备少量降解 DNA 的小标本。
Mol Ecol Resour. 2017 Nov;17(6):1183-1201. doi: 10.1111/1755-0998.12660. Epub 2017 Mar 30.
5
Reinforcing plant evolutionary genomics using ancient DNA.利用古DNA强化植物进化基因组学
Curr Opin Plant Biol. 2017 Apr;36:38-45. doi: 10.1016/j.pbi.2017.01.002. Epub 2017 Feb 1.
6
Evaluation of library preparation methods for Illumina next generation sequencing of small amounts of DNA from foodborne parasites.用于食源寄生虫少量DNA的Illumina下一代测序文库制备方法的评估
J Microbiol Methods. 2016 Nov;130:23-26. doi: 10.1016/j.mimet.2016.08.020. Epub 2016 Aug 21.
7
Temporal patterns of damage and decay kinetics of DNA retrieved from plant herbarium specimens.从植物标本馆标本中提取的 DNA 的损伤和衰变动力学的时间模式。
R Soc Open Sci. 2016 Jun 22;3(6):160239. doi: 10.1098/rsos.160239. eCollection 2016 Jun.
8
All that is gold does not glitter? Age, taxonomy, and ancient plant DNA quality.并非所有金子都会发光?年代、分类学与古代植物DNA质量。
PeerJ. 2015 Jul 23;3:e1087. doi: 10.7717/peerj.1087. eCollection 2015.
9
The use of museum specimens with high-throughput DNA sequencers.博物馆标本与高通量DNA测序仪的联用
J Hum Evol. 2015 Feb;79:35-44. doi: 10.1016/j.jhevol.2014.10.015. Epub 2014 Dec 18.
10
Library construction for next-generation sequencing: overviews and challenges.下一代测序文库构建:概述与挑战。
Biotechniques. 2014 Feb 1;56(2):61-4, 66, 68, passim. doi: 10.2144/000114133. eCollection 2014.