Whole genome wide expression profiles on germination of Verticillium dahliae microsclerotia

Verticillium dahliae is a fungal pathogen causing Verticillium wilt on a range of economically important crops. Microsclerotia are its main survival and dormancy structures and serve as the primary inoculum on many hosts. Studies were conducted to determine the effect of temperature (5 to 50°C), pH...

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Veröffentlicht in:PloS one 2014-06, Vol.9 (6), p.e100046
Hauptverfasser: Hu, Dongfang, Wang, Chunsheng, Tao, Fei, Cui, Qian, Xu, Xiangming, Shang, Wenjing, Hu, Xiaoping
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container_title PloS one
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Wang, Chunsheng
Tao, Fei
Cui, Qian
Xu, Xiangming
Shang, Wenjing
Hu, Xiaoping
description Verticillium dahliae is a fungal pathogen causing Verticillium wilt on a range of economically important crops. Microsclerotia are its main survival and dormancy structures and serve as the primary inoculum on many hosts. Studies were conducted to determine the effect of temperature (5 to 50°C), pH (2 to 12) and nutrient regimes on microsclerotia germination. The optimal condition for microsclerotium germination was 20°C with pH 8.0 whereas nutrient regimes had no significant effect on its germination. The whole genome wide expression profiles during microsclerotium germination were characterized using the Illumina sequencing technology. Approximately 7.4 million of 21-nt cDNA tags were sequenced in the cDNA libraries derived from germinated and non-germinated microsclerotia. About 3.9% and 2.3% of the unique tags were up-regulated and down-regulated at least five-fold, respectively, in the germinated microsclerotia compared with the non-germinated microsclerotia. A total of 1654 genes showing differential expression were identified. Genes that are likely to have played important roles in microsclerotium germination include those encoding G-protein coupled receptor, lipase/esterase, cyclopentanone 1,2-monooxygenase, H(+)/hexose cotransporter 1, fungal Zn(2)-Cys(6) binuclear cluster domain, thymus-specific serine protease, glucan 1,3-beta-glucosidase, and alcohol dehydrogenase. These genes were mainly up-regulated or down-regulated only in germinated microsclerotia, compared with non-germinated microsclerotia. The differential expression of genes was confirmed by qRT-PCR analysis of 20 randomly selected genes from the 40 most differentially expressed genes.
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Microsclerotia are its main survival and dormancy structures and serve as the primary inoculum on many hosts. Studies were conducted to determine the effect of temperature (5 to 50°C), pH (2 to 12) and nutrient regimes on microsclerotia germination. The optimal condition for microsclerotium germination was 20°C with pH 8.0 whereas nutrient regimes had no significant effect on its germination. The whole genome wide expression profiles during microsclerotium germination were characterized using the Illumina sequencing technology. Approximately 7.4 million of 21-nt cDNA tags were sequenced in the cDNA libraries derived from germinated and non-germinated microsclerotia. About 3.9% and 2.3% of the unique tags were up-regulated and down-regulated at least five-fold, respectively, in the germinated microsclerotia compared with the non-germinated microsclerotia. A total of 1654 genes showing differential expression were identified. 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Microsclerotia are its main survival and dormancy structures and serve as the primary inoculum on many hosts. Studies were conducted to determine the effect of temperature (5 to 50°C), pH (2 to 12) and nutrient regimes on microsclerotia germination. The optimal condition for microsclerotium germination was 20°C with pH 8.0 whereas nutrient regimes had no significant effect on its germination. The whole genome wide expression profiles during microsclerotium germination were characterized using the Illumina sequencing technology. Approximately 7.4 million of 21-nt cDNA tags were sequenced in the cDNA libraries derived from germinated and non-germinated microsclerotia. About 3.9% and 2.3% of the unique tags were up-regulated and down-regulated at least five-fold, respectively, in the germinated microsclerotia compared with the non-germinated microsclerotia. A total of 1654 genes showing differential expression were identified. Genes that are likely to have played important roles in microsclerotium germination include those encoding G-protein coupled receptor, lipase/esterase, cyclopentanone 1,2-monooxygenase, H(+)/hexose cotransporter 1, fungal Zn(2)-Cys(6) binuclear cluster domain, thymus-specific serine protease, glucan 1,3-beta-glucosidase, and alcohol dehydrogenase. These genes were mainly up-regulated or down-regulated only in germinated microsclerotia, compared with non-germinated microsclerotia. The differential expression of genes was confirmed by qRT-PCR analysis of 20 randomly selected genes from the 40 most differentially expressed genes.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24927478</pmid><doi>10.1371/journal.pone.0100046</doi><oa>free_for_read</oa></addata></record>
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subjects Alcohol dehydrogenase
Alcohols
Analysis
Aspergillus niger
Biology
Biology and Life Sciences
Crop diseases
Dormancy
Drinking water
Esterase
Fungi
G protein-coupled receptors
Gene expression
Gene Expression Regulation, Fungal
Gene Library
Genes
Genes, Fungal
Genomes
Genomics
Germination
Glucan
Glucan 1,3-b-glucosidase
Glucosidase
Hexose
Inoculum
Laboratories
Lipase
Monooxygenase
Nutrients
pH effects
Physical Sciences
Proteins
Real-Time Polymerase Chain Reaction
Serine
Serine proteinase
Spores, Fungal - genetics
Spores, Fungal - growth & development
Tags
Temperature effects
Thrombin
Thymus
Transcriptome
Verticillium - genetics
Verticillium - growth & development
Verticillium dahliae
Verticillium wilt
Zinc
title Whole genome wide expression profiles on germination of Verticillium dahliae microsclerotia
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