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通过RNA测序对SD-2a对酸休克反应的转录组分析。

Transcriptomic Analysis of SD-2a Response to Acid Shock by RNA-Seq.

作者信息

Liu Longxiang, Zhao Hongyu, Peng Shuai, Wang Tao, Su Jing, Liang Yanying, Li Hua, Wang Hua

机构信息

College of Enology, Northwest A&F UniversityYangling, China.

College of Bioengineering, Sichuan University of Science and EngineeringZigong, China.

出版信息

Front Microbiol. 2017 Aug 22;8:1586. doi: 10.3389/fmicb.2017.01586. eCollection 2017.

DOI:10.3389/fmicb.2017.01586
PMID:28878748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5572241/
Abstract

can be applied to conduct malolactic fermentation (MLF), but also is the main species growing naturally in wine. Due to the high stress tolerance, it is an interesting model for investigating acid response mechanisms. In this study, the changes in the transcriptome of SD-2a during the adaptation period have been studied. RNA-seq was introduced for the transcriptomic analysis of samples treated with pH 4.8 and pH 3.0 at 0 and 1 h, respectively. Gene ontology (GO) and Kyoto encyclopedia of genes and genome (KEGG) were performed to compare the transcriptome data between different treatments. From GO analysis, the majority of differentially expressed genes (DEGs) (pH 3.0_1 h-VS-pH 4.8_1 h, pH 3.0_1 h-VS-pH 4.8_0 h, and pH 4.8_1 h-VS-pH 4.8_0 h) were found to be involved in the metabolic process, catalytic activity, cellular process, and binding. KEGG analysis reveals that the most functional gene categories affected by acid are membrane transport, amino acid metabolism and carbohydrate metabolism. Some genes, like the heat shock protein Hsp20, malate transporter and malate permease, were also over-expressed in response to acid stress. In addition, a considerable proportion of gene indicate a significantly different expression in this study, are novel, which needs to be investigated further. These results provide a new viewpoint and crucial resource on the acid stress response in .

摘要

可用于进行苹果酸-乳酸发酵(MLF),也是葡萄酒中自然生长的主要菌种。由于其高胁迫耐受性,它是研究酸响应机制的一个有趣模型。在本研究中,对SD-2a在适应期的转录组变化进行了研究。分别在0小时和1小时对pH 4.8和pH 3.0处理的样品进行RNA测序以进行转录组分析。进行基因本体论(GO)和京都基因与基因组百科全书(KEGG)分析以比较不同处理之间的转录组数据。从GO分析中发现,大多数差异表达基因(DEGs)(pH 3.0_1小时对pH 4.8_1小时、pH 3.0_1小时对pH 4.8_0小时以及pH 4.8_1小时对pH 4.8_0小时)参与代谢过程、催化活性、细胞过程和结合。KEGG分析表明,受酸影响的最主要功能基因类别是膜转运、氨基酸代谢和碳水化合物代谢。一些基因,如热休克蛋白Hsp20、苹果酸转运蛋白和苹果酸通透酶,也在酸胁迫下过表达。此外,在本研究中相当一部分显示出显著不同表达的基因是新基因,需要进一步研究。这些结果为[具体研究对象]的酸胁迫响应提供了新的观点和关键资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d2/5572241/3aab1c1d36ee/fmicb-08-01586-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d2/5572241/27bf1d6b4483/fmicb-08-01586-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d2/5572241/220a69754baa/fmicb-08-01586-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d2/5572241/9a9ef4f294d7/fmicb-08-01586-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d2/5572241/8c73586403e6/fmicb-08-01586-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d2/5572241/3aab1c1d36ee/fmicb-08-01586-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d2/5572241/27bf1d6b4483/fmicb-08-01586-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d2/5572241/220a69754baa/fmicb-08-01586-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d2/5572241/9a9ef4f294d7/fmicb-08-01586-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d2/5572241/8c73586403e6/fmicb-08-01586-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d2/5572241/3aab1c1d36ee/fmicb-08-01586-g0005.jpg

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