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“秦冠”苹果(苹果属 × 栽培种)叶片响应苹果盘二孢菌接种的动态转录谱

Dynamic transcription profiles of "Qinguan" apple (Malus × domestica) leaves in response to Marssonina coronaria inoculation.

作者信息

Xu Jianhua, Li Miaomiao, Jiao Peng, Tao Hongxia, Wei Ningning, Ma Fengwang, Zhang Junke

机构信息

The Department of Pomology, College of Horticulture, Northwest A&F University Yangling, China.

出版信息

Front Plant Sci. 2015 Oct 13;6:842. doi: 10.3389/fpls.2015.00842. eCollection 2015.

Abstract

Marssonina apple blotch, caused by the fungus Marssonina coronaria, is one of the most destructive apple diseases in China and East Asia. A better understanding of the plant's response to fungi during pathogenesis is urgently needed to improve plant resistance and to breed resistant cultivars. To address this, the transcriptomes of "Qinguan" (a cultivar with high resistance to M. coronaria) apple leaves were sequenced at 12, 24, 48, and 72 h post-inoculation (hpi) with Marssonina coronaria. The comparative results showed that a total of 1956 genes were differentially expressed between the inoculated and control samples at the 4 time points. Gene ontology (GO) term enrichment analysis of differentially expressed genes (DEGs) revealed changes in cellular component, secondary metabolism including chalcone isomerase activity, phytoalexin biosynthetic process, anthocyanin-containing compound biosynthetic process, lignin biosynthetic process, positive regulation of flavonoid biosynthetic process; and molecular functions or biological processes related to the defense response, biotic stimulus response, wounding response and fungus response. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis showed that DEGs were significantly enriched in flavonoid biosynthesis, vitamin B6 metabolism, phenylpropanoid biosynthesis, and the stilbenoid, diarylheptanoid and gingerol biosynthesis pathways. Furthermore, the importance of changes in cellular components and partial polyphenol compounds when encountering M. coronaria are discussed.

摘要

苹果炭疽叶枯病由真菌苹果盘二孢菌引起,是中国和东亚地区最具毁灭性的苹果病害之一。为了提高植物抗性并培育抗病品种,迫切需要深入了解植物在发病过程中对真菌的反应。为此,对接种苹果盘二孢菌后12、24、48和72小时(hpi)的“秦冠”(对苹果盘二孢菌具有高抗性的品种)苹果叶片进行了转录组测序。比较结果表明,在这4个时间点,接种样品和对照样品之间共有1956个基因差异表达。对差异表达基因(DEGs)的基因本体(GO)术语富集分析揭示了细胞成分、包括查尔酮异构酶活性的次生代谢、植保素生物合成过程、含花青素化合物生物合成过程、木质素生物合成过程、类黄酮生物合成过程的正调控;以及与防御反应、生物刺激反应、创伤反应和真菌反应相关的分子功能或生物学过程的变化。京都基因与基因组百科全书(KEGG)通路分析表明,差异表达基因在类黄酮生物合成、维生素B6代谢、苯丙烷生物合成以及芪类、二芳基庚烷类和姜酚生物合成途径中显著富集。此外,还讨论了细胞成分和部分多酚化合物在遇到苹果盘二孢菌时变化的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af42/4602106/0d250e938627/fpls-06-00842-g0001.jpg

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