Colletotrichum siamense infection caused transcripts involved plant hormone signal transduction and phenylpropanoid biosynthesis varied in strawberry

苯丙素 小桶 生物 植物激素 RNA序列 代谢途径 转录组 信号转导 炭疽菌 生物合成 基因表达 基因 植物 生物化学
作者
Rong ZHENG,Bo Shu,Chun Luo
出处
期刊:Notulae botanicae Horti Agrobotanici Cluj-Napoca [Academic Press]
卷期号:50 (3): 12791-12791 被引量:1
标识
DOI:10.15835/nbha50312791
摘要

Colletotrichum siamense infected the petiole and crown of strawberry (Fragaria × ananassa), and this anthracnose threatens strawberry production heavily in Hubei province. Characteristic the variation of transcript caused by C. siamense is important for anthracnose control of strawberry. In this study, RNA-seq analysis was used to monitor the strawberry transcripts in response of C. siamense at 0- and 6-days post-inoculation based on lesion measurement and hypha observation. The number of clean reads achieved for each sample was ranged from 5.68 to 8.12 Gb. The 0DPM vs 0DPI group had seven significantly differentially expressed transcripts, whereas the 6DPM vs 6DPI group exhibited 12,097 significantly differentially expressed transcripts. The differentially expressed transcripts of 6DPM vs 6DPI group were enriched in ‘metabolic process’ and ‘biological process’ in the biological process category and ‘oxidoreductase activity’ in the molecular function category by GO analysis. While ‘Starch and sucrose metabolism’, ‘Plant hormone signal transduction’ and ‘Phenylpropanoid biosynthesis’ pathways were significantly enriched by KEGG analysis. The expression of MYC2 in JA, the ETR in Eth and, the SnRK2 and ABF in ABA signal transduction pathways were promoted, whereas expression of the PR1 in SA, JZA1 in JA, and ERF in Eth signal transduction pathways were inhibited. In addition, the transcripts that encode enzymes involved in the ‘Phenylpropanoid biosynthesis’ pathway, such as PAL, CYP73A, CSE, 4CL, HTC, GSE and COMT were all inhibited showed by RNA-seq and qRT-PCR. This study provided basic information of strawberry responding to C. siamense infection.
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