Transcriptional regulation of the grape cytochrome P450 monooxygenase gene CYP736B expression in response to Xylella fastidiosa infection 英文参考文献.docVIP
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Transcriptional regulation of the grape cytochrome P450 monooxygenase gene CYP736B expression in response to Xylella fastidiosa infection 英文参考文献
Cheng et al. BMC Plant Biology 2010, 10:135
/1471-2229/10/135
RESEARCH ARTICLE
Open Access
Transcriptional regulation of the grape cytochrome Research article
P450 monooxygenase gene CYP736B expression in
response to Xylella fastidiosa infection
Davis W Cheng1,2, Hong Lin*1, Yuri Takahashi3,4, M Andrew Walker3, Edwin L Civerolo1 and Drake C Stenger1
Abstract
Background: Plant cytochrome P450 monooxygenases (CYP) mediate synthesis and metabolism of many
physiologically important primary and secondary compounds that are related to plant defense against a range of
pathogenic microbes and insects. To determine if cytochrome P450 monooxygenases are involved in defense
response to Xylella fastidiosa (Xf) infection, we investigated expression and regulatory mechanisms of the cytochrome
P450 monooxygenase CYP736B gene in both disease resistant and susceptible grapevines.
Results: Cloning of genomic DNA and cDNA revealed that the CYP736B gene was composed of two exons and one
intron with GT as a donor site and AG as an acceptor site. CYP736B transcript was up-regulated in PD-resistant plants
and down-regulated in PD-susceptible plants 6 weeks after Xf inoculation. However, CYP736B expression was very low
in stem tissues at all evaluated time points. 5RACE and 3RACE sequence analyses revealed that there were three
candidate transcription start sites (TSS) in the upstream region and three candidate polyadenylation (PolyA) sites in the
downstream region of CYP736B. Usage frequencies of each transcription initiation site and each polyadenylation site
varied depending on plant genotype, developmental stage, tissue, and treatment. These results demonstrate that
expression of CYP736B is regulated developmentally and in response to Xf infection at both transcriptional and post-
transcriptional levels. Multiple transcription start and polyadenylation sites contribute to regulation of CYP736B
expression.
Conclusions: This report provides evidence that the cytochrome
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