Activation tagging identifies a conserved MYB regulator of phenylpropanoid biosynthesis

被引:1183
作者
Borevitz, JO
Xia, YJ
Blount, J
Dixon, RA
Lamb, C [1 ]
机构
[1] Salk Inst Biol Studies, Plant Biol Lab, La Jolla, CA 92037 USA
[2] Samuel Roberts Noble Fdn Inc, Div Plant Biol, Ardmore, OK 73401 USA
关键词
D O I
10.1105/tpc.12.12.2383
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Plants produce a wide array of natural products, many of which are likely to be useful bioactive structures. Unfortunately, these complex natural products usually occur at very low abundance and with restricted tissue distribution, thereby hindering their evaluation. Here, we report a novel approach for enhancing the accumulation of natural products based on activation tagging by Agrobacterium-mediated transformation with a T-DNA that carries cauliflower mosaic virus 35S enhancer sequences at its right border. Among similar to 5000 Arabidopsis activation-tagged lines, we found a plant that exhibited intense purple pigmentation in many vegetative organs throughout development. This upregulation of pigmentation reflected a dominant mutation that resulted in massive activation of phenylpropanoid biosynthetic genes and enhanced accumulation of lignin, hydroxycinnamic acid esters, and flavonoids, including various anthocyanins that were responsible for the purple color. These phenotypes, caused by insertion of the viral enhancer sequences adjacent to an MYB transcription factor gene, indicate that activation tagging can overcome the stringent genetic controls regulating the accumulation of specific natural products during plant development. Our findings suggest a functional genomics approach to the biotechnological evaluation of phytochemical biodiversity through the generation of massively enriched tissue sources for drug screening and for isolating underlying regulatory and biosynthetic;genes.
引用
收藏
页码:2383 / 2393
页数:11
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