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矮牵牛黄酮醇合酶的克隆与表达

Cloning and expression of flavonol synthase from Petunia hybrida.

作者信息

Holton T A, Brugliera F, Tanaka Y

机构信息

Calgene Pacific Pty Ltd., Collingwood, Victoria, Australia.

出版信息

Plant J. 1993 Dec;4(6):1003-10. doi: 10.1046/j.1365-313x.1993.04061003.x.

Abstract

Flavonols are important co-pigments in flower colour and are also essential for pollen tube growth. In petunia, flavonol synthesis is controlled by the Fl locus. Flavonol synthase (FLS) belongs to the 2-oxoglutarate-dependent dioxygenase family. Dioxygenase gene fragments were amplified by PCR on cDNA made from FlFl and flfl flowers using degenerate primers designed from conserved dioxygenase sequences. A petunia petal cDNA library was screened for clones that hybridized more strongly to the Fl PCR products than the fl PCR products. A full-length cDNA clone identified by this screening exhibited FLS activity when expressed in yeast. FLS gene expression is developmentally regulated during flower development. Antisense expression of an FLS cDNA clone in petunia markedly reduced flavonol synthesis in petals. RFLP mapping showed that the FLS gene is linked to Fl, suggesting that Fl is the structural gene for FLS.

摘要

黄酮醇是花色中重要的共色素,对花粉管生长也至关重要。在矮牵牛中,黄酮醇的合成由Fl位点控制。黄酮醇合酶(FLS)属于依赖2-酮戊二酸的双加氧酶家族。使用根据保守双加氧酶序列设计的简并引物,通过PCR从FlFl和flfl花朵制备的cDNA上扩增双加氧酶基因片段。筛选矮牵牛花瓣cDNA文库,寻找与Fl PCR产物杂交比fl PCR产物更强的克隆。通过该筛选鉴定出的全长cDNA克隆在酵母中表达时表现出FLS活性。FLS基因表达在花发育过程中受到发育调控。矮牵牛中FLS cDNA克隆的反义表达显著降低了花瓣中黄酮醇的合成。RFLP图谱显示FLS基因与Fl连锁,表明Fl是FLS的结构基因。

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