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敲除三个花色苷修饰基因对龙胆花蓝色素的影响。

Effects of knocking out three anthocyanin modification genes on the blue pigmentation of gentian flowers.

机构信息

Iwate Biotechnology Research Center, 22-174-4 Narita, Kitakami, Iwate, 024-0003, Japan.

Tokyo University of Agriculture, Atsugi, Kanagawa, 243-0034, Japan.

出版信息

Sci Rep. 2019 Nov 1;9(1):15831. doi: 10.1038/s41598-019-51808-3.

Abstract

Genome editing by the CRISPR/Cas9 system has recently been used to produce gene knockout lines in many plant species. We applied this system to analyze Japanese gentian plants that produce blue flowers because of the accumulation of a polyacylated anthocyanin, gentiodelphin. Mutant lines in which anthocyanin modification genes were knocked out were examined to assess the contribution of each gene to the blue pigmentation of flowers. The targeted genes encoded anthocyanin 5-O-glycosyltransferase (Gt5GT), anthocyanin 3'-O-glycosyltransferase (Gt3'GT), and anthocyanin 5/3'-aromatic acyltransferase (Gt5/3'AT). The Gt5GT knockout lines accumulated delphinidin 3G, whereas the Gt3'GT knockout lines accumulated delphinidin 3G-5CafG as the major flower pigment. Knocking out Gt5/3'AT resulted in the accumulation of delphinidin 3G-5G-3'G and delphinidin 3G-5G as the primary and secondary pigments, respectively. These results indicated the existence of two pathways mediating the modification of delphinidin 3G-5G in flowers, with one involving a glycosylation by 3'GT and the other involving an acylation by 5/3'AT. The Gt5GT, Gt3'GT, and Gt5/3'AT transformants produced pale red violet, dull pink, and pale mauve flowers, respectively, unlike the vivid blue flowers of wild-type plants. Thus, the glycosylation and subsequent acylation of the 3'-hydroxy group of the B-ring in delphinidin aglycone is essential for the development of blue gentian flowers.

摘要

CRISPR/Cas9 系统的基因组编辑最近被用于许多植物物种中产生基因敲除系。我们应用该系统来分析产生蓝色花的日本龙胆植物,因为其积累了多酰化的花色素苷,即Gentianodelphin。敲除花色素苷修饰基因的突变体系被用来评估每个基因对花的蓝色着色的贡献。靶向基因编码花色素苷 5-O-糖基转移酶(Gt5GT)、花色素苷 3'-O-糖基转移酶(Gt3'GT)和花色素苷 5/3'-芳基酰基转移酶(Gt5/3'AT)。Gt5GT 敲除系积累了飞燕草素 3G,而 Gt3'GT 敲除系则积累了飞燕草素 3G-5CafG 作为主要的花色素。敲除 Gt5/3'AT 导致飞燕草素 3G-5G-3'G 和飞燕草素 3G-5G 分别积累为主要和次要色素。这些结果表明存在两种途径介导花色素苷 3G-5G 的修饰,一种涉及 3'GT 的糖基化,另一种涉及 5/3'AT 的酰化。Gt5GT、Gt3'GT 和 Gt5/3'AT 转化体分别产生淡红色、暗淡粉红色和淡紫色花朵,与野生型植物鲜艳的蓝色花朵不同。因此,花色素苷 3'-羟基的糖基化和随后的酰化对于飞燕草苷元 B 环的蓝色发展至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a0/6825144/dbdaff0a79dd/41598_2019_51808_Fig1_HTML.jpg

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