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CRISRP/Cas9介导的番茄多聚半乳糖醛酸酶基因靶向诱变延迟果实软化

CRISRP/Cas9-Mediated Targeted Mutagenesis of Tomato Polygalacturonase Gene () Delays Fruit Softening.

作者信息

Nie Hongmei, Shi Yu, Geng Xueqing, Xing Guoming

机构信息

College of Horticulture/Collaborative Innovation Center of Improving Quality and Increasing Profits for Protected Vegetables in Shanxi, Shanxi Agricultural University, Taigu, China.

School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Front Plant Sci. 2022 May 19;13:729128. doi: 10.3389/fpls.2022.729128. eCollection 2022.

Abstract

Polygalacturonase (PG) gene has been documented as a key candidate for the improvement of fruit firmness, which is a target trait for tomato production because it facilitates transportation and storage. To reduce the expression of the gene, most of the elite commercial tomato varieties were obtained by RNA interference technology. However, this approach of producing commercialized tomatoes by integration of the exogenous gene is controversial. In this work, CRISPR/Cas9 technology was used to induce the targeted mutagenesis of the gene to delay the softening of tomato fruit. Results showed that the gene was frameshift mutated by 4 bp deletion, 10 bp deletion, and 1 bp insertion, which generated premature translation termination codons. Compared with wild-type (WT), homozygous T-generation tomato plants exhibited late fruit softening under natural conditions. Consistent with this phenomenon, the firmness value of WT fruit was lower in mutant fruit, and the physiological loss of water was higher. Collectively, these data demonstrate that the mutation of the gene delays tomato fruit softening. More importantly, 8 out of 20 transgene-free tomato plants, which were homozygous for null alleles of , were separated in the T-generation of line T-#2. This transgene-free may provide materials for more in-depth research of functions and the molecular mechanism of fruit softening in tomatoes.

摘要

多聚半乳糖醛酸酶(PG)基因已被证明是改善果实硬度的关键候选基因,果实硬度是番茄生产的一个目标性状,因为它有利于运输和储存。为了降低该基因的表达,大多数优良的商业番茄品种是通过RNA干扰技术获得的。然而,这种通过整合外源基因来生产商业化番茄的方法存在争议。在这项工作中,利用CRISPR/Cas9技术诱导该基因的靶向诱变,以延缓番茄果实的软化。结果表明,该基因因4bp缺失、10bp缺失和1bp插入而发生移码突变,产生了提前的翻译终止密码子。与野生型(WT)相比,纯合T代番茄植株在自然条件下果实软化较晚。与此现象一致,WT果实的硬度值在突变果实中较低,水分生理损失较高。总体而言,这些数据表明该基因的突变延缓了番茄果实的软化。更重要的是,在T-#2系的T代中分离出了20株无转基因的番茄植株,其中8株为该基因无效等位基因的纯合子。这种无转基因的植株可能为深入研究番茄中该基因的功能和果实软化的分子机制提供材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5103/9162796/7b92f940726e/fpls-13-729128-g001.jpg

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