Jiangsu Key Laboratory of Crop Genetics and Physiology/Key Laboratory of Plant Functional Genomics of the Ministry of Education/Jiangsu Key Laboratory of Crop Genomics and Molecular Breeding, Yangzhou University, Yangzhou 225009, China.
Int J Mol Sci. 2023 Sep 21;24(18):14360. doi: 10.3390/ijms241814360.
The demand for rice grain quality, particularly in terms of eating and cooking quality, is increasingly concerning at present. However, the limited availability of rice-quality-related gene resources and time-consuming and inefficient traditional breeding methods have severely hindered the pace of rice grain quality improvement. Exploring novel methods for improving rice grain quality and creating new germplasms is an urgent problem that needs to be addressed. In this study, an amino-acid-transporter-encoding gene () mainly expressed in endosperm was selected as the target for gene editing using the CRISPR/Cas9 system in three genetic backgrounds (Wuyungeng30, Nangeng9108, and Yanggeng158, hereafter referred to as WYG30, NG9108, and YG158). We successfully obtained homozygous mutants without transgenic insertion. Subsequently, we conducted comprehensive investigations on the agronomic traits, rice grain quality traits, and transcriptomic analysis of these mutants. The results demonstrate that loss of function led to a reduced amino acid content and total protein content in grains without affecting the agronomic traits of the plants; meanwhile, it significantly increased the peak viscosity, holding viscosity, and final viscosity values during the cooking process, thereby enhancing the eating and cooking quality. This study not only provides valuable genetic resources and fundamental materials for improving rice grain quality but also provides novel technical support for the rapid enhancement of rice grain quality.
目前,人们对稻米品质(特别是食味和蒸煮品质)的需求日益增加。然而,稻米品质相关基因资源有限,传统的选育方法费时低效,严重阻碍了稻米品质改良的步伐。探索改良稻米品质和创造新种质的新方法是亟待解决的问题。本研究以主要在胚乳中表达的氨基酸转运蛋白编码基因()为目标基因,在三个遗传背景(武育粳 30 号、南粳 9108 和扬粳 158,以下分别简称为 WYG30、NG9108 和 YG158)下利用 CRISPR/Cas9 系统进行基因编辑,成功获得了无转基因插入的纯合突变体。随后,我们对这些突变体的农艺性状、稻米品质性状和转录组进行了综合分析。结果表明,功能丧失导致突变体稻米的氨基酸和总蛋白含量降低,但不影响植株的农艺性状;同时,它显著提高了蒸煮过程中的峰值黏度、保持黏度和最终黏度值,从而改善了食味和蒸煮品质。本研究不仅为改良稻米品质提供了有价值的遗传资源和基础材料,也为快速提高稻米品质提供了新的技术支持。