Application of CRISPR/Cas9 system to knock out GluB gene for developing low glutelin rice mutant.

IF 3.4 3区 生物学 Q1 Agricultural and Biological Sciences Botanical Studies Pub Date : 2024-09-03 DOI:10.1186/s40529-024-00432-0
Latifa AlHusnain, Muneera D F AlKahtani, Kotb A Attia, Tayyaba Sanaullah, Dalia E Elsharnoby
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Abstract

The nutritional quality improvement is among the most integral objective for any rice molecular breeding programs. The seed storage proteins (SSPs) have greater role to determine the nutritional quality of any cereal grains. Rice contains relatively balanced amino acid composition and the SSPs are fractioned into albumins (ALB), globulins (GLO), prolamins (PRO) and glutelins (GLU) according to differences in solubility. GLUs are further divided into subfamilies: GluA, GluB, GluC, and GluD depending on resemblance in amino acid. The GLU protein accounts for 60-80% of total protein contents, encoded by 15 genes located on different chromosomes of rice genome. The clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) system was employed to knockout Glu-B (LOC-Os02g15070) gene in non-basmati rice PK386 cultivar. The mutant displayed two base pair and three base pair mutation in the targeted regions. The homozygous mutant plant displayed reduction for both in total protein contents and GLU contents whereas, elevation in GLO, ALB and PRO. Moreover, the mutant plant also displayed reduction in physio-chemical properties e.g., total starch, amylose and gel consistency. The agronomic characteristics of both mutant and wild type displayed non-significant differences along with increase in higher percentage of chalkiness in mutant plants. The results obtained from scanning electron microscopy showed the loosely packed starch granules compared to wild type. The gene expression analysis displayed the lower expression of gene at 5 days after flowering (DAF), 10 DAF, 15 DAF and 20 DAF compared to wild type. GUS sub-cellular localization showed the staining in seed which further validated the results obtained from gene expression. Based on these findings it can be concluded Glu-B gene have significant role in controlling GLU contents and can be utilized in breeding programs to enhance the nutritional quality of rice, and may serve as healthy diet for patient allergic with high GLU contents.

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应用 CRISPR/Cas9 系统敲除 GluB 基因,培育低谷蛋白水稻突变体。
提高营养品质是任何水稻分子育种计划最不可或缺的目标之一。种子贮藏蛋白(SSPs)在决定谷物的营养品质方面发挥着重要作用。水稻含有相对均衡的氨基酸组成,根据溶解度的不同,SSPs 可分为白蛋白(ALB)、球蛋白(GLO)、丙种球蛋白(PRO)和谷蛋白(GLU)。谷蛋白又分为亚家族:根据氨基酸的相似性,GLU 又分为 GluA、GluB、GluC 和 GluD 亚家族。GLU 蛋白占蛋白质总含量的 60-80%,由位于水稻基因组不同染色体上的 15 个基因编码。利用簇状规则间隔短回文重复(CRISPR)/CRISPR相关蛋白9(Cas9)系统敲除了非asmati水稻PK386栽培品种的Glu-B(LOC-Os02g15070)基因。突变体在目标区域出现了两个碱基对和三个碱基对的突变。同源突变植株的总蛋白含量和 GLU 含量均有所降低,而 GLO、ALB 和 PRO 含量则有所升高。此外,突变植株的理化特性(如总淀粉、直链淀粉和凝胶稠度)也有所降低。突变体和野生型的农艺特征差异不大,但突变体植株的垩白度增加了。扫描电子显微镜的结果显示,与野生型相比,突变体的淀粉颗粒松散。基因表达分析表明,与野生型相比,突变体在花后 5 天(DAF)、10 DAF、15 DAF 和 20 DAF 的基因表达量较低。GUS 亚细胞定位显示了种子中的染色,这进一步验证了基因表达的结果。基于这些发现,可以得出结论:Glu-B 基因在控制 GLU 含量方面具有重要作用,可用于育种计划以提高水稻的营养品质,并可作为高 GLU 含量过敏症患者的健康饮食。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Botanical Studies
Botanical Studies 生物-植物科学
CiteScore
5.50
自引率
2.90%
发文量
32
审稿时长
2.4 months
期刊介绍: Botanical Studies is an open access journal that encompasses all aspects of botany, including but not limited to taxonomy, morphology, development, genetics, evolution, reproduction, systematics, and biodiversity of all plant groups, algae, and fungi. The journal is affiliated with the Institute of Plant and Microbial Biology, Academia Sinica, Taiwan.
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