Multiplex CRISPR/Cas12a editing of ROC5, GS3, GW2, and LARGE2 reveals effects on yield-related traits in rice cultivar Kasalath.

IF 1.9 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Teerapong Janthabut, Saengtong Pongjaroenkit, Naruemon Khemkladngoen, Suparat K Lithanatudom, Pornchanan Chanchay, Supachai Vuttipongchaikij, Chotipa Sakulsingharoj
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Abstract

Sustainable improvement of rice yield requires coordinated modification of multiple agronomic traits, yet the agronomic outcomes of multiplex genome editing remain difficult to predict. Here, we applied CRISPR/Cas12a-mediated multiplex editing in the indica rice cultivar Kasalath to target six yield-related genes, Gn1a, TAD1, ROC5, GS3, GW2, and LARGE2, using a single Agrobacterium-delivered construct. Sanger sequencing of 28 T0 plants detected edits in Gn1a (3.57%), ROC5 (7.14%), GS3 (35.71%), and GW2 (10.71%), whereas TAD1 and LARGE2 showed no detectable T0 edits. Single, double, and triple edits were recovered, and homozygous lines were established for four single mutants, two double mutants, and two triple mutants. Molecular analysis showed that the recovered GW2 alleles were intronic and did not alter the GW2 coding sequence. Phenotypic evaluation across 13 agronomic traits showed that allele type and locus combination, rather than simple additive effects, determined agronomic outcome. The gs3-13d frameshift allele caused strong pleiotropic effects, including increased tillering and panicle number but reduced grain length and yield. The roc5-7d gw2-8d gs3-3i triple mutant maintained wild-type-level yield performance with altered leaf architecture, whereas gw2-8d gs3-3i large2-10d showed increased grain width, grain thickness, and 1000-grain weight but severe reductions in plant height, tillering, seed setting, yield per panicle, and yield per plant. These results demonstrate the feasibility of CRISPR/Cas12a multiplex editing in Kasalath and highlight the importance of allele design, locus combination, and source-sink balance in multiplex genome editing targeting yield-related traits.

多重CRISPR/Cas12a编辑ROC5、GS3、GW2和LARGE2揭示了对水稻品种Kasalath产量相关性状的影响。
水稻产量的可持续提高需要对多种农艺性状进行协调修改,但多重基因组编辑的农艺结果仍然难以预测。在本研究中,我们在籼稻品种Kasalath中应用CRISPR/ cas12a介导的多重编辑技术,使用单个农杆菌传递构建体靶向6个产量相关基因Gn1a、TAD1、ROC5、GS3、GW2和LARGE2。28株T0植物的Sanger测序检测到Gn1a(3.57%)、ROC5(7.14%)、GS3(35.71%)和GW2(10.71%)的T0编辑,而TAD1和LARGE2未检测到T0编辑。恢复了单、双和三重编辑,并建立了4个单突变体、2个双突变体和2个三突变体的纯合子系。分子分析表明,恢复的GW2等位基因为内含子基因,未改变GW2的编码序列。13个农艺性状的表型评价表明,决定农艺结果的不是简单的加性效应,而是等位基因类型和位点组合。gs3-13d移码等位基因具有较强的多效性,分蘖数和穗数增加,但粒长和产量减少。三突变体roc5-7d gw2-8d gs3-3i在叶片结构改变的情况下保持了野生型水平的产量表现,而gw2-8d gs3-3i large2-10d的粒宽、粒厚和千粒重均有所增加,但株高、分蘖、结实率、单穗产量和单株产量均显著降低。这些结果证明了CRISPR/Cas12a在Kasalath中多重编辑的可行性,并强调了等位基因设计、位点组合和源库平衡在针对产量相关性状的多重基因组编辑中的重要性。
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来源期刊
Transgenic Research
Transgenic Research 生物-生化研究方法
CiteScore
5.40
自引率
0.00%
发文量
38
审稿时长
4-8 weeks
期刊介绍: Transgenic Research focusses on transgenic and genome edited higher organisms. Manuscripts emphasizing biotechnological applications are strongly encouraged. Intellectual property, ethical issues, societal impact and regulatory aspects also fall within the scope of the journal. Transgenic Research aims to bridge the gap between fundamental and applied science in molecular biology and biotechnology for the plant and animal academic and associated industry communities. Transgenic Research publishes -Original Papers -Reviews: Should critically summarize the current state-of-the-art of the subject in a dispassionate way. Authors are requested to contact a Board Member before submission. Reviews should not be descriptive; rather they should present the most up-to-date information on the subject in a dispassionate and critical way. Perspective Reviews which can address new or controversial aspects are encouraged. -Brief Communications: Should report significant developments in methodology and experimental transgenic higher organisms
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