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Generation of High-Amylose Rice through CRISPR/Cas9-Mediated Targeted Mutagenesis of Starch Branching Enzymes

机译:通过CRISPR / Cas9介导的淀粉分支酶定向诱变产生高直链水稻

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摘要

Cereals high in amylose content (AC) and resistant starch (RS) offer potential health benefits. Previous studies using chemical mutagenesis or RNA interference have demonstrated that starch branching enzyme (SBE) plays a major role in determining the fine structure and physical properties of starch. However, it remains a challenge to control starch branching in commercial lines. Here, we use CRISPR/Cas9 technology to generate targeted mutagenesis in SBEI and SBEIIb in rice. The frequencies of obtained homozygous or bi-allelic mutant lines with indels in SBEI and SBEIIb in T0 generation were from 26.7 to 40%. Mutations in the homozygous T0 lines stably transmitted to the T1 generation and those in the bi-allelic lines segregated in a Mendelian fashion. Transgene-free plants carrying only the frame-shifted mutagenesis were recovered in T1 generation following segregation. Whereas no obvious differences were observed between the sbeI mutants and wild type, sbeII mutants showed higher proportion of long chains presented in debranched amylopectin, significantly increased AC and RS content to as higher as 25.0 and 9.8%, respectively, and thus altered fine structure and nutritional properties of starch. Taken together, our results demonstrated for the first time the feasibility to create high-amylose rice through CRISPR/Cas9-mediated editing of SBEIIb.
机译:直链淀粉含量(AC)和抗性淀粉(RS)高的谷物具有潜在的健康益处。先前使用化学诱变或RNA干扰的研究表明,淀粉支化酶(SBE)在确定淀粉的精细结构和物理性质方面起着重要作用。然而,在商业生产中控制淀粉分支仍然是一个挑战。在这里,我们使用CRISPR / Cas9技术在水稻的SBEI和SBEIIb中产生定向诱变。在T0代中获得的具有SBEI和SBEIIb中插入缺失的纯合或双等位基因突变体系的频率为26.7%至40%。纯合的T0系中的突变稳定地传递给T1世代,而双等位基因系中的突变则以孟德尔方式分离。在分离后的T1代中回收了仅携带移码诱变的无转基因植物。尽管sbeI突变体与野生型之间没有观察到明显差异,但sbeII突变体显示支链支链淀粉中存在的长链比例更高,AC和RS含量分别显着增加至25.0和9.8%,从而改变了精细结构和淀粉的营养特性。综上所述,我们的结果首次证明了通过CRISPR / Cas9介导的SBEIIb编辑创建高直链米饭的可行性。

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