4.7 Article

Different knockout genotypes of OsIAA23 in rice using CRISPR/Cas9 generating different phenotypes

期刊

PLANT MOLECULAR BIOLOGY
卷 100, 期 4-5, 页码 467-479

出版社

SPRINGER
DOI: 10.1007/s11103-019-00871-5

关键词

Oryza sativa; OsIAA23; CRISPR; Cas9; Root development; Alternative splicing

资金

  1. National Natural Science Foundation of China [31570368, 31870204]
  2. National Major Special Project on New Varieties Cultivation for Transgenic Organisms [2016ZX08009001-003]
  3. Jiangsu Collaborative Innovation Center for Modern Crop Production

向作者/读者索取更多资源

Key messageWe have isolated several Osiaa23 rice mutants with different knockout genotypes, resulting in different phenotypes, which suggested that different genetic backgrounds or mutation types influence gene function.AbstractThe Auxin/Indole-3-Acetic Acid (Aux/IAA) gene family performs critical roles in auxin signal transduction in plants. In rice, the gene OsIAA23 (Os06t0597000) is known to affect development of roots and shoots, but previous knockouts in OsIAA23 have been sterile and difficult for research continuously. Here, we isolate new Osiaa23 mutants using the CRISPR/Cas9 system in japonica (Wuyunjing24) and indica (Kasalath) rice, with extensive genome re-sequencing to confirm the absence of off-target effects. In Kasalath, mutants with a 13-amino acid deletion showed profoundly greater dwarfing, lateral root developmental disorder, and fertility deficiency, relative to mutants with a single amino acid deletion, demonstrating that those 13 amino acids in Kasalath are essential to gene function. In Wuyunjing24, we predicted that mutants with a single base-pair frameshift insertion would experience premature termination and strong phenotypic defects, but instead these lines exhibited negligible phenotypic difference and normal fertility. Through RNA-seq, we show here that new mosaic transcripts of OsIAA23 were produced de novo, which circumvented the premature termination and thereby preserved the wild-type phenotype. This finding is a notable demonstration in plants that mutants can mask loss of function CRISPR/Cas9 editing of the target gene through de novo changes in alternative splicing.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据