The Application of a Meiocyte-Specific CRISPR/Cas9 (MSC) System and a Suicide-MSC System in Generating Inheritable and Stable Mutations in Arabidopsis

• Published in: Frontiers in plant science Vol. 9; p. 1007
• Main Authors: Xu, Penghui, Su, Hang, Chen, Wanli, Lu, Pingli
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 13.07.2018
• Subjects: Arabidopsis; CRISPR/Cas9; genome editing; meiocyte-specific promoter; Plant Science; suicide-MSC; genome editing; CRISPR/Cas9; suicide-MSC; Arabidopsis; meiocyte-specific promoter
• ISSN: 1664-462X; 1664-462X
• DOI: 10.3389/fpls.2018.01007

The CRISPR/Cas9 system has been widely used for generating targeted mutations in various species. In Arabidopsis, it largely relies on the edited cells where the Cas9 protein performs its activity to obtain heritable and stable mutated lines. Here, we designed an improved CRISPR/Cas9 system, named as the MSC (meiocyte-specific CRISPR/Cas9) system, in which the expression is driven by an experimentally approved meiocyte-specific promoter ( promoter). Two endogenous genes, including vegetative gene and reproductive gene , were targeted. We obtained heterozygous T1 plants for targeted genes with high efficiency (64%). In the T2 generation, the homozygous plants were abundant with high efficiency (37%). Analysis of Sanger sequencing results of T2 generation revealed that heritable gene mutations were high (52%). Moreover, we showed that the MSC system could sufficiently delete a middle size DNA fragment (∼500 bp) between two cleavage sites with a high rate (64.15%) in the T1 plants, providing direct evidence for making complete knock-out or certain domain-depletion mutations. In addition, we further made a suicide-MSC system, which can edit the targeted endogenous gene and the exogenous gene simultaneously, not only successfully avoiding the further destroy of alleles brought in by molecular complementary or genic allelic test, but also maintaining the stable mutated alleles for functional studies. In short, the two systems provide new approaches to generate mutations for gene functional studies.