Abstract

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.The 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.

Highlights

  • Auxins were the first major phytohormones discovered and orchestrate cardinal plant developmental processes, such as cell elongation, cell division and differentiation, tropic responses to light and gravity, general root and shootMengmeng Jiang and Huaying Hu contributed to this work.Electronic supplementary material The online version of this article contains supplementary material, which is available to authorized users.The Auxin/Indole-3-Acetic Acid (Aux/IAA) gene family members encode short-lived nuclear proteins characterized by four highly conserved domains, designated as domains I, II, III, and IV (Mukesh et al 2006)

  • As Tajima’s D values showed, an excess of low-frequency nucleotide polymorphisms was detected in most IAA genes, in Domain II and IV (Supplementary Table S3)

  • For some genes, including OsIAA2, OsIAA22, OsIAA23, and OsIAA29, strong selection was detected in their Domain II, which plays a major role in the stability of Aux/IAA proteins

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Summary

Introduction

The Aux/IAA gene family members encode short-lived nuclear proteins characterized by four highly conserved domains, designated as domains I, II, III, and IV (Mukesh et al 2006). Domain I harbors an amino-terminal leucine repeat motif (LxLxLx) and functions as a transcriptional repressor of downstream auxin-regulated genes Domain II contains a conserved TIR1/AFB recognition sequence, GWPPV, and plays a major role in the stability of Aux/IAA proteins. Mutations in the GWPPV recognition sequence block rapid degradation of Aux/IAAs, disturbing the auxin signaling pathway (Worley et al 2000; Ni et al 2011). ARF proteins harbor Domains III and IV, which are involved in homo- and heterodimerization of Aux/IAA and/or ARF proteins (Ouellet et al 2001)

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