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ITPK4 和 MRP5 基因的同时突变导致拟南芥中植酸水平降低而不影响其耐盐性。

Simultaneous mutations in ITPK4 and MRP5 genes result in a low phytic acid level without compromising salt tolerance in Arabidopsis.

机构信息

Key Laboratory of Plant Design, National Key Laboratory of Plant Molecular Genetics, Shanghai Center for Plant Stress Biology, CAS Center for Excellence in Molecular Plant Sciences, the Chinese Academy of Sciences, Shanghai, 200032, China.

University of Chinese Academy of Sciences, Beijing, 100190, China.

出版信息

J Integr Plant Biol. 2024 Oct;66(10):2109-2125. doi: 10.1111/jipb.13745. Epub 2024 Jul 19.

Abstract

Generation of crops with low phytic acid (myo-inositol-1,2,3,4,5,6-hexakisphosphate (InsP)) is an important breeding direction, but such plants often display less desirable agronomic traits. In this study, through ethyl methanesulfonate-mediated mutagenesis, we found that inositol 1,3,4-trisphosphate 5/6-kinase 4 (ITPK4), which is essential for producing InsP, is a critical regulator of salt tolerance in Arabidopsis. Loss of function of ITPK4 gene leads to reduced root elongation under salt stress, which is primarily because of decreased root meristem length and reduced meristematic cell number. The itpk4 mutation also results in increased root hair density and increased accumulation of reactive oxygen species during salt exposure. RNA sequencing assay reveals that several auxin-responsive genes are down-regulated in the itpk4-1 mutant compared to the wild-type. Consistently, the itpk4-1 mutant exhibits a reduced auxin level in the root tip and displays compromised gravity response, indicating that ITPK4 is involved in the regulation of the auxin signaling pathway. Through suppressor screening, it was found that mutation of Multidrug Resistance Protein 5 (MRP5)5 gene, which encodes an ATP-binding cassette (ABC) transporter required for transporting InsP from the cytoplasm into the vacuole, fully rescues the salt hypersensitivity of the itpk4-1 mutant, but in the itpk4-1 mrp5 double mutant, InsP remains at a very low level. These results imply that InsP homeostasis rather than its overall amount is beneficial for stress tolerance in plants. Collectively, this study uncovers a pair of gene mutations that confer low InsP content without impacting stress tolerance, which offers a new strategy for creating "low-phytate" crops.

摘要

培育低植酸(肌醇-1,2,3,4,5,6-六磷酸(InsP))作物是一个重要的育种方向,但这类植物通常表现出较差的农艺性状。在这项研究中,通过乙基磺酸甲酯诱变,我们发现肌醇 1,3,4-三磷酸 5/6-激酶 4(ITPK4)是产生 InsP 的必需酶,它是拟南芥盐胁迫耐受的关键调节因子。ITPK4 基因的功能丧失导致盐胁迫下根伸长减少,这主要是由于根分生组织长度变短和分生组织细胞数量减少所致。itpk4 突变还导致根毛密度增加和盐暴露时活性氧积累增加。RNA 测序分析显示,与野生型相比,itpk4-1 突变体中几个生长素响应基因下调。一致地,itpk4-1 突变体在根尖的生长素水平降低,并且表现出重力反应受损,表明 ITPK4 参与了生长素信号通路的调节。通过抑制子筛选,发现多药耐药蛋白 5(MRP5)5 基因突变,该基因编码一种 ABC 转运蛋白,用于将 InsP 从细胞质运入液泡,完全挽救了 itpk4-1 突变体的盐敏感表型,但在 itpk4-1 mrp5 双突变体中,InsP 仍保持在非常低的水平。这些结果表明,InsP 稳态而不是其总量有利于植物的胁迫耐受。总之,本研究揭示了一对基因突变,它们在不影响胁迫耐受的情况下赋予低 InsP 含量,为创造“低植酸”作物提供了新策略。

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