首页> 外文期刊>The Plant Cell >Diurnal Regulation of Plant Epidermal Wax Synthesis through Antagonistic Roles of the Transcription Factors SPL9 and DEWAX
【24h】

Diurnal Regulation of Plant Epidermal Wax Synthesis through Antagonistic Roles of the Transcription Factors SPL9 and DEWAX

机译:通过转录因子SPL9和DEWAX对拮抗作用的植物表皮蜡合成的昼夜调节

获取原文
获取原文并翻译 | 示例
           

摘要

Plant surface waxes form an outer barrier that protects the plant from many forms of environmental stress. The deposition of cuticular waxes on the plant surface is regulated by external environmental changes, including light and dark cycles. However, the underlying molecular mechanisms controlling light regulation of wax production are still poorly understood, especially at the posttranscriptional level. In this paper, we report the regulation of cuticular wax production by the miR156-SPL9 (SQUAMOSA PROMOTER BINDING PROTEIN-LIKE 9) module in Arabidopsis (Arabidopsis thaliana). When compared with wild-type plants, miR156 and SPL9 mutants showed significantly altered cuticular wax amounts in both stems and leaves. Furthermore, it was found that SPL9 positively regulates gene expression of the alkane-forming enzyme ECERIFERUM1 (CER1), as well as the primary (1-) alcohol-forming enzyme ECERIFERUM4 (CER4), to enhance alkane and 1-alcohol synthesis, respectively. Our results indicate that complex formation of SPL9 with a negative regulator of wax synthesis, DEWAX, will hamper SPL9 DNA binding ability, possibly by interfering with SPL9 homodimerization. Combined with their diurnal gene and protein expressions, this dynamic repression-activation transcriptional module defines a dynamic mechanism that may allow plants to optimize wax synthesis during daily cycles. These findings provide a regulatory framework for environmental signal integration in the regulation of wax synthesis.
机译:植物表面蜡形成外屏障,保护植物免受多种形式的环境压力。在植物表面上的切割蜡的沉积由外部环境变化调节,包括光和黑暗循环。然而,控制蜡的光调节的潜在的分子机制仍然是较差的理解,特别是在预追查层面。在本文中,我们报告了拟南芥(Arabidopsis Thaliana)中MiR156-SPL9(Squamosa启动子结合蛋白样9)模块的切割蜡产生的调节。与野生型植物相比,miR156和SPL9突变体显示出显着改变的茎和叶中的内心蜡量。此外,发现SPL9积极地调节烷烃形成酶Eceriferum1(Cer1)的基因表达,以及伯(1-)醇形成酶Eceriferum4(Cer4),分别增强烷烃和1-醇合成。我们的结果表明,用负调节剂的蜡合成的SPL9复杂形成,脱蜡将妨碍SPL9 DNA结合能力,可能是通过干扰SPL9同型化学中化。结合其昼夜基因和蛋白质表达,这种动态镇压激活转录模块定义了一种动态机制,其可以允许植物在日常循环期间优化蜡合成。这些调查结果为蜡合成的调节中的环境信号集成提供了监管框架。

著录项

  • 来源
    《The Plant Cell》 |2019年第11期|共23页
  • 作者单位

    Chinese Acad Sci Key Lab Plant Germplasm Enhancement &

    Specialty A Wuhan Bot Garden Wuhan 430074 Hubei Peoples R China;

    Chinese Acad Sci Key Lab Plant Germplasm Enhancement &

    Specialty A Wuhan Bot Garden Wuhan 430074 Hubei Peoples R China;

    Chinese Acad Sci Key Lab Plant Germplasm Enhancement &

    Specialty A Wuhan Bot Garden Wuhan 430074 Hubei Peoples R China;

    Wuhan Univ Coll Life Sci Wuhan 430072 Hubei Peoples R China;

    Univ Arizona Coll Agr &

    Life Sci Sch Plant Sci Tucson AZ 85721 USA;

    Hubei Univ Sch Life Sci State Key Lab Biocatalysis &

    Enzyme Engn Wuhan 434200 Hubei Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 植物细胞学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号