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BnaC9.DEWAX1 通过转录抑制. 来负调控蜡质生物合成。

BnaC9.DEWAX1 Negatively Regulates Wax Biosynthesis via Transcriptional Suppression of .

机构信息

College of Agronomy, Qingdao Agriculture University, Qingdao 266109, China.

College of Agronomy and Biotechnology, Southwest University, Chongqing 400716, China.

出版信息

Int J Mol Sci. 2023 Feb 21;24(5):4287. doi: 10.3390/ijms24054287.

Abstract

Very-long-chain alkane plays an important role as an aliphatic barrier. We previously reported that was responsible for alkane biosynthesis in and improved plant tolerance to drought. However, how the expression of is regulated is still unknown. Through yeast one-hybrid screening, we identified a transcriptional regulator of , BnaC9.DEWAX1, which encodes AP2\ERF transcription factor. BnaC9.DEWAX1 targets the nucleus and displays transcriptional repression activity. Electrophoretic mobility shift and transient transcriptional assays suggested that BnaC9.DEWAX1 repressed the transcription of by directly interacting with its promoter. was expressed predominantly in leaves and siliques, which was similar to the expression pattern of . Hormone and major abiotic stresses such as drought and high salinity affected the expression of . Ectopic expression of in Arabidopsis plants down-regulated transcription levels and resulted in a reduction in alkanes and total wax loads in leaves and stems when compared with the wild type, whereas the wax depositions in the mutant returned to the wild type level after complementation of in the mutant. Moreover, both altered cuticular wax composition and structure contribute to increased epidermal permeability in overexpression lines. Collectively, these results support the notion that BnaC9.DEWAX1 negatively regulates wax biosynthesis by binding directly to the promoter, which provides insights into the regulatory mechanism of wax biosynthesis in .

摘要

长链烷烃在作为脂肪性障碍方面起着重要作用。我们之前报道过, 负责油菜烷烃的生物合成,并提高了植物对干旱的耐受性。然而, 的表达如何受到调控仍然未知。通过酵母单杂交筛选,我们鉴定到了一个 的转录调控因子 BnaC9.DEWAX1,它编码 AP2/ERF 转录因子。BnaC9.DEWAX1 靶向细胞核并显示转录抑制活性。电泳迁移率变动和瞬时转录测定表明,BnaC9.DEWAX1 通过直接与启动子相互作用来抑制 的转录。 在叶片和角果中表达为主,与 的表达模式相似。激素和主要非生物胁迫,如干旱和高盐度,影响 的表达。与野生型相比,拟南芥中 的异位表达降低了 的转录水平,并导致叶片和茎中的烷烃和总蜡载量减少,而 在突变体中的互补则使蜡沉积恢复到野生型水平。此外,改变的角质层蜡组成和结构导致 过表达系中表皮渗透率增加。总之,这些结果支持 BnaC9.DEWAX1 通过直接结合 启动子负调控蜡生物合成的观点,为油菜蜡生物合成的调控机制提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d7a/10002155/b069ae8d6348/ijms-24-04287-g001.jpg

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