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在拟南芥突变体中,被转座子诱导的 DNA 甲基化所抑制。

Is Repressed by Transgene-Induced DNA Methylation in the Arabidopsis Mutant.

机构信息

Laboratory of Plant Molecular Physiology, Graduate School of Agricultural and Life Sciences, University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan.

Gene Discovery Research Group, RIKEN Center for Sustainable Resource Science, Tsukuba, Ibaraki 305-0074, Japan.

出版信息

Plant Cell. 2020 Apr;32(4):1035-1048. doi: 10.1105/tpc.19.00532. Epub 2020 Feb 7.

Abstract

DREB1/CBFs are key transcription factors involved in plant cold stress adaptation. The expression of s triggers a cold-responsive transcriptional cascade, after which many stress tolerance genes are expressed. Thus, elucidating the mechanisms of cold stress-inducible expression is important to understand the molecular mechanisms of plant cold stress responses and tolerance. We analyzed the roles of a transcription factor, INDUCER OF CBF EXPRESSION1 (ICE1), that is well known as an important transcriptional activator in the cold-inducible expression of in Arabidopsis (). is a widely accepted mutant allele known to abolish cold-inducible expression, and this evidence has strongly supported ICE1- regulation for many years. However, in outcross descendants, we unexpectedly discovered that repression was genetically independent of the allele ICE1(R236H). Moreover, neither overexpression nor double loss-of-function mutation of and its homolog altered expression. Instead, a transgene locus harboring a reporter gene in the genome was responsible for altering expression. The promoter was hypermethylated due to the transgene. We showed that repression in results from transgene-induced silencing and not genetic regulation by ICE1. The ICE1(R236H) mutation has also been reported as , which confers constitutive stomatal differentiation. The phenotype and the expression of a stomatal differentiation marker gene were confirmed to be linked to the ICE1(R236H) mutation. We propose that the current ICE1- regulatory model should be revalidated without the previous assumptions.

摘要

DREB1/CBFs 是参与植物冷胁迫适应的关键转录因子。s 的表达触发了一个冷响应的转录级联反应,之后许多应激耐受基因被表达。因此,阐明冷应激诱导表达的机制对于理解植物冷应激响应和耐受的分子机制非常重要。我们分析了转录因子 INDUCER OF CBF EXPRESSION1(ICE1)的作用,ICE1 作为拟南芥中冷诱导表达的重要转录激活因子而广为人知。是一个广被认可的突变等位基因,已知其能消除冷诱导的表达,多年来这一证据强烈支持 ICE1 对的调控。然而,在 的杂交后代中,我们出人意料地发现 抑制在遗传上与 的等位基因 ICE1(R236H)无关。此外,过表达或双功能缺失突变 及其同源物 均未改变 的表达。相反,在 基因组中含有报告基因的转基因位点负责改变 的表达。由于转基因, 的启动子发生了超甲基化。我们表明,在 中 的抑制是由转基因诱导的沉默引起的,而不是由 ICE1 进行的遗传调控。ICE1(R236H)突变也被报道为 ,它赋予了组成型的气孔分化。气孔分化标记基因的表达和 表型被证实与 ICE1(R236H)突变有关。我们提出,在没有先前假设的情况下,应该重新验证当前的 ICE1-调控模型。

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