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单子叶植物调控蛋白不透明-2定位于玉米胚乳细胞核及转化的烟草植株中。

Monocot regulatory protein Opaque-2 is localized in the nucleus of maize endosperm and transformed tobacco plants.

作者信息

Varagona M J, Schmidt R J, Raikhel N V

机构信息

Department of Energy Plant Research Laboratory, Michigan State University, East Lansing 48824-1312.

出版信息

Plant Cell. 1991 Feb;3(2):105-13. doi: 10.1105/tpc.3.2.105.

Abstract

Protein targeting to the nucleus has been studied extensively in animal and yeast systems; however, nothing is known about nuclear targeting in plants. The Opaque-2 (O2) gene produces a regulatory protein that is responsible for inducing transcription of the alpha-zein class of storage proteins in maize kernels. The cloned O2 gene encodes a protein that contains a leucine zipper DNA binding domain that can interact with zein gene promoters. We have used immunolocalization to show that the O2 protein is present in nuclei in the maize endosperm tissues known to produce alpha-zeins. In addition, neither embryo tissue from wild-type kernels nor endosperm from kernels harboring a null o2 allele contain the O2 protein. Analysis of a transposable, element-induced o2 allele, o2-m20, revealed that sectors of endosperm cells contained the nuclear-localized O2 protein, indicating excision of the transposable element. To study further the nuclear transport of the O2 protein, we have transformed this gene, under the control of a constitutive promoter, into tobacco. Plants were shown to have detectable levels of steady-state O2 mRNA and O2 protein. Immunolocalization of O2 protein in transformed tobacco plants indicated that the O2 protein was transported into tobacco nuclei. Therefore, we have developed a system to study nuclear targeting in plants and have established that the nuclear transport machinery is similar in monocots and dicots.

摘要

蛋白质靶向细胞核的研究在动物和酵母系统中已广泛开展;然而,对于植物中的核靶向却一无所知。不透明-2(O2)基因产生一种调节蛋白,该蛋白负责诱导玉米籽粒中α-醇溶蛋白类贮藏蛋白的转录。克隆的O2基因编码一种含有亮氨酸拉链DNA结合结构域的蛋白,该结构域可与醇溶蛋白基因启动子相互作用。我们利用免疫定位技术表明,O2蛋白存在于已知产生α-醇溶蛋白的玉米胚乳组织的细胞核中。此外,野生型籽粒的胚组织和携带无效o2等位基因的籽粒的胚乳中均不含O2蛋白。对一个由转座元件诱导的o2等位基因o2-m20的分析表明,胚乳细胞的部分区域含有核定位的O2蛋白,这表明转座元件已被切除。为了进一步研究O2蛋白的核运输,我们在组成型启动子的控制下,将该基因转入烟草。结果显示,这些植物中可检测到稳态O2 mRNA和O2蛋白水平。对转基因烟草植株中O2蛋白的免疫定位表明,O2蛋白被转运到烟草细胞核中。因此,我们开发了一个研究植物核靶向的系统,并确定单子叶植物和双子叶植物中的核运输机制是相似的。

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