Mitsuda Nobutaka, Hisabori Toru, Takeyasu Kunio, Sato Masa H
Graduate School of Human and Environmental Studies, Kyoto University, Yoshidanihonmatsu, Sakyo-ku, Kyoto, 606-8501 Japan.
Plant Cell Physiol. 2004 Jul;45(7):845-54. doi: 10.1093/pcp/pch101.
A 38-bp pollen-specific cis-acting region of the AVP1 gene is involved in the expression of the Arabidopsis thaliana V-PPase during pollen development. Here, we report the isolation and structural characterization of AtVOZ1 and AtVOZ2, novel transcription factors that bind to the 38-bp cis-acting region of A. thaliana V-PPase gene, AVP1. AtVOZ1 and AtVOZ2 show 53% amino acid sequence similarity. Homologs of AtVOZ1 and AtVOZ2 are found in various vascular plants as well as a moss, Physcomitrella patens. Promoter-beta-glucuronidase reporter analysis shows that AtVOZ1 is specifically expressed in the phloem tissue and AtVOZ2 is strongly expressed in the root. In vivo transient effector-reporter analysis in A. thaliana suspension-cultured cells demonstrates that AtVOZ1 and AtVOZ2 function as transcriptional activators in the Arabidopsis cell. Two conserved regions termed Domain-A and Domain-B were identified from an alignment of AtVOZ proteins and their homologs of O. sativa and P. patens. AtVOZ2 binds as a dimer to the specific palindromic sequence, GCGTNx7ACGC, with Domain-B, which is comprised of a functional novel zinc coordinating motif and a conserved basic region. Domain-B is shown to function as both the DNA-binding and the dimerization domains of AtVOZ2. From highly the conservative nature among all identified VOZ proteins, we conclude that Domain-B is responsible for the DNA binding and dimerization of all VOZ-family proteins and designate it as the VOZ-domain.
AVP1基因一个38bp的花粉特异性顺式作用区域参与拟南芥V-PPase在花粉发育过程中的表达。在此,我们报告了AtVOZ1和AtVOZ2的分离及结构特征,它们是与拟南芥V-PPase基因AVP1的38bp顺式作用区域结合的新型转录因子。AtVOZ1和AtVOZ2的氨基酸序列相似度为53%。在多种维管植物以及一种苔藓小立碗藓中发现了AtVOZ1和AtVOZ2的同源物。启动子-β-葡萄糖醛酸酶报告基因分析表明,AtVOZ1在韧皮部组织中特异性表达,AtVOZ2在根中强烈表达。在拟南芥悬浮培养细胞中的体内瞬时效应物-报告基因分析表明,AtVOZ1和AtVOZ2在拟南芥细胞中作为转录激活因子发挥作用。通过对AtVOZ蛋白及其水稻和小立碗藓同源物的比对,鉴定出两个保守区域,分别称为结构域A和结构域B。AtVOZ2以二聚体形式与特定的回文序列GCGTNx7ACGC结合,结合区域为结构域B,该结构域由一个功能性的新型锌配位基序和一个保守的碱性区域组成。结构域B被证明同时作为AtVOZ2的DNA结合结构域和二聚化结构域。基于所有已鉴定的VOZ蛋白之间的高度保守性,我们得出结论,结构域B负责所有VOZ家族蛋白的DNA结合和二聚化,并将其命名为VOZ结构域。