Caspar T, Quail P H
UC-Berkeley/USDA Plant Gene Expression Center, Albany 94710.
Plant J. 1993 Jan;3(1):161-74. doi: 10.1046/j.1365-313x.1993.t01-8-00999.x.
Ferredoxin is a nuclear-encoded protein that is involved in a variety of electron transfer reactions in both photosynthetic and non-photosynthetic plastids. We show here that the expression of the ferredoxin A gene (FedA) in Arabidopsis thaliana is light-regulated, with its mRNA level increased 4.5-fold by transfer of dark-grown seedlings to white light for 3 h. A portion of this light regulation is mediated by phytochrome through a very low fluence type of response. In addition, it is likely that another photoreceptor(s) is also involved. The FedA promoter confers a light- and tissue-regulated expression pattern when fused to the beta-glucuronidase (GUS) and luciferase reporter genes, indicating that the gene is transcriptionally regulated. No evidence of cis-acting light-regulatory elements within the 5' untranslated leader region of the gene was detected. Nevertheless, elements within this leader are required for full activity since its deletion reduces expression both in the light and dark by 25-fold. This region includes a sequence, ACAAAA, which is also present in the 5' untranslated leader of the other three ferredoxin leaders that have been sequenced and in the leaders of 31 other plant genes or about 8% of all plant genes in the GenBank database. In addition to mediating light regulation, the FedA promoter also directs GUS expression in aerial tissues at 70-fold higher levels than in roots. GUS activity staining in aerial tissues is observed in both photosynthetic and non-photosynthetic cells. These data indicate that the FedA promoter also carries the information for expression of this gene in a highly tissue- and cell-specific manner.
铁氧化还原蛋白是一种核编码蛋白,参与光合和非光合质体中的各种电子传递反应。我们在此表明,拟南芥中铁氧化还原蛋白A基因(FedA)的表达受光调控,黑暗中生长的幼苗转移至白光下3小时后,其mRNA水平增加4.5倍。这种光调控的一部分是由光敏色素通过极低光通量类型的反应介导的。此外,可能还有其他光感受器也参与其中。当与β-葡萄糖醛酸酶(GUS)和荧光素酶报告基因融合时,FedA启动子赋予光和组织调控的表达模式,表明该基因是转录调控的。在该基因5'非翻译前导区内未检测到顺式作用光调控元件的证据。然而,该前导区内的元件对于完全活性是必需的,因为其缺失会使光下和黑暗中的表达降低25倍。该区域包括一个序列ACAAAA,在已测序的其他三个铁氧化还原蛋白前导区的5'非翻译前导区以及GenBank数据库中31个其他植物基因的前导区中也存在,约占所有植物基因的8%。除了介导光调控外,FedA启动子还指导GUS在地上组织中的表达水平比在根中高70倍。在光合和非光合细胞中均观察到地上组织中的GUS活性染色。这些数据表明,FedA启动子还以高度组织和细胞特异性的方式携带该基因表达的信息。