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乙烯诱导的烟草PR-5中性异构体类渗透素蛋白的基因表达由AGCCGCC顺式序列介导。

Ethylene-induced gene expression of osmotin-like protein, a neutral isoform of tobacco PR-5, is mediated by the AGCCGCC cis-sequence.

作者信息

Sato F, Kitajima S, Koyama T, Yamada Y

机构信息

Department of Agricultural Chemistry, Faculty of Agriculture, Kyoto University, Japan.

出版信息

Plant Cell Physiol. 1996 Apr;37(3):249-55. doi: 10.1093/oxfordjournals.pcp.a028939.

Abstract

Osmotin-like protein (OLP) is a neutral isoform in the group 5 pathogenesis-related (PR) tobacco proteins. The OLP gene, like the basic PR protein genes, is constitutively expressed in tobacco roots and cultured cells. OLP is not naturally present in intact healthy leaves, but ethylene treatment induces a high accumulation there. To study the mechanism of OLP gene expression as induced by ethylene, we cloned the gene from Nicotiana sylvestris, an ancestor of N. tabacum. Sequence analysis showed that it has no intron and that its promoter region contains two AGCCGCC sequences that are conserved in most basic PR-protein genes. The function of the AGCCGCC sequences in transgenic tobacco plants that harbor the wild and mutated OLP promoter::GUS fusion genes was analyzed. Mutation in the AGCCGCC sequences clearly inhibited the GUS expression induced by ethylene, indicative that the AGCCGCC sequence(s) is a DNA element(s) responsive to ethylene. An EREBP2 protein, isolated as one of the proteins binding to the AGCCGCC sequence of the tobacco beta-1,3-glucanase gene, also was found to bind to the AGCCGCC sequence(s) of OLP gene. These results suggest that the ethylene-induced expression of OLP is regulated by a trans-acting factor(s) common to basic PR-proteins.

摘要

类渗透素蛋白(OLP)是烟草病程相关蛋白第5组中的一种中性异构体。与碱性病程相关蛋白基因一样,OLP基因在烟草根和培养细胞中组成型表达。OLP在完整健康的叶片中并非天然存在,但乙烯处理会诱导其在叶片中大量积累。为了研究乙烯诱导OLP基因表达的机制,我们从烟草的祖先野生烟草中克隆了该基因。序列分析表明,它没有内含子,其启动子区域包含两个在大多数碱性病程相关蛋白基因中保守的AGCCGCC序列。分析了含有野生型和突变型OLP启动子::GUS融合基因的转基因烟草植株中AGCCGCC序列的功能。AGCCGCC序列的突变明显抑制了乙烯诱导的GUS表达,表明AGCCGCC序列是乙烯响应性DNA元件。作为与烟草β-1,3-葡聚糖酶基因的AGCCGCC序列结合的蛋白之一分离得到的EREBP2蛋白,也被发现与OLP基因的AGCCGCC序列结合。这些结果表明,乙烯诱导的OLP表达受碱性病程相关蛋白共有的反式作用因子调控。

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