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复苏植物蓝猪耳的两个脱水诱导转录本编码相互作用的同源异型域-亮氨酸拉链蛋白。

Two dehydration-inducible transcripts from the resurrection plant Craterostigma plantagineum encode interacting homeodomain-leucine zipper proteins.

作者信息

Frank W, Phillips J, Salamini F, Bartels D

机构信息

Max-Planck-Institut für Züchtungsforschung, Köln, Germany.

出版信息

Plant J. 1998 Aug;15(3):413-21. doi: 10.1046/j.1365-313x.1998.00222.x.

DOI:10.1046/j.1365-313x.1998.00222.x
PMID:9750352
Abstract

The molecular dissection of desiccation tolerance in the resurrection plant Craterostigma plantagineum led to the isolation of two dehydration-stress inducible homeo-domain-leucine zipper genes (CPHB-1 and -2). When the coding region of CPHB-1 was used as bait in the yeast two-hybrid system, the ability of CPHB-1 to form homodimers was demonstrated. The two-hybrid system was also used to isolate CPHB-2, which heterodimerises with CPHB-1. Both transcripts are inducible by dehydration in leaves and roots, but steady state levels vary in response to exogenously applied ABA. Although expression of CPHB-1 is not inducible by ABA, the transcript level of CPHB-2 increases during ABA-treatment. Both genes are expressed at very early stages of dehydration and thus may be involved in the regulation of gene expression during dehydration. CPHB-1 and -2 differential expression in response to ABA suggests that they act in different branches of the dehydration-induced signalling network. In vitro binding studies revealed that CPHB-1 specifically binds to the pseudopalindromic sequence CAAT(C/G)ATTG. Using this element for in vitro binding studies with nuclear proteins from dehydrated leaves, an inducible DNA-protein complex was identified.

摘要

对复苏植物车前叶蓝芥中耐干燥性的分子解析,导致分离出两个脱水胁迫诱导的同源结构域-亮氨酸拉链基因(CPHB-1和-2)。当将CPHB-1的编码区用作酵母双杂交系统中的诱饵时,证明了CPHB-1形成同二聚体的能力。双杂交系统还用于分离与CPHB-1异二聚化的CPHB-2。两种转录本在叶片和根中均可被脱水诱导,但稳态水平会因外源施加脱落酸(ABA)而有所不同。虽然CPHB-1的表达不能被ABA诱导,但在ABA处理期间CPHB-2的转录水平会增加。这两个基因在脱水的非常早期阶段就表达,因此可能参与脱水过程中基因表达的调控。CPHB-1和-2对ABA的差异表达表明它们在脱水诱导的信号网络的不同分支中起作用。体外结合研究表明,CPHB-1特异性结合假回文序列CAAT(C/G)ATTG。使用该元件对脱水叶片的核蛋白进行体外结合研究,鉴定出一种可诱导的DNA-蛋白质复合物。

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