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14-3-3蛋白是拟南芥中ATEM1启动子转录复合体的组成成分。

14-3-3 Proteins are components of the transcription complex of the ATEM1 promoter in Arabidopsis.

作者信息

del Viso Florencia, Casaretto Jose A, Quatrano Ralph S

机构信息

Department of Biology, Washington University, St Louis, MO 63130, USA.

出版信息

Planta. 2007 Dec;227(1):167-75. doi: 10.1007/s00425-007-0604-1. Epub 2007 Aug 16.

Abstract

The AtEm1 and AtEm6 gene products accumulate exclusively in embryos during Arabidopsis seed maturation. The transcription factor ABI3 and the phytohormone abscisic acid are required for normal expression of both genes. However, the expression of these genes occurs in extremely small embryos limiting the availability of tissue to directly study DNA-protein interactions. We generated callus lines derived from embryos to determine if the regulation of Em expression was similar to wild type embryos. Expression of AtEm1 and AtEm6 was strongly induced by abscisic acid in callus derived from wild type embryos, but not in embryo callus derived from ABI3 mutant embryos (abi3-6). Epitopes to 14-3-3 proteins were found in complexes with the AtEm1 promoter in mobility shift experiments using nuclear extracts derived from both wild type and abi3-6 calli. Using phosphorylated peptides that bind to 14-3-3 proteins, we show that 14-3-3 proteins are required for the maintenance of the transcriptional complex generated in nuclear extracts. Chromatin immunoprecipitation experiments using a 14-3-3 antibody display the expected 241-bp band from the AtEm1 promoter. Hence, 14-3-3 proteins are physically present in the AtEm1 transcriptional complex in vivo and are required for the maintenance of the transcriptional complex in vitro.

摘要

AtEm1和AtEm6基因产物仅在拟南芥种子成熟期间的胚胎中积累。转录因子ABI3和植物激素脱落酸是这两个基因正常表达所必需的。然而,这些基因的表达发生在极小的胚胎中,限制了直接研究DNA-蛋白质相互作用的组织可用性。我们从胚胎中生成了愈伤组织系,以确定Em表达的调控是否与野生型胚胎相似。脱落酸在源自野生型胚胎的愈伤组织中强烈诱导AtEm1和AtEm6的表达,但在源自ABI3突变体胚胎(abi3-6)的胚胎愈伤组织中则不然。在使用源自野生型和abi3-6愈伤组织的核提取物进行的迁移率变动实验中,发现14-3-3蛋白的表位与AtEm1启动子形成复合物。使用与14-3-3蛋白结合的磷酸化肽,我们表明14-3-3蛋白是维持核提取物中产生的转录复合物所必需的。使用14-3-3抗体进行的染色质免疫沉淀实验显示了来自AtEm1启动子的预期241bp条带。因此,14-3-3蛋白在体内物理存在于AtEm1转录复合物中,并且在体外是维持转录复合物所必需的。

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