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植物GATA型锌指蛋白AGP1与创伤诱导型Myb基因NtMyb2的AG基序(AGATCCAA)结合介导的转录激活。

Transcriptional activation mediated by binding of a plant GATA-type zinc finger protein AGP1 to the AG-motif (AGATCCAA) of the wound-inducible Myb gene NtMyb2.

作者信息

Sugimoto Kazuhiko, Takeda Shin, Hirochika Hirohiko

机构信息

Department of Molecular Genetics, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602, Japan.

出版信息

Plant J. 2003 Nov;36(4):550-64. doi: 10.1046/j.1365-313x.2003.01899.x.

Abstract

NtMyb2 is a regulator of the tobacco retrotransposon Tto1 and the defense-related gene phenylalanine ammonia lyase (PAL), which are induced by various stress stimuli such as wounding or elicitor treatment. NtMyb2 is also induced by wounding or elicitor treatment and is regulated at the transcriptional level. In this study, mutational analysis of the promoter of NtMyb2 and gain-of-function analysis in vivo showed that the sequence AGATCCAA, named the AG-motif, is a cis-element sufficient to confer responsiveness to wounding and elicitor treatment. Furthermore, by using the south-western method, we cloned cDNAs encoding a GATA-type zinc finger protein, which can specifically bind to the AG-motif, named AG-motif binding Protein (AGP1). Domain analysis revealed that not only the GATA-type zinc finger region but also the downstream His2 motif of AGP1 is required for binding activity, showing that the AGP has a novel GATA-type zinc finger domain. AGP1 can activate expression from promoters containing the AG-motif in tobacco protoplasts, indicating that AGP1 is a positive regulator of NtMyb2. We also found that the AGP1 binding activity is highly enhanced by adenine methylation of the AG-motif by bacterial dam methylase.

摘要

NtMyb2是烟草反转录转座子Tto1和防御相关基因苯丙氨酸解氨酶(PAL)的调节因子,这些基因可被诸如创伤或激发子处理等各种应激刺激所诱导。NtMyb2也可被创伤或激发子处理所诱导,并在转录水平上受到调控。在本研究中,对NtMyb2启动子的突变分析和体内功能获得分析表明,序列AGATCCAA(命名为AG基序)是一个顺式元件,足以赋予对创伤和激发子处理的响应性。此外,通过使用西南杂交法,我们克隆了编码一种GATA型锌指蛋白的cDNA,该蛋白可特异性结合AG基序,命名为AG基序结合蛋白(AGP1)。结构域分析表明,AGP1的结合活性不仅需要GATA型锌指区域,还需要其下游的His2基序,这表明AGP具有一个新型的GATA型锌指结构域。AGP1可激活烟草原生质体中含有AG基序的启动子的表达,表明AGP1是NtMyb2的正调节因子。我们还发现,细菌dam甲基转移酶对AG基序的腺嘌呤甲基化可高度增强AGP1的结合活性。

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