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拟南芥 AtERF71/HRE2 通过顺式作用 GCC 盒或 DRE/CRT 元件作为转录激活因子发挥作用,通过调节根细胞的扩张参与根发育。

Arabidopsis AtERF71/HRE2 functions as transcriptional activator via cis-acting GCC box or DRE/CRT element and is involved in root development through regulation of root cell expansion.

机构信息

Department of Molecular Biology, Pusan National University, Busan, 609-735, Korea.

出版信息

Plant Cell Rep. 2015 Feb;34(2):223-31. doi: 10.1007/s00299-014-1701-9. Epub 2014 Oct 25.

Abstract

AtERF71/HRE2 binds to GCC box or DRE/CRT as transcription activator and plays an important role in root development via root cell expansion regulation. AtERF71/HRE2 transcription factor, a member of the AP2/ERF family, plays a key role in the stress response. GCC box and DRE/CRT, both essential cis-acting elements, have been shown to be recognized by AP2/ERF family transcription factors. However, it remains unclear whether or not AtERF71/HRE2 directly interacts with GCC box and/or DRE/CRT. Here, we showed that AtERF71/HRE2 binds to GCC box and DRE/CRT by electrophoretic mobility shift assay (EMSA). Binding of AtERF71/HRE2 to GCC box and DRE/CRT was also detected by fluorescence measurement and surface plasmon resonance spectroscopy (BIAcore) experiments. Folding properties of AtERF71/HRE2 proteins were characterized by CD spectroscopy, and AtERF71/HRE2 showed thermal stability as evidenced by two endothermic peaks (T d) at 53 and 65 °C. In addition, AtERF71/HRE2 showed transcriptional activation activity via GCC box and DRE/CRT in Arabidopsis protoplasts. Interestingly, AtERF71/HRE2 OXs showed increased primary root length due to elevated root cell expansion. Our data indicate that AtERF71/HRE2 binds to both GCC box and DRE/CRT, transactivates expression of genes downstream via GCC box or DRE/CRT, and plays an important role in root development through regulation of root cell expansion.

摘要

AtERF71/HRE2 作为转录激活因子与 GCC 框或 DRE/CRT 结合,通过调节根细胞扩展在根发育中发挥重要作用。AtERF71/HRE2 转录因子是 AP2/ERF 家族的成员,在应激反应中发挥关键作用。GCC 框和 DRE/CRT 是两个必需的顺式作用元件,已被证明被 AP2/ERF 家族转录因子识别。然而,AtERF71/HRE2 是否直接与 GCC 框和/或 DRE/CRT 相互作用仍不清楚。在这里,我们通过电泳迁移率变动分析 (EMSA) 表明 AtERF71/HRE2 与 GCC 框和 DRE/CRT 结合。荧光测量和表面等离子体共振光谱 (BIAcore) 实验也检测到 AtERF71/HRE2 与 GCC 框和 DRE/CRT 的结合。通过 CD 光谱学对 AtERF71/HRE2 蛋白质的折叠特性进行了表征,AtERF71/HRE2 表现出热稳定性,证据是在 53 和 65°C 处有两个吸热峰 (T d)。此外,AtERF71/HRE2 在拟南芥原生质体中通过 GCC 框和 DRE/CRT 显示出转录激活活性。有趣的是,AtERF71/HRE2 OXs 由于根细胞扩展增加而导致主根长度增加。我们的数据表明,AtERF71/HRE2 与 GCC 框和 DRE/CRT 结合,通过 GCC 框或 DRE/CRT 转激活下游基因的表达,并通过调节根细胞扩展在根发育中发挥重要作用。

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