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An Autoregulatory Loop Controlling Arabidopsis HsfA2 Expression: Role of Heat Shock-Induced Alternative Splicing

机译:自动调节环控制拟南芥HsfA2表达:热休克诱导的选择性剪接的作用。

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摘要

Heat shock transcription factorA2 (HsfA2) is a key regulator in response to heat stress in Arabidopsis (Arabidopsis thaliana), and its heat shock ()-induced transcription regulation has been extensively studied. Recently, alternative splicing, a critical posttranscriptional event, has been shown to regulate -inducible expression of HsfA2; however, the molecular mechanism remains largely unknown. Here, we demonstrate a new heat stress-induced splice variant, HsfA2-III, is involved in the self-regulation of HsfA2 transcription in Arabidopsis. HsfA2-III is generated through a cryptic 5′ splice site in the intron, which is activated by severe heat (42°C–45°C). We confirmed that HsfA2-III encodes a small truncated HsfA2 isoform (S-HsfA2) by an immunoblot assay with anti-S-HsfA2 antiserum. S-HsfA2 has an extra leucine-rich motif next to its carboxyl-terminal truncated DNA-binding domain. The biological significance of S-HsfA2 was further demonstrated by its nuclear localization and heat shock element (HSE)-binding ability. In yeast (Saccharomyces cerevisiae), the leucine-rich motif can inhibit the transcriptional activation activity of S-HsfA2, while it appears not to be required for the truncated DNA-binding domain-mediated binding ability of S-HsfA2-HSE. Further results reveal that S-HsfA2 could bind to the TATA box-proximal clusters of HSE in the HsfA2 promoter to activate its own transcription. This S-HsfA2-modulated HsfA2 transcription is not mediated through homodimer or heterodimer formation with HsfA1d or HsfA1e, which are known transcriptional activators of HsfA2. Altogether, our findings provide new insights into how posttranscriptionally regulates HsfA2 expression. Severe -induced alternative splicing also occurs in four other -inducible Arabidopsis Hsf genes, suggesting that it is a common feature among Arabidopsis Hsfs.
机译:热休克转录因子A2(HsfA2)是对拟南芥(Arabidopsis thaliana)中的热应激作出反应的关键调节剂,并且已经对其热休克诱导的转录调控进行了广泛研究。最近,替代剪接是一种关键的转录后事件,已显示出它调节HsfA2的诱导型表达。然而,分子机制仍然是未知的。在这里,我们证明了一种新的热应激诱导的剪接变体HsfA2-III,参与拟南芥中HsfA2转录的自我调节。 HsfA2-III是通过内含子中一个隐蔽的5'剪接位点产生的,该位点被强热(42°C–45°C)激活。我们通过使用抗S-HsfA2抗血清的免疫印迹试验证实,HsfA2-III编码一个小的截短的HsfA2亚型(S-HsfA2)。 S-HsfA2在其羧基末端截短的DNA结合结构域旁边具有一个额外的富含亮氨酸的基序。 S-HsfA2的核定位和热激元件(HSE)结合能力进一步证明了其生物学意义。在酵母中(Saccharomyces cerevisiae),富含亮氨酸的基序可以抑制S-HsfA2的转录激活活性,而对于S-HsfA2-HSE的截短的DNA结合域介导的结合能力似乎并不是必需的。进一步的结果表明,S-HsfA2可以与HsfA2启动子中HSE的TATA盒近端簇结合,从而激活其自身的转录。该S-HsfA2调节的HsfA2转录不是通过与HsfA1d或HsfA1e(已知的HsfA2转录激活因子)的同二聚体或异二聚体形成来介导的。总之,我们的发现为转录后调节HsfA2表达的方式提供了新的见解。严重诱导的选择性剪接也出现在其他四个可诱导的拟南芥Hsf基因中,这表明它是拟南芥Hsfs之间的共同特征。

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