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序列保守的上游开放阅读框对拟南芥 HsfB1 转录物主开放阅读框翻译的抑制作用。

An inhibitory effect of the sequence-conserved upstream open-reading frame on the translation of the main open-reading frame of HsfB1 transcripts in Arabidopsis.

机构信息

Graduate School of Life Sciences, Tohoku University, 2-1-1 Katahira, Aoba, Sendai-city, Miyagi 980-8577, Japan.

出版信息

Plant Cell Environ. 2012 Nov;35(11):2014-30. doi: 10.1111/j.1365-3040.2012.02533.x. Epub 2012 May 31.

Abstract

Plants have as many as 20 heat shock factors (Hsfs) grouped into three classes, A, B and C, based on sequence similarity and modular structures. Through screening for cell death-inducing factor(s) in Nicotiana benthamiana, we identified Arabidopsis HsfB2b and thus subjected all other members of Arabidopsis Hsf class B (HsfB1, HsfB2a, HsfB2b, HsfB3 and HsfB4) to the same cell death assay. When expressed in N. benthamiana leaves, only HsfB1 and HsfB2b elicited mild cell death. Simultaneously we found that HsfB1 has a post-transcriptional control mechanism, in which a sequence-conserved upstream open-reading frame (sc-uORF) is involved. The known repressor function of the respective HsfBs was confirmed and the difference in cell death-inducing activity of HsfBs was explained by the fact that HsfB1 and HsfB2b are transcriptional repressors but the others are not. Indeed, the cell death symptom by HsfB1 and HsfB2b required not only their repression activity but also their nuclear localization activity. HsfB1 expression was drastically and transiently induced by heat shock (HS) and the intactness of sc-uORF was required for its HS response. Based on the results, the physiological significance of cell death-inducing activity of HsfB1 and HsfB2b and the sc-uORF in the HsfB1 transcript during HS response is discussed.

摘要

植物有多达 20 种热休克因子 (Hsfs),根据序列相似性和模块结构分为 A、B 和 C 三类。通过在本氏烟中筛选细胞死亡诱导因子,我们鉴定出拟南芥 HsfB2b,并对拟南芥 HsfB 类的其他所有成员(HsfB1、HsfB2a、HsfB2b、HsfB3 和 HsfB4)进行了相同的细胞死亡检测。当在本氏烟叶片中表达时,只有 HsfB1 和 HsfB2b 引发轻微的细胞死亡。同时,我们发现 HsfB1 具有转录后调控机制,其中涉及一个保守的上游开放阅读框(sc-uORF)。确认了各自 HsfB 的已知抑制功能,并且 HsfB 的细胞死亡诱导活性的差异可以通过以下事实来解释:HsfB1 和 HsfB2b 是转录抑制剂,但其他 HsfB 不是。事实上,HsfB1 和 HsfB2b 的细胞死亡症状不仅需要它们的抑制活性,还需要它们的核定位活性。HsfB1 的表达在热休克 (HS) 下急剧且短暂地被诱导,并且 sc-uORF 的完整性是其 HS 反应所必需的。基于这些结果,讨论了 HsfB1 和 HsfB2b 的细胞死亡诱导活性以及 HsfB1 转录物中 sc-uORF 在 HS 反应期间的生理意义。

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