Suppr超能文献

在蜕皮末期蜕皮甾体滴度下降期间,MHR4和多巴脱羧酶相继出现的协调性。

The coordination of the sequential appearance of MHR4 and dopa decarboxylase during the decline of the ecdysteroid titer at the end of the molt.

作者信息

Hiruma Kiyoshi, Riddiford Lynn M

机构信息

Faculty of Agriculture and Life Sciences, Hirosaki University, Hirosaki 036-8561, Japan.

出版信息

Mol Cell Endocrinol. 2007 Sep 30;276(1-2):71-9. doi: 10.1016/j.mce.2007.07.002. Epub 2007 Jul 10.

Abstract

During the last larval molt in Manduca sexta, in response to an increasing, then decreasing ecdysteroid titer, a number of transcription factors such as E75B, MHR3, MHR4, and betaFTZ-F1 appear and disappear in the abdominal epidermis leading to dopa decarboxylase (DDC) expression. Messenger RNAs for both the 20E-induced transcription factors, MHR3 and E75B, are maximal near the peak of the ecdysteroid titer with MHR4 mRNA appearing as the titer declines followed by betaFTZ-F1 and DDC mRNAs. E75B and MHR4 mRNA were not expressed in Manduca GV1 cells, either during exposure to 20E or after its removal. When either MHR3 dsRNA was transfected or E75B was constitutively expressed in these cells, MHR4 mRNA appeared in response to 20E by 6h. E75B was found to form a heterodimer with MHR3 using the BacterioMatch II two-hybrid assay. We conclude that MHR3 apparently suppresses MHR4 expression in the presence of 20E; the appearance of E75B then removes MHR3 by dimerization, allowing MHR4 to be expressed. Because of significant basal activity of the ddc promoter in the GV1 cells, we could perform rescue experiments by adding various factors. Constitutive expression of either E75B or MHR4 in the cells suppressed the significant basal activity of the 3.2kb ddc promoter in the GV1 cells, but 20E had no effect on this activity. Thus, E75B and MHR4 are 20E-induced inhibitory factors that suppress ddc expression and therefore act as ecdysteroid-regulated timers to coordinate the onset of ddc expression at the end of the molt.

摘要

在烟草天蛾最后一次幼虫蜕皮期间,随着蜕皮甾体滴度先升高后降低,一些转录因子如E75B、MHR3、MHR4和βFTZ-F1在腹部表皮中出现和消失,从而导致多巴脱羧酶(DDC)的表达。20E诱导的转录因子MHR3和E75B的信使RNA在蜕皮甾体滴度峰值附近达到最大值,MHR4信使RNA在滴度下降时出现,随后是βFTZ-F1和DDC信使RNA。无论是在暴露于20E期间还是去除20E后,E75B和MHR4信使RNA在烟草天蛾GV1细胞中均未表达。当在这些细胞中转染MHR3双链RNA或组成性表达E75B时,MHR4信使RNA在6小时内对20E产生反应而出现。使用细菌双杂交检测发现E75B与MHR3形成异源二聚体。我们得出结论,在20E存在的情况下,MHR3明显抑制MHR4的表达;然后E75B的出现通过二聚化去除MHR3,使MHR4得以表达。由于ddc启动子在GV1细胞中有显著的基础活性,我们可以通过添加各种因子进行拯救实验。在细胞中组成性表达E75B或MHR4均可抑制GV1细胞中3.2kb ddc启动子的显著基础活性,但20E对此活性没有影响。因此,E75B和MHR4是20E诱导的抑制因子,可抑制ddc表达,因此作为蜕皮甾体调节的定时器来协调蜕皮末期ddc表达的开始。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验