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EcR-A突变体的表型分析表明,EcR亚型在果蝇发育过程中具有独特功能。

Phenotypic analysis of EcR-A mutants suggests that EcR isoforms have unique functions during Drosophila development.

作者信息

Davis Melissa B, Carney Ginger E, Robertson Anne E, Bender Michael

机构信息

Department of Genetics, The University of Georgia, Athens, GA 30602, USA.

出版信息

Dev Biol. 2005 Jun 15;282(2):385-96. doi: 10.1016/j.ydbio.2005.03.019.

Abstract

The steroid hormone ecdysone triggers transitions between developmental stages in Drosophila by acting through a heterodimer consisting of the EcR and USP nuclear receptors. The EcR gene encodes three protein isoforms (EcR-A, EcR-B1, and EcR-B2) that have unique amino termini but that contain a common carboxy-terminal region including DNA-binding and ligand-binding domains. EcR-A and EcR-B1 are expressed in a spatially complementary pattern at the onset of metamorphosis, suggesting that specific responses to ecdysone involve distinct EcR isoforms. Here, we describe phenotypes of EcR-A specific deletion mutants isolated using transposon mutagenesis. Western blot analysis shows that each of these mutants completely lacks EcR-A protein, while the EcR-B1 protein is still present. The EcR(112) strain has a deletion of EcR-A specific non-coding and regulatory sequences but retains the coding exons, while the EcR(139) strain has a deletion of EcR-A specific protein coding exons but retains the regulatory region. In these mutants, the developmental progression of most internal tissues that normally express EcR-B1 is unaffected by the lack of EcR-A. Surprisingly, however, we found that one larval tissue, the salivary gland, fails to degenerate even though EcR-B1 is the predominant isoform. This result may indicate that the low levels of EcR-A in this tissue are in fact required. We identified yet another type of mutation, the EcR(94) deletion, that removes the EcR-A specific protein coding exons as well as the introns between the EcR-A and EcR-B transcription start sites. This deletion places the EcR-A regulatory region adjacent to the EcR-B transcription start site. While EcR(112) and EcR(139) mutant animals die during mid and late pupal development, respectively, EcR(94) mutants arrest prior to pupariation. EcR-A mutant phenotypes and lethal phases differ from those of EcR-B mutants, suggesting that the EcR isoforms have distinct developmental functions.

摘要

类固醇激素蜕皮激素通过作用于由蜕皮激素受体(EcR)和超气门蛋白(USP)核受体组成的异源二聚体,触发果蝇发育阶段之间的转变。EcR基因编码三种蛋白质异构体(EcR-A、EcR-B1和EcR-B2),它们具有独特的氨基末端,但包含一个共同的羧基末端区域,包括DNA结合域和配体结合域。EcR-A和EcR-B1在变态开始时以空间互补模式表达,这表明对蜕皮激素的特定反应涉及不同的EcR异构体。在这里,我们描述了使用转座子诱变分离的EcR-A特异性缺失突变体的表型。蛋白质免疫印迹分析表明,这些突变体中的每一个都完全缺乏EcR-A蛋白,而EcR-B1蛋白仍然存在。EcR(112)菌株缺失了EcR-A特异性非编码和调控序列,但保留了编码外显子,而EcR(139)菌株缺失了EcR-A特异性蛋白质编码外显子,但保留了调控区域。在这些突变体中,大多数正常表达EcR-B1的内部组织的发育进程不受EcR-A缺失的影响。然而,令人惊讶的是,我们发现一个幼虫组织,即唾液腺,即使EcR-B1是主要的异构体,也不会退化。这一结果可能表明该组织中低水平的EcR-A实际上是必需的。我们鉴定出了另一种类型的突变,即EcR(94)缺失,它去除了EcR-A特异性蛋白质编码外显子以及EcR-A和EcR-B转录起始位点之间的内含子。这种缺失使EcR-A调控区域与EcR-B转录起始位点相邻。虽然EcR(112)和EcR(139)突变动物分别在蛹发育中期和后期死亡,但EcR(94)突变体在化蛹前就停滞了。EcR-A突变体表型和致死阶段与EcR-B突变体不同,这表明EcR异构体具有不同的发育功能。

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