Davis Melissa B, Carney Ginger E, Robertson Anne E, Bender Michael
Department of Genetics, The University of Georgia, Athens, GA 30602, USA.
Dev Biol. 2005 Jun 15;282(2):385-96. doi: 10.1016/j.ydbio.2005.03.019.
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.
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。