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Genetic interactions between splicing and RNA editing in Drosophila.

机译:果蝇中剪接和RNA编辑之间的遗传相互作用。

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摘要

Previous work has shown that one region of the para transcription unit requires MLE for normal processing of the transcript (Reenan et al, 2000). This particular region of para contains three A-to-I editing sites and a predicted ECS that forms a duplex with the editing site sequence to target the editing enzyme, dADAR, to the substrate. The mutant helicase, MLEnapts, causes skipping of the edited exon of para. We hypothesized that since RNA editing requires a RNA secondary structure, the MLE helicase is necessary to facilitate resolution of the structure at this region of para.; To study the interactions of RNA editing and splicing at this site in para, experiments were designed to (1) identify the mutation(s) in mle that cause the napts phenotype and (2) identify cis-acting suppressors of the mle napts phenotype.; Two potential mutations were identified, a 7 bp insertion in the intron and T415S mutation near the ATPase motif. Wild type and mle napts transgenes were made. Wild type transgenic flies were able to complement male lethality associated with the null allele of mle and reduce the skipping of the edited exon of para in a mlenapts background. The mle napts transgene did not complement male lethality associated with the null allele of mle or cause skipping of the edited exon indicating that the MLEnapts protein was not being expressed. We, therefore, were unable to confirm the mlenapts mutation.; A mini reporter construct was created to recapitulate the skipping that occurs in a mlenapts background in order to find cis-acting suppressors. Within this reporter construct three conserved elements were found using comparative sequence analysis of other Drosophilidae species: the ECS, DCS (donor site complementary sequence), and a hairpin (HP). These elements were deleted individually or in combination to determine the effect of MLEnapts. Deletion of the HP significantly reduced the skipping while deletions of the ECS and DCS did not. Reporter constructs that deleted all three conserved elements and deletion of the DCS and HP together were the only complete suppressors of the skipping, indicating that the HP is responsible for the skipping.
机译:先前的工作表明,对转录单元的一个区域需要MLE才能正常处理转录本(Reenan等,2000)。对位的这个特定区域包含三个A-to-I编辑位点和一个预测的ECS,该ECS与编辑位点序列形成双链体,以将编辑酶dADAR靶向底物。突变解旋酶MLEnapts导致对位的已编辑外显子的跳过。我们假设,由于RNA编辑需要RNA二级结构,因此MLE解旋酶对于促进解析该段区域的结构是必需的。为了研究对等位点上RNA编辑和剪接的相互作用,设计了以下实验:(1)识别引起幼虫表型的多发性骨髓瘤突变,以及(2)鉴定多发性n小体表型的顺式作用抑制剂。 ;鉴定出两个潜在的突变,内含子插入了7 bp,ATPase基序附近的T415S突变。产生了野生型和m虫转基因。野生型转基因果蝇能够补充与mle无效等位基因相关的雄性致死性,并减少在mlenapts背景中对位外显子的编辑遗漏。 mle napts转基因不能补充与mle无效等位基因相关的男性致死力,或导致编辑的外显子跳过,表明MLEnapts蛋白未表达。因此,我们无法确定mlenapts突变。创建了一个微型报告基因构建体,以概括在mlenapts背景中发生的跳跃,以发现顺式作用抑制剂。使用其他果蝇科的比较序列分析,在该报告基因构建体中发现了三个保守元件:ECS,DCS(供体位点互补序列)和发夹(HP)。这些元素被单独删除或组合删除以确定MLEnapts的效果。删除HP可显着减少跳过,而删除ECS和DCS则不会。删除所有三个保守元素并同时删除DCS和HP的Reporter构造是唯一完整的跳过抑制器,表明HP负责跳过。

著录项

  • 作者

    Smith, Lee Ann.;

  • 作者单位

    University of Connecticut.;

  • 授予单位 University of Connecticut.;
  • 学科 Biology Molecular.; Biology Genetics.
  • 学位 Ph.D.
  • 年度 2004
  • 页码 140 p.
  • 总页数 140
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子遗传学;遗传学;
  • 关键词

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