首页> 外文期刊>Heredity: An International Journal of Genetics >Genetic variation of copia suppression in Drosophila melanogaster.
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Genetic variation of copia suppression in Drosophila melanogaster.

机译:果蝇黑斑病抑制的遗传变异。

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Transposable elements (TEs) are genomic parasites that propagate by exploiting its host reproductive machinery. However, some hosts have evolved the ability to silence TE activity, whereas others have not. We are investigating the population dynamics of TE host-silencing pathways, particularly copia long terminal repeat retrotransposon in Drosophila melanogaster. Here, we identify large effect genes involved in copia suppression by using a semi-quantitative analysis to assay levels of copia plasmids (believed to be an intermediate of transposition) in 98 recombinant inbred lines constructed from a line exhibiting high copia transpositions and a line exhibiting no transpositions. The results revealed that the influence of copia copy number and transcription level on copia plasmid concentrations are weak and that genomic factors, presumably encoded by the host, have stronger effects on transposition rates. We mapped a QTL affecting copia plasmid concentration within the 33A-43E cytological region of the second chromosome and applied a quantitative deficiency complementation analysis on this chromosomal region. One out of the two large effect deficiencies on copia plasmid concentrations corresponded to the vasa gene, an important component of the nuage-piwi RNA TE-silencing machinery. We hypothesize that copia suppression occurs by the joint action of several post-transcriptional mechanisms with at least one of the blocks taking place in the nuage.
机译:转座因子(TEs)是基因组寄生虫,可通过利用其宿主生殖机制繁殖。但是,有些主持人已发展出使TE活动沉默的能力,而另一些则没有。我们正在调查果蝇的TE宿主沉默途径,尤其是果蝇长末端重复反转录转座子的种群动态。在这里,我们通过使用半定量分析来测定98个重组自交系中的Copia质粒(被认为是转座的中间产物)的水平,确定了影响Copia抑制的大效应基因,该重组自交系由表现出高Copia转座的品系​​和没有换位。结果表明,仿禽的拷贝数和转录水平对仿禽质粒浓度的影响较弱,推测由宿主编码的基因组因子对转座率的影响更大。我们在第二条染色体的33A-43E细胞学区域内绘制了一个影响胸腔质粒浓度的QTL,并对该染色体区域进行了定量缺陷互补分析。在对Copia质粒浓度的两个较大影响缺陷中,有一个对应于vasa基因,该基因是nuage-piwi RNA TE沉默机制的重要组成部分。我们假设,由于几种转录后机制的共同作用而发生了鸦片抑制作用,其中至少一个发生在小核中。

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