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Dosage Compensation of the Copia Retrotransposon in Drosophila Melanogaster

机译:果蝇黑斑逆转录转座子的剂量补偿

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摘要

Dosage compensation in Drosophila has been studied at the steady state RNA level for several single-copy genes; however, an important point is addressed by analyzing a repetitive, transposable element for dosage compensation. The two issues of gene-specific cis control and genomic position can be studied by determining the extent of dosage compensation of a transposable element at different chromosomal locations. To determine whether the multicopy copia transposable element can dosage compensate, we used the X-linked white-apricot (w(a)) mutation in which a copia element is present. The extent of dosage compensation was determined for the white and copia promoters in larvae and adults in two different genomic locations of the w(a) allele. We conclude that copia is able to dosage compensate, and that the white promoter and the copia promoter are not coordinate in their dosage compensation abilities when assayed under these various conditions. Thus, two transcriptional units, one within the other, both of which are able to dosage compensate, do so differently in response to developmental stage and genomic position.
机译:果蝇的剂量补偿已经在稳态RNA水平研究了几种单拷贝基因。然而,重要的一点是通过分析用于剂量补偿的重复的,易位的元件来解决的。可以通过确定转座因子在不同染色体位置的剂量补偿程度来研究基因特异性顺式控制和基因组位置这两个问题。为了确定多拷贝的copia转座元件是否可以剂量补偿,我们使用了其中存在copia元件的X连锁白杏(w(a))突变。在w(a)等位基因的两个不同基因组位置,确定了幼虫和成虫中白色和Copia启动子的剂量补偿程度。我们得出的结论是,鸦片能够补偿剂量,并且在这些不同条件下测定时,白色启动子和鸦片启动子在剂量补偿能力上并不​​协调。因此,响应于发育阶段和基因组位置,两个转录单位,一个在另一个内,两者都能够剂量补偿,所以其作用不同。

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