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转座因子插入对黑腹果蝇乙醇脱氢酶表达的影响。

Effects of a transposable element insertion on alcohol dehydrogenase expression in Drosophila melanogaster.

作者信息

Dunn R C, Laurie C C

机构信息

Department of Zoology, Duke University, Durham, North Carolina 27708, USA.

出版信息

Genetics. 1995 Jun;140(2):667-77. doi: 10.1093/genetics/140.2.667.

Abstract

Variation in the DNA sequence and level of alcohol dehydrogenase (Adh) gene expression in Drosophila melanogaster have been studied to determine what types of DNA polymorphisms contribute to phenotypic variation in natural populations. The Adh gene, like many others, shows a high level of variability in both DNA sequence and quantitative level of expression. A number of transposable element insertions occur in the Adh region and one of these, a copia insertion in the 5' flanking region, is associated with unusually low Adh expression. To determine whether this insertion (called R142) causes the low expression level, the insertion was excised from the cloned R142 Adh gene and the effect was assessed by P-element transformation. Removal of this insertion causes a threefold increase in the level of ADH, clearly showing that it contributes to the naturally occurring variation in expression at this locus. Removal of all but one LTR also causes a threefold increase, indicating that the mechanism is not a simple sequence disruption. Furthermore, this copia insertion, which is located between the two Adh promoters and their upstream enhancer sequences, has differential effects on the levels of proximal and distal transcripts. Finally, a test for the possible modifying effects of two suppressor loci, su(wa) and su(f), on this insertional mutation was negative, in contrast to a previous report in the literature.

摘要

为了确定哪些类型的DNA多态性导致自然种群中的表型变异,研究了黑腹果蝇中酒精脱氢酶(Adh)基因的DNA序列变异和表达水平。与许多其他基因一样,Adh基因在DNA序列和表达定量水平上都表现出高度变异性。在Adh区域发生了许多转座元件插入,其中一个是在5'侧翼区域的copia插入,与异常低的Adh表达相关。为了确定这种插入(称为R142)是否导致低表达水平,从克隆的R142 Adh基因中切除该插入,并通过P元件转化评估其效果。去除该插入导致ADH水平增加了三倍,清楚地表明它促成了该基因座自然发生的表达变异。去除除一个LTR之外的所有LTR也导致三倍的增加,表明该机制不是简单的序列破坏。此外,这种位于两个Adh启动子及其上游增强子序列之间的copia插入,对近端和远端转录本的水平有不同的影响。最后,与文献中先前的报告相反,对两个抑制位点su(wa)和su(f)对这种插入突变的可能修饰作用的测试为阴性。

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