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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Positive and negative regulatory elements control expression of the yeast retrotransposon Ty3.
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Positive and negative regulatory elements control expression of the yeast retrotransposon Ty3.

机译:正调控元件和负调控元件控制酵母逆转录转座子Ty3的表达。

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摘要

We report the results of an analysis of Ty3 transcription and identification of Ty3 regions that mediate pheromone and mating-type regulation to coordinate its expression with the yeast life cycle. A set of strains was constructed which was isogenic except for the number of Ty3 elements, which varied from zero to three. Analysis of Ty3 expression in these strains showed that each of the three elements was transcribed and that each element was regulated. Dissection of the long terminal repeat regulatory region by Northern blot analysis of deletion mutants and reporter gene analysis showed that the upstream junction of Ty3 with flanking chromosomal sequences contained a negative control region. A 19-bp fragment (positions 56-74) containing one consensus copy and one 7 of 8-bp match to the pheromone response element (PRE) consensus was sufficient to mediate pheromone induction in either haploid cell type. Deletion of this region, however, did not abolish expression, indicating that other sequences also activate transcription. A 24-bp block immediately downstream of the PRE region contained a sequence similar to the a1-alpha 2 consensus that conferred mating-type control. A single base pair mutation in the region separating the PRE and a1-alpha 2 sequences blocked pheromone induction, but not mating-type control. Thus, the long terminal repeat of Ty3 is a compact, highly regulated, mobile promoter which is responsive to cell type and mating.
机译:我们报告分析Ty3转录和Ty3区域的分析结果,该区域介导信息素和交配型调节以协调其与酵母生命周期的表达。构建了一组同基因的菌株,除了Ty3元素的数量从零到三不等。在这些菌株中Ty3表达的分析表明,三个元件中的每一个都被转录并且每个元件都被调控。通过缺失突变体的Northern印迹分析和报道基因分析,对长末端重复调控区进行解剖,发现Ty3的上游连接与侧翼的染色体序列含有一个阴性对照区。一个19 bp的片段(第56-74位)包含一个共有拷贝和一个7个8 bp匹配信息素应答元件(PRE)共有序列,足以介导单倍体细胞类型中的信息素诱导。然而,该区域的删除并没有消除表达,表明其他序列也激活了转录。 PRE区域下游的一个24 bp的区块包含一个类似于赋予交配型控制的a1-alpha 2共有序列的序列。在分隔PRE和a1-alpha 2序列的区域中的单个碱基对突变阻止了信息素的诱导,但没有阻止交配型控制。因此,Ty3的长末端重复序列是紧凑的,高度调节的,可移动的启动子,对细胞类型和交配有响应。

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