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正负调控元件控制酵母逆转录转座子Ty3的表达。

Positive and negative regulatory elements control expression of the yeast retrotransposon Ty3.

作者信息

Bilanchone V W, Claypool J A, Kinsey P T, Sandmeyer S B

机构信息

Department of Microbiology and Molecular Genetics, University of California, Irvine 92717.

出版信息

Genetics. 1993 Jul;134(3):685-700. doi: 10.1093/genetics/134.3.685.

Abstract

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.

摘要

我们报告了对Ty3转录的分析结果以及对介导信息素和交配型调控以使其表达与酵母生命周期相协调的Ty3区域的鉴定。构建了一组菌株,除了Ty3元件的数量不同(从零到三个)外,其余均为同基因。对这些菌株中Ty3表达的分析表明,三个元件中的每一个都被转录且每个元件都受到调控。通过对缺失突变体的Northern印迹分析和报告基因分析对长末端重复调控区域进行剖析,结果表明Ty3与侧翼染色体序列的上游连接处包含一个负调控区域。一个19 bp的片段(位置56 - 74),包含一个与信息素反应元件(PRE)共有序列一致的拷贝以及一个与PRE共有序列8 bp匹配中的7 bp匹配,足以介导任一单倍体细胞类型中的信息素诱导。然而,该区域的缺失并未消除表达,这表明其他序列也能激活转录。PRE区域下游紧邻的一个24 bp的片段包含一个与a1 - alpha 2共有序列相似的序列,该序列赋予了交配型调控。PRE和a1 - alpha 2序列之间区域的一个单碱基对突变阻断了信息素诱导,但未阻断交配型调控。因此,Ty3的长末端重复是一个紧凑的、高度受调控的、可移动的启动子,它对细胞类型和交配有反应。

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