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上游序列调节果蝇卵黄蛋白基因I和II的体外转录。

Upstream sequences modulate in vitro transcription from Drosophila yolk protein genes I and II.

作者信息

Voss D, Pongs O

出版信息

Eur J Biochem. 1986 Jul 1;158(1):25-32. doi: 10.1111/j.1432-1033.1986.tb09716.x.

Abstract

A Drosophila transcription system was employed to study transcription in vitro from templates carrying yolk polypeptide I and II (YPI, YPII) promoter regions. The transcription start sites of YPI and YPII genes are linked by 1225 base pairs of intergenic DNA and the genes are transcribed in divergent directions. Transcription was studied in vitro from templates carrying YPI or YPII promoter regions separately. We have successively deleted intergenic DNA upstream of the YPI or the YPII transcription start site and have assayed the dependence of transcription efficiency an template concentration. The results indicate that in vitro YPI and YPII transcript synthesis is controlled by separate cis-acting DNA sequence elements, which are located between 86 and 159 base pairs upstream of the YPI transcription start site and between 161 and 341 base pairs upstream of the YPII transcription start site. These elements stimulate in vitro transcription up to fivefold. Transcription was also studied with templates which contained both YP promoters. The transcription data indicate that the intergenic DNA contains additional DNA motif(s), which apparently modulate in vitro transcription coordinately from both YP promoters in an orientation-dependent manner.

摘要

采用果蝇转录系统,从携带卵黄蛋白多肽I和II(YPI、YPII)启动子区域的模板进行体外转录研究。YPI和YPII基因的转录起始位点由1225个碱基对的基因间DNA相连,且这两个基因以相反方向转录。分别从携带YPI或YPII启动子区域的模板进行体外转录研究。我们相继删除了YPI或YPII转录起始位点上游的基因间DNA,并检测了转录效率对模板浓度的依赖性。结果表明,体外YPI和YPII转录本的合成受独立的顺式作用DNA序列元件控制,这些元件位于YPI转录起始位点上游86至159个碱基对之间以及YPII转录起始位点上游161至341个碱基对之间。这些元件可将体外转录刺激高达五倍。还使用包含两个YP启动子的模板进行了转录研究。转录数据表明,基因间DNA包含其他DNA基序,这些基序显然以方向依赖的方式协调调节来自两个YP启动子的体外转录。

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