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小鼠APRT基因表达所需DNA序列的鉴定。

Identification of DNA sequences required for mouse APRT gene expression.

作者信息

Dush M K, Briggs M R, Royce M E, Schaff D A, Khan S A, Tischfield J A, Stambrook P J

机构信息

Department of Anatomy and Cell Biology, University of Cincinnati College of Medicine, OH 45267.

出版信息

Nucleic Acids Res. 1988 Sep 12;16(17):8509-24. doi: 10.1093/nar/16.17.8509.

Abstract

The mouse aprt promoter contains four GC boxes, which bind transcription factor Spl in vitro, and lacks both TATA and CCAAT boxes. Removal of the two most distal GC boxes of this promoter had little effect on APRT enzyme levels produced in a transient expression assay. Deletion of the distal three GC boxes resulted in a 50% reduction, and deletion of all GC boxes resulted in essentially complete loss of APRT activity. There are two predominant transcription start sites which are located within the region containing the GC boxes. The promoter behaved as a relatively strong promoter when compared to the RSV LTR promoter in a transient CAT assay, and operated in one orientation only. No upstream anti-sense transcripts were detected in either mouse CAK or liver cells, confirming that the mouse aprt promoter, unlike some other GC-rich promoters appears not to support bidirectional transcription.

摘要

小鼠aprt启动子包含四个GC框,它们在体外与转录因子Spl结合,并且缺乏TATA框和CCAAT框。去除该启动子的两个最远端的GC框对瞬时表达试验中产生的APRT酶水平几乎没有影响。删除远端的三个GC框导致减少50%,而删除所有GC框则导致APRT活性基本完全丧失。有两个主要的转录起始位点,位于包含GC框的区域内。在瞬时CAT试验中,与RSV LTR启动子相比,该启动子表现为相对较强的启动子,并且仅以一种方向起作用。在小鼠CAK或肝细胞中均未检测到上游反义转录本,证实与其他一些富含GC的启动子不同,小鼠aprt启动子似乎不支持双向转录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df14/338573/c56d306e4f5f/nar00159-0315-a.jpg

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