Kim S, Mellor J, Kingsman A J, Kingsman S M
Mol Cell Biol. 1986 Dec;6(12):4251-8. doi: 10.1128/mcb.6.12.4251-4258.1986.
The TRP1 promoter generates two groups of mRNAs, transcript I and transcript II. The difference in size between the largest and smallest mRNAs is about 200 base pairs. A series of one-sided and internal deletions were constructed in vitro throughout the TRP1 promoter, and the effect of each deletion on transcription was assessed by Northern blotting. We showed that 395 base pairs of the TRP1 promoter were sufficient for the normal transcription of all RNAs and that the promoter contained two control domains. The control domain for transcript I consisted of one positive element and one negative element, while the control domain for transcript II contained two positive elements. The negative element, mapped between -293 and -318, expression of transcript I. Two regions of transcript I. Two regions (-280 to -236 and -235 to -209) were required for accurate initiation of transcript I. Each region contained sequences homologous to known consensus sequences of the TATA box.
TRP1启动子产生两组mRNA,即转录本I和转录本II。最大和最小mRNA之间的大小差异约为200个碱基对。在体外构建了一系列贯穿TRP1启动子的单侧和内部缺失,并通过Northern印迹法评估每个缺失对转录的影响。我们发现,TRP1启动子的395个碱基对足以实现所有RNA的正常转录,并且该启动子包含两个控制域。转录本I的控制域由一个正调控元件和一个负调控元件组成,而转录本II的控制域包含两个正调控元件。负调控元件位于-293至-318之间,影响转录本I的表达。转录本I的两个区域(-280至-236和-235至-209)是转录本I准确起始所必需的。每个区域都包含与TATA盒已知共有序列同源的序列。