Bull P, Thorikay M, Moenne A, Wilkens M, Sánchez H, Valenzuela P, Venegas A
Laboratorio de Bioquimica, Facultad de Ciencias Biologicas, Pontificia Universidad Catolica de Chile, Santiago.
DNA. 1987 Aug;6(4):353-62. doi: 10.1089/dna.1987.6.353.
Several cloned members of the yeast tRNA(Phe) gene family were transcribed in vitro using a HeLa extract and a yeast extract. The optimum DNA concentration was determined and kinetic experiments were performed for each clone to compare transcription levels. Both extract systems were able to splice the intervening sequence, but only the yeast extract produced the mature product. Some genes were not transcribed with the homologous system while they were transcribed with the HeLa extract, suggesting a control mechanism that is not operating in the heterologous system. Competition experiments demonstrated that the intragenic promoters of the inactive genes were able to bind transcription factor(s), but not as efficiently as active genes. This binding was not so strong when using linear DNA and was dependent on the presence of the 3' intragenic control region. DNA sequencing and computer analysis indicated the presence of short conserved sequences upstream from the genes. These sequences, which are not related to the intragenic promoters, are direct repeats of part of the 3' coding region in those genes that are transcribed in the homologous system. The relevance of these sequences on homologous transcription in vitro remains to be established.
使用人宫颈癌细胞系提取物(HeLa提取物)和酵母提取物对酵母苯丙氨酸转运RNA(tRNA(Phe))基因家族的几个克隆成员进行了体外转录。确定了最佳DNA浓度,并对每个克隆进行了动力学实验以比较转录水平。两种提取物系统都能够剪接间隔序列,但只有酵母提取物产生成熟产物。一些基因在同源系统中不转录,而在用HeLa提取物时却能转录,这表明存在一种在异源系统中不起作用的控制机制。竞争实验表明,无活性基因的基因内启动子能够结合转录因子,但效率不如活性基因。使用线性DNA时,这种结合不那么强,并且依赖于3'基因内控制区的存在。DNA测序和计算机分析表明,基因上游存在短保守序列。这些序列与基因内启动子无关,是在同源系统中被转录的那些基因的3'编码区部分的直接重复序列。这些序列在体外同源转录中的相关性仍有待确定。