Drabent B, Genthe A, Benecke B J
Nucleic Acids Res. 1986 Nov 25;14(22):8933-48. doi: 10.1093/nar/14.22.8933.
A cDNA clone homologous to HeLa cell mRNA encoding the 70 kDa human heat shock protein (hsp 70) was used to isolate a recombinant phage containing an entire human hsp 70 gene. Sequence analysis of the 5' and 3' flanking regions revealed the structural integrity of the regulatory elements. The functional integrity of this hsp 70 gene was substantiated by in vitro transcription studies with nuclear extracts. Specific run-off transcripts, synthesized by RNA polymerase II, were obtained with extracts prepared from heat-shocked cells. Extracts from non-heat-shocked cells were found inactive in hsp 70 gene transcription. However, 5' deletion mutants lacking the heat shock element (HSE) were transcribed by both heat shock and nonheat shock HeLa extracts.
一个与编码70kDa人热休克蛋白(hsp 70)的HeLa细胞mRNA同源的cDNA克隆被用于分离一个包含完整人hsp 70基因的重组噬菌体。对5'和3'侧翼区域的序列分析揭示了调控元件的结构完整性。该hsp 70基因的功能完整性通过用核提取物进行的体外转录研究得到证实。用热休克细胞制备的提取物获得了由RNA聚合酶II合成的特异性径流转录本。发现非热休克细胞的提取物在hsp 70基因转录中无活性。然而,缺乏热休克元件(HSE)的5'缺失突变体在热休克和非热休克的HeLa提取物中均被转录。