Han J, Unlap T, Rado T A
Laboratory of Medical Genetics, University of Alabama, Birmingham 35294.
Biochem Biophys Res Commun. 1991 Dec 31;181(3):1462-8. doi: 10.1016/0006-291x(91)92104-r.
The structure and position of cis-acting DNA sequences which regulate tissue specific expression of the human neutrophil elastase (HNE) gene have been investigated. We have identified a positive and a negative regulatory element upstream from the promoter region. The ability of these sequences to regulate transcription in myeloid and non-myeloid cells was studied by inserting varying lengths of HNE 5'-flanking sequence into a reporter plasmid containing the bacterial chloramphenicol acetyltransferase (CAT) gene. CAT activity in U937 was minimal in the absence of promoter and in the presence of HNE sequence to -102 bp. Inclusion of sequence up to -153 bp resulted in a 5.6-fold increase in CAT activity that was not observed in non-myeloid transfectants. Extension of the insert to include additional HNE sequence to -196 bp resulted in a decrease in CAT activity to control levels.
对调控人中性粒细胞弹性蛋白酶(HNE)基因组织特异性表达的顺式作用DNA序列的结构和位置进行了研究。我们在启动子区域上游鉴定出一个正调控元件和一个负调控元件。通过将不同长度的HNE 5'侧翼序列插入含有细菌氯霉素乙酰转移酶(CAT)基因的报告质粒中,研究了这些序列在髓系和非髓系细胞中调控转录的能力。在没有启动子且存在至-102 bp的HNE序列时,U937中的CAT活性最低。包含至-153 bp的序列导致CAT活性增加5.6倍,这在非髓系转染子中未观察到。将插入片段延伸以包含额外的至-196 bp的HNE序列导致CAT活性降至对照水平。