Pentecost B T, Mattheiss L, Dickerman H W, Kumar S A
Wadsworth Center for Laboratories and Research, New York State Department of Health, Albany 12201-0509.
Mol Endocrinol. 1990 Jul;4(7):1000-10. doi: 10.1210/mend-4-7-1000.
Creatine kinase-B (CKB) synthesis is rapidly and specifically induced by estrogen in the uterus of the immature rat. This study indicates that this elevation is due at least in part to increases in the levels of mRNA for CKB. The stimulation of CKB mRNA levels is rapid (a 7- to 10-fold increase is detected 1-3 h after estrogen administration), but transient, as levels return to near control values by 6 h. Analysis of cDNAs to both uterine and brain CKB mRNA indicate that the same sequence is expressed in both tissues despite earlier observations of heterogeneity of the protein isolated from the two tissues. A 1.7-kilobasepair DNA fragment containing the CKB promoter and 5' flanking sequences confers estrogen sensitivity on expression of the bacterial chloramphenicol acetyl transferase gene in HeLa cells on cotransfection with an estrogen-receptor expression vector. However, the CKB promoter sequences lack any motif with convincing similarity to the currently accepted consensus estrogen response element GGTCAnnnTGACC.
在未成熟大鼠子宫中,肌酸激酶-B(CKB)的合成可被雌激素迅速且特异性地诱导。本研究表明,这种升高至少部分归因于CKB mRNA水平的增加。CKB mRNA水平的刺激迅速(雌激素给药后1-3小时检测到增加7至10倍),但具有短暂性,因为6小时后水平恢复到接近对照值。对子宫和脑CKB mRNA的cDNA分析表明,尽管早期观察到从这两种组织中分离的蛋白质存在异质性,但相同的序列在两种组织中均有表达。一个包含CKB启动子和5'侧翼序列的1.7千碱基对DNA片段,与雌激素受体表达载体共转染时,可使HeLa细胞中细菌氯霉素乙酰转移酶基因的表达具有雌激素敏感性。然而,CKB启动子序列缺乏与目前公认的共有雌激素反应元件GGTCAnnnTGACC有令人信服的相似性的任何基序。