Erlander M G, Tobin A J
Neuroscience Program, University of California, Los Angeles 90024-1606.
J Neurochem. 1992 Jun;58(6):2182-90. doi: 10.1111/j.1471-4159.1992.tb10962.x.
We have isolated the 5' flanking DNA sequences of the human gene encoding the 67,000-M(r) form of glutamate decarboxylase (GAD67), the gamma-aminobutyric acid synthetic enzyme. Transcription begins at a single promoter (P1) in adult brain but at two tandem promoters, P1 and P2, in fetal brain. P1, which is 3' to P2, resembles the promoter regions of many constitutively expressed genes, whereas P2 resembles a tissue-specific promoter. P1 contains a 10-base sequence (dec-1) that closely matches the element I cis-regulatory sequence identified in the promoter region of Drosophila 3,4-dihydroxyphenylalanine decarboxylase. Gel shift and transient expression assays demonstrate that the dec-1 sequence plays a role in the transcription of the human GAD67 gene.
我们已经分离出编码67,000道尔顿分子量的谷氨酸脱羧酶(GAD67)(γ-氨基丁酸合成酶)的人类基因的5'侧翼DNA序列。在成人大脑中,转录起始于单个启动子(P1),而在胎儿大脑中,转录起始于两个串联启动子P1和P2。位于P2下游3'端的P1类似于许多组成型表达基因的启动子区域,而P2则类似于组织特异性启动子。P1包含一个10碱基序列(dec-1),该序列与在果蝇3,4-二羟基苯丙氨酸脱羧酶启动子区域中鉴定出的元件I顺式调控序列紧密匹配。凝胶迁移和瞬时表达分析表明,dec-1序列在人类GAD67基因的转录中发挥作用。