Sabol S Z, Hu S, Hamer D
Laboratory of Biochemistry, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Hum Genet. 1998 Sep;103(3):273-9. doi: 10.1007/s004390050816.
We describe a new polymorphism upstream of the gene for monoamine oxidase A (MAOA), an important enzyme in human physiology and behavior. The polymorphism, which is located 1.2 kb upstream of the MAOA coding sequences, consists of a 30-bp repeated sequence present in 3, 3.5, 4, or 5 copies. The polymorphism is in linkage disequilibrium with other MAOA and MAOB gene markers and displays significant variations in allele frequencies across ethnic groups. The polymorphism has been shown to affect the transcriptional activity of the MAOA gene promoter by gene fusion and transfection experiments involving three different cell types. Alleles with 3.5 or 4 copies of the repeat sequence are transcribed 2-10 times more efficiently than those with 3 or 5 copies of the repeat, suggesting an optimal length for the regulatory region. This promoter region polymorphism may be useful as both a functional and an anonymous genetic marker for MAOA.
我们描述了一种位于单胺氧化酶A(MAOA)基因上游的新多态性,MAOA是人类生理和行为中的一种重要酶。该多态性位于MAOA编码序列上游1.2 kb处,由一个30 bp的重复序列组成,该重复序列以3、3.5、4或5个拷贝的形式存在。该多态性与其他MAOA和MAOB基因标记处于连锁不平衡状态,并且在不同种族群体中的等位基因频率存在显著差异。通过涉及三种不同细胞类型的基因融合和转染实验表明,该多态性会影响MAOA基因启动子的转录活性。具有3.5或4个拷贝重复序列的等位基因的转录效率比具有3或5个拷贝重复序列的等位基因高2至10倍,这表明调控区域存在一个最佳长度。这种启动子区域多态性可能作为MAOA的功能性和匿名性遗传标记都很有用。