Danciger E, Mettling C, Vidal M, Morris R, Margolis F
Department of Neurosciences, Roche Research Center, Nutley, NJ 07110.
Proc Natl Acad Sci U S A. 1989 Nov;86(21):8565-9. doi: 10.1073/pnas.86.21.8565.
Olfactory marker protein (OMP) genomic clones were isolated from a Charon 4A phage lambda rat genomic library. A 16.5-kilobase (kb) fragment of the rat genome containing the gene was isolated and characterized. Sequence analysis of the gene showed the absence of introns and the lack of CAAT and TATA boxes in the 5' flanking region. The transcription initiation site was mapped, and two sites 55 and 58 base pairs upstream of the ATG were observed. The 5' flanking region is rich in G+C residues and contains a G+C-rich motif as well as direct and inverted repeats. Functional OMP regulatory sequences were demonstrated in transgenic mice. An 11-kb chimeric gene was constructed in which the coding region for OMP was replaced with that for Thy-1.1. In Thy-1.2 mice carrying this transgene, Thy-1.1 was expressed solely by olfactory receptor neurons and their axons and terminals in the olfactory bulb.
从Charon 4A噬菌体λ大鼠基因组文库中分离出嗅觉标记蛋白(OMP)基因组克隆。分离并鉴定了包含该基因的大鼠基因组16.5千碱基(kb)片段。该基因的序列分析表明其缺乏内含子,且在5'侧翼区域没有CAAT盒和TATA盒。确定了转录起始位点,在ATG上游55和58个碱基对处观察到两个位点。5'侧翼区域富含G + C残基,包含一个富含G + C的基序以及正向和反向重复序列。在转基因小鼠中证实了功能性OMP调控序列。构建了一个11 kb的嵌合基因,其中OMP的编码区被Thy-1.1的编码区取代。在携带该转基因的Thy-1.2小鼠中,Thy-1.1仅在嗅觉受体神经元及其在嗅球中的轴突和终末中表达。