Chiu M I, Nathans J
Department of Molecular Biology and Genetics, Johns Hopkins-University School of Medicine, Baltimore, MD 21205.
Vis Neurosci. 1994 Jul-Aug;11(4):773-80. doi: 10.1017/s0952523800003072.
A 6.4-kb sequence upstream of the mouse blue visual pigment gene has been assayed in transgenic mice for the ability to direct cell-type-specific expression of a linked beta-galactosidase (lacZ) reporter. The construct is expressed specifically in cone photoreceptors in three independent lines. Transgene expression is found in the developing retina on the first postnatal day, increases rapidly in subsequent days, and persists through adulthood. A gradient of transgene expression is observed across the retina, with the transgene-expressing cones found almost exclusively in the lower retina and rarely in the upper retina, a pattern that parallels the distribution of blue cones in the mouse retina. Double-labeling with anti-cone pigment antibodies shows that transgene expression is confined to blue cones. These results imply that all of the sequence elements necessary for the control of blue cone-specific expression are encoded within the 6.4-kb DNA fragment tested.
在转基因小鼠中,对小鼠蓝色视觉色素基因上游6.4 kb的序列进行了检测,以评估其指导连接的β-半乳糖苷酶(lacZ)报告基因进行细胞类型特异性表达的能力。该构建体在三个独立品系的视锥光感受器中特异性表达。在出生后的第一天,转基因在发育中的视网膜中表达,在随后的几天中迅速增加,并持续到成年期。在整个视网膜中观察到转基因表达的梯度,表达转基因的视锥几乎只存在于视网膜下部,很少出现在视网膜上部,这种模式与小鼠视网膜中蓝色视锥的分布相似。用抗视锥色素抗体进行双重标记表明,转基因表达仅限于蓝色视锥。这些结果表明,控制蓝色视锥特异性表达所需的所有序列元件都编码在所测试的6.4 kb DNA片段中。