Takeuchi S, Yamamoto H, Takeuchi T
Biological Institute, Tohoku University, Sendai, Japan.
Biochem Biophys Res Commun. 1988 Aug 30;155(1):470-5. doi: 10.1016/s0006-291x(88)81110-0.
In order to study the molecular aspects of albinism, we analyzed the expression of tyrosinase gene in some amelanotic mutant mice by Northern blotting using mouse tyrosinase cDNA as a probe. It hybridized with a species of 2.1 kilobase RNA prepared from the skin of wild-type mice and two albino strains in the same quantity. In black-eyed white mouse, however, no RNA transcript encoding tyrosinase was detected. Our results suggest that these albinism is due to a point mutation in the structural region of the tyrosinase gene, not to a deficiency of tyrosinase gene expression and that the black-eyed white mouse has a deficiency in the gene expression possibly related to melanocyte differentiation.
为了研究白化病的分子机制,我们以小鼠酪氨酸酶cDNA为探针,通过Northern印迹法分析了一些无黑素突变小鼠中酪氨酸酶基因的表达情况。它与从野生型小鼠皮肤和两个白化病品系皮肤中制备的等量2.1千碱基RNA杂交。然而,在黑眼白鼠中,未检测到编码酪氨酸酶的RNA转录本。我们的结果表明,这些白化病是由于酪氨酸酶基因结构区域的点突变,而非酪氨酸酶基因表达缺陷所致,并且黑眼白鼠在基因表达方面存在缺陷,可能与黑素细胞分化有关。