Mori T, Wanaka A, Taguchi A, Matsumoto K, Tohyama M
Department of Anatomy and Neuroscience, Osaka University Medical School, Japan.
Brain Res Mol Brain Res. 1995 Dec 1;34(1):154-60. doi: 10.1016/0169-328x(95)00154-k.
In the course of studies to identify new members of the eph family of receptor tyrosine kinases, MDK1 and one of its splicing variants lacking a kinase domain, MDK1-T1, were identified. To gain insight into the functions of these subtypes, expression patterns of their mRNAs in the developing mouse nervous system were examined by Northern blotting and in situ hybridization histochemistry. Colocalization of their mRNAs was observed, but the levels of expression of each mRNA were developmentally regulated. These findings suggest functional differences between full-length and truncated forms of MDK1 receptor tyrosine kinase.
在鉴定受体酪氨酸激酶Eph家族新成员的研究过程中,发现了MDK1及其一个缺少激酶结构域的剪接变体MDK1-T1。为深入了解这些亚型的功能,通过Northern印迹法和原位杂交组织化学法检测了它们的mRNA在发育中的小鼠神经系统中的表达模式。观察到它们的mRNA共定位,但每种mRNA的表达水平受发育调控。这些发现提示MDK1受体酪氨酸激酶全长形式和截短形式之间存在功能差异。