Valenzuela David M, Maisonpierre Peter C, Glass David J, Rojas Eduardo, Nuñez Lorna, Kong Yuan, Gies David R, Stitt Trevor N, Ip Nancy Y, Yancopoulos George D
Regeneron Pharmaceuticals, Inc. Tarrytown, New York 10591.
Neuron. 1993 May;10(5):963-74. doi: 10.1016/0896-6273(93)90211-9.
We have identified transcripts encoding several different forms of rat TrkC, a member of the Trk family of receptor tyrosine kinases that serves as a receptor for neurotrophin-3. Some forms of TrkC lack the intracytoplasmic kinase domain and thus resemble previously defined truncated variants of TrkB. Other forms of TrkC contain variable-sized amino acid insertions within the tyrosine kinase domain. Transcripts encoding all forms of TrkC can be detected throughout the nervous system, displaying substantial overlap as well as mutually exclusive distribution patterns with transcripts for TrkB. Strikingly, only transcripts encoding the truncated forms of TrkB and TrkC are found in astrocytes, peripheral nerve, and nonneural tissues. Finally, forms of TrkC containing insertions within the kinase domain retain their ability to autophosphorylate in response to neurotrophin-3, but cannot mediate proliferation in fibroblasts or neuronal differentiation in PC12 cells.
我们已经鉴定出编码大鼠TrkC几种不同形式的转录本,TrkC是受体酪氨酸激酶Trk家族的成员,作为神经营养蛋白-3的受体。某些形式的TrkC缺乏胞质内激酶结构域,因此类似于先前定义的TrkB截短变体。其他形式的TrkC在酪氨酸激酶结构域内含有大小可变的氨基酸插入。编码所有形式TrkC的转录本在整个神经系统中都能检测到,与TrkB的转录本显示出大量重叠以及相互排斥的分布模式。引人注目的是,仅在星形胶质细胞、外周神经和非神经组织中发现编码TrkB和TrkC截短形式的转录本。最后,在激酶结构域内含有插入的TrkC形式保留了其响应神经营养蛋白-3进行自身磷酸化的能力,但不能介导成纤维细胞的增殖或PC12细胞的神经元分化。