Suvanto P, Wartiovaara K, Lindahl M, Arumae U, Moshnyakov M, Horelli-Kuitunen N, Airaksinen M S, Palotie A, Sariola H, Saarma M
Institute of Biotechnology, University of Helsinki, Finland.
Hum Mol Genet. 1997 Aug;6(8):1267-73. doi: 10.1093/hmg/6.8.1267.
Glial cell line-derived neurotrophic factor (GDNF) is a potent survival factor for central dopaminergic neurons, motor neurons and several other populations of neurons in the central and peripheral nervous system. GDNF and its receptor complex of c-RET tyrosine kinase and a glycosyl-phosphatidylinositol linked protein GDNFR-alpha are of great interest due to their potential use in the therapy of Parkinson's and motoneuron diseases. We have cloned the human and rat cDNA sequences of GDNFR-beta, a new gene encoding for a 464 amino acid long homologue of GDNFR-alpha, and assign the locus of this new gene to human chromosome 8p21-22 and mouse chromosome 14D3-E1. Similarly to GDNFR-alpha, GDNFR-beta mediates GDNF-induced Ret autophosphorylation in transfected cells. By northern hybridisation we show that the transcript level of human GDNFR-beta mRNA is high in the adult brain, intestine and placenta and in fetal brain, lung and kidney. Studied by in situ hybridisation, GDNFR-beta mRNA shows in E17 rat embryo different distribution to that of GDNFR-alpha mRNA, especially, in adrenal gland, kidney and gut. In the developing nervous system, GDNFR-beta mRNA expression is restricted to certain neuronal populations, while GDNFR-alpha mRNA is widely expressed also in non-neuronal cells. The distinct tissue distribution of GDNFR-beta mRNA and its ability to mediate GDNF signal in transfected cells suggest a role in signal transduction of GDNF and, possibly, related neurotrophic factors in vivo.
胶质细胞系源性神经营养因子(GDNF)是中枢多巴胺能神经元、运动神经元以及中枢和外周神经系统中其他几类神经元的强效存活因子。由于GDNF及其c-RET酪氨酸激酶和糖基磷脂酰肌醇连接蛋白GDNFR-α的受体复合物在帕金森病和运动神经元疾病治疗中的潜在用途,它们备受关注。我们克隆了GDNFR-β的人类和大鼠cDNA序列,这是一个编码464个氨基酸的GDNFR-α同源物的新基因,并将该新基因的基因座定位到人类染色体8p21 - 22和小鼠染色体14D3 - E1。与GDNFR-α类似,GDNFR-β在转染细胞中介导GDNF诱导的Ret自磷酸化。通过Northern杂交,我们发现人类GDNFR-β mRNA的转录水平在成人大脑、肠道和胎盘以及胎儿大脑、肺和肾脏中较高。通过原位杂交研究发现,GDNFR-β mRNA在E17大鼠胚胎中的分布与GDNFR-α mRNA不同,特别是在肾上腺、肾脏和肠道中。在发育中的神经系统中,GDNFR-β mRNA的表达仅限于某些神经元群体,而GDNFR-α mRNA在非神经元细胞中也广泛表达。GDNFR-β mRNA独特的组织分布及其在转染细胞中介导GDNF信号的能力表明它在体内GDNF以及可能相关的神经营养因子的信号转导中发挥作用。