Reddy U R, Phatak S, Pleasure D
Division of Neurology Research, The Children's Hospital of Philadelphia, Pennsylvania 19104, USA.
Oncogene. 1996 Oct 3;13(7):1555-9.
Human heart, lung and kidney express a 6 kb mRNA encoding Ror1, a member of the receptor tyrosine kinase (RTK) family with as yet unknown ligand specificity. We used a Ror1 cDNA probe to screen a cDNA library prepared from the human neuronogenic teratocarcinoma line, NTera2, and cloned a 2373 nucleotide transcript. This transcript contains an open reading frame that encodes a 388 amino acid protein identical with the cytosolic, C-terminal region of ror1 but lacking the ror1 transmembrane and entire extracellular domains. Northern blots demonstrate that mRNA encoding this truncated Ror1 ('t-Rorl') is abundantly expressed in fetal and adult human CNS, in human leukemia, lymphoma cell lines, and in a variety of human cancers derived from neuroectoderm. While previous studies have documented alternative splicing patterns within 5' and 3' regions of mRNAs encoding various RTKs altering their ligand binding specificity or their intracellular signaling, the present report is the first to demonstrate tissue-specific alternative mRNA splicing causing loss of the entire extracellular and transmembrane regions of an RTK.
人类心脏、肺和肾脏表达一种6 kb的mRNA,该mRNA编码Ror1,它是受体酪氨酸激酶(RTK)家族的成员,其配体特异性尚不清楚。我们使用Ror1 cDNA探针筛选从人类神经源性畸胎瘤细胞系NTera2制备的cDNA文库,并克隆了一个2373个核苷酸的转录本。该转录本包含一个开放阅读框,编码一种388个氨基酸的蛋白质,该蛋白质与ror1的胞质C末端区域相同,但缺少ror1的跨膜和整个细胞外结构域。Northern印迹显示,编码这种截短的Ror1(“t-Ror1”)的mRNA在胎儿和成人人类中枢神经系统、人类白血病、淋巴瘤细胞系以及多种源自神经外胚层的人类癌症中大量表达。虽然先前的研究记录了编码各种RTK的mRNA的5'和3'区域内的可变剪接模式会改变其配体结合特异性或细胞内信号传导,但本报告首次证明了组织特异性可变mRNA剪接导致RTK的整个细胞外和跨膜区域缺失。