Human tenascin-C: Identification of a novel type III repeat in oral cancer and of novel splice variants in normal, malignant and reactive oral mucosae

选择性拼接 剪接 Tenascin公司 生物 藤黄蛋白C 癌症 RNA剪接 克拉斯 基因亚型 纤维连接蛋白 癌症研究 分子生物学 遗传学 基因 细胞外基质 结直肠癌 核糖核酸
作者
Alan J. Mighell,John Thompson,William J. Hume,Alexander F. Markham,Philip A. Robinson
出处
期刊:International Journal of Cancer [Wiley]
卷期号:72 (2): 236-240 被引量:52
标识
DOI:10.1002/(sici)1097-0215(19970717)72:2<236::aid-ijc6>3.0.co;2-s
摘要

Tenascin-C is a mosaic, linear glycoprotein that is up-regulated during many normal and pathological processes involving either cell migration or tissue morphogenesis, such as invasion of malignant cells and wound healing. Human tenascin-C contains 8 consecutive type III fibronectin (TNCfn) domains that are involved in alternative splicing and potentially generate a large number of isoforms that code for tenascin-C proteins with subtly different functions. Human tenascin-C splice variants were investigated by RT-PCR in a range of normal and pathological oral mucosal tissues. A novel, 9th human TNCfn domain involved in alternative splicing was identified. It shares 70% nucleic acid and 55% protein sequence homology with chicken TNCfn-ad2. As in avians, this novel repeat was located between TNCfn-B and TNCfn-ad1 and accordingly was designated human TNCfn-ad2. Human TNCfn-ad2 was detected in only 2 of 10 oral cancers. However, TNCfn-ad2 was absent from 40 normal, reactive, pre-malignant and other oral mucosal specimens investigated. Previous studies have described 8 splice variant transcripts for human tenascin-C. By systematic investigation we identified further novel splice variants for human tenascin-C. Furthermore, our results indicate that many potential splice variants probably do not exist in the tissues investigated. Thus, we have demonstrated that human tenascin-C transcripts generate a complex but selected repertoire of different alternative splice products. Int. J. Cancer 72:236–240, 1997. © 1997 Wiley-Liss, Inc.
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