首页> 外国专利> ISOLATION AND CHARACTERIZATION OF EPIDERMAL GROWTH FACTOR RELATED PROTEIN

ISOLATION AND CHARACTERIZATION OF EPIDERMAL GROWTH FACTOR RELATED PROTEIN

机译:表皮生长因子相关蛋白的分离与鉴定

摘要

A cDNA fragment clone of 1583 base pairs with 90-95 % sequence homology to the mouse EGFR and a truncated rat EGFR was isolated. The isolated cDNA lacked the "termination" codon, rapid amplification of cDNA ends (RACE) was applied to obtain the 3'-terminal end. The full-length cDNA revealed 1753 base pairs that contained 227 base pairs of 5' untranslated region and an open reading frame encoding 473 amino acids which showed an 84 % and 91 % homology, respectively, to a rat truncated EGFR and the mouse EGFR. We refer to the product of the newly isolated cDNA as ERRP (uE/uGF-uR/ueceptor uR/uelated uP/urotein). In Northern-blot analysis with poly A+ RNA from different rat tissues, ERRP cDNA hybridized strongly to a mRNA transcript of about 1.8 kb. Maximal expression was noted in the small intestine, followed by colon, liver, gastric mucosa and other tissues. Transfection of ERRP cDNA in HCT-116 cells, a colon cancer cell line, markedly inhibits proliferation in monolayer and in soft agar and attenuates EGF-R tyrosine kinase activity. Transfection of ERRP in HCT-116 also delays tumor growth in SCID mice injected with these cells compared to the vector-transfected control cells. On the other hand, proliferation of the vector-transfected control, but not ERRP transfected HCT cells could be stimulated by TGF- alpha (10-10M and 10-9M). The ERRP cDNA represents a new member of the EGFR gene family, and its protein product plays a key role in modulating the function of EGFR.
机译:分离出与小鼠EGFR具有90-95%序列同源性的1583个碱基对的cDNA片段克隆,并分离出了截短的大鼠EGFR。分离的cDNA缺少“终止”密码子,将cDNA末端的快速扩增(RACE)用于获得3'-末端。全长cDNA揭示了1753个碱基对,其中包含227个碱基对的5'非翻译区和一个开放阅读框,其编码473个氨基酸,与大鼠截短的EGFR和小鼠EGFR分别具有84%和91%的同源性。我们将新分离的cDNA的产物称为ERRP( E GF- R 受体 R elated P rotein )。在用来自不同大鼠组织的poly A + RNA的Northern印迹分析中,ERRP cDNA与约1.8 kb的mRNA转录物强烈杂交。在小肠中发现最大的表达,其次是结肠,肝,胃粘膜和其他组织。 ERRP cDNA在结肠癌细胞系HCT-116细胞中的转染显着抑制单层和软琼脂中的增殖,并减弱EGF-R酪氨酸激酶活性。与载体转染的对照细胞相比,HCT-116中ERRP的转染也延迟了注射了这些细胞的SCID小鼠的肿瘤生长。另一方面,可以通过TGF-α(10 -10 M和10 -9 M)刺激载体转染的对照而不是ERRP转染的HCT细胞的增殖。 ERRP cDNA代表EGFR基因家族的新成员,其蛋白质产物在调节EGFR功能中起关键作用。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号