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首页> 外文期刊>American Journal of Physiology >Cloning of a novel EGFR-related peptide: a putative negative regulator of EGFR.
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Cloning of a novel EGFR-related peptide: a putative negative regulator of EGFR.

机译:新型EGFR相关肽的克隆:EGFR的负调节剂。

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Although epidermal growth factor receptor (EGFR) plays a key role in regulating cell proliferation, differentiation, and transformation in many tissues, little is known about the factor(s) that may modulate its function. We have isolated a cDNA clone from the rat gastroduodenal mucosa whose full length revealed 1,958 bp that contained 227 bp of 5'-untranslated region (UTR) and an open-reading frame encoding 479 amino acids, followed by 290 bp of 3'-UTR. It showed ~85% nucleotide homology to the external domain of the rat EGFR. We refer to the product of the newly isolated cDNA as EGFR-related protein (ERRP). In Northern blot analysis with poly(A)(+) RNA from different rat tissues, ERRP cDNA hybridized to several mRNA transcripts with the strongest reaction noted with a transcript of approximately 2 kb. Maximal expression of the 2-kb mRNA transcript was observed in the small intestine, followed by colon, liver, gastric mucosa, and other tissues. Transfection of ERRP cDNA into a colon cancer cell line, HCT116, resulted in a marked reduction in proliferation in monolayer and colony formation in soft agar compared with the vector-transfected controls. In another colon cancer cell line, Caco-2, with a tetracycline-regulated promoter system, induction of ERRP expression in the absence of doxycycline was associated with a marked reduction in EGFR activation and proliferation. We conclude that the ERRP cDNA may represent a new member of the EGFR gene family and that ERRP plays a role in regulating cell proliferation by modulating the function of EGFR.
机译:尽管表皮生长因子受体(EGFR)在许多组织中调节细胞增殖,分化和转化中起着关键作用,但对于可能调节其功能的因子知之甚少。我们从大鼠胃十二指肠粘膜中分离出一个cDNA克隆,其全长显示1,958 bp,其中包含227 bp的5'-非翻译区(UTR)和一个开放阅读框,编码479个氨基酸,随后是290 bp的3'-UTR 。它显示出与大鼠EGFR外部结构域〜85%的核苷酸同源性。我们将新分离的cDNA的产物称为EGFR相关蛋白(ERRP)。用来自不同大鼠组织的poly(A)(+)RNA进行Northern印迹分析时,ERRP cDNA与数个mRNA转录本杂交,其中最强的反应约为2 kb。在小肠中观察到2-kb mRNA转录的最大表达,其次是结肠,肝脏,胃粘膜和其他组织。与载体转染的对照相比,将ERRP cDNA转染到结肠癌细胞系HCT116中导致软琼脂中单层增殖和集落形成的明显减少。在具有四环素调节的启动子系统的另一种结肠癌细胞系Caco-2中,在没有强力霉素的情况下诱导ERRP表达与EGFR激活和增殖的显着降低有关。我们得出的结论是,ERRP cDNA可能代表了EGFR基因家族的新成员,并且ERRP通过调节EGFR的功能在调节细胞增殖中发挥了作用。

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