Cloning of a novel EGFR-related peptide: a putative negative regulator of EGFR

Citation
Yj. Yu et al., Cloning of a novel EGFR-related peptide: a putative negative regulator of EGFR, AM J P-CELL, 280(5), 2001, pp. C1083-C1089
Citations number
27
Categorie Soggetti
Cell & Developmental Biology
Journal title
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
ISSN journal
03636143 → ACNP
Volume
280
Issue
5
Year of publication
2001
Pages
C1083 - C1089
Database
ISI
SICI code
0363-6143(200105)280:5<C1083:COANEP>2.0.ZU;2-H
Abstract
Although epidermal growth factor receptor (EGFR) plays a key role in regula ting cell proliferation, differentiation, and transformation in many tissue s, little is known about the factor(s) that may modulate its function. We h ave isolated a cDNA clone from the rat gastroduodenal mucosa whose full len gth 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 similar to 85% nucleotide homology to the external domain of the rat EGFR. We refer to the product of the newly isolated cDNA as EGF R-related protein (ERRP). In Northern blot analysis with poly(A)(+) RNA fro m different rat tissues, ERRP cDNA hybridized to several mRNA transcripts w ith the strongest reaction noted with a transcript of similar to2 kb. Maxim al expression of the 2-kb mRNA transcript was observed in the small intesti ne, followed by colon, liver, gastric mucosa, and other tissues. Transfecti on 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 c DNA 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.