Identification and characterization of a novel gene EOLA1 stimulating ECV304 cell proliferation.
- Author:
Zi-wen LIANG
1
;
Zong-cheng YANG
;
Yue-ming LIU
;
Yu CHEN
;
Xiang-dong LUO
Author Information
- Publication Type:Journal Article
- MeSH: Amino Acid Sequence; Base Sequence; Blotting, Northern; Blotting, Western; Cell Line; Cell Proliferation; Chromosomes, Human, X; genetics; Exons; genetics; Humans; Immunoprecipitation; Membrane Proteins; genetics; metabolism; physiology; Metallothionein; genetics; metabolism; Molecular Sequence Data; Protein Binding; Sequence Alignment; Two-Hybrid System Techniques
- From: Chinese Journal of Medical Genetics 2005;22(5):518-523
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo amplify the full-length cDNA and characterize the structure and biological function of a novel expression sequence tag ST55 (GenBank Accession No. BM121646).
METHODSRapid amplification of cDNA ends was used to clone the full-length of cDNA of ST55 in this study. Then, its tissue distribution was checked by Northern blots, and the associated protein was screened by GAL 4-based yeast two-hybrid. The effect of stable transfection of the cDNA on cell proliferation was evaluated in ECV304 cells.
RESULTSA full-length 1404 bp cDNA was cloned, and it was accepted as a novel human mRNA by GenBank (No. AY074889), named endothelial-overexpressed lipopolysaccharide-associated factor 1 (EOLA1). Bioinformatic analysis found that the EOLA1 encoded 158 amino acids, 17.89 kDa protein, and mapped to chromosome Xq27.4 with 5 exons. EOLA1 expressed in different human normal tissues and cancer cell lines. Using the EOLA1 cDNA as bait, we performed a yeast two-hybrid screening of a human liver cDNA library and identified metallothionein 2A (MT2A) as associated protein. The interaction between EOLA1 and MT2A was confirmed by co-immunoprecipitation experiments. Stable transfection of EOLA1 was noted to stimulate ECV304 cell proliferation (P < 0.05).
CONCLUSIONThe findings suggest that EOLA1 is a novel gene and the interaction of EOLA1 and MT2A may play an important role in cell protection in inflammation reaction.