Screening of augmenter of liver regeneration-binding proteins by yeast-two hybrid technique
Cheng, J.; Wang, L.; Li, K.; Lu, Y.-Y.; Wang, G.; Liu, Y.; Zhong, Y.-W.; Duan, H.-J.; Hong, Y.; Li, L.; Zhang, L.-X.; Chen, J.-M.
Hepatobiliary and Pancreatic Diseases International Hbpd Int 2(1): 81-84
2003
ISSN/ISBN: 1499-3872 PMID: 14607653 Document Number: 555886
To investigate the biological function of augmenter of liver regeneration (ALR), we used yeast-two hybrid technique to detect proteins in hepatocytes interacting with ALR. ALR bait plasmid was constructed by using yeast-two hybrid system 3, then transformed into yeast AH109. The transformed yeast was mated with yeast Y187 containing liver cDNA library plasmid in a 2XYPDA medium. Diploid yeast was plated on a synthetic dropout nutrient medium (SD/-Trp-Leu-His-Ade) containing x-alpha-gal for selection and screening. After extracting and sequencing of the plasmid from blue colonies. Analysis was performed by bioinformatics. Of 36 colonies sequenced, 14 are metallothionein, 12 albumin, and 3 selenoprotein P. One colony is a new gene with unknown function. The successful cloning of gene of ALR interacting protein has paved the way for studying the physiological function of ALR and associated proteins.