Screening and identification of candidate proteins interacting with lung cancer metastasis-related protein 1 of human 95D cell line cDNA library by yeast two hybridization
LI Yanqin, LIU Yang, LIANG Liling, and XU Yang.
Department of Respiratory Medicine, PLA General Hospital, Beijing 100853, China
Abstract:Objective To screen and identify the proteins that interact with LCMR1 from human 95D cell line library by the yeast two-hybrid system.Methods The bait plasmid, pGBKT7-LCMR1 , which expressed LCMR1 fusion protein, was transformed into AH109 yeast strains before yeast two-hybrid screening was performed by mating AH109 with Y187 containing human 95D cell cDNA library plasmids. SD/-Ade/-His/-Leu/-Trp medium and X-α-Gal were used for selecting and screening the interacting proteins.Moreover, back-cross was performed to confirm the positive clones .The vectors of Myc-tagged fusion protein and flag-tagged interacting proteins were constructed, identified and cotransfected into human embryo kidney 293 cells.The interactions between them were investigated by the immunoprecipitation(CO-IP) and GST pull-down system.Results The bait plasmid pGBKT7-LCMR1 was identified and transformed into AH109 and six true positive proteins with known functions were obtained through sequencing and bioinformatics analysis, which were GNG5, RPL29, DEK, CCAR1, G3BP1 and LGMN. GNG5 and RPL29 were selected for further study. The eukaryotic expression vectors of pcDNA3.0-flag -RPL29, pcDNA3.0 -flag-GNG5 and pCMV-Myc-LCMR1 were constructed and confirmed with double restriction enzyme digestion and co-transfected into 293 cell line.The interactions between RPL29 and LCMR1 were identified with Western blot after Co-IP, andno interactions between GNG5 and LCMR1 were detected.The same results were found in the subsequent experiment of GST pull down.Conclusions Proteins in 95D cell line library that can interact with LCMR1 are successfully screened out and identified.The interactions between LCMR1 and RPL29 are confirmed by the CO-IP and GST pull-down system.
李彦芹, 刘扬, 梁丽玲, 许阳. 酵母双杂交技术筛选人95D细胞中肺癌转移相关蛋白1相互作用蛋白及其验证[J]. 武警医学, 2018, 29(9): 895-900.
LI Yanqin, LIU Yang, LIANG Liling, and XU Yang.. Screening and identification of candidate proteins interacting with lung cancer metastasis-related protein 1 of human 95D cell line cDNA library by yeast two hybridization. Med. J. Chin. Peop. Armed Poli. Forc., 2018, 29(9): 895-900.
Chen L,Liang Z,Tian Q,et al. Overexpression of LCMR1 is significantly associated with clinical stage in human NSCLC[J]. J Exp Clin Cancer Res,2011, 30:18.
[2]
Xu Y, Li C, Tian Q, et al. Suppression of lung cancer metastasis-related protein 1 promotes apoptosis in lung cancer cells[J]. Int J Mol Med. 2012 ,30(6):1481-1486.
[3]
Aga sse G, Barbollat-Boutrand L, Sulpice E, et al. A large-scale RNAi screen identifies LCMR1 as a critical regulator of Tspan8-mediated melanoma invasion[J].Oncogene, 2017, 36(35):5084.
[4]
Chien C T,Bartel P L,Sternglanz R,et al. The two-hybrid system :a method to identify and clone genes for proteins that interact with a protein of interest[J]. Proc Natl Acad Sci USA,1991, 88(21):9578-9582.
[5]
Xu J, Yang H, Zhou X, et al .Bisdemethoxycurcumin suppresses migration and invasion of highly metastatic 95D lung cancer cells by regulating E-cadherin and vimentin expression, and inducing autophagy[J]. Mol Med Rep, 2015,12(5):7603-7608.
[6]
Tian Q, Chen L, Liu Y. Study on high-rate and low-rate metastatic large-cell lung cancer cell lines via differential display reverse transcript PCR[J]. Zhongguo Fei Ai Za Zhi, 2003,6(5):347-351.