Screening of proteins binding to FXR1P using yeast two-hybrid technique.
- Author:
	        		
		        		
		        		
			        		Jiao SU
			        		
			        		
			        		
			        			1
			        			,
			        		
			        			2
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Shu-ya HE
			        		
			        		;
		        		
		        		
		        		
			        		Bin-yuan LI
			        		
			        		;
		        		
		        		
		        		
			        		Yun MA
			        		
			        		;
		        		
		        		
		        		
			        		Chang-shun YU
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Journal Article
 - MeSH: Autoantigens; genetics; metabolism; Estradiol Dehydrogenases; genetics; metabolism; Ferritins; genetics; metabolism; Gene Library; Humans; Membrane Proteins; genetics; metabolism; Protein Binding; Protein Interaction Domains and Motifs; genetics; RNA-Binding Proteins; genetics; metabolism; Two-Hybrid System Techniques
 - From: Journal of Southern Medical University 2009;29(12):2394-2400
 - CountryChina
 - Language:Chinese
 - 
		        	Abstract:
			       	
			       		
				        
				        	
OBJECTIVETo screen the proteins interacting with FXR1P for functional investigation of FXR1P.
METHODSThe yeast strain AH109 transformed with the recombinant expression vector pGBKT7/FXR1 was mated with the yeast strain Y187 pretransformed with human fetal brain cDNA library. The positive clones were screened and identified by sequence analysis.
RESULTSThe recombinant expression vector pGBKT7/FXR1 was constructed successfully. Five proteins binding to FXR1P were screened from human fetal brain cDNA library using the yeast two-hybrid system, including CMAS, FTH1, GOLGA4, HSD17B1 and CSH1.
CONCLUSIONSThese results provide new clues for investigating the biological functions of FXR1P and the pathogenesis of Fragile X syndrome.
 
            