Hrs inhibits citron kinase-mediated HIV-1 budding via its FYVE domain.
	    		
		   		
		   			
		   		
	    	
    	 
    	10.1007/s13238-011-1053-y
   		
        
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Jiwei DING
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Lishan SU
			        		
			        		;
		        		
		        		
		        		
			        		Guangxia GAO
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. Key Laboratory of Infection and Immunity, Institute of Biophysics, Chinese Academy of Sciences, Beijing.
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
            
            	- MeSH:
            	
	        			
	        				
	        				
				        		
					        		Down-Regulation;
				        		
			        		
				        		
					        		Endosomal Sorting Complexes Required for Transport;
				        		
			        		
				        		
					        		genetics;
				        		
			        		
				        		
					        		metabolism;
				        		
			        		
				        		
					        		Endosomes;
				        		
			        		
				        		
					        		metabolism;
				        		
			        		
				        		
					        		Exocytosis;
				        		
			        		
				        		
					        		Gene Expression;
				        		
			        		
				        		
					        		Gene Silencing;
				        		
			        		
				        		
					        		drug effects;
				        		
			        		
				        		
					        		HEK293 Cells;
				        		
			        		
				        		
					        		HIV Infections;
				        		
			        		
				        		
					        		genetics;
				        		
			        		
				        		
					        		metabolism;
				        		
			        		
				        		
					        		virology;
				        		
			        		
				        		
					        		HIV-1;
				        		
			        		
				        		
					        		drug effects;
				        		
			        		
				        		
					        		genetics;
				        		
			        		
				        		
					        		growth & development;
				        		
			        		
				        		
					        		Humans;
				        		
			        		
				        		
					        		Immunoprecipitation;
				        		
			        		
				        		
					        		Intracellular Signaling Peptides and Proteins;
				        		
			        		
				        		
					        		genetics;
				        		
			        		
				        		
					        		metabolism;
				        		
			        		
				        		
					        		Microscopy, Fluorescence;
				        		
			        		
				        		
					        		Phosphoproteins;
				        		
			        		
				        		
					        		genetics;
				        		
			        		
				        		
					        		metabolism;
				        		
			        		
				        		
					        		Plasmids;
				        		
			        		
				        		
					        		Protein Binding;
				        		
			        		
				        		
					        		drug effects;
				        		
			        		
				        		
					        		genetics;
				        		
			        		
				        		
					        		Protein Interaction Domains and Motifs;
				        		
			        		
				        		
					        		Protein Structure, Tertiary;
				        		
			        		
				        		
					        		Protein Transport;
				        		
			        		
				        		
					        		Protein-Serine-Threonine Kinases;
				        		
			        		
				        		
					        		genetics;
				        		
			        		
				        		
					        		metabolism;
				        		
			        		
				        		
					        		RNA, Small Interfering;
				        		
			        		
				        		
					        		pharmacology;
				        		
			        		
				        		
					        		Transfection;
				        		
			        		
				        		
					        		Virion;
				        		
			        		
				        		
					        		drug effects;
				        		
			        		
				        		
					        		genetics;
				        		
			        		
				        		
					        		growth & development;
				        		
			        		
				        		
					        		Virus Release;
				        		
			        		
				        		
					        		drug effects;
				        		
			        		
				        		
					        		Virus Replication;
				        		
			        		
				        		
					        		drug effects
				        		
			        		
	        			
	        			
            	
            	
 
            
            
            	- From:
	            		
	            			Protein & Cell
	            		
	            		 2011;2(6):470-476
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:English
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Hepatocyte growth factor-regulated tyrosine kinase substrate (Hrs) is a key component of the endosomal sorting complexes required for transport and has been demonstrated to play a regulatory role in endocytosis/exocytosis and the accumulation of internal vesicles in multivesicular bodies. Citron kinase is a Ser/The kinase that we previously reported to enhance human immunodeficiency virus type 1 (HIV-1) virion production. However, the relationship between Hrs and citron kinase in HIV-1 production remains elusive. Here, we report that Hrs interacts with citron kinase via its FYVE domain. Overexpression of Hrs or the FYVE domain resulted in a significant decrease in HIV-1 virion production. Depletion of Hrs by RNA interference in HEK293T cells increased HIV-1 virion production and enhanced the activity of citron kinase. These data suggest that Hrs inhibits HIV-1 production by inhibiting citron kinase-mediated exocytosis.