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    A novel family of repeat sequences in the mouse genome responsive to retinoic acid.
        
        Mamm. Genome 7, 741-748 (1996)
    
    
    
	    Repetitive DNA sequences form a substantial portion of eukaryotic genomes and exist as members of families that differ in copy number, length, and sequence. Various functions, including chromosomal integrity, gene regulation, and gene rearrangement have been ascribed to repetitive DNA. Although there is evidence that some repetitive sequences may participate in gene regulation, little is known about how their own expression may be regulated. During the course of gene trapping experiments with embryonic stem (ES) cells, we identified a novel class of expressed repetitive sequences in the mouse, using 5' rapid amplification of cDNA ends-polymerase chain reaction (5' RACE-PCR) to clone fusion transcripts from these lines. The expression of these repeats was induced by retinoic acid (RA) in cultured ES cells examined by Northern blot analyses. In vivo, their expression was spatially restricted in embryos and in the adult brain as determined by RNA in situ hybridization. We designated this family of sequences as Dr (developmentally regulated) repeats. The members of the Dr family, identified by cDNA cloning and through database search, are highly similar in sequence and show peculiar structural features. Our results suggest the expression of Dr-containing transcripts may be part of an ES cell differentiation program triggered by RA.
	
	
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        Publication type
        Article: Journal article
    
 
    
        Document type
        Scientific Article
    
 
     
    
     
     
    
    
        Language
        english
    
 
    
        Publication Year
        1996
    
 
     
    
        HGF-reported in Year
        0
    
 
    
    
        ISSN (print) / ISBN
        0938-8990
    
 
    
        e-ISSN
        1432-1777
    
 
    
     
     
	     
	 
	 
    
        Journal
        Mammalian Genome
    
 
	
    
        Quellenangaben
        
	    Volume: 7,  
	    Issue: 10,  
	    Pages: 741-748 
	    
	    
	
    
 
    
         
        
            Publisher
            Springer
        
 
         
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Reviewing status
        Peer reviewed
    
 
    
        Institute(s)
        Institute of Developmental Genetics (IDG)
    
 
     
     
     
     
     	
    
        PubMed ID
        8854861
    
    
        Erfassungsdatum
        1996-12-31