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The fragile X mental retardation protein, FMRP, recognizes G‐quartets

 

作者: Jennifer C. Darnell,   Stephen T. Warren,   Robert B. Darnell,  

 

期刊: Mental Retardation and Developmental Disabilities Research Reviews  (WILEY Available online 2004)
卷期: Volume 10, issue 1  

页码: 49-52

 

ISSN:1080-4013

 

年代: 2004

 

DOI:10.1002/mrdd.20008

 

出版商: Wiley Subscription Services, Inc., A Wiley Company

 

关键词: fragile X mental retardation protein (FMRP);RNA binding protein;intramolecular G‐quartet;in vitro RNA selection;translational control

 

数据来源: WILEY

 

摘要:

AbstractFragile X mental retardation is a disease caused by the loss of function of a single RNA‐binding protein, FMRP. Identifying the RNA targets recognized by FMRP is likely to reveal much about its functions in controlling some aspects of memory and behavior. Recent evidence suggests that one of the predominant RNA motifs recognized by the FMRP protein is an intramolecular G‐quartet and that the RGG box of FMRP mediates this interaction. Searching databases of mRNA sequence information, as well as compiled sequences of predicted FMRP targets based on biochemical identification, has revealed that many of these predicted FMRP targets contain intramolecular G‐quartets. Interestingly, many of the G‐quartet containing RNA targets encode proteins involved in neuronal development and synaptic function. Defects in the metabolism of this set of RNAs, presumably in the translation of their protein products, is likely to underlie the behavioral and cognitive changes seen in the disease. MRDD Research Reviews 2004;10:49–52. © 2004 Wiley

 

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