1ei2

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(New page: 200px<br /><applet load="1ei2" size="450" color="white" frame="true" align="right" spinBox="true" caption="1ei2" /> '''STRUCTURAL BASIS FOR RECOGNITION OF THE RNA ...)
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[[Image:1ei2.gif|left|200px]]<br /><applet load="1ei2" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1ei2.gif|left|200px]]<br /><applet load="1ei2" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1ei2" />
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'''STRUCTURAL BASIS FOR RECOGNITION OF THE RNA MAJOR GROOVE IN THE TAU EXON 10 SPLICING REGULATORY ELEMENT BY AMINOGLYCOSIDE ANTIBIOTICS'''<br />
'''STRUCTURAL BASIS FOR RECOGNITION OF THE RNA MAJOR GROOVE IN THE TAU EXON 10 SPLICING REGULATORY ELEMENT BY AMINOGLYCOSIDE ANTIBIOTICS'''<br />
==Overview==
==Overview==
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Drug-like molecules that bind RNA with sequence selectivity would provide, valuable tools to elucidate gene expression pathways and new avenues to, the treatment of degenerative and chronic conditions. Efforts at, discovering such agents have been hampered, until recently, by the limited, knowledge of RNA recognition principles. Several recent structures of, aminoglycoside-RNA complexes have begun to reveal the structural basis for, RNA-drug recognition. However, the absence of suitable chemical scaffolds, known to bind the RNA major groove, where specificity could be provided by, the diversity of functional groups exposed on the RNA bases, has, represented a major obstacle. Here we report an investigation of the, structural basis for recognition of an RNA stem-loop by neomycin, a, naturally occurring aminoglycoside antibiotic. We found that neomycin, binds the RNA stem-loop that regulates alternative splicing of exon 10, within the gene coding for human tau protein. Mutations within this, splicing regulatory element destabilise the RNA structure and cause, frontotemporal dementia and Parkinsonism linked to chromosome 17, (FTDP-17), an autosomal dominant condition leading to neurodegeneration, and death. The three-dimensional structure of the RNA-neomycin complex, shows interaction of the drug in the major groove of the short RNA duplex, where familial mutations cluster. Analysis of the structure shows how, aminoglycosides and related drugs bind to the RNA major groove, adding to, our understanding of the principles of drug-RNA recognition.
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Drug-like molecules that bind RNA with sequence selectivity would provide valuable tools to elucidate gene expression pathways and new avenues to the treatment of degenerative and chronic conditions. Efforts at discovering such agents have been hampered, until recently, by the limited knowledge of RNA recognition principles. Several recent structures of aminoglycoside-RNA complexes have begun to reveal the structural basis for RNA-drug recognition. However, the absence of suitable chemical scaffolds known to bind the RNA major groove, where specificity could be provided by the diversity of functional groups exposed on the RNA bases, has represented a major obstacle. Here we report an investigation of the structural basis for recognition of an RNA stem-loop by neomycin, a naturally occurring aminoglycoside antibiotic. We found that neomycin binds the RNA stem-loop that regulates alternative splicing of exon 10 within the gene coding for human tau protein. Mutations within this splicing regulatory element destabilise the RNA structure and cause frontotemporal dementia and Parkinsonism linked to chromosome 17 (FTDP-17), an autosomal dominant condition leading to neurodegeneration and death. The three-dimensional structure of the RNA-neomycin complex shows interaction of the drug in the major groove of the short RNA duplex, where familial mutations cluster. Analysis of the structure shows how aminoglycosides and related drugs bind to the RNA major groove, adding to our understanding of the principles of drug-RNA recognition.
==About this Structure==
==About this Structure==
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1EI2 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with NMY as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1EI2 OCA].
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1EI2 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with <scene name='pdbligand=NMY:'>NMY</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1EI2 OCA].
==Reference==
==Reference==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Goedert, M]]
[[Category: Goedert, M]]
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[[Category: Spillantini, M.G.]]
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[[Category: Spillantini, M G.]]
[[Category: Varani, G.]]
[[Category: Varani, G.]]
[[Category: Varani, L.]]
[[Category: Varani, L.]]
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[[Category: tau]]
[[Category: tau]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sat Nov 24 22:19:08 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:27:58 2008''

Revision as of 10:28, 21 February 2008


1ei2

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STRUCTURAL BASIS FOR RECOGNITION OF THE RNA MAJOR GROOVE IN THE TAU EXON 10 SPLICING REGULATORY ELEMENT BY AMINOGLYCOSIDE ANTIBIOTICS

Overview

Drug-like molecules that bind RNA with sequence selectivity would provide valuable tools to elucidate gene expression pathways and new avenues to the treatment of degenerative and chronic conditions. Efforts at discovering such agents have been hampered, until recently, by the limited knowledge of RNA recognition principles. Several recent structures of aminoglycoside-RNA complexes have begun to reveal the structural basis for RNA-drug recognition. However, the absence of suitable chemical scaffolds known to bind the RNA major groove, where specificity could be provided by the diversity of functional groups exposed on the RNA bases, has represented a major obstacle. Here we report an investigation of the structural basis for recognition of an RNA stem-loop by neomycin, a naturally occurring aminoglycoside antibiotic. We found that neomycin binds the RNA stem-loop that regulates alternative splicing of exon 10 within the gene coding for human tau protein. Mutations within this splicing regulatory element destabilise the RNA structure and cause frontotemporal dementia and Parkinsonism linked to chromosome 17 (FTDP-17), an autosomal dominant condition leading to neurodegeneration and death. The three-dimensional structure of the RNA-neomycin complex shows interaction of the drug in the major groove of the short RNA duplex, where familial mutations cluster. Analysis of the structure shows how aminoglycosides and related drugs bind to the RNA major groove, adding to our understanding of the principles of drug-RNA recognition.

About this Structure

1EI2 is a Protein complex structure of sequences from [1] with as ligand. Full crystallographic information is available from OCA.

Reference

Structural basis for recognition of the RNA major groove in the tau exon 10 splicing regulatory element by aminoglycoside antibiotics., Varani L, Spillantini MG, Goedert M, Varani G, Nucleic Acids Res. 2000 Feb 1;28(3):710-9. PMID:10637322

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