1pdq: Difference between revisions

New page: left|200px<br /> <applet load="1pdq" size="450" color="white" frame="true" align="right" spinBox="true" caption="1pdq, resolution 1.76Å" /> '''Polycomb chromodoma...
 
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[[Image:1pdq.gif|left|200px]]<br />
[[Image:1pdq.gif|left|200px]]<br /><applet load="1pdq" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1pdq" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1pdq, resolution 1.76&Aring;" />
caption="1pdq, resolution 1.76&Aring;" />
'''Polycomb chromodomain complexed with the histone H3 tail containing trimethyllysine 27.'''<br />
'''Polycomb chromodomain complexed with the histone H3 tail containing trimethyllysine 27.'''<br />


==Overview==
==Overview==
On the histone H3 tail, Lys 9 and Lys 27 are both methylation sites, associated with epigenetic repression, and reside within a highly related, sequence motif ARKS. Here we show that the chromodomain proteins Polycomb, (Pc) and HP1 (heterochromatin protein 1) are highly discriminatory for, binding to these sites in vivo and in vitro. In Drosophila S2 cells, and, on polytene chromosomes, methyl-Lys 27 and Pc are both excluded from areas, that are enriched in methyl-Lys 9 and HP1. Swapping of the chromodomain, regions of Pc and HP1 is sufficient for switching the nuclear localization, patterns of these factors, indicating a role for their chromodomains in, both target site binding and discrimination. To better understand the, molecular basis for the selection of methyl-lysine binding sites, we, solved the 1.8 A structure of the Pc chromodomain in complex with a H3, peptide bearing trimethyl-Lys 27, and compared it with our previously, determined structure of the HP1 chromodomain in complex with a H3 peptide, bearing trimethyl-Lys 9. The Pc chromodomain distinguishes its methylation, target on the H3 tail via an extended recognition groove that binds five, additional residues preceding the ARKS motif.
On the histone H3 tail, Lys 9 and Lys 27 are both methylation sites associated with epigenetic repression, and reside within a highly related sequence motif ARKS. Here we show that the chromodomain proteins Polycomb (Pc) and HP1 (heterochromatin protein 1) are highly discriminatory for binding to these sites in vivo and in vitro. In Drosophila S2 cells, and on polytene chromosomes, methyl-Lys 27 and Pc are both excluded from areas that are enriched in methyl-Lys 9 and HP1. Swapping of the chromodomain regions of Pc and HP1 is sufficient for switching the nuclear localization patterns of these factors, indicating a role for their chromodomains in both target site binding and discrimination. To better understand the molecular basis for the selection of methyl-lysine binding sites, we solved the 1.8 A structure of the Pc chromodomain in complex with a H3 peptide bearing trimethyl-Lys 27, and compared it with our previously determined structure of the HP1 chromodomain in complex with a H3 peptide bearing trimethyl-Lys 9. The Pc chromodomain distinguishes its methylation target on the H3 tail via an extended recognition groove that binds five additional residues preceding the ARKS motif.


==About this Structure==
==About this Structure==
1PDQ is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Drosophila_melanogaster Drosophila melanogaster]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1PDQ OCA].  
1PDQ is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Drosophila_melanogaster Drosophila melanogaster]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PDQ OCA].  


==Reference==
==Reference==
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[[Category: Drosophila melanogaster]]
[[Category: Drosophila melanogaster]]
[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Allis, C.D.]]
[[Category: Allis, C D.]]
[[Category: Fischle, W.]]
[[Category: Fischle, W.]]
[[Category: Jacobs, S.A.]]
[[Category: Jacobs, S A.]]
[[Category: Khorasanizadeh, S.]]
[[Category: Khorasanizadeh, S.]]
[[Category: Kim, Y.]]
[[Category: Kim, Y.]]
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[[Category: trimethyllysine]]
[[Category: trimethyllysine]]


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