Nucleosome structure: Difference between revisions

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[[es:Nucleosome structure (spanish)]]
[[es:Nucleosome structure (Spanish)]]
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<Structure load='1aoi' size='800' frame='true' align='right' caption='Nucleosoma' scene='60/602771/Proteinas/5'/>
<Structure load='1aoi' size='450' frame='true' align='right' caption='Nucleosome [[1aoi]]' scene='60/602771/Nucleosoma/3'/>
<big><big>'''Nucleosome''' is the basic structure of '''chromatin fiber'''. A nucleosome consists of a core with a '''histonic proteins octamer''' and a '''DNA''' molecule 146 bp long  wound around this core in two complete turns.
<big><big>'''Nucleosomes''' are the basic building blocks of '''chromatin fibers'''. A nucleosome consists of a core containing '''an octamer of histone proteins''' and a '''DNA''' molecule 146 bp long  wound around this core in two complete turns.
Histonic protein octamer includes four types of proteins: <scene name='60/602771/Histonah2a/1'>H2A</scene>, <scene name='60/602771/Histonah2b/1'>H2B</scene>, <scene name='60/602771/Histonah3/1'>H3</scene> y <scene name='60/602771/Histonah4/1'>H4</scene>. Histonic proteins are organized in dimers so:
The <scene name='60/602771/Proteinas/5'>histone protein octamer</scene>  includes four types of proteins: <scene name='60/602771/Histonah2a/1'>H2A</scene>, <scene name='60/602771/Histonah2b/1'>H2B</scene>, <scene name='60/602771/Histonah3/1'>H3</scene> and <scene name='60/602771/Histonah4/1'>H4</scene>. Histone proteins are organized in dimers so:


*Two H3-H4 dimers
*Two H3-H4 dimers
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*<scene name='60/602771/Octamero/1'>Whole octamer</scene>
*<scene name='60/602771/Octamero/1'>Whole octamer</scene>
*<scene name='60/602771/Nucleosoma/3'>DNA</scene> molecule wound in <scene name='60/602771/Nucleosoma/4'>two complete turns</scene> around octamer. Some<scene name='60/602771/Nucleosoma/5'>manganese ions</scene> complete the whole structure.
*<scene name='60/602771/Nucleosoma/3'>DNA</scene> molecule wound in <scene name='60/602771/Nucleosoma/4'>two complete turns</scene> around octamer. Some <scene name='60/602771/Nucleosoma/5'>manganese ions</scene> complete the whole structure.


The more widespread secondary structure in <scene name='60/602771/Octamero/2'>histonic proteins</scene> is <scene name='60/602771/Secondarystructure/1'>alfa helix</scene>.
The main secondary structure in <scene name='60/602771/Octamero/2'>histones</scene> is <scene name='60/602771/Secondarystructure/1'>alpha helices</scene>.


If we situate the different types of amino acid residues in <scene name='60/602771/Esqueleto/1'>protein skeleton</scene> we can see that <scene name='60/602771/Residuosnegativos/1'>negatively charged residues</scene> and <scene name='60/602771/Residuospositivos/1'>positively charged residues</scene> are arranged so positively  charged residues are in <scene name='60/602771/Periferia/1'>peripherycal positions</scene>, where they can stablish ionic interations with <scene name='60/602771/Interacciones/1'>phosphate groups on DNA molecule</scene>. Such electric charges distribution, gives stability to the whole structure.
If we highlight the different types of amino acid residues on the <scene name='60/602771/Esqueleto/1'>protein backbone</scene> we can see that <scene name='60/602771/Residuosnegativos/1'>negatively charged residues</scene> and <scene name='60/602771/Residuospositivos/1'>positively charged residues</scene> are arranged so positively  charged residues are in <scene name='60/602771/Periferia/1'>peripheral positions</scene>, where they can form ionic interactions ([[salt bridges]]) with <scene name='60/602771/Interacciones/1'>phosphate groups on the DNA molecule</scene>. This distribution of electric charges stabilizes the whole structure.


<small>
<small>
==See Also==
*[[Nucleosome structure (Spanish)]]
*[[Nucleosomes]]
*[[User:Eric Martz/Nucleosomes]]
== References ==
== References ==
<references/>
<references/>

Latest revision as of 19:21, 2 March 2016


Nucleosome 1aoi

Drag the structure with the mouse to rotate

Nucleosomes are the basic building blocks of chromatin fibers. A nucleosome consists of a core containing an octamer of histone proteins and a DNA molecule 146 bp long wound around this core in two complete turns. The histone protein octamer includes four types of proteins: H2A, H2B, H3 and H4. Histone proteins are organized in dimers so:

The main secondary structure in histones is alpha helices.

If we highlight the different types of amino acid residues on the protein backbone we can see that negatively charged residues and positively charged residues are arranged so positively charged residues are in peripheral positions, where they can form ionic interactions (salt bridges) with phosphate groups on the DNA molecule. This distribution of electric charges stabilizes the whole structure.

See Also

References

This page is based on 1aoi file from Proteopedia.

1aoi is a 10 chain structure with sequence from Xenopus laevis. The July 2000 RCSB PDB Molecule of the Month feature on Nucleosome by David S. Goodsell is 10.2210/rcsb_pdb/mom_2000_7. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.

Proteopedia Page Contributors and Editors (what is this?)

Alejandro Porto, Eric Martz, Michal Harel