Difference between revisions of "KSH 0610 Epigenomics"

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imported>Seung-hoon Kim
(Created page with "<p><span style="font-size:18px"><strong> Epigenomics - Epi(Outside) + Genomics(The study of genome, especially function and structure analysis)</strong></span></p> <ul> <l...")
 
imported>Seung-hoon Kim
 
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<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ex) It could affect Tumorigenesis</p>
 
<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ex) It could affect Tumorigenesis</p>
  
<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ex) DNA imprinting </p>
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<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ex) DNA imprinting - Parent generations put tags to next generation&nbsp;using DNA&nbsp;methylation</p>
  
 
<ul>
 
<ul>
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</ol>
 
</ol>
  
<p>&nbsp;</p>
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<ul>
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<li>How do we study epigenomics and DNA methylation?</li>
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</ul>
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<ol>
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<li>Bisulfite treatment on DNA - Treatment of DNA with bisulfite converts Cytosine to Uracil. It cannot convert methylcytosine.</li>
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<li>Sequencing</li>
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</ol>
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<ul>
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<li>Protein - Switch - On and off - Energy(ATP, GTP, etc.) makes switching(acetylation, phosphorylation etc.)</li>
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<li>To detect protein structure</li>
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</ul>
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 +
<ol>
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<li>X-ray crystallography</li>
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<li>Nuclear Magnetic Resonance</li>
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<li>Cryoelectron microscopy</li>
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<li>Microscope</li>
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<li>Sequence</li>
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<li>Mass spectroscopy</li>
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</ol>
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 +
<ul>
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<li>Protein secondary structure - the primary polypeptide chain (sequence of specific amino acid) gets properly foled in the form of</li>
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</ul>
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 +
<ol>
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<li>alpha helix - scaffold</li>
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<li>beta sheet - scaffold</li>
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<li>coil (randomly coiled, irregular) - for binding to attack something Ex) Venom, Immunoglobulin (antibody) antigen binding site</li>
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</ol>
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 +
<ul>
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<li>&nbsp;Interaction proteomics - using chips, microarray</li>
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</ul>

Latest revision as of 16:57, 10 June 2016

 Epigenomics - Epi(Outside) + Genomics(The study of genome, especially function and structure analysis)

  • The study of the complete set of epigenetic modifications on the genetic material of a cell
  • Epigenetic modification
  1. DNA methylation by DNMT (DNA methyltransferase)
  2. Histone modification - acetylation, methylation, phosphorylation and so on
  • Epigenetic modifications play an important role in gene expression and regulation

         Ex) It could affect Tumorigenesis

         Ex) DNA imprinting - Parent generations put tags to next generation using DNA methylation

  • The effects of chromatin structure on the function of the included genes
  • Chromatin structure
  1. Euchromatin - a lightly packed form of chromatin. It is often under active transcription state.
  2. Heterochromatin - a tightly packed form of chromatin - inaccessible to polymerase and not transcribed
  3. Nucleosome - a basic unit of DNA packing in eukaryotes, consisting of 8 histone proteins and a segment of DNA (around 147bp)
  • How do we study epigenomics and DNA methylation?
  1. Bisulfite treatment on DNA - Treatment of DNA with bisulfite converts Cytosine to Uracil. It cannot convert methylcytosine.
  2. Sequencing
  • Protein - Switch - On and off - Energy(ATP, GTP, etc.) makes switching(acetylation, phosphorylation etc.)
  • To detect protein structure
  1. X-ray crystallography
  2. Nuclear Magnetic Resonance
  3. Cryoelectron microscopy
  4. Microscope
  5. Sequence
  6. Mass spectroscopy
  • Protein secondary structure - the primary polypeptide chain (sequence of specific amino acid) gets properly foled in the form of
  1. alpha helix - scaffold
  2. beta sheet - scaffold
  3. coil (randomly coiled, irregular) - for binding to attack something Ex) Venom, Immunoglobulin (antibody) antigen binding site
  •  Interaction proteomics - using chips, microarray