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> Ex) It could affect Tumorigenesis</p> | <p> Ex) It could affect Tumorigenesis</p> | ||
− | <p> Ex) DNA imprinting </p> | + | <p> Ex) DNA imprinting - Parent generations put tags to next generation using DNA methylation</p> |
<ul> | <ul> | ||
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</ol> | </ol> | ||
− | < | + | <ul> |
+ | <li>How do we study epigenomics and DNA methylation?</li> | ||
+ | </ul> | ||
+ | |||
+ | <ol> | ||
+ | <li>Bisulfite treatment on DNA - Treatment of DNA with bisulfite converts Cytosine to Uracil. It cannot convert methylcytosine.</li> | ||
+ | <li>Sequencing</li> | ||
+ | </ol> | ||
+ | |||
+ | <ul> | ||
+ | <li>Protein - Switch - On and off - Energy(ATP, GTP, etc.) makes switching(acetylation, phosphorylation etc.)</li> | ||
+ | <li>To detect protein structure</li> | ||
+ | </ul> | ||
+ | |||
+ | <ol> | ||
+ | <li>X-ray crystallography</li> | ||
+ | <li>Nuclear Magnetic Resonance</li> | ||
+ | <li>Cryoelectron microscopy</li> | ||
+ | <li>Microscope</li> | ||
+ | <li>Sequence</li> | ||
+ | <li>Mass spectroscopy</li> | ||
+ | </ol> | ||
+ | |||
+ | <ul> | ||
+ | <li>Protein secondary structure - the primary polypeptide chain (sequence of specific amino acid) gets properly foled in the form of</li> | ||
+ | </ul> | ||
+ | |||
+ | <ol> | ||
+ | <li>alpha helix - scaffold</li> | ||
+ | <li>beta sheet - scaffold</li> | ||
+ | <li>coil (randomly coiled, irregular) - for binding to attack something Ex) Venom, Immunoglobulin (antibody) antigen binding site</li> | ||
+ | </ol> | ||
+ | |||
+ | <ul> | ||
+ | <li> Interaction proteomics - using chips, microarray</li> | ||
+ | </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
- DNA methylation by DNMT (DNA methyltransferase)
- 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
- Euchromatin - a lightly packed form of chromatin. It is often under active transcription state.
- Heterochromatin - a tightly packed form of chromatin - inaccessible to polymerase and not transcribed
- 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?
- Bisulfite treatment on DNA - Treatment of DNA with bisulfite converts Cytosine to Uracil. It cannot convert methylcytosine.
- Sequencing
- Protein - Switch - On and off - Energy(ATP, GTP, etc.) makes switching(acetylation, phosphorylation etc.)
- To detect protein structure
- X-ray crystallography
- Nuclear Magnetic Resonance
- Cryoelectron microscopy
- Microscope
- Sequence
- Mass spectroscopy
- Protein secondary structure - the primary polypeptide chain (sequence of specific amino acid) gets properly foled in the form of
- alpha helix - scaffold
- beta sheet - scaffold
- coil (randomly coiled, irregular) - for binding to attack something Ex) Venom, Immunoglobulin (antibody) antigen binding site
- Interaction proteomics - using chips, microarray