TLS Online TPP Program

#Id: 6891


The Xist transcript is regulated in a negative manner by Tsix, its antisense partner.



#Unit 3. Fundamental Processes #Chromatin Remodelling & Epigenetics #Part B Pointers
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TLS Online TPP Program

#Id: 2766

#Unit 13. Methods in Biology

DNase footprinting relies on the fact that a protein, by binding to DNA, covers the binding site and so protects it from attack by DNase. 






TLS Online TPP Program

#Id: 2767

#Unit 13. Methods in Biology

We perform DNase footprinting by binding the protein to its DNA target, then digesting the DNA–protein complex with DNase. 

When we electrophorese the resulting DNA fragments, the protein binding site shows up as a gap, or “footprint,” in the pattern where the protein protected the 

DNA from degradation.


TLS Online TPP Program

#Id: 2768

#Unit 13. Methods in Biology

Footprinting is a means of finding the target DNA sequence, or binding site, of a DNA-binding protein.






TLS Online TPP Program

#Id: 2769

#Unit 13. Methods in Biology

DNase footprinting gives a good idea of the location of the binding site for the protein, but DNase is a macromolecule and is therefore a rather blunt instrument for probing the fine details of the binding site.


TLS Online TPP Program

#Id: 2770

#Unit 13. Methods in Biology

DNA-binding proteins frequently perturb the DNA within the binding region, distorting the double helix. These perturbations are interesting, but are not generally detected by DNase footprinting because the protein keeps the DNase away.



TLS Online TPP Program

#Id: 2771

#Unit 13. Methods in Biology

More detailed footprinting requires a smaller molecule that can

fit into the nooks and crannies of the DNA–protein complex and reveal more of the subtleties of the interaction. A favorite tool for this job is the methylating agent dimethyl sulfate (DMS).