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In cellulo DNA analysis (LMPCR footprinting).
- Source :
-
Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2009; Vol. 543, pp. 293-336. - Publication Year :
- 2009
-
Abstract
- The in cellulo analysis of DNA protein interactions and chromatin structure is very important to better understand the mechanisms involved in the regulation of gene expression. The nuclease-hypersensitive sites and sequences bound by transcription factors often correspond to genetic regulatory elements. Using the Ligation-mediated polymerase chain reaction (LMPCR) technology, it is possible to precisely analyze these DNA sequences to demonstrate the existence of DNA-protein interactions or unusual DNA structures directly in living cells. Indeed, the ideal chromatin substrate is, of course, found inside intact cells. LMPCR, a genomic-sequencing, technique that map DNA single-strand breaks at the sequence level of resolution, is the method of choice for in cellulo footprinting and DNA structure studies because it can be used to investigate any complex genomes, including human. The detailed conventional and automated LMPCR protocols are presented in this chapter.
- Subjects :
- Base Sequence
Cell Survival drug effects
Cell Survival radiation effects
DNA analysis
DNA Breaks, Single-Stranded drug effects
DNA Breaks, Single-Stranded radiation effects
DNA Methylation drug effects
DNA Methylation radiation effects
Deoxyribonuclease I metabolism
Molecular Sequence Data
Protein Binding
Pyrimidine Dimers
Sequence Analysis, DNA
Sulfuric Acid Esters pharmacology
Templates, Genetic
Ultraviolet Rays
Chromatin genetics
Chromatin metabolism
DNA genetics
DNA metabolism
DNA Footprinting methods
Polymerase Chain Reaction
Subjects
Details
- Language :
- English
- ISSN :
- 1064-3745
- Volume :
- 543
- Database :
- MEDLINE
- Journal :
- Methods in molecular biology (Clifton, N.J.)
- Publication Type :
- Academic Journal
- Accession number :
- 19378174
- Full Text :
- https://doi.org/10.1007/978-1-60327-015-1_20