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or chemically (Micrococcal nuclease (MNase) enzyme). The protein-DNA
complex is precipitated using antibodies produced particularly for the
desired protein. Acid treatment is employed for the release of precipitated
DNA, which is then detected by either sequencing, microarray or amplified
via polymerase chain reaction (PCR) (Park, 2009).
12.5.1.2 CHIP-SEQUENCING (CHIP-SEQ)
ChIP assay coupled with the next-generation sequencing methods is an
effective approach for locating the different sites across the whole genome
where DNA binds with transcription factors and other proteins. The use of
next-generation sequencing (NGS) on ChIP has provided useful data on gene
regulatory events involved in a variety of biological processes. ChIP-Seq
may be utilized for global mapping of protein-DNA interacting regions
genome-wide. Unlike arrays and other epigenome-related methods, which
are biased by the use of probes produced from known sequences, ChIP-Seq
does not require any previous information. ChIP-Seq uses massively parallel
sequencing to do genome-wide profiling, yielding millions of counts across
many samples enabling a cost-effective, precise, and impartial examination
of epigenetic profile (Park, 2009).
12.5.1.3 CHIP PCR
In this protocol analysis of protein-bound DNA sequences are immuno
precipitated then the DNA fragments are detected and/or quantified in
ChIP-PCR with specific primers using TaqMan or Sybr Green Technologies.
In this technique, histone modifications and/or protein binding to a known
selected of desired loci in the genome are investigated using PCR. ChIP
qPCR allows rapid and quantitative comparisons of a particular area within
the genome across numerous samples. This approach is less expensive and
faster than whole-genome sequencing.
12.5.1.4 CHIP MICROARRAY (CHIP-CHIP)
ChIP microarray (ChIP-Chip), or genome-wide mapping, integrates chro
matin immunoprecipitation (ChIP) with DNA microarray for discovering
cellular protein-DNA associations. The antibody pulled down DNA is labeled