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ChIP-Seq:

ChIP-Seq combines chromatin immunoprecipitation with DNA sequencing, to obtain the DNA sequences which are able to interact with the immunoprecipitated proteins. This is very useful to identify transcription factors and nucleosome-associated sequences. Workflow is very simple: first, the cells need to be treated with formaldehyde, to create cross-link between the proteins and the DNA. Then, cells have to be lysed, DNA is extracted and fragmented with sonication; an antibody against the protein of interest is added. Precipitation could be achieved via beads associated to A/G proteins and centrifugation. Subsequently the pellet needs to be eluted and treated with high ionic force or high temperature, to resolve the cross-links and dissociate DNA fragments from the protein of interest. DNA has to be purified from contaminants (RNA and proteins). Finally, adapters have to be added at the ends of the fragments: ends must be blunted to allow ligase reaction between the fragments and the adapters. Specific primers for PCR phase (able to recognize these adapters) will be used to amplify and sequence each fragments. Also, a library can be created.

(Samuele Irudal)

ATAC-Seq

DNase-seq

DNase-seq (DNase I hypersensitive sites sequencing) is a technique used to identify the location of cis-regulatory regions (eg promoters, enhancers, silencers) in the genome. These regulatory areas are nucleosome-free and, therefore, are accessible and sensitive to DNase I. DNase I is an E. coli’s endonuclease which only shows specificity for DNA regions not wrapped on histones, independently from the nucleotidic composition.

Briefly, cells are lysed, chromatin in extracted and DNase I digestion occur. Then the solution is deproteinized so only DNA fragments are cleaved by restriction enzymes. The remaining fragments are now separated on electrophoresis gel. In the classical DNase hypersensitivity assay the following step is Southern blot with very ends probes; on the contrary, in DNase-seq it is necessary to amplify cleavage products by PCR and prepare a library for high-throughput next generation sequencing. NGS will give the precise nucleotidic sequence of nucleosome-depleted DNA regions, which are the regulatory ones.

FAIRE-seq is a DNA-seq successor.

(Giada Cipollina)

FAIRE

Nucleosome positioning

Different assay can bu used to assess nucleosoe positioning, but two can be the more relevant: one is an in tube assay, the other is an in vivo one. Both are single locus analysis, so the focus will be only one one gene.

• In the first, DNA associated to nucleosomes have to be extracted; then, nucleosomes are dissociated from the main sequence. After a fixed time, a specific RE is used to cut a restriction site in our gene of reference; the samples are then separeted on gel-electrophoresis and cut is spotted via Southern-blot, using a probe against our gene. Different output can be observed, according to the new position taken by the nucleosomes: if the nucleosomes covered the RE site, one high band will be observed; if nuclesomes moved on the sequence, different bands with different MW will be observed. Nucleosomes positioning can be forced to change adding Tfs to the tube, causing (e.g.) the coverage of the RE site. Fig. 1 show the point of the assay. (I'm not pretty confident about this description, so help is welcome!)

• The second assay involves the use of Micrococcus Nuclease (MNase 1). First, nuclei are extracted from the cell colture and then treatment with MNase 1 occurs. This enzyme is an endonuclease, able to cut in the middle of the sequence and to digest DNA until an obstacle is encountered (e.g.: nucleosome associated to DNA). After this passage, the samples are deproteinized and RE treatment is followed: this will grant a point of reference for MW misuration in the next passage. Subsequently, separation on gel-electrophoresis is executed with a following Southern blot analysis. Being a single locus analysis, a probe against a specific gene is used. Different output can be observed: if in a sample nucleosome positioning is random, many bands will be shown according to the different length of the fragments (Fig.2a). If nucleosomes positioning in the sample is ordered, bands number will be indeed fixed and and lower (Fig.2b).

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