Javascript must be enabled to continue!
An improved ChEC-seq method for mapping the genome-wide binding of S. cerevisiae transcription factors v2
View through CrossRef
ChEC-seq and other nuclease-based methods such as Cut&Run map protein locations on DNA by targeting nuclease activity to specific transcription factors and mapping the resulting DNA cleavages (Schmid et al. 2004; Skene and Henikoff 2017; Zentner et al. 2015). For ChEC-seq, yeast cells expressing a protein-micrococcal nuclease (MNase) fusion are permeabilized, MNase is activated by the addition of calcium, and the resulting DNA fragments are mapped. Potential advantages of this approach include avoiding non-specific protein-DNA crosslinking in highly transcribed regions, efficient mapping of factors that do not directly bind DNA and, more sensitive detection of protein-DNA interactions. We optimized the original ChEC-seq protocol to minimize non-specific DNA cleavage, avoid over digestion at authentic binding sites, and efficiently assay large numbers of factors. We also created a robust data analysis pipeline that incorporates peak calling to map binding sites and quantitative analysis, based on utilization of spike-in DNA, to compare factor-DNA binding under different conditions. We used this modified approach to map genome-wide distributions of the transcription coactivators TFIID and SAGA (Donczew et al. 2020) as well as transcription factors Abf1 and Rap1 (Donczew et al, submitted to Mol Cell). References Donczew R, Warfield L, Pacheco D, Erijman A, Hahn S. 2020. Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA.eLife 9: e50109. Schmid M, Durussel T, Laemmli UK. 2004. ChIC and ChEC; genomic mapping of chromatin proteins.Mol Cell 16: 147–157. Skene PJ, Henikoff S. 2017. An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sites.eLife 6: e21856. Warfield L, Ramachandran S, Baptista T, Devys D, Tora L, Hahn S. 2017. Transcription of nearly all yeast RNA Polymerase II-transcribed genes is dependent on transcription factor TFIID.Mol Cell. 68:118-129 Zentner GE, Kasinathan S, Xin B, Rohs R, Henikoff S. 2015. ChEC-seq kinetics discriminates transcription factor binding sites by DNA sequence and shape in vivo.Nat Commun 6: 8733.
Title: An improved ChEC-seq method for mapping the genome-wide binding of S. cerevisiae transcription factors v2
Description:
ChEC-seq and other nuclease-based methods such as Cut&Run map protein locations on DNA by targeting nuclease activity to specific transcription factors and mapping the resulting DNA cleavages (Schmid et al.
2004; Skene and Henikoff 2017; Zentner et al.
2015).
For ChEC-seq, yeast cells expressing a protein-micrococcal nuclease (MNase) fusion are permeabilized, MNase is activated by the addition of calcium, and the resulting DNA fragments are mapped.
Potential advantages of this approach include avoiding non-specific protein-DNA crosslinking in highly transcribed regions, efficient mapping of factors that do not directly bind DNA and, more sensitive detection of protein-DNA interactions.
We optimized the original ChEC-seq protocol to minimize non-specific DNA cleavage, avoid over digestion at authentic binding sites, and efficiently assay large numbers of factors.
We also created a robust data analysis pipeline that incorporates peak calling to map binding sites and quantitative analysis, based on utilization of spike-in DNA, to compare factor-DNA binding under different conditions.
We used this modified approach to map genome-wide distributions of the transcription coactivators TFIID and SAGA (Donczew et al.
2020) as well as transcription factors Abf1 and Rap1 (Donczew et al, submitted to Mol Cell).
References Donczew R, Warfield L, Pacheco D, Erijman A, Hahn S.
2020.
Two roles for the yeast transcription coactivator SAGA and a set of genes redundantly regulated by TFIID and SAGA.
eLife 9: e50109.
Schmid M, Durussel T, Laemmli UK.
2004.
ChIC and ChEC; genomic mapping of chromatin proteins.
Mol Cell 16: 147–157.
Skene PJ, Henikoff S.
2017.
An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sites.
eLife 6: e21856.
Warfield L, Ramachandran S, Baptista T, Devys D, Tora L, Hahn S.
2017.
Transcription of nearly all yeast RNA Polymerase II-transcribed genes is dependent on transcription factor TFIID.
Mol Cell.
68:118-129 Zentner GE, Kasinathan S, Xin B, Rohs R, Henikoff S.
2015.
ChEC-seq kinetics discriminates transcription factor binding sites by DNA sequence and shape in vivo.
Nat Commun 6: 8733.
Related Results
An improved ChEC-seq method for mapping the genome-wide binding of S. cerevisiae transcription factors v3
An improved ChEC-seq method for mapping the genome-wide binding of S. cerevisiae transcription factors v3
ChEC-seq and other nuclease-based methods such as Cut&Run map protein locations on DNA by targeting nuclease activity to specific transcription factors and mapping the resultin...
High resolution genome-wide occupancy in
Candida spp
. using ChEC-seq
High resolution genome-wide occupancy in
Candida spp
. using ChEC-seq
Abstract
To persist in their hostile and dynamic human host environments, fungal pathogens has to sense and adapt by modulating their gene expres...
ChEC-seq2: an improved Chromatin Endogenous Cleavage sequencing method and bioinformatic analysis pipeline for mapping
in vivo
protein-DNA interactions
ChEC-seq2: an improved Chromatin Endogenous Cleavage sequencing method and bioinformatic analysis pipeline for mapping
in vivo
protein-DNA interactions
Abstract
Defining the
in vivo
DNA binding specificity of transcription factors (TFs) has relied nearly exclus...
Chromatin Endogenous Cleavage and high-throughput sequencing (ChEC-seq) inS. cerevisiae v1
Chromatin Endogenous Cleavage and high-throughput sequencing (ChEC-seq) inS. cerevisiae v1
Genome-wide mapping of protein-DNA interactions is critical for understanding gene regulation, chromatin remodeling, and other chromatin-resident processes. Formaldehyde crosslinki...
Chromatin endogenous cleavage provides a global view of RNA polymerase II transcription kinetics
Chromatin endogenous cleavage provides a global view of RNA polymerase II transcription kinetics
Abstract
Chromatin immunoprecipitation (ChIP-seq) is the most common approach to observe global binding of proteins to DNA in vivo. The occupancy of transcription f...
Chromatin endogenous cleavage provides a global view of yeast RNA polymerase II transcription kinetics
Chromatin endogenous cleavage provides a global view of yeast RNA polymerase II transcription kinetics
Abstract
Chromatin immunoprecipitation (ChIP-seq) is the most common approach to observe global binding of proteins to DNA in vivo. The occupancy of transcription f...
Chromatin endogenous cleavage provides a global view of yeast RNA polymerase II transcription kinetics
Chromatin endogenous cleavage provides a global view of yeast RNA polymerase II transcription kinetics
Chromatin immunoprecipitation (ChIP-seq) is the most common approach to observe global binding of proteins to DNA in vivo. The occupancy of transcription factors (TFs) from ChIP-se...
Budding yeast ChEC v1
Budding yeast ChEC v1
Genome-wide mapping of protein-DNA interactions is critical for understanding gene regulation, chromatin remodeling, and other chromatin-resident processes. Formaldehyde crosslinki...

