Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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ChIP-Seq of six Drosophila species with anti-Drosophila melanogaster Twist and anti-Snail antibodies using different library fragment sizes


ABSTRACT: The binding patterns of some transcription factors have been shown to diverge substantially between closely related species. Here, we show that the binding pattern of the developmental transcription factor Twist is highly conserved across six Drosophila species, revealing strong functional constraints at developmental enhancers. Conserved binding correlates with sequence motifs for Twist and its partners, permitting the de novo discovery of their cooperative binding. It also includes over 10,000 low-occupancy sites near the detection limit, which tend to mark enhancers of later developmental stages. We predict that conservation, dynamic occupancy, and combinatorial regulation will be generally true for developmental enhancers.

ORGANISM(S): Drosophila ananassae

SUBMITTER: Ariel Paulson 

PROVIDER: E-MTAB-376 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Identification of transcription factor binding sites from ChIP-seq data at high resolution.

Bardet Anaïs F AF   Steinmann Jonas J   Bafna Sangeeta S   Knoblich Juergen A JA   Zeitlinger Julia J   Stark Alexander A  

Bioinformatics (Oxford, England) 20130824 21


<h4>Motivation</h4>Chromatin immunoprecipitation coupled to next-generation sequencing (ChIP-seq) is widely used to study the in vivo binding sites of transcription factors (TFs) and their regulatory targets. Recent improvements to ChIP-seq, such as increased resolution, promise deeper insights into transcriptional regulation, yet require novel computational tools to fully leverage their advantages.<h4>Results</h4>To this aim, we have developed peakzilla, which can identify closely spaced TF bin  ...[more]

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