Abstract

Chromosome conformation capture (3C) is a biochemical technology to analyse contact frequencies between selected genomic sites in a cell population. Its recent genomic variants, e.g. Hi-C/ chromatin interaction analysis by paired-end tag (ChIA-PET), have enabled the study of nuclear organization at an unprecedented level. However, due to the inherent low resolution and ultrahigh cost of Hi-C/ChIA-PET, 3C is still the gold standard for determining interactions between given regulatory DNA elements, such as enhancers and promoters. Therefore, we developed a database of 3C determined functional chromatin interactions (3CDB; http://3cdb.big.ac.cn). To construct 3CDB, we searched PubMed and Google Scholar with carefully designed keyword combinations and retrieved more than 5000 articles from which we manually extracted 3319 interactions in 17 species. Moreover, we proposed a systematic evaluation scheme for data reliability and classified the interactions into four categories. Contact frequencies are not directly comparable as a result of various modified 3C protocols employed among laboratories. Our evaluation scheme provides a plausible solution to this long-standing problem in the field. A user-friendly web interface was designed to assist quick searches in 3CDB. We believe that 3CDB will provide fundamental information for experimental design and phylogenetic analysis, as well as bridge the gap between molecular and systems biologists who must now contend with noisy high-throughput data.Database URL: http://3cdb.big.ac.cn

Highlights

  • Gene expression in eukaryotes is tightly regulated by both cis- and trans-regulatory elements [1]

  • The data generated from genome-wide, high-throughput variations of 3C, i.e. Hi-C [9] and chromatin interaction analysis by paired-end tag (ChIA-PET) sequencing [10] have revealed nuclear organization at an unprecedented level

  • In addition to raw 3C interaction pairs, we developed a systematic evaluation scheme based on data reliability and classified the interactions into four categories

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Summary

Introduction

Gene expression in eukaryotes is tightly regulated by both cis- and trans-regulatory elements [1]. Multiple columns are given, including name and genome locus of the genes of interest, DNA sequences and primer strands, species name and genome version, name of cell line, number of experimental repetitions, name of restriction enzyme used and the name and publication date of the citation. By our data evaluation scheme, 524 and 669 interactions are in classes I and II, respectively, as defined by gel image.

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