Format

Send to

Choose Destination
G3 (Bethesda). 2018 Jan 4;8(1):219-229. doi: 10.1534/g3.117.300296.

Comparison of ChIP-Seq Data and a Reference Motif Set for Human KRAB C2H2 Zinc Finger Proteins.

Author information

1
Terrence Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Ontario M5S 1A8, Canada.
2
Department of Molecular Genetics, University of Toronto, Ontario M5S 1A8, Canada.
3
Terrence Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Ontario M5S 1A8, Canada t.hughes@utoronto.ca.
4
Canadian Institutes for Advanced Research, Toronto, Ontario M5G 1M1, Canada.

Abstract

KRAB C2H2 zinc finger proteins (KZNFs) are the largest and most diverse family of human transcription factors, likely due to diversifying selection driven by novel endogenous retroelements (EREs), but the vast majority lack binding motifs or functional data. Two recent studies analyzed a majority of the human KZNFs using either ChIP-seq (60 proteins) or ChIP-exo (221 proteins) in the same cell type (HEK293). The ChIP-exo paper did not describe binding motifs, however. Thirty-nine proteins are represented in both studies, enabling the systematic comparison of the data sets presented here. Typically, only a minority of peaks overlap, but the two studies nonetheless display significant similarity in ERE binding for 32/39, and yield highly similar DNA binding motifs for 23 and related motifs for 34 (MoSBAT similarity score >0.5 and >0.2, respectively). Thus, there is overall (albeit imperfect) agreement between the two studies. For the 242 proteins represented in at least one study, we selected a highest-confidence motif for each protein, utilizing several motif-derivation approaches, and evaluating motifs within and across data sets. Peaks for the majority (158) are enriched (96% with AUC >0.6 predicting peak vs. nonpeak) for a motif that is supported by the C2H2 "recognition code," consistent with intrinsic sequence specificity driving DNA binding in cells. An additional 63 yield motifs enriched in peaks, but not supported by the recognition code, which could reflect indirect binding. Altogether, these analyses validate both data sets, and provide a reference motif set with associated quality metrics.

KEYWORDS:

C2H2 recognition code; ChIP-seq; DNA-binding motif; KRAB C2H2 zinc finger proteins; endogenous retroelements

PMID:
29146583
PMCID:
PMC5765350
DOI:
10.1534/g3.117.300296
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for HighWire Icon for PubMed Central
Loading ...
Support Center