Study / S31SP5EYS2020-02-26

Candidate silencer elements for the human and mouse genomes

Naresh Doni Jayavelu, Ajay Jajodia, Arpit Mishra, R. David Hawkins

About this study

The study of gene regulation is dominated by a focus on the control of gene activation or increase in the level of expression. Just as critical is the process of gene repression or silencing. Chromatin signatures have identified enhancers, however, genome-wide identification of silencers by computational or experimental approaches are lacking. Here, we first define uncharacterized cis-regulatory elements likely containing silencers and find that 41.5% of ~7500 tested elements show silencer activity using massively parallel reporter assay (MPRA). We trained a support vector machine classifier based on MPRA data to predict candidate silencers in over 100 human and mouse cell or tissue types. The predicted candidate silencers exhibit characteristics expected of silencers. Leveraging promoter-capture HiC data, we find that over 50% of silencers are interacting with gene promoters having very low to no expression. Our results suggest a general strategy for genome-wide identification and characterization of silencer elements.

Full author list & citation

Naresh Doni Jayavelu, Ajay Jajodia, Arpit Mishra, R. David Hawkins. Candidate silencer elements for the human and mouse genomes. 2020-02-26. https://doi.org/10.1038/s41467-020-14853-5

Experiments 1

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K562 silencer activity screen of human uncharacterized CREs

A plasmid STARR-seq-style silencer MPRA tested 7,440 human uncharacterized cis-regulatory elements alongside known enhancer, known silencer, and random-region controls in K562 cells. The library used 200-nt genomic inserts downstream of the SCP1 super core promoter and was measured in five biological RNA/DNA replicate pairs.

Silencer / Repressor MPRAHumanhg19
Explore data

Raw source data 4 files

Original supplemental and deposited inputs retained for this study. Download files individually or together as a ZIP; nested folders are preserved. Source reuse terms apply, and sequencing reads may be omitted.

Download all 4 files (ZIP)41467_2020_14853_MOESM2_ESM_Supplementary_Information.pdf41467_2020_14853_MOESM5_ESM_Supplementary_Data_2_MPRA.xlsx41467_2020_14853_MOESM6_ESM_Supplementary_Data_3_reporter_validation.xlsxGSE142207_Processed_data_raw_read_counts_RNA_DNA_libraries_at_peaks.txt.gz

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