Evidence map›Paper›PMID 30002158›Full record

ArticleGenome research2018

A common pattern of DNase I footprinting throughout the human mtDNA unveils clues for a chromatin-like organization.

Amit Blumberg, Charles G Danko, Anshul Kundaje, Dan Mishmar

Abstract read
In one paragraph

Article in Genome research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

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  5. Polycomb Repressive Complex 1 and USP16 localize to the mitochondrion and influence its function.Proceedings of the National Academy of Sciences of the United States of America · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Amit BlumbergDepartment of Life Sciences, Ben-Gurion University of the Negev, Beer Sheva 84105 Israel.
Charles G DankoBaker Institute for Animal Health, Cornell University, Ithaca, New York 14853, USA.ORCID 0000-0002-1999-7125
Anshul KundajeDepartment of Genetics, Stanford University, Stanford, California 94305-5120, USA.ORCID 0000-0003-3084-2287
Dan MishmarDepartment of Life Sciences, Ben-Gurion University of the Negev, Beer Sheva 84105 Israel.ORCID 0000-0003-3488-8792

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human mitochondrial DNA (mtDNA) is believed to lack chromatin and histones. Instead, it is coated solely by the transcription factor TFAM. We asked whether mtDNA packaging is more regulated than once thought. To address this, we analyzed DNase-seq experiments in 324 human cell types and found, for the first time, a pattern of 29 mtDNA Genomic footprinting (mt-DGF) sites shared by ∼90% of the samples. Their syntenic conservation in mouse DNase-seq experiments reflect selective constraints. Colocalization with known mtDNA regulatory elements, with G-quadruplex structures, in TFAM-poor sites (in HeLa cells) and with transcription pausing sites, suggest a functional regulatory role for such mt-DGFs. Altered mt-DGF pattern in interleukin 3-treated CD34

Indexed as

Genome, HumanAnimalsCell LineChromatinDeoxyribonucleasesDNA-Binding ProteinsDNA FootprintingDNA, MitochondrialGene Expression RegulationG-QuadruplexesHeLa CellsHumansMiceMitochondriaMitochondrial ProteinsTranscription FactorsChromatinDeoxyribonucleasesDNA-Binding ProteinsDNA, MitochondrialMitochondrial ProteinsTFAM protein, humanTranscription Factors

Identifiers

PMID30002158
PMCPMC6071632

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.