Evidence map›Paper›PMID 37479688›Full record

ArticleNature communications2023

MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters.

Dongmei Wang, Haimin Li, Navdeep S Chandel, Yali Dou, Rui Yi

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.8field-weighted citation impact, top 9% of its field
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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. bioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Targeting lysine acetylation readers and writers.Nature reviews. Drug discovery · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Acetyltransferase in cardiovascular disease and aging.The journal of cardiovascular aging · 2024
    Article
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

5 authors at 2 institutions in 1 country.

Dongmei WangDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.ORCID 0000-0002-3923-8951
Haimin LiDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.
Navdeep S ChandelRobert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.ORCID 0000-0001-7208-3886
Yali DouDepartment of Medicine, University of Southern California, Los Angeles, CA, 90033, USA.ORCID 0000-0002-4040-1429
Rui YiDepartment of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA. yir@northwestern.edu.ORCID 0000-0002-6934-7091
Northwestern University · USUniversity of Southern California · US

Funding

Tissue resident macrophages regulate proteostasis in the aging lungP01AG049665 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GR Scott Budinger · 2015 to 2026
$26.9M
Northwestern University Skin Disease Research Center Resource-based CenterP30AR075049 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Amy S Paller · 2019 to 2026
$6.6M
Transcriptional regulation of skin stem cells and their nicheR01AR071435 · NIAMS · UNIVERSITY OF COLORADO · PI Rui Yi · 2017 to 2026
$3.8M
Modeling p63-associated human birth defects with systems developmental biology approachesR01HD107841 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Rui Yi · 2022 to 2026
$2.3M
Investigate MOF regulated epigenetic mechanisms of skin developmentR01AR081103 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Rui Yi · 2022 to 2026
$2.2M
NIAMS NIH HHS P30 AR075049NIAMS NIH HHS R01 AR071435NIAMS NIH HHS R01 AR081103NIA NIH HHS P01 AG049665NICHD NIH HHS R01 HD107841
6 · The paper itself

Abstract

Histone H4 lysine 16 acetylation (H4K16ac), governed by the histone acetyltransferase MOF, orchestrates gene expression regulation and chromatin interaction. However, the roles of MOF and H4K16ac in controlling cellular function and regulating mammalian tissue development remain unclear. Here we show that conditional deletion of Mof in the skin, but not Kansl1, causes severe defects in the self-renewal of basal epithelial progenitors, epidermal differentiation, and hair follicle growth, resulting in barrier defects and perinatal lethality. MOF-regulated genes are highly enriched for essential functions in the mitochondria and cilia. Genetic deletion of Uqcrq, an essential subunit for the electron transport chain (ETC) Complex III, in the skin, recapitulates the defects in epidermal differentiation and hair follicle growth observed in MOF knockout mouse. Together, this study reveals the requirement of MOF-mediated epigenetic mechanism for regulating mitochondrial and ciliary gene expression and underscores the important function of the MOF/ETC axis for mammalian skin development.

Indexed as

HistonesLysineAcetylationAnimalsChromatinHistone AcetyltransferasesMammalsMiceMitochondriaChromatinHistone AcetyltransferasesHistonesLysine

Identifiers

PMID37479688
PMCPMC10362062
OpenAlexW4385064796

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.