Evidence map›Paper›PMID 31267707›Full record

ReviewEMBO reports2019

The non-specific lethal (NSL) complex at the crossroads of transcriptional control and cellular homeostasis.

Bilal N Sheikh, Sukanya Guhathakurta, Asifa Akhtar

Open access · hybridAbstract readReview
In one paragraph

Review in EMBO reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

74 citing papers in PubMed, 1 synthesis or guideline pooled it, 108 citations in OpenAlex.

  1. Pooled it
  2. Review
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  13. Fto-mediated mJournal of biomedical science · 2025
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  15. Hierarchical small molecule inhibition of MYST acetyltransferases.bioRxiv : the preprint server for biology · 2025
    Article
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  17. N-terminus ofeLife · 2024
    Article
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14 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Bilal N SheikhMax Planck Institute for Immunobiology and Epigenetics, Freiburg im Breisgau, Germany.ORCID 0000-0002-1970-6236
Sukanya GuhathakurtaMax Planck Institute for Immunobiology and Epigenetics, Freiburg im Breisgau, Germany.
Asifa AkhtarMax Planck Institute for Immunobiology and Epigenetics, Freiburg im Breisgau, Germany.ORCID 0000-0001-8973-6193
Max Planck Institute of Immunobiology and Epigenetics · DEUniversity of Freiburg · DE

Funding

German Research Foundation CIBSS-EXC-2189-Project ID 390939984German Research Foundation CRC 992
6 · The paper itself

Abstract

The functionality of chromatin is tightly regulated by post-translational modifications that modulate transcriptional output from target loci. Among the post-translational modifications of chromatin, reversible ε-lysine acetylation of histone proteins is prominent at transcriptionally active genes. Lysine acetylation is catalyzed by lysine acetyltransferases (KATs), which utilize the central cellular metabolite acetyl-CoA as their substrate. Among the KATs that mediate lysine acetylation, males absent on the first (MOF/KAT8) is particularly notable for its ability to acetylate histone 4 lysine 16 (H4K16ac), a modification that decompacts chromatin structure. MOF and its non-specific lethal (NSL) complex members have been shown to localize to gene promoters and enhancers in the nucleus, as well as to microtubules and mitochondria to regulate key cellular processes. Highlighting their importance, mutations or deregulation of NSL complex members has been reported in both human neurodevelopmental disorders and cancer. Based on insight gained from studies in human, mouse, and Drosophila model systems, this review discusses the role of NSL-mediated lysine acetylation in a myriad of cellular functions in both health and disease. Through these studies, the importance of the NSL complex in regulating core transcriptional and signaling networks required for normal development and cellular homeostasis is beginning to emerge.

Indexed as

Chromatin Assembly and DisassemblyEpigenesis, GeneticTranscriptional ActivationAnimalsHistone AcetyltransferasesHomeostasisHumansHistone AcetyltransferasesepigeneticsHATKANSL1Koolen de-Vriestranscription

Identifiers

PMID31267707
PMCPMC6607013
OpenAlexW2948536289

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.