Evidence map›Paper›PMID 38058280›Full record

ArticleProtein science : a publication of the Protein Society2024

KMT2D preferentially binds mRNAs of the genes it regulates, suggesting a role in RNA processing.

Harem Muhamad Amin, Rawan Abukhairan, Beata Szabo, Mevan Jacksi, Gyorgy Varady, Rita Lozsa, Eva Schad, Agnes Tantos

Open access · bronzeAbstract read
In one paragraph

Article in Protein science : a publication of the Protein Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

8 authors at 2 institutions in 2 countries.

Harem Muhamad AminInstitute of Enzymology, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.ORCID 0009-0003-8723-3041
Rawan AbukhairanInstitute of Enzymology, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.ORCID 0000-0003-4802-3802
Beata SzaboInstitute of Enzymology, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.ORCID 0000-0003-2287-0827
Mevan JacksiInstitute of Enzymology, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.ORCID 0000-0003-4659-9015
Gyorgy VaradyInstitute of Enzymology, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.ORCID 0000-0003-2012-9680
Rita LozsaInstitute of Enzymology, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.ORCID 0000-0001-5957-906X
Eva SchadInstitute of Enzymology, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.ORCID 0000-0002-3006-2910
Agnes TantosInstitute of Enzymology, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.ORCID 0000-0003-1273-9841
Institute of Molecular Life Sciences · HUEötvös Loránd University · HU

Funding

National Research, Development and Innovation Office NKFI-K142851
6 · The paper itself

Abstract

Histone lysine methyltransferases (HKMTs) perform vital roles in cellular life by controlling gene expression programs through the posttranslational modification of histone tails. Since many of them are intimately involved in the development of different diseases, including several cancers, understanding the molecular mechanisms that control their target recognition and activity is vital for the treatment and prevention of such conditions. RNA binding has been shown to be an important regulatory factor in the function of several HKMTs, such as the yeast Set1 and the human Ezh2. Moreover, many HKMTs are capable of RNA binding in the absence of a canonical RNA binding domain. Here, we explored the RNA binding capacity of KMT2D, one of the major H3K4 monomethyl transferases in enhancers, using RNA immunoprecipitation followed by sequencing. We identified a broad range of coding and non-coding RNAs associated with KMT2D and confirmed their binding through RNA immunoprecipitation and quantitative PCR. We also showed that a separated RNA binding region within KMT2D is capable of binding a similar RNA pool, but differences in the binding specificity indicate the existence of other regulatory elements in the sequence of KMT2D. Analysis of the bound mRNAs revealed that KMT2D preferentially binds co-transcriptionally to the mRNAs of the genes under its control, while also interacting with super enhancer- and splicing-related non-coding RNAs. These observations, together with the nuclear colocalization of KMT2D with differentially phosphorylated forms of RNA Polymerase II suggest a so far unexplored role of KMT2D in the RNA processing of the nascent transcripts.

Indexed as

HistonesNeoplasmsHumansRNARNA, MessengerRNA Processing, Post-TranscriptionalHistonesRNARNA, Messengercotranscriptional RNA bindinghistone lysine methyltransferaseKMT2DMLL4mRNA splicingnon-coding RNARIP-sequencingRNA polymerase II

Identifiers

PMID38058280
PMCPMC10731558
OpenAlexW4389453070

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.