Evidence map›Paper›PMID 24234443›Full record

ArticleNucleic acids research2014

RNA-dependent dynamic histone acetylation regulates MCL1 alternative splicing.

Dilshad H Khan, Carolina Gonzalez, Charlton Cooper, Jian-Min Sun, Hou Yu Chen, Shannon Healy, Wayne Xu, Karen T Smith, Jerry L Workman, Etienne Leygue and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

34 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. HDAC11 Regulates RNA Splicing via De-Fatty Acylation of SF3B2.bioRxiv : the preprint server for biology · 2026
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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

11 authors at 2 institutions in 2 countries.

Dilshad H KhanDepartment of Biochemistry and Medical Genetics, University of Manitoba, Manitoba Institute of Child Health, Winnipeg, Manitoba, R3E 3P4, Canada, Department of Biochemistry and Medical Genetics, University of Manitoba, Manitoba Institute of Cell Biology, Winnipeg, Manitoba, R3E0V9, Canada and Stowers Institute for Medical Research, Kansas City, Missouri 64110, USA.
Carolina Gonzalez
Charlton Cooper
Jian-Min Sun
Hou Yu Chen
Shannon Healy
Wayne Xu
Karen T Smith
Jerry L Workman
Etienne Leygue
James R Davie
University of Manitoba · CAChildren's Hospital Research Institute of Manitoba · CA

Funding

MECHANISMS OF TRANSCRIPTIONAL REGULATION IN CHROMATINR01GM047867 · NIGMS · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI WORKMAN, JERRY L · 1992 to 2014
$1.5M
CIHR MOP-9186NIGMS NIH HHS 1R01 GM047867NIGMS NIH HHS R01 GM047867
6 · The paper itself

Abstract

Histone deacetylases (HDACs) and lysine acetyltransferases (KATs) catalyze dynamic histone acetylation at regulatory and coding regions of transcribed genes. Highly phosphorylated HDAC2 is recruited within corepressor complexes to regulatory regions, while the nonphosphorylated form is associated with the gene body. In this study, we characterized the nonphosphorylated HDAC2 complexes recruited to the transcribed gene body and explored the function of HDAC-complex-mediated dynamic histone acetylation. HDAC1 and 2 were coimmunoprecipitated with several splicing factors, including serine/arginine-rich splicing factor 1 (SRSF1) which has roles in alternative splicing. The co-chromatin immunoprecipitation of HDAC1/2 and SRSF1 to the gene body was RNA-dependent. Inhibition of HDAC activity and knockdown of HDAC1, HDAC2 or SRSF1 showed that these proteins were involved in alternative splicing of MCL1. HDAC1/2 and KAT2B were associated with nascent pre-mRNA in general and with MCL1 pre-mRNA specifically. Inhibition of HDAC activity increased the occupancy of KAT2B and acetylation of H3 and H4 of the H3K4 methylated alternative MCL1 exon 2 nucleosome. Thus, nonphosphorylated HDAC1/2 is recruited to pre-mRNA by splicing factors to act at the RNA level with KAT2B and other KATs to catalyze dynamic histone acetylation of the MCL1 alternative exon and alter the splicing of MCL1 pre-mRNA.

Indexed as

Alternative SplicingAcetylationCell LineChromatinHistone Deacetylase 1Histone Deacetylase 2Histone Deacetylase InhibitorsHistonesHumansMyeloid Cell Leukemia Sequence 1 ProteinNuclear Proteinsp300-CBP-Associated Factorp300-CBP Transcription FactorsRNA-Binding ProteinsRNA, MessengerRNA Polymerase IIChromatinHistone Deacetylase 1Histone Deacetylase 2Histone Deacetylase InhibitorsHistonesMCL1 protein, humanMyeloid Cell Leukemia Sequence 1 ProteinNuclear Proteinsp300-CBP-Associated Factorp300-CBP Transcription FactorsRNA-Binding ProteinsRNA, MessengerRNA Polymerase IIRNA PrecursorsSerine-Arginine Splicing Factors

Identifiers

PMID24234443
PMCPMC3919583
OpenAlexW2166381886

What OpenQuestion 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 OpenQuestion graph.