Evidence map›Paper›PMID 35325203›Full record

ArticleNucleic acids research2022

ZWC complex-mediated SPT5 phosphorylation suppresses divergent antisense RNA transcription at active gene promoters.

Kihyun Park, Jian Zhong, Jin Sung Jang, Jihyun Kim, Hye-Jung Kim, Jeong-Heon Lee, Jaehoon Kim

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

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  16. Premature transcription termination complex proteins PCF11 and WDR82 silence HIV-1 expression in latently infected cells.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. Article
  18. Article
  19. Natural antisense transcripts as drug targets.Frontiers in molecular biosciences · 2022
    Review
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

7 authors at 2 institutions in 2 countries.

Kihyun ParkDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon 34141, South Korea.
Jian ZhongEpigenomics Program, Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Jin Sung JangMedical Genome Facility, Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Jihyun KimDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon 34141, South Korea.
Hye-Jung KimNew Drug Development Center, OSONG Medical Innovation Foundation, Cheongju 28160, South Korea.
Jeong-Heon LeeEpigenomics Program, Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Jaehoon KimDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon 34141, South Korea.ORCID 0000-0003-4035-0438
Korea Advanced Institute of Science and Technology · KRMayo Clinic · US

Funding

Physiological Characterization and Data Integration CoreP01DK068055 · NIDDK · MAYO CLINIC ROCHESTER · PI BHARUCHA, ADIL E. · 2004 to 2019
$23.8M
NIDDK NIH HHS P01 DK068055
6 · The paper itself

Abstract

The human genome encodes large numbers of non-coding RNAs, including divergent antisense transcripts at transcription start sites (TSSs). However, molecular mechanisms by which divergent antisense transcription is regulated have not been detailed. Here, we report a novel ZWC complex composed of ZC3H4, WDR82 and CK2 that suppresses divergent antisense transcription. The ZWC complex preferentially localizes at TSSs of active genes through direct interactions of ZC3H4 and WDR82 subunits with the S5p RNAPII C-terminal domain. ZC3H4 depletion leads to increased divergent antisense transcription, especially at genes that naturally produce divergent antisense transcripts. We further demonstrate that the ZWC complex phosphorylates the previously uncharacterized N-terminal acidic domain of SPT5, a subunit of the transcription-elongation factor DSIF, and that this phosphorylation is responsible for suppressing divergent antisense transcription. Our study provides evidence that the newly identified ZWC-DSIF axis regulates the direction of transcription during the transition from early to productive elongation.

Indexed as

Chromosomal Proteins, Non-HistoneNuclear ProteinsRNA, AntisenseTranscriptional Elongation FactorsTranscription, GeneticDNA-Binding ProteinsHumansPhosphorylationRNA Polymerase IITranscription FactorsChromosomal Proteins, Non-HistoneDNA-Binding ProteinsNuclear ProteinsRNA, AntisenseRNA Polymerase IISUPT5H protein, humanTranscriptional Elongation FactorsTranscription FactorsWDR82 protein, humanZC3H4 protein, human

Identifiers

PMID35325203
PMCPMC9023261
OpenAlexW4220752221

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.