Evidence map›Paper›PMID 34890234›Full record

ArticleScience advances2021

The nuclear transcription factor, TAF7, is a cytoplasmic regulator of protein synthesis.

Dan Cheng, Kevin Semmens, Elizabeth McManus, Qingrong Chen, Daoud Meerzaman, Xiantao Wang, Markus Hafner, Brian A Lewis, Hidehisa Takahashi, Ballachanda N Devaiah and 2 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  8. Article
  9. Review
  10. Deciphering the RNA-binding protein network during endosomal mRNA transport.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Enhanced gene regulation by cooperation between mRNA decay and gene transcription.Biochimica et biophysica acta. Gene regulatory mechanisms · 2023
    Article
  16. Article
  17. 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

12 authors at 4 institutions in 2 countries.

Dan ChengExperimental Immunology Branch, National Cancer Institute, NIH, Bethesda, MD 20892, USA.ORCID 0000-0001-5302-950X
Kevin SemmensSchool of Medicine, University of Utah, Salt Lake City, UT 84132, USA.ORCID 0000-0001-5496-1067
Elizabeth McManusExperimental Immunology Branch, National Cancer Institute, NIH, Bethesda, MD 20892, USA.
Qingrong ChenCenter for Biomedical Informatics and Information Technology, National Cancer Institute, NIH, Rockville, MD 20850, USA.
Daoud MeerzamanCenter for Biomedical Informatics and Information Technology, National Cancer Institute, NIH, Rockville, MD 20850, USA.
Xiantao WangLaboratory of Muscle Stem Cells and Gene Regulation, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD 20892, USA.
Markus HafnerLaboratory of Muscle Stem Cells and Gene Regulation, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD 20892, USA.ORCID 0000-0002-4336-6518
Brian A LewisLaboratory of Pathology, National Cancer Institute, NIH, Bethesda, MD 20892, USA.ORCID 0000-0002-8321-0665
Hidehisa TakahashiDepartment of Molecular Biology, Yokohama City University Graduate School of Medical Science, Fukuura 3-9, Kanazawa-ku, Yokohama, Kanagawa 216-0004, Japan.
Ballachanda N DevaiahExperimental Immunology Branch, National Cancer Institute, NIH, Bethesda, MD 20892, USA.
Anne GegonneExperimental Immunology Branch, National Cancer Institute, NIH, Bethesda, MD 20892, USA.
Dinah S SingerExperimental Immunology Branch, National Cancer Institute, NIH, Bethesda, MD 20892, USA.ORCID 0000-0002-7369-3018
National Cancer Institute · USNational Institute of Arthritis and Musculoskeletal and Skin Diseases · USUniversity of Utah · USYokohama City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The TFIID component, TAF7, has been extensively characterized as essential for transcription and is critical for cell proliferation and differentiation. Here, we report that TAF7 is a previously unknown RNA chaperone that contributes to the regulation of protein synthesis. Mechanistically, TAF7 binds RNAs in the nucleus and delivers them to cytoplasmic polysomes. A broad spectrum of target RNA species, including the HIV-1 transactivation response element, binds TAF7 through consensus CUG motifs within the 3′ untranslated region. Export to the cytoplasm depends on a TAF7 nuclear export signal and occurs by an exportin 1–dependent pathway. Notably, disrupting either TAF7’s RNA binding or its export from the nucleus results in retention of target messenger RNAs in the nucleus and reduced levels of the protein products of TAF7-target RNAs. Thus, TAF7, an essential transcription factor, plays a key role in the regulation of RNA translation, thereby potentially connecting these processes.

Identifiers

PMID34890234
PMCPMC8664259
OpenAlexW4200378358

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.