Evidence map›Paper›PMID 27172002›Full record

ArticleAutophagy2016

TP53INP2/DOR, a mediator of cell autophagy, promotes rDNA transcription via facilitating the assembly of the POLR1/RNA polymerase I preinitiation complex at rDNA promoters.

Yinfeng Xu, Wei Wan, Xin Shou, Rui Huang, Zhiyuan You, Yanhong Shou, Lingling Wang, Tianhua Zhou, Wei Liu

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.9field-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

25 citing papers in PubMed, 48 citations in OpenAlex.

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  12. Review
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  14. Autophagy regulates rRNA synthesis.Nucleus (Austin, Tex.) · 2022
    Article
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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

9 authors at 1 institution in 1 country.

Yinfeng Xua Department of Biochemistry and Molecular Biology , Program in Molecular and Cell Biology, Zhejiang University School of Medicine , Hangzhou , China.
Wei Wana Department of Biochemistry and Molecular Biology , Program in Molecular and Cell Biology, Zhejiang University School of Medicine , Hangzhou , China.
Xin Shoua Department of Biochemistry and Molecular Biology , Program in Molecular and Cell Biology, Zhejiang University School of Medicine , Hangzhou , China.
Rui Huanga Department of Biochemistry and Molecular Biology , Program in Molecular and Cell Biology, Zhejiang University School of Medicine , Hangzhou , China.
Zhiyuan Youa Department of Biochemistry and Molecular Biology , Program in Molecular and Cell Biology, Zhejiang University School of Medicine , Hangzhou , China.
Yanhong Shoua Department of Biochemistry and Molecular Biology , Program in Molecular and Cell Biology, Zhejiang University School of Medicine , Hangzhou , China.
Lingling Wanga Department of Biochemistry and Molecular Biology , Program in Molecular and Cell Biology, Zhejiang University School of Medicine , Hangzhou , China.
Tianhua Zhoua Department of Biochemistry and Molecular Biology , Program in Molecular and Cell Biology, Zhejiang University School of Medicine , Hangzhou , China.
Wei Liua Department of Biochemistry and Molecular Biology , Program in Molecular and Cell Biology, Zhejiang University School of Medicine , Hangzhou , China.
Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cells control their metabolism through modulating the anabolic and catabolic pathways. TP53INP2/DOR (tumor protein p53 inducible nuclear protein 2), participates in cell catabolism by serving as a promoter of autophagy. Here we uncover a novel function of TP53INP2 in protein synthesis, a major biosynthetic and energy-consuming anabolic process. TP53INP2 localizes to the nucleolus through its nucleolar localization signal (NoLS) located at the C-terminal domain. Chromatin immunoprecipitation (ChIP) assays detected an association of TP53INP2 with the ribosomal DNA (rDNA), when exclusion of TP53INP2 from the nucleolus repressed rDNA promoter activity and the production of ribosomal RNA (rRNA) and proteins. The removal of TP53INP2 also impaired the association of the POLR1/RNA polymerase I preinitiation complex (PIC) with rDNA. Further, TP53INP2 interacts directly with POLR1 PIC, and is required for the assembly of the complex. These data indicate that TP53INP2 promotes ribosome biogenesis through facilitating rRNA synthesis at the nucleolus, suggesting a dual role of TP53INP2 in cell metabolism, assisting anabolism on the nucleolus, and stimulating catabolism off the nucleolus.

Indexed as

AutophagyDNA, RibosomalHumansMCF-7 CellsNuclear ProteinsPromoter Regions, GeneticProtein BindingRNA Polymerase ITranscription, GeneticDNA, RibosomalNuclear ProteinsRNA Polymerase ITP53INP2 protein, humanautophagynucleoluspreinitiation complexrDNATP53INP2/DOR

Identifiers

PMID27172002
PMCPMC4990990
OpenAlexW2355269937

What OpenQuestion holds

Textmetadata
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.