Evidence map›Paper›PMID 21078665›Full record

ArticleThe Journal of biological chemistry2011

A small ribosomal subunit (SSU) processome component, the human U3 protein 14A (hUTP14A) binds p53 and promotes p53 degradation.

Lelin Hu, Jiangnan Wang, Yun Liu, Ying Zhang, Liangliang Zhang, Ruirui Kong, Zongfang Zheng, Xiaojuan Du, Yang Ke

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

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  10. [Expression of hUTP14a in non-small cell lung cancer].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2019
    Article
  11. Article
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  16. Review
  17. Human diseases of the SSU processome.Biochimica et biophysica acta · 2014
    Review
  18. Does not hUTP14a promoter form a regulation feedback loop with P53?Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2014
    Article
  19. 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 3 institutions in 2 countries.

Lelin HuDepartment of Cell Biology, Peking University Health Science Center, Beijing 100191, China.
Jiangnan Wang
Yun Liu
Ying Zhang
Liangliang Zhang
Ruirui Kong
Zongfang Zheng
Xiaojuan Du
Yang Ke
Peking University · CNMinistry of Education · ETPeking University Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ribosome biogenesis is required for normal cell function, and aberrant ribosome biogenesis can lead to p53 activation. However, how p53 is activated by defects of ribosome biogenesis remains to be determined. Here, we identified human UTP14a as an SSU processome component by showing that hUTP14a is nucleolar, associated with U3 snoRNA and involved in 18 S rRNA processing. Interestingly, ectopic expression of hUTP14a resulted in a decrease and knockdown of hUTP14a led to an increase of p53 protein levels. We showed that hUTP14a physically interacts with p53 and functionally promotes p53 turn-over, and that hUTP14a promotion of p53 destabilization is sensitive to a proteasome inhibitor but independent of ubiquitination. Significantly, knockdown of hUTP14a led to cell cycle arrest and apoptosis. Our data identified a novel pathway for p53 activation through a defect in rRNA processing and suggest that a ribosome biogenesis factor itself could act as a sensor for nucleolar stress to regulate p53.

Indexed as

ApoptosisCell CycleGene Knockdown TechniquesHeLa CellsHumansProteasome Endopeptidase ComplexProtein StabilityRibonucleoproteins, Small NucleolarRibosomesRNA Processing, Post-TranscriptionalRNA, Ribosomal, 18SRNA, Small NucleolarTumor Suppressor Protein p53Proteasome Endopeptidase ComplexRibonucleoproteins, Small Nucleolarribonucleoprotein, U3 small nucleolarRNA, Ribosomal, 18SRNA, Small NucleolarRNA, U3 small nucleolarTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID21078665
PMCPMC3024804
OpenAlexW2051369825

What OpenQuestion holds

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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.