Evidence map›Paper›PMID 39036955›Full record

ArticleNucleic acids research2024

A UTP3-dependent nucleolar translocation pathway facilitates pre-rRNA 5'ETS processing.

Jiayang Bao, Baochun Su, Zheyan Chen, Zhaoxiang Sun, Jinrong Peng, Shuyi Zhao

Abstract read
In one paragraph

Article in Nucleic acids research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jiayang BaoMOE Key Laboratory for Molecular Animal Nutrition, College of Animal Sciences, Zhejiang University, Hangzhou 310058, China.ORCID 0009-0008-5665-8799
Baochun SuMOE Key Laboratory for Molecular Animal Nutrition, College of Animal Sciences, Zhejiang University, Hangzhou 310058, China.ORCID 0009-0005-6604-0165
Zheyan ChenCollege of Life Sciences, Zhejiang University, Hangzhou 310058, China.ORCID 0009-0009-4684-1378
Zhaoxiang SunCollege of Life Sciences, Zhejiang University, Hangzhou 310058, China.ORCID 0009-0008-5732-4571
Jinrong PengMOE Key Laboratory for Molecular Animal Nutrition, College of Animal Sciences, Zhejiang University, Hangzhou 310058, China.ORCID 0000-0002-0793-4848
Shuyi ZhaoMOE Key Laboratory for Molecular Animal Nutrition, College of Animal Sciences, Zhejiang University, Hangzhou 310058, China.ORCID 0000-0003-1774-5415

Funding

National Key R&D Program of China 2018YFA0800502National Natural Science Foundation of China U21A20198
6 · The paper itself

Abstract

The ribosome small subunit (SSU) is assembled by the SSU processome which contains approximately 70 non-ribosomal protein factors. Whilst the biochemical mechanisms of the SSU processome in 18S rRNA processing and maturation have been extensively studied, how SSU processome components enter the nucleolus has yet to be systematically investigated. Here, in examining the nucleolar localization of 50 human SSU processome components, we found that UTP3, together with another 24 proteins, enter the nucleolus autonomously. For the remaining 25 proteins we found that UTP3/SAS10 assists the nucleolar localization of five proteins (MPP10, UTP25, EMG1 and the two UTP-B components UTP12 and UTP13), likely through its interaction with nuclear importin α. This 'ferrying' function of UTP3 was then confirmed as conserved in the zebrafish. We also found that knockdown of human UTP3 impairs cleavage at the A0-site while loss-of-function of either utp3/sas10 or utp13/tbl3 in zebrafish causes the accumulation of aberrantly processed 5'ETS products, which highlights the crucial role of UTP3 in mediating 5'ETS processing. Mechanistically, we found that UTP3 facilitates the degradation of processed 5'ETS by recruiting the RNA exosome component EXOSC10 to the nucleolus. These findings lay the groundwork for studying the mechanism of cytoplasm-to-nucleolus trafficking of SSU processome components.

Indexed as

Cell NucleolusRNA PrecursorsRNA Processing, Post-TranscriptionalZebrafishAnimalsHEK293 CellsHeLa CellsHumansNuclear ProteinsNuclear ProteinsRNA Precursors

Identifiers

PMID39036955
PMCPMC11381329

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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.