Evidence map›Paper›PMID 33689394›Full record

ArticleMolecular biology of the cell2021

Increased numbers of nucleoli in a genome-wide RNAi screen reveal proteins that link the cell cycle to RNA polymerase I transcription.

Lisa M Ogawa, Amber F Buhagiar, Laura Abriola, Bryan A Leland, Yulia V Surovtseva, Susan J Baserga

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2021. 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
2.2field-weighted citation impact, top 11% 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, 37 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Lisa M OgawaDepartment of Molecular Biophysics & Biochemistry, Yale University School of Medicine, New Haven, CT 06520.
Amber F BuhagiarDepartment of Molecular Biophysics & Biochemistry, Yale University School of Medicine, New Haven, CT 06520.
Laura AbriolaYale Center for Molecular Discovery, Yale University, West Haven, CT 06516.
Bryan A LelandYale Center for Molecular Discovery, Yale University, West Haven, CT 06516.
Yulia V SurovtsevaYale Center for Molecular Discovery, Yale University, West Haven, CT 06516.
Susan J BasergaDepartment of Molecular Biophysics & Biochemistry, Yale University School of Medicine, New Haven, CT 06520.
Yale University · US

Funding

Skill Development for Diverse Scientific Careers: A New Course Predoctoral Program in Cellular and Molecular BiologyT32GM007223 · NIGMS · YALE UNIVERSITY · PI BASERGA, SUSAN J · 1985 to 2019
$31.0M
Novel regulatory networks driving human ribosome biogenesisR35GM131687 · NIGMS · YALE UNIVERSITY · PI Susan J Baserga · 2019 to 2026
$5.1M
The intersection of Alzheimer’s disease and ribosome biogenesis through Amyloid Beta Precursor Protein Binding Family B Member 1 (APBB1; FE65)F31AG058405 · NIA · YALE UNIVERSITY · PI MCLEAN, LISA OGAWA · 2017 to 2020
$128k
NIA NIH HHS F31 AG058405NIGMS NIH HHS R35 GM131687NIGMS NIH HHS T32 GM007223
6 · The paper itself

Abstract

Nucleoli are dynamic nuclear condensates in eukaryotic cells that originate through ribosome biogenesis at loci that harbor the ribosomal DNA. These loci are known as nucleolar organizer regions (NORs), and there are 10 in a human diploid genome. While there are 10 NORs, however, the number of nucleoli observed in cells is variable. Furthermore, changes in number are associated with disease, with increased numbers and size common in aggressive cancers. In the near-diploid human breast epithelial cell line, MCF10A, the most frequently observed number of nucleoli is two to three per cell. Here, to identify novel regulators of ribosome biogenesis we used high-throughput quantitative imaging of MCF10A cells to identify proteins that, when depleted, increase the percentage of nuclei with ≥5 nucleoli. Unexpectedly, this unique screening approach led to identification of proteins associated with the cell cycle. Functional analysis on a subset of hits further revealed not only proteins required for progression through the S and G2/M phase, but also proteins required explicitly for the regulation of RNA polymerase I transcription and protein synthesis. Thus, results from this screen for increased nucleolar number highlight the significance of the nucleolus in human cell cycle regulation, linking RNA polymerase I transcription to cell cycle progression.

Indexed as

Breast NeoplasmsCell CycleCell Line, TumorCell NucleolusCell NucleusDNA, RibosomalHumansMicroscopy, FluorescenceNucleolus Organizer RegionProtein BiosynthesisProteinsRNA Polymerase IDNA, RibosomalProteinsRNA Polymerase I

Identifiers

PMID33689394
PMCPMC8108525
OpenAlexW3134241172

What OpenQuestion holds

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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.