Evidence map›Paper›PMID 29959231›Full record

ArticleThe Journal of cell biology2018

CLIP and cohibin separate rDNA from nucleolar proteins destined for degradation by nucleophagy.

Md Golam Mostofa, Muhammad Arifur Rahman, Naoki Koike, Akter Mst Yeasmin, Nafisa Islam, Talukdar Muhammad Waliullah, Shun Hosoyamada, Mitsugu Shimobayashi, Takehiko Kobayashi, Michael N Hall and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 81 citations in OpenAlex.

  1. Prevention of ubiquitination at K6 and K9 in mutant huntingtin exacerbates disease pathology in a knock-in mouse model.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  10. A Yeast Mitotic Tale for the Nucleus and the Vacuoles to Embrace.International journal of molecular sciences · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Md Golam MostofaGraduate School of Science and Technology, Shizuoka University, Shizuoka, Japan.ORCID 0000-0002-0488-9121
Muhammad Arifur RahmanGraduate School of Science and Technology, Shizuoka University, Shizuoka, Japan.ORCID 0000-0002-9908-1474
Naoki KoikeGraduate School of Science and Technology, Shizuoka University, Shizuoka, Japan.
Akter Mst YeasminGraduate School of Science and Technology, Shizuoka University, Shizuoka, Japan.
Nafisa IslamCourse of Biological Science, Department of Science, Graduate School of Integrated Science and Technology, Shizuoka University, Shizuoka, Japan.
Talukdar Muhammad WaliullahGraduate School of Science and Technology, Shizuoka University, Shizuoka, Japan.ORCID 0000-0001-9951-2871
Shun HosoyamadaLaboratory of Genome Regeneration, Institute of Molecular and Cellular Biosciences, University of Tokyo, Tokyo, Japan.
Mitsugu ShimobayashiBiozentrum, University of Basel, Basel, Switzerland.ORCID 0000-0002-6936-0990
Takehiko KobayashiLaboratory of Genome Regeneration, Institute of Molecular and Cellular Biosciences, University of Tokyo, Tokyo, Japan.ORCID 0000-0002-7990-3741
Michael N HallBiozentrum, University of Basel, Basel, Switzerland.
Takashi UshimaruGraduate School of Science and Technology, Shizuoka University, Shizuoka, Japan takashi.ushimaru@gmail.com.ORCID 0000-0003-4589-7408
Shizuoka University · JPThe University of Tokyo · JPUniversity of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nutrient starvation or inactivation of target of rapamycin complex 1 (TORC1) in budding yeast induces nucleophagy, a selective autophagy process that preferentially degrades nucleolar components. DNA, including ribosomal DNA (rDNA), is not degraded by nucleophagy, even though rDNA is embedded in the nucleolus. Here, we show that TORC1 inactivation promotes relocalization of nucleolar proteins and rDNA to different sites. Nucleolar proteins move to sites proximal to the nuclear-vacuolar junction (NVJ), where micronucleophagy (or piecemeal microautophagy of the nucleus) occurs, whereas rDNA dissociates from nucleolar proteins and moves to sites distal to NVJs. CLIP and cohibin, which tether rDNA to the inner nuclear membrane, were required for repositioning of nucleolar proteins and rDNA, as well as effective nucleophagic degradation of the nucleolar proteins. Furthermore, micronucleophagy itself was necessary for the repositioning of rDNA and nucleolar proteins. However, rDNA escaped from nucleophagic degradation in CLIP- or cohibin-deficient cells. This study reveals that rDNA-nucleolar protein separation is important for the nucleophagic degradation of nucleolar proteins.

Indexed as

AutophagyCell SurvivalChromatin ImmunoprecipitationDNA, RibosomalNuclear ProteinsProteolysisSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTranscription FactorsDNA, RibosomalNuclear ProteinsSaccharomyces cerevisiae ProteinsTORC1 protein complex, S cerevisiaeTranscription Factors

Identifiers

PMID29959231
PMCPMC6080932
OpenAlexW2809901305

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.