Evidence map›Paper›PMID 30995177›Full record

ArticleMolecular biology of the cell2019

REEP3 and REEP4 determine the tubular morphology of the endoplasmic reticulum during mitosis.

Darshan Kumar, Banafsheh Golchoubian, Ilya Belevich, Eija Jokitalo, Anne-Lore Schlaitz

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In one paragraph

Article in Molecular biology of the cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 51 citations in OpenAlex.

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  12. Regulation of organelle size and organization during development.Seminars in cell & developmental biology · 2023
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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

5 authors at 2 institutions in 2 countries.

Darshan KumarCell and Molecular Biology Program, University of Helsinki, FI-00014 Helsinki, Finland.
Banafsheh GolchoubianCenter for Molecular Biology of Heidelberg University (ZMBH), D-69120 Heidelberg, Germany.
Ilya BelevichCell and Molecular Biology Program, University of Helsinki, FI-00014 Helsinki, Finland.
Eija JokitaloCell and Molecular Biology Program, University of Helsinki, FI-00014 Helsinki, Finland.
Anne-Lore SchlaitzCenter for Molecular Biology of Heidelberg University (ZMBH), D-69120 Heidelberg, Germany.
University of Helsinki · FIHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endoplasmic reticulum (ER) is extensively remodeled during metazoan open mitosis. However, whether the ER becomes more tubular or more cisternal during mitosis is controversial, and dedicated factors governing the morphology of the mitotic ER have remained elusive. Here, we describe the ER membrane proteins REEP3 and REEP4 as major determinants of ER morphology in metaphase cells. REEP3/4 are specifically required for generating the high-curvature morphology of mitotic ER and promote ER tubulation through their reticulon homology domains (RHDs). This ER-shaping activity of REEP3/4 is distinct from their previously described function to clear ER from metaphase chromatin. We further show that related REEP proteins do not contribute to mitotic ER shaping and provide evidence that the REEP3/4 carboxyterminus mediates regulation of the proteins. These findings confirm that ER converts to higher curvature during mitosis, identify REEP3/4 as specific and crucial morphogenic factors mediating ER tubulation during mitosis, and define the first cell cycle-specific role for RHD proteins.

Indexed as

MitosisAmino Acid SequenceChromatinEndoplasmic ReticulumHeLa CellsHumansMembrane Transport ProteinsMetaphaseProtein DomainsChromatinMembrane Transport ProteinsREEP3 protein, humanREEP4 protein, human

Identifiers

PMID30995177
PMCPMC6724692
OpenAlexW2938350367

What OpenQuestion holds

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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.