Evidence map›Paper›PMID 34449766›Full record

ArticlePLoS genetics2021

AKTIP interacts with ESCRT I and is needed for the recruitment of ESCRT III subunits to the midbody.

Chiara Merigliano, Romina Burla, Mattia La Torre, Simona Del Giudice, Hsiangling Teo, Chong Wai Liew, Alexandre Chojnowski, Wah Ing Goh, Yolanda Olmos, Klizia Maccaroni and 10 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. ESCRT-III function in membrane fission and repair.Nature reviews. Molecular cell biology · 2026
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  14. Mechanics and regulation of cytokinetic abscission.Frontiers in cell and developmental biology · 2022
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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

20 authors at 6 institutions in 4 countries.

Chiara MeriglianoSapienza University Dept. Biology and Biotechnology, Rome, Italy.ORCID 0000-0002-0658-2609
Romina BurlaSapienza University Dept. Biology and Biotechnology, Rome, Italy.ORCID 0000-0002-5640-4464
Mattia La TorreSapienza University Dept. Biology and Biotechnology, Rome, Italy.ORCID 0000-0002-1178-6948
Simona Del GiudiceSapienza University Dept. Biology and Biotechnology, Rome, Italy.ORCID 0000-0002-4573-269X
Hsiangling TeoInstitute of Structural Biology, Nanyang Technological University, Singapore.ORCID 0000-0002-3849-809X
Chong Wai LiewInstitute of Structural Biology, Nanyang Technological University, Singapore.ORCID 0000-0002-4343-818X
Alexandre ChojnowskiA*STAR, Developmental and Regenerative Biology, ASLR, Agency for Science, Technology and Research, Singapore.ORCID 0000-0002-0669-2146
Wah Ing GohA*STAR Microscopy Platform, Research Support Centre, Agency for Science, Technology and Research, Singapore.ORCID 0000-0001-6594-0640
Yolanda OlmosSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.ORCID 0000-0002-5952-1607
Klizia MaccaroniSapienza University Dept. Biology and Biotechnology, Rome, Italy.ORCID 0000-0003-3856-8470
Maria GiubettiniCrestOptics S.p.A., Rome, Italy.
Irene ChioloUniversity of Southern California, Molecular and Computational Biology Dept., Los Angeles, California, United States of America.
Jeremy G CarltonSchool of Cancer and Pharmaceutical Sciences, King's College London, London, United Kingdom.ORCID 0000-0002-7255-1894
Domenico RaimondoSapienza University Dept. Molecular Medicine, Rome, Italy.
Fiammetta VernìSapienza University Dept. Biology and Biotechnology, Rome, Italy.ORCID 0000-0001-8866-3324
Colin L StewartA*STAR, Developmental and Regenerative Biology, ASLR, Agency for Science, Technology and Research, Singapore.ORCID 0000-0002-4988-536X
Daniela RhodesInstitute of Structural Biology, Nanyang Technological University, Singapore.
Graham D WrightA*STAR Microscopy Platform, Research Support Centre, Agency for Science, Technology and Research, Singapore.ORCID 0000-0003-2362-1312
Brian E BurkeA*STAR, Singapore Nuclear Dynamics and Architecture, ASLR Skin Research Labs, Agency for Science, Technology and Research, Singapore.ORCID 0000-0002-6887-7154
Isabella SaggioSapienza University Dept. Biology and Biotechnology, Rome, Italy.ORCID 0000-0002-9497-7415
Sapienza University of Rome · ITAgency for Science, Technology and Research · SGNanyang Technological University · SGKing's College London · GBInstitute of Molecular Biology and Pathology · ITUniversity of Southern California · US

Funding

Roles of nuclear architecture and phase separation in heterochromatin repair dynamicsR01GM117376 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHIOLO, IRENE E · 2015 to 2023
$3.3M
Cancer Research UK FC001002NIGMS NIH HHS R01 GM117376Wellcome Trust
6 · The paper itself

Abstract

To complete mitosis, the bridge that links the two daughter cells needs to be cleaved. This step is carried out by the endosomal sorting complex required for transport (ESCRT) machinery. AKTIP, a protein discovered to be associated with telomeres and the nuclear membrane in interphase cells, shares sequence similarities with the ESCRT I component TSG101. Here we present evidence that during mitosis AKTIP is part of the ESCRT machinery at the midbody. AKTIP interacts with the ESCRT I subunit VPS28 and forms a circular supra-structure at the midbody, in close proximity with TSG101 and VPS28 and adjacent to the members of the ESCRT III module CHMP2A, CHMP4B and IST1. Mechanistically, the recruitment of AKTIP is dependent on MKLP1 and independent of CEP55. AKTIP and TSG101 are needed together for the recruitment of the ESCRT III subunit CHMP4B and in parallel for the recruitment of IST1. Alone, the reduction of AKTIP impinges on IST1 and causes multinucleation. Our data altogether reveal that AKTIP is a component of the ESCRT I module and functions in the recruitment of ESCRT III components required for abscission.

Indexed as

Adaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsCell Cycle ProteinsCytokinesisDNA-Binding ProteinsEndosomal Sorting Complexes Required for TransportHeLa CellsHumansMitosisProtein TransportSpindle ApparatusTranscription FactorsTsg101 ProteinAdaptor Proteins, Signal TransducingAKTIP protein, humanApoptosis Regulatory ProteinsCell Cycle ProteinsCep55 protein, humanCHMP4B protein, humanDNA-Binding ProteinsEndosomal Sorting Complexes Required for TransportTranscription FactorsTsg101 ProteinVPS28 protein, human

Identifiers

PMID34449766
PMCPMC8428793
OpenAlexW3194247542

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.