Evidence map›Paper›PMID 35952650›Full record

ArticleACS chemical biology2022

Proximity Labeling Reveals Spatial Regulation of the Anaphase-Promoting Complex/Cyclosome by a Microtubule Adaptor.

Xiaofu Cao, Adnan Shami Shah, Ethan J Sanford, Marcus B Smolka, Jeremy M Baskin

Open access · greenAbstract read
In one paragraph

Article in ACS chemical biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

6 citing papers in PubMed, 8 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

5 authors at 1 institution in 1 country.

Xiaofu CaoDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14850, United States.ORCID 0000-0002-2417-5652
Adnan Shami ShahDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14850, United States.
Ethan J SanfordWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, New York 14850, United States.
Marcus B SmolkaWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, New York 14850, United States.ORCID 0000-0001-9952-2885
Jeremy M BaskinDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14850, United States.ORCID 0000-0003-2939-3138
Cornell University · US

Funding

Signaling Mechanisms in Genome Maintenance (Equipment Supplement 2023)R35GM141159 · NIGMS · CORNELL UNIVERSITY · PI Marcus Smolka · 2021 to 2026
$3.5M
Phosphoinositide-Binding Proteins as Regulators of Ubiquitination and Wnt SignalingR01GM131101 · NIGMS · CORNELL UNIVERSITY · PI BASKIN, JEREMY · 2018 to 2022
$1.7M
Spatiotemporal control of ubiquitination by phosphoinositide-binding proteinsR01GM143367 · NIGMS · CORNELL UNIVERSITY · PI BASKIN, JEREMY · 2022 to 2025
$1.3M
NIGMS NIH HHS R01 GM131101NIGMS NIH HHS R01 GM143367NIGMS NIH HHS R35 GM141159
6 · The paper itself

Abstract

The anaphase-promoting complex/cyclosome (APC/C) coordinates advancement through mitosis via temporally controlled polyubiquitination events. Despite the long-appreciated spatial organization of key events in mitosis mediated largely by cytoskeletal networks, the spatial regulation of APC/C, the major mitotic E3 ligase, is poorly understood. We describe a microtubule-resident protein, PLEKHA5, as an interactor of APC/C and spatial regulator of its activity in mitosis. Microtubule-localized proximity biotinylation tools revealed that PLEKHA5 depletion decreased APC/C association with the microtubule cytoskeleton, which prevented efficient loading of APC/C with its coactivator CDC20 and led to reduced APC/C E3 ligase activity. PLEKHA5 knockdown delayed mitotic progression, causing accumulation of APC/C substrates dependent upon the PLEKHA5-APC/C interaction in microtubules. We propose that PLEKHA5 functions as an adaptor of APC/C that promotes its subcellular localization to microtubules and facilitates its activation by CDC20, thus ensuring the timely turnover of key mitotic APC/C substrates and proper progression through mitosis.

Indexed as

AnaphaseMitosisAnaphase-Promoting Complex-CyclosomeCdc20 ProteinsCell Cycle ProteinsMicrotubulesUbiquitin-Protein LigasesAnaphase-Promoting Complex-CyclosomeCdc20 ProteinsCell Cycle ProteinsUbiquitin-Protein Ligases

Identifiers

PMID35952650
PMCPMC9933862
OpenAlexW4291012057

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.