Evidence map›Paper›PMID 32936885›Full record

ArticleThe Journal of cell biology2020

An antibody toolbox to track complex I assembly defines AIF's mitochondrial function.

Anjaneyulu Murari, Shauna-Kay Rhooms, Naga Sri Goparaju, Maximino Villanueva, Edward Owusu-Ansah

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. ATP synthase subunits e and g are essential for CaCell death and differentiation · 2026
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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.

Anjaneyulu MurariDepartment of Physiology and Cellular Biophysics, Columbia University Medical Center, New York, NY.
Shauna-Kay RhoomsDepartment of Physiology and Cellular Biophysics, Columbia University Medical Center, New York, NY.
Naga Sri GoparajuDepartment of Physiology and Cellular Biophysics, Columbia University Medical Center, New York, NY.
Maximino VillanuevaDepartment of Physiology and Cellular Biophysics, Columbia University Medical Center, New York, NY.
Edward Owusu-AnsahDepartment of Physiology and Cellular Biophysics, Columbia University Medical Center, New York, NY.
Columbia University Irving Medical Center · US

Funding

Identifying Remote Regulators of Complex I Biogenesis in DrosophilaR35GM124717 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI OWUSU-ANSAH, EDWARD · 2017 to 2021
$2.2M
IGFBP-Mediated Local and Systemic Effects of Mitochondrial Dysfunction in Skeletal MusclesR21DK112074 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI OWUSU-ANSAH, EDWARD · 2016 to 2018
$594k
Genetic Dissection of OXPHOS Assembly in Skeletal MusclesR21AR077312 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI OWUSU-ANSAH, EDWARD · 2020 to 2021
$387k
NIAMS NIH HHS R21 AR077312NIDDK NIH HHS R21 DK112074NIGMS NIH HHS R35 GM124717
6 · The paper itself

Abstract

An ability to comprehensively track the assembly intermediates (AIs) of complex I (CI) biogenesis in Drosophila will enable the characterization of the precise mechanism(s) by which various CI regulators modulate CI assembly. Accordingly, we generated 21 novel antibodies to various mitochondrial proteins and used this resource to characterize the mechanism by which apoptosis-inducing factor (AIF) regulates CI biogenesis by tracking the AI profile observed when AIF expression is impaired. We find that when the AIF-Mia40 translocation complex is disrupted, the part of CI that transfers electrons to ubiquinone is synthesized but fails to progress in the CI biosynthetic pathway. This is associated with a reduction in intramitochondrial accumulation of the Mia40 substrate, MIC19. Importantly, knockdown of either MIC19 or MIC60, components of the mitochondrial contact site and cristae organizing system (MICOS), fully recapitulates the AI profile observed when AIF is inhibited. Thus, AIF's effect on CI assembly is principally due to compromised intramitochondrial transport of the MICOS complex.

Indexed as

AnimalsApoptosis Inducing FactorDrosophila melanogasterElectron Transport Complex IMitochondriaMitochondrial MembranesMitochondrial Membrane Transport ProteinsMitochondrial ProteinsProtein BindingApoptosis Inducing FactorElectron Transport Complex IMitochondrial Membrane Transport ProteinsMitochondrial Proteins

Identifiers

PMID32936885
PMCPMC7659709
OpenAlexW3084739147

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.