Evidence map›Paper›PMID 28669756›Full record

ArticleCurrent biology : CB2017

A Splice Variant of Centrosomin Converts Mitochondria to Microtubule-Organizing Centers.

Jieyan V Chen, Rebecca A Buchwalter, Ling-Rong Kao, Timothy L Megraw

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.7field-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

43 citing papers in PubMed, 66 citations in OpenAlex.

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  8. Mitochondrial Differentiation during Spermatogenesis: Lessons fromInternational journal of molecular sciences · 2024
    Review
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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

4 authors at 1 institution in 1 country.

Jieyan V ChenDepartment of Biomedical Sciences, Florida State University, 1115 West Call Street, Tallahassee, FL 32306, USA. Electronic address: jc09n@my.fsu.edu.
Rebecca A BuchwalterDepartment of Biomedical Sciences, Florida State University, 1115 West Call Street, Tallahassee, FL 32306, USA.
Ling-Rong KaoDepartment of Biomedical Sciences, Florida State University, 1115 West Call Street, Tallahassee, FL 32306, USA.
Timothy L MegrawDepartment of Biomedical Sciences, Florida State University, 1115 West Call Street, Tallahassee, FL 32306, USA. Electronic address: timothy.megraw@med.fsu.edu.
Florida State University · US

Funding

Centrosomin and Centrosomes in Cell DivisionR01GM068756 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI MEGRAW, TIMOTHY L · 2003 to 2012
$2.8M
Control of Autophagy by Centrosome ProteinsR15GM119078 · NIGMS · FLORIDA STATE UNIVERSITY · PI MEGRAW, TIMOTHY L · 2016 to 2016
$434k
NIGMS NIH HHS R01 GM068756NIGMS NIH HHS R15 GM119078
6 · The paper itself

Abstract

Non-centrosomal microtubule organizing centers (MTOCs) direct microtubule (MT) organization to exert diverse cell-type-specific functions. In Drosophila spermatids, the giant mitochondria provide structural platforms for MT reorganization to support elongation of the extremely long sperm. However, the molecular basis for this mitochondrial MTOC and other non-centrosomal MTOCs has not been discerned. Here we report that Drosophila centrosomin (cnn) expresses two major protein variants: the centrosomal form (CnnC) and a non-centrosomal form in testes (CnnT). CnnC is established as essential for functional centrosomes, the major MTOCs in animal cells. We show that CnnT is expressed exclusively in testes by alternative splicing and localizes to giant mitochondria in spermatids. In cell culture, CnnT targets to the mitochondrial surface, recruits the MT nucleator γ-tubulin ring complex (γ-TuRC), and is sufficient to convert mitochondria to MTOCs independent of core pericentriolar proteins that regulate MT assembly at centrosomes. We mapped two separate domains in CnnT: one that is necessary and sufficient to target it to mitochondria and another that is necessary and sufficient to recruit γ-TuRCs and nucleate MTs. In elongating spermatids, CnnT forms speckles on the giant mitochondria that are required to recruit γ-TuRCs to organize MTs and support spermiogenesis. This molecular characterization of the mitochondrial MTOC defines a minimal molecular requirement for MTOC generation and implicates the potent role of Cnn (or its related) proteins in the direct regulation of MT assembly and organization of non-centrosomal MTOCs.

Indexed as

AnimalsDrosophila melanogasterDrosophila ProteinsHomeodomain ProteinsMaleMicrotubule-Organizing CenterMitochondriaProtein IsoformsSpermatidsTestiscnn protein, DrosophilaDrosophila ProteinsHomeodomain ProteinsProtein Isoformscentriolecentrosomecentrosomingamma tubulinmicrotubulemitochondrianon-centrosomal MTOCspermatidspermatogenesisγ-TuRC

Identifiers

PMID28669756
PMCPMC6147254
OpenAlexW2734077890

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Registered trials

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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.