Evidence map›Paper›PMID 27646273›Full record

ArticleThe Journal of cell biology2016

Transition zone assembly and its contribution to axoneme formation in Drosophila male germ cells.

Jennifer Vieillard, Marie Paschaki, Jean-Luc Duteyrat, Céline Augière, Elisabeth Cortier, Jean-André Lapart, Joëlle Thomas, Bénédicte Durand

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.3field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 69 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

8 authors at 3 institutions in 1 country.

Jennifer VieillardUniversité Claude Bernard Lyon 1, Institut National de la Santé et de la Recherche Médicale U1217, Institut NeuroMyoGène, Centre National de la Recherche Scientifique UMR 5310, F-69100 Lyon, France.
Marie PaschakiUniversité Claude Bernard Lyon 1, Institut National de la Santé et de la Recherche Médicale U1217, Institut NeuroMyoGène, Centre National de la Recherche Scientifique UMR 5310, F-69100 Lyon, France.
Jean-Luc DuteyratUniversité Claude Bernard Lyon 1, Institut National de la Santé et de la Recherche Médicale U1217, Institut NeuroMyoGène, Centre National de la Recherche Scientifique UMR 5310, F-69100 Lyon, France.
Céline AugièreUniversité Claude Bernard Lyon 1, Institut National de la Santé et de la Recherche Médicale U1217, Institut NeuroMyoGène, Centre National de la Recherche Scientifique UMR 5310, F-69100 Lyon, France.
Elisabeth CortierUniversité Claude Bernard Lyon 1, Institut National de la Santé et de la Recherche Médicale U1217, Institut NeuroMyoGène, Centre National de la Recherche Scientifique UMR 5310, F-69100 Lyon, France.
Jean-André LapartUniversité Claude Bernard Lyon 1, Institut National de la Santé et de la Recherche Médicale U1217, Institut NeuroMyoGène, Centre National de la Recherche Scientifique UMR 5310, F-69100 Lyon, France.
Joëlle ThomasUniversité Claude Bernard Lyon 1, Institut National de la Santé et de la Recherche Médicale U1217, Institut NeuroMyoGène, Centre National de la Recherche Scientifique UMR 5310, F-69100 Lyon, France.
Bénédicte DurandUniversité Claude Bernard Lyon 1, Institut National de la Santé et de la Recherche Médicale U1217, Institut NeuroMyoGène, Centre National de la Recherche Scientifique UMR 5310, F-69100 Lyon, France durand-b@univ-lyon1.fr.
Université Claude Bernard Lyon 1 · FRInstitut NeuroMyoGène · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ciliary transition zone (TZ) is a complex structure found at the cilia base. Defects in TZ assembly are associated with human ciliopathies. In most eukaryotes, three protein complexes (CEP290, NPHP, and MKS) cooperate to build the TZ. We show that in Drosophila melanogaster, mild TZ defects are observed in the absence of MKS components. In contrast, Cby and Azi1 cooperate to build the TZ by acting upstream of Cep290 and MKS components. Without Cby and Azi1, centrioles fail to form the TZ, precluding sensory cilia assembly, and no ciliary membrane cap associated with sperm ciliogenesis is made. This ciliary cap is critical to recruit the tubulin-depolymerizing kinesin Klp59D, required for regulation of axonemal growth. Our results show that Drosophila TZ assembly in sensory neurons and male germ cells involves cooperative actions of Cby and Dila. They further reveal that temporal control of membrane cap assembly by TZ components and microtubule elongation by kinesin-13 is required for axoneme formation in male germ cells.

Indexed as

AnimalsAxonemeCentriolesCiliaDrosophila melanogasterDrosophila ProteinsFertilityMaleSpermatogenesisSpermatozoaDrosophila Proteins

Identifiers

PMID27646273
PMCPMC5037411
OpenAlexW2521166179

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.