Evidence map›Paper›PMID 26965374›Full record

ArticleDevelopment (Cambridge, England)2016

aura (mid1ip1l) regulates the cytoskeleton at the zebrafish egg-to-embryo transition.

Celeste Eno, Bharti Solanki, Francisco Pelegri

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2016. 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
–field-weighted citation impact
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.

  1. Review
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  6. Review
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  11. Review
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  16. Aggregation, segregation, and dispersal of homotypic germ plasm RNPs in the early zebrafish embryo.Developmental dynamics : an official publication of the American Association of Anatomists · 2019
    Article
  17. Review
  18. Article
  19. Article
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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

3 authors.

Celeste EnoLaboratory of Genetics, University of Wisconsin - Madison, 425-G Henry Mall, Room 2455 Genetics, Madison, WI 53706, USA.
Bharti SolankiLaboratory of Genetics, University of Wisconsin - Madison, 425-G Henry Mall, Room 2455 Genetics, Madison, WI 53706, USA.
Francisco PelegriLaboratory of Genetics, University of Wisconsin - Madison, 425-G Henry Mall, Room 2455 Genetics, Madison, WI 53706, USA fjpelegri@wisc.edu.

Funding

Diversity Supplement: Cytokinesis and RNA segregation in zebrafish developmentR01GM065303 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI PELEGRI, FRANCISCO J · 2002 to 2023
$4.7M
Cytokinesis and RNA Segregation in Zebrafish DevelopmentR56GM065303 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI PELEGRI, FRANCISCO J · 2007 to 2007
$254k
Germ Plasm Aggregation and Compaction in the Early Zebrafish EmbryoF31GM108449 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI ENO, CELESTE CHLOE · 2014 to 2016
$55k
NIGMS NIH HHS F31 GM108449NIGMS NIH HHS R01 GM065303NIGMS NIH HHS R56 GM065303
6 · The paper itself

Abstract

Embryos from females homozygous for a recessive maternal-effect mutation in the gene aura exhibit defects including reduced cortical integrity, defective cortical granule (CG) release upon egg activation, failure to complete cytokinesis, and abnormal cell wound healing. We show that the cytokinesis defects are associated with aberrant cytoskeletal reorganization during furrow maturation, including abnormal F-actin enrichment and microtubule reorganization. Cortical F-actin prior to furrow formation fails to exhibit a normal transition into F-actin-rich arcs, and drug inhibition is consistent with aura function promoting F-actin polymerization and/or stabilization. In mutants, components of exocytic and endocytic vesicles, such as Vamp2, Clathrin and Dynamin, are sequestered in unreleased CGs, indicating a need for CG recycling in the normal redistribution of these factors. However, the exocytic targeting factor Rab11 is recruited to the furrow plane normally at the tip of bundling microtubules, suggesting an alternative anchoring mechanism independent of membrane recycling. A positional cloning approach indicates that the mutation in aura is associated with a truncation of Mid1 interacting protein 1 like (Mid1ip1l), previously identified as an interactor of the X-linked Opitz G/BBB syndrome gene product Mid1. A Cas9/CRISPR-induced mutant allele in mid1ip1l fails to complement the originally isolated aura maternal-effect mutation, confirming gene assignment. Mid1ip1l protein localizes to cortical F-actin aggregates, consistent with a direct role in cytoskeletal regulation. Our studies indicate that maternally provided aura (mid1ip1l) acts during the reorganization of the cytoskeleton at the egg-to-embryo transition and highlight the importance of cytoskeletal dynamics and membrane recycling during this developmental period.

Indexed as

ActinsAnimalsClathrinCytokinesisCytoplasmic GranulesCytoskeletal ProteinsCytoskeletonDynaminsMicrotubulesrab11 GTP-Binding Proteinsrab GTP-Binding ProteinsVesicle-Associated Membrane Protein 2ZebrafishZebrafish ProteinsActinsClathrinCytoskeletal ProteinsDynaminsmid1ip1l protein, zebrafishrab11 GTP-Binding Proteinsrab GTP-Binding ProteinsVesicle-Associated Membrane Protein 2Zebrafish ProteinsCortical granulesCytokinesisCytoskeletonF-actinMembrane exocytosisMid1Mid1ip1lOpitz G/BBB syndromeZebrafish

Identifiers

PMID26965374
PMCPMC4986165

What OpenQuestion holds

Textmetadata
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.