Evidence map›Paper›PMID 21060807›Full record

ArticlePLoS genetics2010

Actin depolymerizing factors cofilin1 and destrin are required for ureteric bud branching morphogenesis.

Satu Kuure, Cristina Cebrian, Quentin Machingo, Benson C Lu, Xuan Chi, Deborah Hyink, Vivette D'Agati, Christine Gurniak, Walter Witke, Frank Costantini

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.6field-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

38 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
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  4. Integrins in the kidney - beyond the matrix.Nature reviews. Nephrology · 2025
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  7. Overexpression of long noncoding RNAFrontiers in cell and developmental biology · 2023
    Article
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  10. Review
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  12. Article
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  14. Review
  15. Article
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  17. 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

10 authors at 3 institutions in 2 countries.

Satu KuureDepartment of Genetics and Development, Columbia University Medical Center, New York, New York, United States of America.
Cristina Cebrian
Quentin Machingo
Benson C Lu
Xuan Chi
Deborah Hyink
Vivette D'Agati
Christine Gurniak
Walter Witke
Frank Costantini
Columbia University Irving Medical Center · USUniversity of Bonn · DEIcahn School of Medicine at Mount Sinai · US

Funding

Branching Morphogenesis of Urinary Epithelia: from Genes to Cellular BehaviorsR01DK083289 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI COSTANTINI, FRANKLIN D · 2009 to 2018
$4.9M
Genetic analysis of Pea3 transcription factors and kidney developmentR01DK075578 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI COSTANTINI, FRANKLIN D · 2006 to 2014
$4.1M
NIDDK NIH HHS 1R01DK075578NIDDK NIH HHS 1R01DK083289NIDDK NIH HHS R01 DK075578NIDDK NIH HHS R01 DK083289
6 · The paper itself

Abstract

The actin depolymerizing factors (ADFs) play important roles in several cellular processes that require cytoskeletal rearrangements, such as cell migration, but little is known about the in vivo functions of ADFs in developmental events like branching morphogenesis. While the molecular control of ureteric bud (UB) branching during kidney development has been extensively studied, the detailed cellular events underlying this process remain poorly understood. To gain insight into the role of actin cytoskeletal dynamics during renal branching morphogenesis, we studied the functional requirements for the closely related ADFs cofilin1 (Cfl1) and destrin (Dstn) during mouse development. Either deletion of Cfl1 in UB epithelium or an inactivating mutation in Dstn has no effect on renal morphogenesis, but simultaneous lack of both genes arrests branching morphogenesis at an early stage, revealing considerable functional overlap between cofilin1 and destrin. Lack of Cfl1 and Dstn in the UB causes accumulation of filamentous actin, disruption of normal epithelial organization, and defects in cell migration. Animals with less severe combinations of mutant Cfl1 and Dstn alleles, which retain one wild-type Cfl1 or Dstn allele, display abnormalities including ureter duplication, renal hypoplasia, and abnormal kidney shape. The results indicate that ADF activity, provided by either cofilin1 or destrin, is essential in UB epithelial cells for normal growth and branching.

Indexed as

MorphogenesisActinsAnimalsCell MovementCofilin 1DestrinEpithelial CellsEpitheliumFemaleFluorescent Antibody TechniqueGenotypeGlial Cell Line-Derived Neurotrophic FactorIn Situ HybridizationKidneyMaleMiceActinsCfl1 protein, mouseCofilin 1DestrinDstn protein, mouseGlial Cell Line-Derived Neurotrophic Factor

Identifiers

PMID21060807
PMCPMC2965756
OpenAlexW2086026094

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.