Evidence map›Paper›PMID 20944551›Full record

ArticleKidney international2011

Dicer regulates the development of nephrogenic and ureteric compartments in the mammalian kidney.

Vidya K Nagalakshmi, Qun Ren, Margaret M Pugh, M Todd Valerius, Andrew P McMahon, Jing Yu

Open access · bronzeAbstract read
In one paragraph

Article in Kidney international, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
4.9field-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

99 citing papers in PubMed, 163 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. The genetics and pathogenesis of CAKUT.Nature reviews. Nephrology · 2023
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. DICER1 tumor predisposition syndrome: an evolving story initiated with the pleuropulmonary blastoma.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Review
  14. Role of microRNAs in Obesity-Related Kidney Disease.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Review
  17. Non-Coding RNAs in Hereditary Kidney Disorders.International journal of molecular sciences · 2021
    Review
  18. Review
  19. Organ-Specific Branching Morphogenesis.Frontiers in cell and developmental biology · 2021
    Review
  20. Article

39 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Vidya K NagalakshmiDepartment of Cell Biology, University of Virginia School of Medicine, Charlottesville, Virginia 22908, USA.
Qun Ren
Margaret M Pugh
M Todd Valerius
Andrew P McMahon
Jing Yu
University of Virginia · USHarvard Stem Cell Institute · US

Funding

Cell Interactions in Development of the Mammalian KidneyR37DK054364 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MCMAHON, ANDREW P. · 2008 to 2017
$7.0M
CELL INTERACTIONS IN DEVELOPMENT OF THE MAMMALIAN KIDNEYR01DK054364 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MCMAHON, ANDREW P. · 1998 to 2022
$6.9M
Molecular and Cellular Regulation of Mammalian Renal Medulla DevelopmentR01DK085080 · NIDDK · UNIVERSITY OF VIRGINIA · PI YU, JING · 2010 to 2014
$1.7M
NIDDK NIH HHS DK054364NIDDK NIH HHS R01 DK054364NIDDK NIH HHS R01 DK085080NIDDK NIH HHS R37 DK054364
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are a large and growing class of small, non-coding, regulatory RNAs that control gene expression predominantly at the post-transcriptional level. The production of most functional miRNAs depends on the enzymatic activity of Dicer, an RNase III class enzyme. To address the potential action of Dicer-dependent miRNAs in mammalian kidney development, we conditionally ablated Dicer function within cells of nephron lineage and the ureteric bud-derived collecting duct system. Six2Cre-mediated removal of Dicer activity from the progenitors of the nephron epithelium led to elevated apoptosis and premature termination of nephrogenesis. Thus, Dicer action is important for maintaining the viability of this critical self-renewing progenitor pool and, consequently, development of a normal nephron complement. HoxB7Cre-mediated removal of Dicer function from the ureteric bud epithelium led to the development of renal cysts. This was preceded by excessive cell proliferation and apoptosis, and accompanied by disrupted ciliogenesis within the ureteric bud epithelium. Dicer removal also disrupted branching morphogenesis with the phenotype correlating with downregulation of Wnt11 and c-Ret expression at ureteric tips. Thus Dicer, and by inference Dicer-dependent miRNA activity, have distinct regulatory roles within different components of the developing mouse kidney. Furthermore, an understanding of miRNA action may provide new insights into the etiology and pathogenesis of renal cyst-based kidney disease.

Indexed as

AnimalsAnimals, NewbornApoptosisCell ProliferationCell SurvivalDEAD-box RNA HelicasesEndoribonucleasesEpithelial CellsGene Expression Regulation, DevelopmentalGenotypeGestational AgeGlial Cell Line-Derived Neurotrophic FactorKidney Diseases, CysticMiceMice, KnockoutMicroRNAsDEAD-box RNA HelicasesDicer1 protein, mouseEndoribonucleasesGlial Cell Line-Derived Neurotrophic FactorMicroRNAsProto-Oncogene Proteins c-retRibonuclease IIIRNA, MessengerWnt11 protein, mouseWnt Proteins

Identifiers

PMID20944551
PMCPMC3214622
OpenAlexW2061477448

What OpenQuestion holds

Textmetadata
LicenceTDM
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.