Evidence map›Paper›PMID 16464245›Full record

ArticleBMC nephrology2006

Gene expression profiles in developing nephrons using Lim1 metanephric mesenchyme-specific conditional mutant mice.

You-Tzung Chen, Akio Kobayashi, Kin Ming Kwan, Randy L Johnson, Richard R Behringer

Open access · goldAbstract read
In one paragraph

Article in BMC nephrology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

11 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Transcriptional control of terminal nephron differentiation.American journal of physiology. Renal physiology · 2008
    Review
  10. Article
  11. Molecular insights into segmentation along the proximal-distal axis of the nephron.Journal of the American Society of Nephrology : JASN · 2007
    Review
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

5 authors at 1 institution in 1 country.

You-Tzung ChenDepartment of Molecular Genetics, University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA. ytchen@mdanderson.org
Akio Kobayashi
Kin Ming Kwan
Randy L Johnson
Richard R Behringer
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Molecular Genetics of Female Reproductive TractR01HD030284 · NICHD · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BEHRINGER, RICHARD R · 1994 to 2013
$4.5M
Female Reproductive Tract Development in the MouseR37HD030284 · NICHD · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BEHRINGER, RICHARD R · 2014 to 2023
$4.2M
MOLECULAR MECHANISM OF OCULAR MORPHOGENESIS--THE ANT SEGR01EY012311 · NEI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI JOHNSON, RANDY L. · 1998 to 2005
$2.1M
NCI NIH HHS CA16672NCI NIH HHS P30 CA016672NEI NIH HHS EY012311NEI NIH HHS R01 EY012311NICHD NIH HHS HD30284NICHD NIH HHS R01 HD030284NICHD NIH HHS R37 HD030284
6 · The paper itself

Abstract

backgroundLim1 is a homeobox gene that is essential for nephrogenesis. During metanephric kidney development, Lim1 is expressed in the nephric duct, ureteric buds, and the induced metanephric mesenchyme. Conditional ablation of Lim1 in the metanephric mesenchyme blocks the formation of nephrons at the nephric vesicle stage, leading to the production of small, non-functional kidneys that lack nephrons.

methodsIn the present study, we used Affymetrix probe arrays to screen for nephron-specific genes by comparing the expression profiles of control and Lim1 conditional mutant kidneys. Kidneys from two developmental stages, embryonic day 14.5 (E14.5) and 18.5 (E18.5), were examined.

resultsComparison of E18.5 kidney expression profiles generated a list of 465 nephron-specific gene candidates that showed a more than 2-fold increase in their expression level in control kidney versus the Lim1 conditional mutant kidney. Computational analysis confirmed that this screen enriched for kidney-specific genes. Furthermore, at least twenty-eight of the top fifty (56%) candidates (or their vertebrate orthologs) were previously reported to have a nephron-specific expression pattern. Our analysis of E14.5 expression data yielded 41 candidate genes that are up-regulated in the control kidneys compared to the conditional mutants. Three of them are related to the Notch signaling pathway that is known to be important in cell fate determination and nephron patterning.

conclusionTherefore, we demonstrate that Lim1 conditional mutant kidneys serve as a novel tissue source for comprehensive expression studies and provide a means to identify nephron-specific genes.

Indexed as

Gene Expression ProfilingAnimalsEmbryo, MammalianEmbryonic DevelopmentHomeodomain ProteinsLIM-Homeodomain ProteinsMiceMice, Mutant StrainsNephronsOligonucleotide Array Sequence AnalysisReceptors, NotchSignal TransductionTranscription FactorsUp-RegulationHomeodomain ProteinsLhx1 protein, mouseLIM-Homeodomain ProteinsReceptors, NotchTranscription Factors

Identifiers

PMID16464245
PMCPMC1413522
OpenAlexW1501475362

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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.