Evidence map›Paper›PMID 24143253›Full record

ArticlePloS one2013

MADM-ML, a mouse genetic mosaic system with increased clonal efficiency.

Astra Henner, P Britten Ventura, Ying Jiang, Hui Zong

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Tuning mitotic recombination with patterned DNA nicks for precision mosaic analysis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Critical role of cell competition in gliomagenesis.bioRxiv : the preprint server for biology · 2026
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  10. In Vivo Methods to Monitor Cardiomyocyte Proliferation.Journal of cardiovascular development and disease · 2022
    Review
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  19. Article
  20. Cardiac Regeneration and Stem Cells.Physiological reviews · 2015
    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

4 authors at 1 institution in 1 country.

Astra HennerInstitute of Molecular Biology, University of Oregon, Eugene, Oregon, United States of America.
P Britten Ventura
Ying Jiang
Hui Zong
University of Oregon · US

Funding

DEVELOPMENTAL BIOLOGY TRAINING PROGRAMT32HD007348 · NICHD · UNIVERSITY OF OREGON · PI Chris Q Doe, KRYN STANKUNAS · 1989 to 2026
$6.8M
Characterizing the glioma cell of origin in vivo using MADM, a mouse genetic mosaR01CA136495 · NCI · UNIVERSITY OF VIRGINIA · PI ZONG, HUI · 2010 to 2015
$1.7M
The essential role of supporting cells in medulloblastoma tumorigenicityF31NS076313 · NINDS · UNIVERSITY OF VIRGINIA · PI VENTURA, PATRICK BRITTEN · 2011 to 2012
$84k
NCI NIH HHS R01 CA136495NCI NIH HHS R01-CA136495NICHD NIH HHS T32 HD007348NINDS NIH HHS 7F31NS076313NINDS NIH HHS F31 NS076313
6 · The paper itself

Abstract

Mosaic Analysis with Double Markers (MADM) is a mouse genetic system that allows simultaneous gene knockout and fluorescent labeling of sparse, clonally-related cells within an otherwise normal mouse, thereby circumventing embryonic lethality problems and providing single-cell resolution for phenotypic analysis in vivo. The clonal efficiency of MADM is intrinsically low because it relies on Cre/loxP-mediated mitotic recombination between two homologous chromosomes rather than within the same chromosome, as in the case of conditional knockout (CKO). Although sparse labeling enhances in vivo resolution, the original MADM labels too few or even no cells when a low-expressing Cre transgene is used or a small population of cells is studied. Recently, we described the usage of a new system, MADM-ML, which contains three mutually exclusive, self-recognizing loxP variant sites as opposed to a single loxP site present in the original MADM system (referred to as MADM-SL in this paper). Here we carefully compared the recombination efficiency between MADM-SL and MADM-ML using the same Cre transgene, and found that the new system labels significantly more cells than the original system does. When we established mouse medulloblastoma models with both the original and the new MADM systems, we found that, while the MADM-SL model suffered from varied tumor progression and incomplete penetrance, the MADM-ML model had consistent tumor progression and full penetrance of tumor formation. Therefore MADM-ML, with its higher recombination efficiency, will broaden the applicability of MADM for studying many biological questions including normal development and disease modeling at cellular resolution in vivo.

Indexed as

MosaicismAnimalsChromatidsClone CellsDisease ProgressionGene Knockout TechniquesGenetic MarkersIntegrasesMedulloblastomaMiceRecombination, GeneticTransgenesCre recombinaseGenetic MarkersIntegrases

Identifiers

PMID24143253
PMCPMC3797059
OpenAlexW2037584877

What OpenQuestion holds

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LicenceCC BY
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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.