Evidence map›Paper›PMID 20156285›Full record

ArticleEvolution & development

Phylogenetic analysis of developmental and postnatal mouse cell lineages.

Stephen J Salipante, Arnold Kas, Eva McMonagle, Marshall S Horwitz

Open access · bronzeAbstract read
In one paragraph

Article in Evolution & development. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  3. PolyG-DS: An ultrasensitive polyguanine tract-profiling method to detect clonal expansions and trace cell lineage.Proceedings of the National Academy of Sciences of the United States of America · 2021
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  11. Hypermutable DNA chronicles the evolution of human colon cancer.Proceedings of the National Academy of Sciences of the United States of America · 2014
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Stephen J SalipanteDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98109, USA.
Arnold Kas
Eva McMonagle
Marshall S Horwitz
University of Washington · US

Funding

University of Washington Medical Scientist Training Program: MD/PhDT32GM007266 · NIGMS · UNIVERSITY OF WASHINGTON · PI HORWITZ, MARSHALL S. · 1985 to 2023
$30.4M
Medical Genetics Training GrantT32GM007454 · NIGMS · UNIVERSITY OF WASHINGTON · PI Gail Pairitz Jarvik, Andrew Ben Stergachis · 1985 to 2026
$6.9M
NIH Director's Pioneer AwardDP1OD003278 · OD · UNIVERSITY OF WASHINGTON · PI HORWITZ, MARSHALL S. · 2007 to 2011
$3.9M
Genomic Fate MapsR01DK078340 · NIDDK · UNIVERSITY OF WASHINGTON · PI HORWITZ, MARSHALL S. · 2008 to 2012
$1.7M
Phylogenetic Fate Mapping: Following Cellular Lineages in Embryogenesis and AgingF30AG030316 · NIA · UNIVERSITY OF WASHINGTON · PI SALIPANTE, STEPHEN J · 2007 to 2010
$127k
NIA NIH HHS F30 AG030316NIA NIH HHS F30AG030316NIDDK NIH HHS R01 DK078340NIDDK NIH HHS R01DK078340NIGMS NIH HHS T32 GM007266NIGMS NIH HHS T32GM007266NIGMS NIH HHS T32 GM007454NIH HHS DP1 OD003278NIH HHS DP1OD003278
6 · The paper itself

Abstract

Fate maps depict how cells relate together through past lineage relationships, and are useful tools for studying developmental and somatic processes. However, with existing technologies, it has not been possible to generate detailed fate maps of complex organisms such as the mouse. We and others have therefore proposed a novel approach, "phylogenetic fate mapping," where patterns of somatic mutation carried by the individual cells of an animal are used to retrospectively deduce lineage relationships through phylogenetic inference. Here, we have cataloged genomic polymorphisms at 324 mutation-prone polyguanine tracts for nearly 300 cells isolated from a single mouse, and have explored the cells' lineage relationships both phylogenetically and through a network-based approach. We present a model of mouse embryogenesis, where an early period of substantial cell mixing is followed by more coherent growth of clones later. We find that cells from certain tissues have greater numbers of close relatives in other specific tissues than expected from chance, suggesting that those populations arise from a similar pool of ancestral lineages. Finally, we have investigated the dynamics of cell turnover (the frequency of cell loss and replacement) in postnatal tissues. This work offers a longitudinal study of developmental lineages, from conception to adulthood, and provides insight into basic questions of mouse embryology as well as the somatic processes that occur after birth.

Indexed as

PhylogenyAnimalsAntigens, Polyomavirus TransformingBase SequenceBayes TheoremCells, CulturedDNA PrimersEmbryonic DevelopmentGene Regulatory NetworksGenotypeMaleMiceMice, TransgenicMitosisModels, BiologicalZygoteAntigens, Polyomavirus TransformingDNA Primers

Identifiers

PMID20156285
PMCPMC2824914
OpenAlexW2135610271

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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.