Evidence map›Paper›PMID 21364958›Full record

ArticlePloS one2011

Dramatic repositioning of c-Myb to different promoters during the cell cycle observed by combining cell sorting with chromatin immunoprecipitation.

Anita M Quintana, Ye E Zhou, Janeth J Pena, John P O'Rourke, Scott A Ness

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. 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
1.4field-weighted citation impact, top 20% 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, 27 citations in OpenAlex.

  1. Review
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  8. Dual Mechanism ofMolecular and cellular biology · 2017
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  14. Analysis of a Genetic Polymorphism in the Costimulatory Molecule TNFSF4 with Hematopoietic Stem Cell Transplant Outcomes.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2016
    Article
  15. Runx2 regulates endochondral ossification through control of chondrocyte proliferation and differentiation.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2014
    Article
  16. Article
  17. Review
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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

5 authors at 1 institution in 1 country.

Anita M QuintanaDepartment of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, United States of America.
Ye E Zhou
Janeth J Pena
John P O'Rourke
Scott A Ness
University of New Mexico · US

Funding

WOMEN'S CANCERS RESEARCH PROGRAMP30CA118100 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Yolanda Sanchez · 2005 to 2026
$57.1M
CORE--VECTOR PRODUCTIONP30DK056465 · NIDDK · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HEIMFELD, SHELLY · 1999 to 2014
$14.9M
UNM PREP (Post-baccalaureate Research Education ProgramR25GM075149 · NIGMS · UNIVERSITY OF NEW MEXICO · PI Kelly Miller · 2005 to 2026
$7.3M
TRANSFORMING FUNCTIONS OF THE V-MYB ONCOGENE PRODUCTR01CA058443 · NCI · UNIVERSITY OF NEW MEXICO · PI NESS, SCOTT A. · 1995 to 2010
$2.6M
Myb protein specificity in human hematopoietic cellsR01CA105257 · NCI · UNIVERSITY OF NEW MEXICO · PI NESS, SCOTT A. · 2005 to 2009
$1.3M
Post-translational modifications affect c-Myb specificity.F31HL090024 · NHLBI · UNIVERSITY OF NEW MEXICO · PI QUINTANA, ANITA M · 2007 to 2009
$87k
NCI NIH HHS 5R01CA058443NCI NIH HHS 5R01CA105257NCI NIH HHS P30 CA118100NCI NIH HHS R01 CA058443NCI NIH HHS R01 CA105257NHLBI NIH HHS 5F31HL090024-03NHLBI NIH HHS F31 HL090024NIDDK NIH HHS DK56465NIDDK NIH HHS P30 DK056465NIGMS NIH HHS R25 GM075149
6 · The paper itself

Abstract

The c-Myb transcription factor is a critical regulator of proliferation and stem cell differentiation, and mutated alleles of c-Myb are oncogenic, but little is known about changes in c-Myb activity during the cell cycle. To map the association of c-Myb with specific target genes during the cell cycle, we developed a novel Fix-Sort-ChIP approach, in which asynchronously growing cells were fixed with formaldehyde, stained with Hoechst 33342 and separated into different cell cycle fractions by flow sorting, then processed for chromatin immunoprecipitation (ChIP) assays. We found that c-Myb actively repositions, binding to some genes only in specific cell cycle phases. In addition, the specificity of c-Myb is dramatically different in small subpopulations of cells, for example cells in the G2/M phase of the cell cycle, than in the bulk population. The repositioning of c-Myb during the cell cycle is not due to changes in its expression and also occurs with ectopically expressed, epitope-tagged versions of c-Myb. The repositioning occurs in established cell lines, in primary human CD34+ hematopoietic progenitors and in primary human acute myeloid leukemia cells. The combination of fixation, sorting and ChIP analysis sheds new light on the dynamic nature of gene regulation during the cell cycle and provides a new type of tool for the analysis of gene regulation in small subsets of cells, such as cells in a specific phase of the cell cycle.

Indexed as

Chromatin ImmunoprecipitationFlow CytometryPromoter Regions, GeneticAntineoplastic AgentsCell CycleCells, CulturedChromatinCombinatorial Chemistry TechniquesGene Expression RegulationHumansHydroxyureaJurkat CellsNocodazoleProtein BindingProto-Oncogene Proteins c-mybAntineoplastic AgentsChromatinHydroxyureaNocodazoleProto-Oncogene Proteins c-myb

Identifiers

PMID21364958
PMCPMC3043100
OpenAlexW1991004739

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.