Evidence map›Paper›PMID 15317935›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2004

Orthogonal analysis of C/EBPbeta targets in vivo during liver proliferation.

Joshua R Friedman, Brian Larris, Phillip P Le, T Harshani Peiris, Athanasios Arsenlis, Jonathan Schug, John W Tobias, Klaus H Kaestner, Linda E Greenbaum

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  8. Beta-catenin signaling in hepatic development and progenitors: which way does the WNT blow?Developmental dynamics : an official publication of the American Association of Anatomists · 2011
    Review
  9. Article
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  15. Hepatocyte nuclear factor-1alpha regulates glucocorticoid receptor expression to control postnatal body growth.American journal of physiology. Gastrointestinal and liver physiology · 2008
    Article
  16. Article
  17. Article
  18. Liver regeneration.Journal of cellular physiology · 2007
    Review
  19. Article
  20. Article
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

9 authors at 1 institution in 1 country.

Joshua R FriedmanDepartment of Genetics, Bioinformatics Core, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Brian Larris
Phillip P Le
T Harshani Peiris
Athanasios Arsenlis
Jonathan Schug
John W Tobias
Klaus H Kaestner
Linda E Greenbaum
University of Pennsylvania · US

Funding

ZINC FINGER PROTEINS IN EARLY KIDNEY DEVELOPMENTP01DK049210 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI BIRNBAUM, MORRIS J · 1995 to 2016
$26.9M
FUNCTIONAL GENOMICS OF THE BETA-CELLU01DK056947 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI KAESTNER, KLAUS H. · 2002 to 2007
$10.7M
MEDICAL GENETICS RESEARCH TRAINING GRANTT32GM008638 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI Rebecca Ganetzky · 1997 to 2026
$8.7M
FUNCTIONAL GENOMICS OF THE DEVELOPING ENDOCRINE PANCREASR24DK056947 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI KAESTNER, KLAUS H. · 1999 to 2001
$3.2M
Transcriptional Control in Hepatocyte ProliferationR01DK056669 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI GREENBAUM, LINDA E · 2001 to 2011
$2.8M
NIDDK NIH HHS DK056669NIDDK NIH HHS DK49210NIDDK NIH HHS DK56947NIDDK NIH HHS P01 DK049210NIDDK NIH HHS R01 DK056669NIDDK NIH HHS R24 DK056947NIDDK NIH HHS U01 DK056947NIGMS NIH HHS 5T32GM008638NIGMS NIH HHS T32 GM008638
6 · The paper itself

Abstract

CCAAT enhancer-binding protein beta (C/EBPbeta), a basic-leucine zipper transcription factor, is an important effector of signals in physiologic growth and cancer. The identification of direct C/EBPbeta targets in vivo has been limited by functional compensation by other C/EBP family proteins and the low stringency of the consensus sequence. Here we use the combined power of expression profiling and high-throughput chromatin immunoprecipitation to identify direct and biologically relevant targets of C/EBPbeta. We identified 25 potential C/EBPbeta targets, of which 88% of those tested were confirmed as in vivo C/EBPbeta-binding sites. Six of these genes also displayed differential expression in C/EBPbeta-/- livers. Computational analysis revealed that bona fide C/EBPbeta target genes can be distinguished by the presence of binding motifs for specific additional transcription factors in the vicinity of the C/EBPbeta site. This approach is generally applicable to the discovery of direct, biologically relevant targets of mammalian transcription factors.

Indexed as

AnimalsCCAAT-Enhancer-Binding Protein-betaCell DivisionGene Expression RegulationLiverLiver RegenerationMiceMutationCCAAT-Enhancer-Binding Protein-beta

Identifiers

PMID15317935
PMCPMC516505
OpenAlexW2168447817

What OpenQuestion holds

Textmetadata
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.