Evidence map›Paper›PMID 7544436›Full record

ArticleMolecular and cellular biology1995

Individual mouse alpha-fetoprotein enhancer elements exhibit different patterns of tissue-specific and hepatic position-dependent activities.

T M Ramesh, A W Ellis, B T Spear

Abstract readComparative Study
In one paragraph

Article in Molecular and cellular biology, 1995. 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
1.1field-weighted citation impact, top 21% 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, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Tg(Afp-GFP) expression marks primitive and definitive endoderm lineages during mouse development.Developmental dynamics : an official publication of the American Association of Anatomists · 2006
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  10. Position-dependent activity of alpha -fetoprotein enhancer element III in the adult liver is due to negative regulation.Proceedings of the National Academy of Sciences of the United States of America · 2000
    Article
  11. 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

3 authors at 1 institution in 1 country.

T M RameshDepartment of Microbiology and Immunology, University of Kentucky College of Medicine, Lexington 40536-0084, USA.
A W Ellis
B T Spear
University of Kentucky · US

Funding

GENETIC SCHEMES TO CLONE MAMMALIAN TRANSCRIPTION FACTORSR29GM045253 · NIGMS · UNIVERSITY OF KENTUCKY · PI SPEAR, BRETT T · 1991 to 1995
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NIGMS NIH HHS GM-45253
6 · The paper itself

Abstract

Transcription of the mouse alpha-fetoprotein (AFP) gene, which is expressed at high levels in the visceral endoderm of the yolk sac and fetal liver and at low levels in the fetal gut, is regulated by three distinct upstream enhancer regions. To investigate the activities of these regions, each enhancer was individually linked to a heterologous human beta-globin promoter fused to the mouse class I H-2Dd structural gene. When tested in transgenic mice, the beta-globin promoter alone has minimal activity. We find that all three enhancers activate the beta-globin promoter in an AFP-like pattern; i.e., activity is detected in the yolk sac, fetal liver, and fetal gut. The enhancers remain active in the livers and guts of adult mice, consistent with previous studies showing that postnatal AFP repression is due not to the loss of enhancer activity but to a dominant repressor region. Enhancer III also functions in the brain. In addition, these studies reveal that the three enhancers exhibit different position-dependent activities in the adult liver. Enhancers I and II are most active in hepatocytes surrounding the central vein, with a gradual decrease in activity along the hepatic plates toward the portal triad. Enhancer III is active exclusively in hepatocytes surrounding the central vein. These data represent the first examples of individual control elements exhibiting positionally regulated activity in adult liver.

Indexed as

Gene Expression Regulation, Developmentalalpha-FetoproteinsAnimalsEnhancer Elements, GeneticGlobinsH-2 AntigensHistocompatibility Antigen H-2DHumansImmunohistochemistryLiverMiceMice, Inbred StrainsMice, TransgenicRNA, MessengerTissue DistributionYolk Sacalpha-FetoproteinsGlobinsH-2 AntigensHistocompatibility Antigen H-2DRNA, Messenger

Identifiers

PMID7544436
PMCPMC230741
OpenAlexW2138941172

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.