Evidence map›Paper›PMID 11376130›Full record

ArticleMolecular pathology : MP2001

5' flanking sequence of the human immediate early responsive gene ccn1 (cyr61) and mapping of polymorphic CA repeat sequence motifs in the human ccn1 (cyr61) locus.

N Schütze, N Rücker, J Müller, J Adamski, F Jakob

Open access · bronzeAbstract read
In one paragraph

Article in Molecular pathology : MP, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

12 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. CYR61/CCN1 Regulates Sclerostin Levels and Bone Maintenance.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2018
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. CCN1 secretion and cleavage regulate the lung epithelial cell functions after cigarette smoke.American journal of physiology. Lung cellular and molecular physiology · 2014
    Article
  10. Article
  11. Article
  12. 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

5 authors at 3 institutions in 2 countries.

N SchützeOrthopädische Klinik, König-Ludwig-Haus, Labor für Molekulare Experimentelle Orthopädie, Brettreichstrasse 11, 97074 Würzburg, Germany. n-schuetze.klh@mail.uni-wuerzburg.de
N Rücker
J Müller
J Adamski
F Jakob
Klinik König-Ludwig Haus · DEUniversity of Würzburg · DEAmt für Umwelt · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThe human ccn1 (hccn; hcyr61) gene has been identified previously at the mRNA and protein level as a 1,25-dihydroxyvitamin D(3) and growth factor regulated gene in human osteoblasts. This study aimed to analyse genomic clones containing the human ccn1 (cyr61) gene and to provide the 5' flanking region.

methodsGenomic clones were isolated by screening a lambda library and by array filter hybridisations of a genomic library. Sequencing was performed using the dye terminator method. Promoter activity was measured after transient transfection using a beta galactosidase assay. CA repeat motifs were studied by a combined PCR/fragment analysis protocol.

resultsThe human 5' flanking region of 870 nucleotides contains several stretches with high homology to the mouse promoter as well as CA repeat motifs. This first report on the human 5' flanking sequence of the hccn1 (hcyr61) gene provides important insights into regulation pathways for the expression of this 1,25-dihydroxyvitamin D(3) and growth factor responsive early gene. A genomic clone containing the hccn1 (hcyr61) gene region also yielded a CA sequence located 3' of the ccn1 (cyr61) gene. This CA repeat and one of the CA repeat motifs in the promoter were studied in detail and found to be polymorphic.

conclusionsThe 5' flanking sequence of the hccn1 (hcyr61) gene provides insights into the mechanisms of regulation of this immediate early gene product. The CA repeat polymorphisms within the gene region will be useful in the genetic study of disorders affecting bone metabolism.

Indexed as

Chromosome MappingCyclinsPolymorphism, GeneticPromoter Regions, GeneticSequence Analysis, DNAbeta-GalactosidaseClone CellsFungal ProteinsGenomic LibraryHumansPhotometryPolymerase Chain ReactionTransfectionbeta-GalactosidaseCLN1 protein, Candida albicansCyclinsFungal Proteins

Identifiers

PMID11376130
PMCPMC1187057
OpenAlexW1993325779

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.