Evidence map›Paper›PMID 24184271›Full record

ArticleBiochimica et biophysica acta2013

Regulation of HFE expression by poly(ADP-ribose) polymerase-1 (PARP1) through an inverted repeat DNA sequence in the distal promoter.

Christopher Pelham, Tamara Jimenez, Marianna Rodova, Angela Rudolph, Elizabeth Chipps, M Rafiq Islam

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2013. 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
1.2field-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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Experimental Drugs for Chemotherapy- and Cancer-Related Anemia.Journal of experimental pharmacology · 2021
    Review
  5. Okamoto model for necrosis and its expansions, CD38-cyclic ADP-ribose signal system for intracellular CaProceedings of the Japan Academy. Series B, Physical and biological sciences · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. A bouquet of DNA structures: Emerging diversity.Biochemistry and biophysics reports · 2016
    Review
  11. Review
  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

6 authors at 1 institution in 1 country.

Christopher Pelham *Biochemistry Laboratory, Northwest Missouri State University, Maryville, MO 64468.
Tamara Jimenez *Biochemistry Laboratory, Northwest Missouri State University, Maryville, MO 64468.
Marianna RodovaBiochemistry Laboratory, Northwest Missouri State University, Maryville, MO 64468.
Angela RudolphBiochemistry Laboratory, Northwest Missouri State University, Maryville, MO 64468.
Elizabeth ChippsBiochemistry Laboratory, Northwest Missouri State University, Maryville, MO 64468.
M Rafiq IslamBiochemistry Laboratory, Northwest Missouri State University, Maryville, MO 64468.
Northwest Missouri State University · US

Funding

Novel Mekk1-p53 mediated transcriptional regulation: mechanism and genome wide stR15DK069897 · NIDDK · NORTHWEST MISSOURI STATE UNIVERSITY · PI ISLAM, M. RAFIQ · 2005 to 2010
$404k
NIDDK NIH HHS R15 DK069897
6 · The paper itself

Abstract

Hereditary hemochromatosis (HH) is a common autosomal recessive disorder of iron overload among Caucasians of northern European descent. Over 85% of all cases with HH are due to mutations in the hemochromatosis protein (HFE) involved in iron metabolism. Although the importance in iron homeostasis is well recognized, the mechanism of sensing and regulating iron absorption by HFE, especially in the absence of iron response element in its gene, is not fully understood. In this report, we have identified an inverted repeat sequence (ATGGTcttACCTA) within 1700bp (-1675/+35) of the HFE promoter capable to form cruciform structure that binds PARP1 and strongly represses HFE promoter. Knockdown of PARP1 increases HFE mRNA and protein. Similarly, hemin or FeCl3 treatments resulted in increase in HFE expression by reducing nuclear PARP1 pool via its apoptosis induced cleavage, leading to upregulation of the iron regulatory hormone hepcidin mRNA. Thus, PARP1 binding to the inverted repeat sequence on the HFE promoter may serve as a novel iron sensing mechanism as increased iron level can trigger PARP1 cleavage and relief of HFE transcriptional repression.

Indexed as

Gene Expression RegulationInverted Repeat SequencesTranscription, GeneticBlotting, WesternChloridesElectrophoretic Mobility Shift AssayFerric CompoundsHCT116 CellsHEK293 CellsHeLa CellsHemochromatosis ProteinHep G2 CellsHistocompatibility Antigens Class IHumansLuciferasesMembrane ProteinsChloridesferric chlorideFerric CompoundsHemochromatosis ProteinHFE protein, humanHistocompatibility Antigens Class ILuciferasesMembrane ProteinsNoxaePARP1 protein, humanPeptide FragmentsPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesRNA, MessengerCruciformHAMPhemochromatosishemochromatosis proteinHFEHHInverted repeatNegative elementPARP1poly(ADP-ribose) polymerase-1

Identifiers

PMID24184271
PMCPMC3889151
OpenAlexW2038040163

What OpenQuestion holds

Textmetadata
LicenceTDM
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.