Evidence map›Paper›PMID 22575231›Full record

ArticleToxicology and applied pharmacology2012

Identification of an S-adenosylmethionine (SAM) dependent arsenic methyltransferase in Danio rerio.

Mohamad Hamdi, Masafumi Yoshinaga, Charles Packianathan, Jie Qin, Janell Hallauer, Joseph R McDermott, Hung-Chi Yang, Kan-Jen Tsai, Zijuan Liu

Open access · greenAbstract read
In one paragraph

Article in Toxicology and applied pharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.3field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Integration of epigenetics into ecotoxicology: insights and fundamental research needs.Biological reviews of the Cambridge Philosophical Society · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
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  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Zebrafish in Toxicology and Environmental Health.Current topics in developmental biology · 2017
    Review
  16. Article
  17. Zebrafish as a model to study the role of DNA methylation in environmental toxicology.Environmental science and pollution research international · 2015
    Review
  18. Review
  19. Arsenic binding to proteins.Chemical reviews · 2013
    Review
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 4 institutions in 2 countries.

Mohamad HamdiDepartment of Biological Sciences, Oakland University, Rochester, MI 48309, USA.
Masafumi Yoshinaga
Charles Packianathan
Jie Qin
Janell Hallauer
Joseph R McDermott
Hung-Chi Yang
Kan-Jen Tsai
Zijuan Liu
Oakland University · USFlorida International University · USChang Gung University · TWChung Shan Medical University · TW

Funding

Mechanisms of arsenical transportR37GM055425 · NIGMS · WAYNE STATE UNIVERSITY · PI ROSEN, BARRY P. · 2005 to 2014
$4.4M
Mechanisms of Arsenic Transport and BiotransformationsR01GM055425 · NIGMS · WAYNE STATE UNIVERSITY · PI ROSEN, BARRY P. · 1997 to 2019
$3.8M
Arsenic accumulation by aquaglyceroporins and phosphate transporters in zebrafishR15ES016856 · NIEHS · OAKLAND UNIVERSITY · PI LIU, ZIJUAN · 2009 to 2009
$238k
NIEHS NIH HHS ES016856NIEHS NIH HHS R15 ES016856NIGMS NIH HHS GM55425NIGMS NIH HHS R01 GM055425NIGMS NIH HHS R37 GM055425
6 · The paper itself

Abstract

Arsenic methylation is an important cellular metabolic process that modulates arsenic toxicity and carcinogenicity. Biomethylation of arsenic produces a series of mono-, di- and tri-methylated arsenic metabolites that can be detected in tissues and excretions. Here we report that zebrafish exposed to arsenite (As(III)) produces organic arsenicals, including MMA(III), MMA(V) and DMA(V) with characteristic tissue ratios, demonstrating that an arsenic methylation pathway exists in zebrafish. In mammals, cellular inorganic arsenic is methylated by a SAM-dependent arsenic methyltransferase, AS3MT. A zebrafish arsenic methyltransferase homolog, As3mt, was identified by sequence alignment. Western blotting analysis showed that As3mt was universally expressed in zebrafish tissues. Prominent expression in liver and intestine correlated with methylated arsenic metabolites detected in those tissues. As3mt was expressed in and purified from Escherichia coli for in vitro functional studies. Our results demonstrated that As3mt methylated As(III) to DMA(V) as an end product and produced MMA(III) and MMA(V) as intermediates. The activity of As3mt was inhibited by elevated concentrations of the substrate As(III) as well as the metalloid selenite, which is a well-known antagonistic micronutrient of arsenic toxicity. The activity As3mt was abolished by substitution of either Cys160 or Cys210, which corresponds to conserved cysteine residues in AS3MT homologs, suggesting that they are involved in catalysis. Expression in zebrafish of an enzyme that has a similar function to human and rodent orthologs in catalyzing intracellular arsenic biomethylation validates the applicability of zebrafish as a valuable vertebrate model for understanding arsenic-associated diseases in humans.

Indexed as

Amino Acid SequenceAnimalsArsenicalsArsenitesBase SequenceCloning, MolecularFemaleMaleMethylationMethyltransferasesModels, MolecularMolecular Sequence DataRecombinant ProteinsRNA, MessengerS-AdenosylmethionineSequence AlignmentArsenicalsarseniteArsenitesMethyltransferasesRecombinant ProteinsRNA, MessengerS-AdenosylmethionineSodium Selenite

Identifiers

PMID22575231
PMCPMC3394433
OpenAlexW2016503875

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.