Component

Stress-responsive DNA elements

DNA sequences recognized in SELENOH binding experiments.

1 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What acts on it

  1. SELENOH showed redox-responsive association with stress-responsive DNA sequences.

    SELENOH → Stress-responsive DNA elements source_derived_draftliterature_reviewed:direct_experimental
    Experimental context and source evidence
    cell_type
    HT22
    experimental_model
    DNA-binding and expression assays
    limitations
    Not a universal genomic target map.
    organism
    human protein in mouse cells

    Selenium: literature corrections and mechanism additions · lines 858–868

    Metabolic Ledger literature curation, 17 September 2026; primary papers linked individually · supports · DNA-binding and expression assays · secondary_verified · secondary_verified

    ## selenoh-associates-with-stress-dna SELENOH can associate with DNA in a redox-sensitive manner. SELENOH showed redox-responsive association with stress-responsive DNA sequences. Organism: human protein in mouse cells Cell type: HT22 Experimental model: DNA-binding and expression assays Limitations: Not a universal genomic target map. Primary reference: [Selenoprotein H is a redox-sensing high mobility group family DNA-binding protein that up-regulates genes involved in glutathione synthesis and phase II detoxification](https://pubmed.ncbi.nlm.nih.gov/17526492/)
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards