Component

DIO3

Independent protein record for Iodothyronine deiodinase 3.

3 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 it acts on

  1. DIO3 catalyzes inner-ring deiodination of T4 to reverse T3 in functional placental-enzyme studies.

    DIO3 → rT3 source_derived_draftliterature_reviewed:direct_experimental
    Experimental context and source evidence
    experimental_model
    Human placental DIO3 cloning and functional expression.
    limitations
    This experiment-specific relationship does not establish a human dietary-deficiency threshold or supplementation benefit.
    organism
    Human placental protein in an expression system

    Selenium: literature corrections and mechanism additions · lines 1020–1029

    Metabolic Ledger literature curation, 17 September 2026; primary papers linked individually · supports · Human placental DIO3 cloning and functional expression. · secondary_verified · secondary_verified

    ## dio3-thyroxine-inactivation DIO3 lowers thyroid-hormone activity by converting T4 to reverse T3. DIO3 catalyzes inner-ring deiodination of T4 to reverse T3 in functional placental-enzyme studies. Experimental model: Human placental DIO3 cloning and functional expression. Organism: Human placental protein in an expression system Limitations: This experiment-specific relationship does not establish a human dietary-deficiency threshold or supplementation benefit. Primary reference: [Type 3 iodothyronine deiodinase: cloning, in vitro expression, and functional analysis of the placental selenoenzyme](https://www.jci.org/articles/view/118299)
    Complete structured claim and evidence
  2. DIO3 catalyzes inner-ring deiodination of T3 to 3,3-prime-T2 in functional placental-enzyme studies.

    DIO3 → 3,3-prime-T2 source_derived_draftliterature_reviewed:direct_experimental
    Experimental context and source evidence
    experimental_model
    Human placental DIO3 cloning and functional expression.
    limitations
    This experiment-specific relationship does not establish a human dietary-deficiency threshold or supplementation benefit.
    organism
    Human placental protein in an expression system

    Selenium: literature corrections and mechanism additions · lines 1031–1040

    Metabolic Ledger literature curation, 17 September 2026; primary papers linked individually · supports · Human placental DIO3 cloning and functional expression. · secondary_verified · secondary_verified

    ## dio3-triiodothyronine-inactivation DIO3 lowers thyroid-hormone activity by converting T3 to 3,3-prime-T2. DIO3 catalyzes inner-ring deiodination of T3 to 3,3-prime-T2 in functional placental-enzyme studies. Experimental model: Human placental DIO3 cloning and functional expression. Organism: Human placental protein in an expression system Limitations: This experiment-specific relationship does not establish a human dietary-deficiency threshold or supplementation benefit. Primary reference: [Type 3 iodothyronine deiodinase: cloning, in vitro expression, and functional analysis of the placental selenoenzyme](https://www.jci.org/articles/view/118299)
    Complete structured claim and evidence

What acts on it

  1. The 3-prime-untranslated-region SECIS element was required for expression of cloned human placental DIO3, which incorporated 75Se in transfected cells.

    Human DIO3 3-prime-UTR SECIS element → DIO3 source_derived_draftungraded
    Experimental context and source evidence
    cross_nutrient
    Selenium incorporation supports an enzyme that inactivates iodine-containing hormones.
    evidence_locator
    Primary abstract
    evidence_spans
    [{"source_document": "artifacts/iodine-metabolism-sources/7593630.json", "source_field": "resultList.result[0].abstractText", "start_char": 0, "end_char": 1405}]
    experimental_model
    Human placental DIO3 cDNA and heterologous expression, selenium labeling and SECIS manipulation
    exposure
    Cloned 2.1-kb DIO3 cDNA; 75Se labeling and SECIS-dependent expression.
    limitations
    Expression machinery experiment; not evidence for selenium dosing in pregnancy.
    nutrient_topic
    Iodine research collection; topical membership is not evidence of a direct dietary effect. · Iodine
    organism
    Human placental protein in transfected cells
    plain_language
    The hormone-inactivating enzyme also needs the cellular system that incorporates selenium into proteins.
    primary_references
    [i-met-7593630] Type 3 lodothyronine deiodinase: cloning, in vitro expression, and functional analysis of the placental selenoenzyme. (1995). https://pubmed.ncbi.nlm.nih.gov/7593630/ DOI: 10.1172/jci118299
    tissue_or_cell_type
    DIO3 expression system

    Iodine: thyroid hormone production, deficiency, excess and nutrient interactions (2026-09-17) · lines 1129–1142

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Human placental DIO3 cDNA and heterologous expression, selenium labeling and SECIS manipulation · source_derived_draft · unverified_draft

    ### i-met-dio3-secis-expression The 3-prime-untranslated-region SECIS element was required for expression of cloned human placental DIO3, which incorporated 75Se in transfected cells. Condition category: normal nutrient_topic: Iodine research collection; topical membership is not evidence of a direct dietary effect. plain_language: The hormone-inactivating enzyme also needs the cellular system that incorporates selenium into proteins. organism: Human placental protein in transfected cells tissue_or_cell_type: DIO3 expression system experimental_model: Human placental DIO3 cDNA and heterologous expression, selenium labeling and SECIS manipulation limitations: Expression machinery experiment; not evidence for selenium dosing in pregnancy. exposure: Cloned 2.1-kb DIO3 cDNA; 75Se labeling and SECIS-dependent expression. cross_nutrient: Selenium incorporation supports an enzyme that inactivates iodine-containing hormones. evidence_locator: Primary abstract evidence_spans: [{"source_document": "artifacts/iodine-metabolism-sources/7593630.json", "source_field": "resultList.result[0].abstractText", "start_char": 0, "end_char": 1405}] [i-met-7593630] Type 3 lodothyronine deiodinase: cloning, in vitro expression, and functional analysis of the placental selenoenzyme. (1995). https://pubmed.ncbi.nlm.nih.gov/7593630/ DOI: 10.1172/jci118299
    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