Component

Mouse Shmt1 gene

Gene-level perturbation target; individual exposure and alleles are recorded in scenario metadata.

2 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. Control-diet Shmt1-transgenic mice showed approximately twice the hepatic nuclear-DNA uracil of wild-type mice.

    Mouse Shmt1 gene → Uracil incorporation in nuclear DNA source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    evidence_location
    Table 2, control-diet comparison.
    experimental_model
    Nuclear DNA uracil measurement
    exposure
    Assay conditions described in the linked primary study.
    limitations
    Association within a transgenic model; control diet contains folate and choline.
    nutrient_topic
    Folate and folic acid research collection; topical membership is not evidence of a direct dietary effect. · Folate (vitamin B9)
    organism
    Mus musculus
    plain_language
    Incorrect enzyme placement was accompanied by more uracil in DNA.
    primary_references
    [macfarlane-2011] Nuclear localization of de novo thymidylate biosynthesis pathway is required to prevent uracil accumulation in DNA (2011). https://pubmed.ncbi.nlm.nih.gov/22057276/ DOI: 10.1074/jbc.m111.307629
    tissue_or_cell_type
    Liver
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Folate and folic acid: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 1157–1168

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Nuclear DNA uracil measurement · source_derived_draft · unverified_draft

    ### shmt1-transgene-dna-uracil Control-diet Shmt1-transgenic mice showed approximately twice the hepatic nuclear-DNA uracil of wild-type mice. Condition category: machinery_impairment nutrient_topic: Folate and folic acid research collection; topical membership is not evidence of a direct dietary effect. plain_language: Incorrect enzyme placement was accompanied by more uracil in DNA. organism: Mus musculus tissue_or_cell_type: Liver experimental_model: Nuclear DNA uracil measurement limitations: Association within a transgenic model; control diet contains folate and choline. exposure: Assay conditions described in the linked primary study. evidence_location: Table 2, control-diet comparison. [macfarlane-2011] Nuclear localization of de novo thymidylate biosynthesis pathway is required to prevent uracil accumulation in DNA (2011). https://pubmed.ncbi.nlm.nih.gov/22057276/ DOI: 10.1074/jbc.m111.307629
    Complete structured claim and evidence
  2. Shmt1-transgenic mouse liver had lower nuclear SHMT1/TYMS and lower nuclear de novo dTMP synthesis despite higher total enzyme abundance.

    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    experimental_model
    Transgene and isolated-nuclei assays
    exposure
    Assay conditions described in the linked primary study.
    limitations
    Overexpression phenotype must not be generalized to supplementation.
    nutrient_topic
    Folate and folic acid research collection; topical membership is not evidence of a direct dietary effect. · Folate (vitamin B9)
    organism
    Mus musculus
    plain_language
    More enzyme in the whole cell did not mean more at DNA-replication sites.
    primary_references
    [macfarlane-2011] Nuclear localization of de novo thymidylate biosynthesis pathway is required to prevent uracil accumulation in DNA (2011). https://pubmed.ncbi.nlm.nih.gov/22057276/ DOI: 10.1074/jbc.m111.307629
    tissue_or_cell_type
    Liver nuclei
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Folate and folic acid: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 1145–1155

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Transgene and isolated-nuclei assays · source_derived_draft · unverified_draft

    ### shmt1-transgene-nuclear-mislocalization Shmt1-transgenic mouse liver had lower nuclear SHMT1/TYMS and lower nuclear de novo dTMP synthesis despite higher total enzyme abundance. Condition category: machinery_impairment nutrient_topic: Folate and folic acid research collection; topical membership is not evidence of a direct dietary effect. plain_language: More enzyme in the whole cell did not mean more at DNA-replication sites. organism: Mus musculus tissue_or_cell_type: Liver nuclei experimental_model: Transgene and isolated-nuclei assays limitations: Overexpression phenotype must not be generalized to supplementation. exposure: Assay conditions described in the linked primary study. [macfarlane-2011] Nuclear localization of de novo thymidylate biosynthesis pathway is required to prevent uracil accumulation in DNA (2011). https://pubmed.ncbi.nlm.nih.gov/22057276/ DOI: 10.1074/jbc.m111.307629
    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