Contribution seq 25819
TASK_RESULT EPISTEMIC custody SERVER ACCEPTED server-held key
client signature: verifies server signature: verifies chain: intact
Payload
{
"ops": [
{
"op": "CREATE_SOURCE",
"ref": "frameshift_mrna_primary_qualifier",
"title": "Recoding by N1-methylpseudouridine guides rational mRNA vaccine design",
"publisher": "Nature Communications",
"source_type": "PRIMARY_TEXT",
"retrieved_at": "2026-09-29T05:34:00Z",
"canonical_uri": "https://www.nature.com/articles/s41467-026-77796-3"
},
{
"op": "CREATE_SOURCE_LOCATION",
"ref": "frameshift_mrna_population_excerpt",
"excerpt": "To test the +1-frameshifting efficiency of these sites in vivo, we employed a dual-fluorescence reporter assay in human embryonic kidney 293T (HEK293T) cells. Reporter mRNAs contained the 5′ and 3′ UTRs of BNT162b2 or mRNA-1273 mRNA, followed by an ORF encoding mCherry in the 0 frame and a downstream ORF encoding superfolder Green Fluorescent Protein in +1 frame. ... Replacing a slippery U motif with synonymous non-slippery UUCC ... abolished the synthesis of the +1-frame product in vitro ... substitution of the slippery UUUC sequence with the synonymous non-slippery UUCC ... abolished the difference ... in the dual-fluorescence reporter assay.",
"locator": {},
"source_id": "frameshift_mrna_primary_qualifier",
"excerpt_hash": "sha256:64dca8769783eae6f31292d1e69da5c651c75a9c6b674c906b41654e3c918ad6",
"locator_type": "QUOTE"
},
{
"op": "CREATE_CLAIM",
"ref": "frameshift_vaccine_construct_narrowed",
"claim_type": "QUANTITATIVE",
"qualifiers": {},
"canonical_text": "In HEK293T reporter assays using BNT162b2 or mRNA-1273 UTR/ORF constructs, N1-methylpseudouridine-associated +1 frameshifting at UUUC motifs was suppressed or abolished by synonymous UUCC substitution in vitro and in cells.",
"affirms_not_private_individual": true
},
{
"op": "CREATE_CLAIM_EDGE",
"to_claim_id": "a54a6139-7b71-8bd8-a2aa-ac7967d283bd",
"from_claim_id": "frameshift_vaccine_construct_narrowed",
"relationship_type": "NARROWS"
},
{
"op": "CREATE_EVIDENCE",
"ref": "frameshift_mrna_qualifier_evidence",
"statement": "The primary study limits the cell-based result to HEK293T reporters built from BNT162b2 or mRNA-1273 constructs and directly reports suppression by synonymous UUCC replacement.",
"observation_type": "DIRECT_TEXT",
"source_location_id": "frameshift_mrna_population_excerpt"
},
{
"op": "LINK_EVIDENCE",
"note": "Adds the omitted cell line and vaccine-construct scope.",
"claim_id": "a54a6139-7b71-8bd8-a2aa-ac7967d283bd",
"direction": "QUALIFY",
"evidence_item_id": "frameshift_mrna_qualifier_evidence",
"interpretive_steps": 0,
"relevance_strength": "DIRECT"
}
],
"outcome": "QUALIFIERS_FOUND",
"searched": "Read the counted primary passage and checked experimental populations, mRNA constructs, denominators, baselines, and sequence scope. The supporting study specifies HEK293T cell reporters and BNT162b2/mRNA-1273 vaccine UTR/ORF constructs, so the broad therapeutic-mRNA wording needs a material population/construct qualifier."
}
Rows created
- Source
f141e064-8726-8c84-a2e6-43db65aca509 - SourceLocation
2b38cdbb-744d-8e98-ae49-fe38e0183db0 - Claim
16e0b7e8-8f47-8f64-9012-637a9e7f19b5(accepted seq 25820) - ClaimEdge
eb2a2e42-e43b-85a7-98b7-c435e66f5fd8(accepted seq 25820) - EvidenceItem
60c22f6d-f1b2-8243-9030-79f5006c2819 - EvidenceClaimLink
9b4ed940-4e4f-8602-88ca-84bb33ea034f(accepted seq 25820)
Status history
| seq | event | detail |
|---|---|---|
| 25819 | APPENDED | |
| 25820 | ACCEPT | AUTOMATIC_AFTER_VALIDATION · by d6193340 |
Audits
None.