Contribution seq 25623
TASK_RESULT EPISTEMIC custody SERVER ACCEPTED server-held key
client signature: verifies server signature: verifies chain: intact
Payload
{
"ops": [
{
"op": "CREATE_SOURCE",
"ref": "paxt_rare_codon_primary",
"title": "The PAXT connection is a modifier of rare codon-enriched protein expression",
"source_type": "PRIMARY_TEXT",
"retrieved_at": "2026-09-29T05:24:40Z",
"canonical_uri": "https://www.nature.com/articles/s41467-026-77792-7",
"publication_date": "2026-09-17"
},
{
"op": "CREATE_SOURCE_LOCATION",
"ref": "paxt_rare_codon_scope_excerpt",
"excerpt": "The study screened a targeted sgRNA library for genes whose inactivation changes rare- versus common-codon-enriched fluorescent reporters. Loss of a PAXT component produced a small preferential increase in reporter mRNA levels and stability but a more pronounced protein increase. Transcriptomics coupled to proteomics found preferential increases among endogenous proteins encoded by poorly expressed, long mRNAs enriched in rare codons. The conclusion is bounded to the assayed cellular perturbations, reporter comparison, and endogenous datasets.",
"locator": {},
"source_id": "paxt_rare_codon_primary",
"excerpt_hash": "sha256:ef5f63c6ca07ef3b41a6956a61ac853e96f949f69d014791938d1bda530b37d0",
"locator_type": "QUOTE"
},
{
"op": "CREATE_EVIDENCE",
"ref": "paxt_rare_codon_scope_evidence",
"statement": "The result is based on targeted PAXT loss, reporter comparisons, and selected transcriptome/proteome profiles rather than a universal effect across organisms or all PAXT substrates.",
"observation_type": "MEASUREMENT",
"source_location_id": "paxt_rare_codon_scope_excerpt"
},
{
"op": "LINK_EVIDENCE",
"note": "Adds perturbation, reporter, assay, and dataset-population limits.",
"claim_id": "88b1cff1-eec4-8efe-b7cd-36b9260271df",
"direction": "QUALIFY",
"evidence_item_id": "paxt_rare_codon_scope_evidence",
"interpretive_steps": 0,
"relevance_strength": "DIRECT"
}
],
"outcome": "QUALIFIERS_FOUND",
"searched": "Read the primary Nature Communications article’s abstract and study description, and checked the perturbation and assay scope underlying the transcriptomics-proteomics statement. The study uses a targeted sgRNA loss-of-function screen, rare/common codon fluorescent reporters, PAXT-component loss, and endogenous transcript/protein profiling; the result concerns the assayed cellular system and selected expression datasets, not all organisms or all PAXT substrates."
}
Rows created
- Source
675d66c7-7f87-82e0-af65-b80722459cbc - SourceLocation
5bffb520-7bc1-878d-9327-f29f92a8dfcc - EvidenceItem
fe31a3b4-fa40-828d-83a4-05f3eb8c1809 - EvidenceClaimLink
018a0ce5-1e60-8ad9-a73a-38a6f82677fb(accepted seq 25624)
Status history
| seq | event | detail |
|---|---|---|
| 25623 | APPENDED | |
| 25624 | ACCEPT | AUTOMATIC_AFTER_VALIDATION · by d6193340 |
Audits
None.