Gene Regulation Landscape node-audit synthesis
Generated: 2026-06-18
Coverage
All 37 node reports were written in this directory. Reports use the current DOT, technical notes, and blog post as graph claims and audit them against literature-level evidence and assay caveats.
Nodes to keep as-is or with only wording caveats
BRIDGES, SILENCER, OPENER, WRITER-R, SHUFFLER, KEYS, SCRIBE, SHIELD, SPLICER, TRIMMER, RECODER, READERS, DARTS, CENSOR, TIMER, FORGE, BRAKE, DECOY, INSPECTOR, SWITCH, ROUTER, TETHER, LICENSE
Nodes to rename or make more literal
Most code names can remain as mnemonic labels, but the technical notes should prefer literal names in definitions. Highest-value literal renames: FENCES -> INSULATORS/DOMAINS, WRITER-A -> ACTIVE-HISTONE-MARKS, WRITER-R -> REPRESSIVE-HISTONE-MARKS, SHUFFLER -> REMODELER, GUIDES -> CHROMATIN-ncRNA, SHIELD -> CAPPING, TRIMMER -> APA, STAMP -> m6A, READERS -> RBPs, FORGE -> CAP-INITIATION, BRAKE -> ISR, TEMPO -> DECODING-TEMPO, MATURE -> PROTEOSTASIS, PAR -> ADP-RIBOSE.
Nodes to split
- HUBS: split super-enhancers from transcriptional condensates, or at minimum caveat that one is a ChIP-seq enhancer class and the other is a physical model.
- DESTROY: split proteasome and selective autophagy if graph space allows.
- Optional detailed-map splits: WRITER-A into H3K4-associated promoter/enhancer marks and H3K36 elongation marks; GUIDES into piRNA-guided DNA methylation and lncRNA chromatin scaffolds; BYPASS into viral IRES and cellular noncanonical initiation; MATURE into cytosolic chaperones and ER UPR.
Nodes to merge
- Consider merging SPONGE into DARTS as a dashed/contextual “RNA competitors/ceRNA” submechanism unless the map intentionally wants a skeptical lncRNA node.
- LICENSE could be merged into ROUTER for a smaller map, but current separation is biologically defensible because neddylation specifically licenses CRL ubiquitin ligases.
Major issue nodes
- SPONGE: ceRNA/sponging is heavily overclaimed without abundance, affinity, and localization evidence.
- BYPASS: viral IRESs are strong, but many cellular IRES claims are reporter-artifact-prone and need strict controls.
Edges to add
- KEYS -> BRIDGES: enhancer-bound TFs help establish or stabilize enhancer-promoter communication.
- GUIDES -> WRITER-R: XIST and some nuclear lncRNA contexts recruit Polycomb/repressive histone systems.
- SHIELD -> TIMER: the cap protects from 5-prime decay; decapping commits many RNAs to turnover.
- SPLICER <-> TRIMMER: terminal exon choice and splicing are coupled to cleavage/polyadenylation.
- READERS -> TRIMMER and READERS -> VAULT: RBPs regulate APA and RNP-granule partitioning.
- BRAKE -> VAULT: eIF2alpha-P/ISR commonly promotes stress-granule assembly through translation repression.
- TEMPO -> TIMER: codon optimality and translation elongation affect mRNA stability.
- INSPECTOR -> TIMER: NGD/NSD produce mRNA decay outputs, not only nascent-chain destruction.
- MATURE -> ROUTER: CHIP/ERAD/chaperone triage connects proteostasis to ubiquitination.
- PAR -> SHUFFLER/repair-chromatin context: PARP/PAR recruits chromatin remodelers and repair assemblies.
Edges to remove or caveat
- ZONES -> FENCES: change to coexistence/interplay; compartments do not simply create TADs.
- FENCES -> BRIDGES: change “delimits” to probabilistically constrains/biases.
- BRIDGES -> HUBS: caveat; super-enhancers are not simply anchored by individual loops.
- STAMP -> TIMER/FORGE/BYPASS: route through reader context and YTHDF redundancy rather than one-reader-one-output arrows.
- DARTS -> FORGE: caveat that mammalian miRNA repression often proceeds through deadenylation/decay, with translational repression context-dependent.
- TIMER <-> VAULT: granule localization is not proof of decay; storage and exchange are common.
- BRAKE -> BYPASS: mark as contextual; stress does not generally activate all IRES-like translation.
- FORGE -> INSPECTOR: initiation does not itself cause RQC; stalls/defective elongation do.
- FORGE -> SWITCH: fix mTOR/AKT directionality; AKT is often upstream of mTORC1, while mTORC1 signals through S6K/4E-BP.
- PAR -> DESTROY: narrow to PAR-dependent repair-factor recruitment, ubiquitin crosstalk, or local turnover; broad proteolytic-condensate output is too strong.
Literature-risk notes
- Condensates/LLPS: require direct material-property and functional evidence; puncta, overexpression, and 1,6-hexanediol sensitivity are weak alone.
- lncRNA mechanisms: distinguish localization and abundance; PRC2 binding or miRNA-site prediction alone is not mechanism.
- Reporter assays: cellular IRES, miRNA sponging, and enhancer claims are especially vulnerable to cryptic promoter/splicing/overexpression artifacts.
- Omics readouts: Hi-C, ChIP-seq, CLIP, Ribo-seq, m6A maps, and half-life assays are powerful but assay-biased; perturbation and endogenous validation should carry more weight.
- Context specificity: many mechanisms are strong in one lineage, stress, developmental stage, or locus but should not be generalized to a universal edge.
Priority patch plan for DOT/details/blog
- Patch the DOT relation labels first for caveated edges: ZONES->FENCES, FENCES->BRIDGES, BRIDGES->HUBS, STAMP outputs, BRAKE->BYPASS, FORGE->INSPECTOR, FORGE->SWITCH, PAR->DESTROY.
- Add the highest-confidence missing edges: KEYS->BRIDGES, GUIDES->WRITER-R, SHIELD->TIMER, SPLICER<->TRIMMER, BRAKE->VAULT, TEMPO->TIMER, INSPECTOR->TIMER, MATURE->ROUTER.
- Decide whether to split HUBS and DESTROY before editing layout, because those changes affect node count and rank width.
- Revise the technical notes with skepticism boxes for LLPS, ceRNA, cellular IRES, specialized ribosomes, and m6A reader specificity.
- Update the blog post after DOT/details are patched so the public narrative emphasizes that the map is a high-level control architecture with confidence/caveat annotations, not a claim that every arrow is universal.
Completed node reports
ZONES, FENCES, BRIDGES, HUBS, SILENCER, OPENER, WRITER-A, WRITER-R, SHUFFLER, GUIDES, KEYS, SCRIBE, SHIELD, SPLICER, TRIMMER, RECODER, STAMP, READERS, DARTS, SPONGE, CENSOR, TIMER, CLIPS, VAULT, FORGE, BRAKE, DECOY, BYPASS, TEMPO, INSPECTOR, SWITCH, ROUTER, TETHER, LICENSE, DESTROY, MATURE, PAR