Function
Processes
Locations
COOLAIR binding and recruitment of RNA-processing/chromatin partners. Condensate behavior is established separately from RNA-binding assays.
Arabidopsis autonomous flowering regulators promote floral transition through overlapping mechanisms that reduce FLOWERING LOCUS C (FLC) expression. FCA and FY couple processing of COOLAIR antisense RNA to chromatin-associated and termination machinery involving FLD, LD, SDG26/ASHH1, APRF1 and TOPP4. FPA contributes through a distinct RNA-processing route; FLK recognizes modified FLC sense mRNA; FVE/MSI4 supports chromatin-regulatory associations. These relationships vary with genetic background, dosage and locus. Reduced FLC can release repression of FT and SOC1, while FVE also has a distinct direct regulatory effect at FT. Conserved proteins in other plants share biochemical features without necessarily sharing this native RNA-target and chromatin circuit.
Native mechanistic envelope is Arabidopsis thaliana. All 13 native sampled gene products have complete individual reviews; rice FCA Q6K271 and OsFY Q0R3J2 are reviewed comparative evidence only and are not annoton representatives. Family descriptors document verified classification of exact GENE_PRODUCT selections and do not transfer FLC-specific function across broad families. COOLAIR is a lncRNA, so its processing uses GO:0031123 RNA 3'-end processing rather than an mRNA-specific term. The sampled route is not an exhaustive protein complex or a universal knockout-necessity rule. Quantitative feedback and graded versus Polycomb ON/OFF regulation are not reduced to an unvalidated kinetic simulation. FRIGIDA, photoperiod, cold-triggered vernalization and complete downstream floral identity programs remain outside the boundary. No cached GO-CAM index rows matched the 13 native accessions at audit time. Source-access and provider-failure details, exact logic scope and comparative evidence are in the companion notes.
knowledge_gaps[0].provenance[0] · reference_section_type
(0/1)✗ none found
No MODULE:autonomous_flowering_pathway deep-research report alongside the module YAML.
✓ every leaf node grounds to a representative protein.
✓ every declared conforms_to bundle matches its template motif.
11 gene-function check(s) reflected in core functions · 0 conflict(s) · 11 evidence or coverage gap(s) (22 comparison(s))
Retained noncore functions are reported separately; they do not require promotion to core functions. Support from representative genes does not establish conservation across the whole family. Missing reviews or identifiers leave a claim unverified.
| Annoton | Participant | Function | Assessment |
|---|---|---|---|
| fca_coolair_binding | FCA UniProtKB:O04425 Gene |
lncRNA binding GO:0106222 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| fld_h3k4_demethylase | FLD UniProtKB:Q9CAE3 Gene |
histone H3K4 demethylase activity GO:0032453 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| sdg26_dna_binding | ASHH1 UniProtKB:Q84WW6 Gene |
double-stranded DNA binding GO:0003690 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| aprf1_chromatin_scaffold | APRF1 UniProtKB:Q9LYK6 Gene |
chromatin binding GO:0003682 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| topp4_phosphatase | TOPP4 UniProtKB:P48484 Gene |
protein serine/threonine phosphatase activity GO:0004722 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| fpa_rna_processing | FPA UniProtKB:Q8LPQ9 Gene |
RNA binding GO:0003723 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| flk_sense_rna_reader | FLK UniProtKB:Q9SR13 Gene |
N6-methyladenosine-containing RNA reader activity GO:1990247 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| fve_chromatin_association | FVE UniProtKB:O22607 Gene |
histone binding GO:0042393 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| flc_repressor | FLC UniProtKB:Q9S7Q7 Gene |
DNA-binding transcription factor activity, RNA polymerase II-specific GO:0000981 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| ft_coactivator | FT UniProtKB:Q9SXZ2 Gene |
transcription coactivator activity GO:0003713 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| soc1_transcription_factor | SOC1 UniProtKB:O64645 Gene |
DNA-binding transcription factor activity, RNA polymerase II-specific GO:0000981 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| fca_coolair_binding | RNA BINDING PROTEIN PANTHER:PTHR24012 Family |
lncRNA binding GO:0106222 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR24012. |
| fld_h3k4_demethylase | PROTEIN FLOWERING LOCUS D PANTHER:PTHR10742:SF260 Family |
histone H3K4 demethylase activity GO:0032453 |
Family Function Unreviewed
The family review has no applicable adjudication supporting or excluding GO:0032453. |
| sdg26_dna_binding | SET DOMAIN PROTEINS PANTHER:PTHR22884 Family |
double-stranded DNA binding GO:0003690 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR22884. |
| aprf1_chromatin_scaffold | PROTEIN ANTHESIS POMOTING FACTOR 1 PANTHER:PTHR19861:SF9 Family |
chromatin binding GO:0003682 |
Family Function Unreviewed
The family review has no applicable adjudication supporting or excluding GO:0003682. |
| topp4_phosphatase | SERINE_THREONINE-PROTEIN PHOSPHATASE PP1 ISOZYME 4 PANTHER:PTHR11668:SF490 Family |
protein serine/threonine phosphatase activity GO:0004722 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR11668:SF490. |
| fpa_rna_processing | RNA RECOGNITION MOTIF-CONTAINING PANTHER:PTHR23189 Family |
RNA binding GO:0003723 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR23189. |
| flk_sense_rna_reader | KH DOMAIN CONTAINING RNA BINDING PROTEIN PANTHER:PTHR10288 Family |
N6-methyladenosine-containing RNA reader activity GO:1990247 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR10288. |
| fve_chromatin_association | WD40 REPEAT FAMILY PANTHER:PTHR22850 Family |
histone binding GO:0042393 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR22850. |
| flc_repressor | SERUM RESPONSE FACTOR HOMOLOG PANTHER:PTHR48019 Family |
DNA-binding transcription factor activity, RNA polymerase II-specific GO:0000981 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR48019. |
| ft_coactivator | PROTEIN FLOWERING LOCUS T-RELATED PANTHER:PTHR11362:SF9 Family |
transcription coactivator activity GO:0003713 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR11362:SF9. |
| soc1_transcription_factor | SERUM RESPONSE FACTOR HOMOLOG PANTHER:PTHR48019 Family |
DNA-binding transcription factor activity, RNA polymerase II-specific GO:0000981 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR48019. |
✓ every negative regulator described as feedback has an upstream edge closing the loop.
7 complete review(s) · 3 with deep research · 0 missing review · 10 reviewed but lacking deep research
| Gene | Review | Complete | Deep research |
|---|---|---|---|
| APRF1 Q9LYK6 | ✓ | 7/11 | ✗ |
| ASHH1 Q84WW6 | ✓ | 15/17 | ✗ |
| FCA O04425 | ✓ | 20/22 | ✗ |
| FLC Q9S7Q7 | ✓ | ✓ | ✓ |
| FLD Q9CAE3 | ✓ | 12/15 | ✗ |
| FLK Q9SR13 | ✓ | ✓ | ✗ |
| FPA Q8LPQ9 | ✓ | 12/13 | ✗ |
| FT Q9SXZ2 | ✓ | ✓ | ✓ |
| FVE O22607 | ✓ | 39/42 | ✗ |
| FY Q6NLV4 | ✓ | ✓ | ✗ |
| LD Q38796 | ✓ | ✓ | ✗ |
| SOC1 O64645 | ✓ | ✓ | ✓ |
| TOPP4 P48484 | ✓ | ✓ | ✗ |
FLC-regulatory contributions are selectable overlapping implementations, not universally interchangeable complete pathways. At least one nonempty upstream route and the FLC target are required to recognize a represented route; FT/SOC1 are optional readouts.
ONE_OR_MORE means a represented contribution is present, not that a single factor is sufficient to recreate wild-type flowering or compensate for every other pathway lesion.
A selected native mechanistic implementation combining the experimentally characterized RNA-processing, AuPC and CPF-like contributions. Requiring its sampled participants defines this implementation, not universal necessity of every participant in every autonomous response.
The directly characterized antisense substrate is COOLAIR. Its proximal cleavage/polyadenylation uses the RNA-level GO term. The later processivity feedback model concerns productive transcription and early termination at the locus, rather than an exclusively COOLAIR-specific feedback measurement. Constitutive CPSF, CstF64/77 and FLL2 are relevant partners outside the sampled gene panel; FCA and FY are not a complete catalytic machine.
COOLAIR binding and recruitment of RNA-processing/chromatin partners. Condensate behavior is established separately from RNA-binding assays.
Noncatalytic CPSF partner for FCA and SDG26. No isolated plant FY RNA-binding or cleavage activity is asserted.
Native association and chromatin changes support this selected complex implementation. ASHH1 conserved-site Y118A rescue argues catalytic dispensability in the tested flowering assay; mutant catalytic inactivity itself was not directly measured. EFL2/EFL4 and PRC2 enzymes are not sampled here.
LSD1-family demethylase inference with native H3K4me1/chromatin evidence. This is not presented as a purified target-enzyme kinetic assay.
Noncatalytic scaffold connecting FLD-associated chromatin and APRF1/TOPP4 termination assemblies. No DNA binding or phosphatase activity is assigned from its historical protein/family name.
SDG26/ASHH1 contributes DNA association and contacts FY. Its C-terminal region binds FLC-derived dsDNA in vitro; it is not assigned the FLD demethylase reaction. Older methyltransferase evidence is retained in its gene review.
LD is represented once in the linked chromatin part and also participates in this assembly. RNA Pol II phosphorylation changes do not distinguish a CTD substrate from an elongation-factor substrate. These sampled subassemblies need not form one obligatory stoichiometric supercomplex.
Noncatalytic chromatin-associated scaffold of the APRF1/LD/TOPP4 termination module; no COMPASS methyltransferase activity is inferred from Swd2 homology.
PP1-type catalytic phosphatase associated with the CPF-like module. Direct target activity is established on other substrates; its substrate in FLC regulation remains unknown, so no Pol II CTD phosphatase term or direct CTD edge is asserted.
This variant tracks a distinct documented contribution, not an assertion that FPA alone reconstructs wild-type repression without cofactors. Genetic bypass evidence is 35S overexpression; native necessity and dosage are context-dependent.
Distinct RNA-processing regulator affecting FLC antisense poly(A)-site usage. FPA need not bind COOLAIR or assemble with FCA/FY to reproduce every effect; gene-silencing and direct RNA-contact mechanisms are not equated.
The m6A reader mechanism requires a modified target transcript and other RNA machinery. It does not establish an interchangeable FCA/FY pathway or a generic activity of all KH proteins.
m6A-dependent recognition of FLC sense mRNA affecting its stability and splicing. This is distinct from antisense COOLAIR processing.
This route records the FVE-dependent contribution with associated catalytic partners outside the sampled selector. FVE also affects FT chromatin directly, so its entire biological effect is not forced through FLC.
MSI4/FVE contributes to chromatin complexes associated with deacetylation and CLF-dependent regulation. It is not a catalytic HDAC or a demonstrated universal stoichiometric PRC2 core subunit.
RNA/chromatin edges decrease FLC expression, thereby reducing availability of its repressor activity. This coarse causal node does not claim direct inhibition of FLC protein by RNA-processing factors.
FLC expression supplies a DNA-binding repressor of FT and SOC1 in the modeled branch. Other FLC targets can be activated, so a universally negative transcriptional function is not asserted.
Output readout; other photoperiod inputs and FD-mediated activation machinery are not modeled.
Downstream florigen/coactivator whose expression in leaves is repressed by FLC and whose partnership with FD acts at the shoot apex. Transport and complete meristem activation machinery are outside scope.
Output readout integrating multiple pathways, not an obligate serial step after FT in every tissue.
Downstream MADS transcription factor contributing to meristem transition with partners such as AGL24. Its nuclear DNA-binding role is distinct from FLC binding to the SOC1 promoter.