Function
Locations
Auxin stabilizes the receptor–Aux/IAA interface; InsP6 is an integral structural cofactor, not a separately modeled obligatory biosynthetic supply step.
Canonical nuclear auxin signaling couples TIR1/AFB–Aux/IAA co-receptor assembly to regulated transcription by ARF proteins. Auxin enhances receptor–degron association, enabling SCF-dependent Aux/IAA turnover and reducing corepression of class-A ARFs. This circuit is represented by native Arabidopsis and Marchantia implementations within land plants; older algal ARF DNA-binding systems alone do not establish the complete circuit. Arabidopsis TIR1 also produces cAMP, and separation-of-function experiments show that substrate degradation alone does not guarantee transcriptional activation. The downstream cAMP effector remains unidentified, and MpTIR1 AC activity is untested. Marchantia class-B MpARF2 provides an additional active TOPLESS-recruiting repression and DNA-competition branch. Paralog combinations, expression domains and promoter/chromatin contexts determine output; neither all ARFs nor all Aux/IAAs share one regulatory behavior. Auxin synthesis/transport, rapid cytoplasmic or cell-surface pathways, noncanonical receptor routes and the downstream developmental programs are outside this boundary.
Exact gene-product selectors constrain functional claims; verified PANTHER subfamilies record classification without transferring activity to all members. Each native implementation requires receptor/adaptor, corepressor machinery and activator-ARF roles; the characterized TIR1 arm additionally requires its AC atom. AFB2 and Marchantia AC dependence remains unresolved, so their structural coverage is not a claim of AC-independent sufficiency. Feedback and MpARF2 modulation are optional contexts and cannot satisfy the circuit alone. No degradation-to-activation CAUSES edge is asserted. Generic SCF core, E1/E2, ubiquitin, proteasome, transcription machinery and ligand/cofactor supply are required boundary assumptions. MpTPL participation in canonical MpIAA repression includes conserved inference; engineered fusions and added-NLS promoter reporters are not native interaction/localization proofs. Current provider runs failed authentication/quota; manual primary-source research is documented. No bounded-index GO-CAM match was found for the 14 selected accessions. PR5076 overlaps earlier broad family additions; exact-member classification avoids its implied broad functional transfer. The required adenylate-cyclase activity in the assayed Arabidopsis TIR1 implementation rests on the 2025 AC-mutant transcriptional study (PMID:40044868); independent confirmation and the physiological significance of low purified catalytic rates remain open. The alternative AFB2 implementation does not inherit an unmeasured cyclase requirement.
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(0/1)✗ none found
No MODULE:auxin_nuclear_signaling deep-research report alongside the module YAML.
✓ every leaf node grounds to a representative protein.
✓ every declared conforms_to bundle matches its template motif.
19 gene-function check(s) reflected in core functions · 0 conflict(s) · 19 evidence or coverage gap(s) (38 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 |
|---|---|---|---|
| tir1_receptor | TIR1 UniProtKB:Q570C0 Gene |
auxin receptor activity GO:0038198 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| tir1_adaptor | TIR1 UniProtKB:Q570C0 Gene |
ubiquitin-like ligase-substrate adaptor activity GO:1990756 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| tir1_adenylate_cyclase | TIR1 UniProtKB:Q570C0 Gene |
adenylate cyclase activity GO:0004016 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| afb2_receptor | AFB2 UniProtKB:Q9LW29 Gene |
auxin receptor activity GO:0038198 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| afb2_adaptor | AFB2 UniProtKB:Q9LW29 Gene |
ubiquitin-like ligase-substrate adaptor activity GO:1990756 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| iaa12_corepressor | IAA12 UniProtKB:Q38830 Gene |
transcription corepressor activity GO:0003714 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| iaa17_corepressor | IAA17 UniProtKB:P93830 Gene |
transcription corepressor activity GO:0003714 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| tpl_corepressor | TPL UniProtKB:Q94AI7 Gene |
transcription corepressor activity GO:0003714 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| arf5_activator | ARF5 UniProtKB:P93024 Gene |
DNA-binding transcription activator activity GO:0001216 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| arf7_activator | ARF7 UniProtKB:P93022 Gene |
DNA-binding transcription activator activity GO:0001216 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| arf19_activator | ARF19 UniProtKB:Q8RYC8 Gene |
DNA-binding transcription activator activity GO:0001216 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| iaa19_feedback_corepressor | IAA19 UniProtKB:O24409 Gene |
transcription corepressor activity GO:0003714 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| mptir1_receptor | MpTIR1 UniProtKB:A0A0K2QW32 Gene |
auxin receptor activity GO:0038198 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| mptir1_adaptor | MpTIR1 UniProtKB:A0A0K2QW32 Gene |
ubiquitin-like ligase-substrate adaptor activity GO:1990756 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| mpiaa_corepressor | MpIAA UniProtKB:A0A0G3FNI9 Gene |
transcription corepressor activity GO:0003714 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| mptpl_corepressor | MpTPL UniProtKB:A0A0G3FGV9 Gene |
transcription corepressor activity GO:0003714 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| mparf1_activator | MpARF1 UniProtKB:A0A0G3FLP1 Gene |
DNA-binding transcription activator activity GO:0001216 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| mparf2_repressor | MpARF2 UniProtKB:A0A0G3FH20 Gene |
DNA-binding transcription repressor activity GO:0001217 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| mptpl_class_b_corepressor | MpTPL UniProtKB:A0A0G3FGV9 Gene |
transcription corepressor activity GO:0003714 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| tir1_receptor | TIR1 verified PANTHER classification PANTHER:PTHR16134:SF66 Family |
auxin receptor activity GO:0038198 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR16134:SF66. |
| tir1_adaptor | TIR1 verified PANTHER classification PANTHER:PTHR16134:SF66 Family |
ubiquitin-like ligase-substrate adaptor activity GO:1990756 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR16134:SF66. |
| tir1_adenylate_cyclase | TIR1 verified PANTHER classification PANTHER:PTHR16134:SF66 Family |
adenylate cyclase activity GO:0004016 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR16134:SF66. |
| afb2_receptor | AFB2 verified PANTHER classification PANTHER:PTHR16134:SF132 Family |
auxin receptor activity GO:0038198 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR16134:SF132. |
| afb2_adaptor | AFB2 verified PANTHER classification PANTHER:PTHR16134:SF132 Family |
ubiquitin-like ligase-substrate adaptor activity GO:1990756 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR16134:SF132. |
| iaa12_corepressor | IAA12 verified PANTHER classification PANTHER:PTHR31734:SF131 Family |
transcription corepressor activity GO:0003714 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR31734:SF131. |
| iaa17_corepressor | IAA17 verified PANTHER classification PANTHER:PTHR31734:SF126 Family |
transcription corepressor activity GO:0003714 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR31734:SF126. |
| tpl_corepressor | TPL verified PANTHER classification PANTHER:PTHR44083:SF27 Family |
transcription corepressor activity GO:0003714 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR44083:SF27. |
| arf5_activator | ARF5 verified PANTHER classification PANTHER:PTHR31384:SF10 Family |
DNA-binding transcription activator activity GO:0001216 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR31384:SF10. |
| arf7_activator | ARF7 verified PANTHER classification PANTHER:PTHR31384:SF93 Family |
DNA-binding transcription activator activity GO:0001216 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR31384:SF93. |
| arf19_activator | ARF19 verified PANTHER classification PANTHER:PTHR31384:SF21 Family |
DNA-binding transcription activator activity GO:0001216 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR31384:SF21. |
| iaa19_feedback_corepressor | IAA19 verified PANTHER classification PANTHER:PTHR31734:SF121 Family |
transcription corepressor activity GO:0003714 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR31734:SF121. |
| mptir1_receptor | MpTIR1 verified PANTHER classification PANTHER:PTHR16134:SF148 Family |
auxin receptor activity GO:0038198 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR16134:SF148. |
| mptir1_adaptor | MpTIR1 verified PANTHER classification PANTHER:PTHR16134:SF148 Family |
ubiquitin-like ligase-substrate adaptor activity GO:1990756 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR16134:SF148. |
| mpiaa_corepressor | MpIAA verified PANTHER classification PANTHER:PTHR31734:SF28 Family |
transcription corepressor activity GO:0003714 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR31734:SF28. |
| mptpl_corepressor | MpTPL verified PANTHER classification PANTHER:PTHR44083:SF45 Family |
transcription corepressor activity GO:0003714 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR44083:SF45. |
| mparf1_activator | MpARF1 verified PANTHER classification PANTHER:PTHR31384:SF115 Family |
DNA-binding transcription activator activity GO:0001216 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR31384:SF115. |
| mparf2_repressor | MpARF2 verified PANTHER classification PANTHER:PTHR31384:SF1 Family |
DNA-binding transcription repressor activity GO:0001217 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR31384:SF1. |
| mptpl_class_b_corepressor | MpTPL verified PANTHER classification PANTHER:PTHR44083:SF45 Family |
transcription corepressor activity GO:0003714 |
Family Review Missing
No supported structured family review is available for PANTHER:PTHR44083:SF45. |
✓ every negative regulator described as feedback has an upstream edge closing the loop.
12 complete review(s) · 3 with deep research · 0 missing review · 11 reviewed but lacking deep research
| Gene | Review | Complete | Deep research |
|---|---|---|---|
| AFB2 Q9LW29 | ✓ | 16/17 | ✗ |
| ARF19 Q8RYC8 | ✓ | ✓ | ✓ |
| ARF5 P93024 | ✓ | ✓ | ✓ |
| ARF7 P93022 | ✓ | ✓ | ✗ |
| IAA12 Q38830 | ✓ | ✓ | ✗ |
| IAA17 P93830 | ✓ | ✓ | ✗ |
| IAA19 O24409 | ✓ | ✓ | ✗ |
| MpARF1 A0A0G3FLP1 | ✓ | ✓ | ✗ |
| MpARF2 A0A0G3FH20 | ✓ | ✓ | ✗ |
| MpIAA A0A0G3FNI9 | ✓ | ✓ | ✗ |
| MpTIR1 A0A0K2QW32 | ✓ | ✓ | ✗ |
| MpTPL A0A0G3FGV9 | ✓ | ✓ | ✗ |
| TIR1 Q570C0 | ✓ | ✓ | ✓ |
| TPL Q94AI7 | ✓ | 123/124 | ✗ |
The nucleus scopes the transcriptional circuit, not exclusive localization of every component; AFB2 has a cytoplasmic pool and MpTPL localization is not established by an added-NLS reporter.
The nucleus scopes the transcriptional circuit, not exclusive localization of every component; AFB2 has a cytoplasmic pool and MpTPL localization is not established by an added-NLS reporter.
Presence of an alternative establishes a supported role, not unique necessity or equivalence of every interaction pair.
Required receptor-specific mechanism, Aux/IAA–TOPLESS repression machinery and activator-ARF output. TIR1’s characterized mechanism additionally requires its AC activity; the AFB2 alternative records established roles with explicitly unresolved AC dependence. Structural coverage of the AFB2 alternative is not evidence of AC-independent sufficiency.
Receptor roles are coupled within a variant to prevent a TIR1 perception route from dropping its experimentally required AC contribution or borrowing a different receptor’s adaptor atom.
The characterized TIR1 implementation requires receptor recognition, SCF substrate recruitment and demonstrated AC activity. Removing the AC atom fails this implementation even though substrate turnover remains biochemically possible. AC-mutant DR5 and full-length Aux/IAA assays distinguish these outcomes.
TIR1 structural and biochemical co-receptor evidence.
Auxin stabilizes the receptor–Aux/IAA interface; InsP6 is an integral structural cofactor, not a separately modeled obligatory biosynthetic supply step.
Auxin-dependent recruitment of substrates to SCF.
Presents the Aux/IAA degron to SCF for ubiquitination and subsequent proteasomal degradation.
TIR1 catalyzes ATP-to-cAMP conversion. Auxin plus Aux/IAA can enhance this activity. AC-deficient mutants retain substrate degradation while impairing transcription. AFB2 and MpTIR1 catalytic capacity is not established by these studies; an untested family member is neither a positive nor a negative assay result.
Source-specific Arabidopsis cAMP output. The observed low purified rate is not equated with native flux, and AFB5 metal preference is not transferred to TIR1.
Native receptor/adaptor and auxin-response evidence establish these AFB2 contributions. Direct AC catalysis or an AC-independent sufficient transcription mechanism has not been demonstrated for AFB2; lack of an AC atom records an unknown, not biochemical dispensability. The shared output machinery represents observed signaling involvement, not a reconstituted sufficient AFB2-only system.
Native genetics and direct Aux/IAA interaction support AFB2 receptor function.
Auxin-dependent Aux/IAA recognition; AFB2 also has an observed cytoplasmic pool, but this leaf selects its nuclear signaling contribution.
Auxin-dependent recruitment of substrates to SCF.
Presents the Aux/IAA degron to SCF for ubiquitination and subsequent proteasomal degradation.
At low effective auxin signaling, Aux/IAA repressors restrain activator ARFs. Direct pairwise evidence is strongest for IAA12/TPL/ARF5 and IAA17/ARF7; specific promoter/chromatin configurations differ.
IAA12 and IAA17 illustrate canonical repression. Their transcription-factor and receptor interactions are source- and pair-specific; this choice does not assert every possible receptor/ARF pairing in every tissue.
Presence of an alternative establishes a supported role, not unique necessity or equivalence of every interaction pair.
Aux/IAA repression through interaction with ARFs and repression machinery.
IAA12–ARF5 and IAA17–ARF7 provide distinct direct interaction examples; the role is active corepression.
Aux/IAA repression through interaction with ARFs and repression machinery.
IAA12–ARF5 and IAA17–ARF7 provide distinct direct interaction examples; the role is active corepression.
TPL is recruited by repression motifs; Mediator and chromatin effects depend on assay and context.
IAA12 EAR-dependent recruitment directly supports the auxin role. Mediator engagement was tested in synthetic yeast and plant systems; no universal obligate HDAC/Mediator stoichiometry is imposed.
Loss of Aux/IAA repression can permit class-A ARF activity; it is not asserted to be sufficient for activation. TIR1 cAMP separation experiments reveal an additional requirement in the tested contexts, and coactivators/chromatin contribute. Repressor/noncanonical ARFs are not activator alternatives.
Presence of an alternative establishes a supported role, not unique necessity or equivalence of every interaction pair.
A context-selected activator ARF; class-A behavior is not assigned to all ARFs.
Binds auxin-response DNA elements and promotes tested transcriptional outputs. AuxRE sequence, spacing and chromatin context matter; TGTCTC is an example rather than the only site.
A context-selected activator ARF; class-A behavior is not assigned to all ARFs.
Binds auxin-response DNA elements and promotes tested transcriptional outputs. AuxRE sequence, spacing and chromatin context matter; TGTCTC is an example rather than the only site.
A context-selected activator ARF; class-A behavior is not assigned to all ARFs.
Binds auxin-response DNA elements and promotes tested transcriptional outputs. AuxRE sequence, spacing and chromatin context matter; TGTCTC is an example rather than the only site.
ARF7-dependent induction replenishes a repressor that directly binds ARF7. The 65% induction reduction is specific to the tested nph4/arf7 context.
IAA19 binds ARF7 and supplies a demonstrated feedback example; it is not a mandatory part of every represented response.
Native receptor, repressor and class-A output evidence supplies a complete comparative implementation, with an additional class-B repression context. Knockout loss of normal organogenesis is distinguished from viable cell-mass survival. cAMP activity/dependence is untested for MpTIR1.
Native MpTIR1 recruitment of MpIAA DII is auxin dependent.
Plant-expressed MpTIR1 with recombinant MpIAA C-terminal fragments provides direct co-receptor evidence; functional fusion localization is reported as nucleus-like regions in sporelings.
Conditional receptor loss stabilizes the native DII reporter; conserved SCF architecture connects recruitment to proteolysis.
Substrate-adaptor activity is corroborated directly; complete native SCF purification and ubiquitin-transfer reconstitution were not performed in the cited study.
Native MpIAA-dependent repression is established. MpTPL is a conserved repression component; forced MpTPL–MpIAA fusions demonstrate imposed repression, not an independently measured native binary recruitment interaction.
828-aa KP877968 exemplar; independent 825-aa same-locus constructs corroborate native repression without being treated as identical sequences.
Native-circuit TPL contribution is a conserved mechanistic inference supported by repression constructs. Direct MpARF2–MpTPL interaction is separately documented in heterologous cells; promoter-NLS reporters do not measure native MpTPL localization.
Native MpARF1 contributes to auxin-dependent transcription. DBD swaps show some shared DNA recognition with MpARF2, but do not convert the native class-B protein into an activator.
Full-length class-A activator. Native mutant transcriptomics and domain-interface tests support the output; a short isolated peptide can repress without overturning the full protein’s principal activity.
MpARF2 actively recruits MpTPL through LFG and can compete with MpARF1 at shared DNA sites. This branch modulates output independently of the canonical MpIAA degradation gate; it is not an interchangeable activator.
Full MpARF2–MpTPL interaction was measured by FRET–FLIM in Arabidopsis protoplasts; induced repression and conditional-loss phenotypes were tested in native Marchantia. Short-peptide tobacco assays and DBD chimeras are distinct evidence.
LFG-dependent corepressor recruitment by MpARF2; inferred nuclear role is not supported by the added-NLS promoter reporter.