filament shaped
METPO:1000674 · CLASS · REVIEWED
A cell shape in which an organism grows as elongated filamentous cells or hypha-like structures.
Filament-shape Streptomyces polar growth mechanism
Edge evidence
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DivIVA
localizes to
apical polarisome
biolink:located_inDivIVA localizes at hyphal tips as part of the polar growth machinery.
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DOI:10.1016/j.mib.2010.10.002polarity determinant DivIVA
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Scy
part of
apical polarisome
biolink:part_ofScy is a component of the tip-organizing center controlling polar growth.
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DOI:10.1371/journal.pgen.1002423tip organizing center
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apical polarisome
recruits
apical peptidoglycan synthesis
The apical polarisome recruits cell-wall synthesis machinery to hyphal tips.
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DOI:10.1016/j.mib.2012.10.012polarisome-like complex involving the essential polarity protein DivIVA
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apical peptidoglycan synthesis
regulates
hyphal tip extension
RO:0002211Localized wall synthesis at the tip drives filament extension.
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DOI:10.1038/s41564-025-02080-xDivIVA drives growth at the hyphal poles
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hyphal tip extension
manifests as
filament shaped
METPO:2007400Hyphal tip extension manifests filamentous morphology.
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DOI:10.1016/j.mib.2010.10.002Streptomyces hyphae
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RecA/LexA SOS response
induces
SulA
DNA damage activates the RecA/LexA SOS response, inducing the division inhibitor SulA.
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DOI:10.1002/advs.202203260
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SulA
inhibits
FtsZ polymerization
RO:0002212SulA blocks FtsZ polymerization, preventing Z-ring assembly and septation.
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DOI:10.1002/advs.202203260
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FtsZ polymerization
regulates
filament shaped
RO:0002211Inhibited FtsZ polymerization blocks septation, causing non-septate filamentation.
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DOI:10.1002/advs.202203260
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apical polarisome
enables
polar hyphal growth
RO:0002327The DivIVA/polarisome assembly mediates polar growth at hyphal tips.
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DOI:10.1128/jb.00153-23
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apical polarisome
promotes
hyphal branch emergence
RO:0002213Splitting of polarisomes at tips produces daughter polarisomes that coordinate new branch emergence.
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DOI:10.1093/femsml/uqad020
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CglA
enables
cell-wall glycopolymer attachment
RO:0002327CglA is the glycopolymer ligase mediating attachment of glycopolymers to the cell wall.
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DOI:10.1128/mbio.01492-24
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cell-wall glycopolymer attachment
regulates
filament shaped
RO:0002211Reduced glycopolymer attachment results in enlarged vegetative hyphae and loss of hyphal cell shape.
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DOI:10.1128/mbio.01492-24
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Provenance
- Source
- METPO (2025-11-25)
- Author
- Luke Wang
- Definition source
- DOI:10.1016/j.mib.2010.10.002
Parent traits (1)
Synonyms (3)
- S_filament
- filament
- filament-shaped
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1000674[+1.704, -8.992, +4.797, -2.737, …]
Nearest neighbors in embedding space
- morphology fusiform shaped 0.384
- morphology branched shaped 0.361
- morphology tailed shaped 0.324
- morphology spore forming 0.313
- morphology sporulation 0.292
- environment non halophilic 0.275
- morphology disc shaped 0.263
- morphology spore shaped 0.251
Deep research
# Curation report: filament shaped ## Trait record and scope - **Trait:** filament shaped - **Identifier:** **METPO:1000674** - **Category / kind / status:** MORPHOLOGY / CLASS / REVIEWED - **Definition:** an organism grows as elongated filamentous cells or hypha-like structures. - **Parent:** METPO:1000666 - **Synonyms:** S_filament; filament; filament-shaped For the proposed Streptomyces graph, the clearest operational phenotype is **sustained vegetative growth by apical cell-wall extension, accompanied by lateral branching to produce multinucleoid hyphae/mycelia**. DivIVA-containing apical complexes—polarisomes—concentrate envelope assembly at growing tips and are central to this growth mode. Importantly, Streptomyces polar growth is mechanistically separable from cell division. (sen2024adispensablesepiva pages 10-12, sen2024adispensablesepiva pages 1-2) ### Boundary cases 1. **Rod-shaped cells are not filaments merely because they elongate before binary fission.** The trait should require conspicuously elongated, hypha-like growth. 2. **Transient division-inhibition filamentation is a distinct implementation.** For example, antibiotic-, SOS-, or host-induced elongation of ordinarily rod-shaped bacteria may satisfy the observed morphology but should not be merged mechanistically with constitutive Streptomyces hyphal growth. 3. **Aerial hyphae are filamentous, but their conversion into chains of spores is a developmental transition, not the mechanism that originally produces vegetative filaments.** SsgB, SepG, FtsZ ladders, and related division proteins therefore belong principally in a boundary or transition subgraph. (zhang2020branchingofsporogenic pages 27-41, sen2024adispensablesepiva pages 1-2) 4. **Branching is associated but not definitionally required.** An unbranched elongated cell can still be filament-shaped; hyperbranching is an altered topology rather than stronger evidence of the trait. 5. **Pellets, clumps, and mycelial aggregates are population-scale morphologies.** They arise from filament interactions and are important in fermentation, but should not be used as synonyms for cellular filament shape. 6. **SepIVA tip localization is insufficient to infer necessity.** Its deletion causes no detectable defect in S. venezuelae tip extension, branching, growth pattern, or wall composition. (sen2024adispensablesepiva pages 10-12) ## Recommended causal architecture The most defensible core is: **DivIVA/polarisome organization → localized apical envelope synthesis → hyphal tip extension → elongated vegetative hyphae**, with **Scy and FilP** supporting tip organization and branching, and **CglA-mediated wall glycopolymer attachment** maintaining normal filament width, integrity, and division-site organization. (sen2024adispensablesepiva pages 10-12, sen2024adispensablesepiva pages 1-2, bhowmick2024cellshapeand pages 8-10, bhowmick2024cellshapeand pages 1-2) | module | candidate subject | predicate | object | evidence class | recommended action | |---|---|---|---|---|---| | Apical polar growth | DivIVA | organizes/localizes | polar cell-wall assembly at hyphal tips | foundational Streptomyces mechanism; strong but mostly background in retrieved set (sen2024adispensablesepiva pages 10-12, sen2024adispensablesepiva pages 1-2) | Curate as core trait mechanism; link to apical extension and lateral branching, but add a direct primary DivIVA perturbation paper in final YAML | | Tip extension outcome | polar cell-wall assembly at hyphal tips | enables | apical extension / filamentous vegetative growth | supported by Streptomyces polar-growth summaries and tip-localization data (sen2024adispensablesepiva pages 10-12, sen2024adispensablesepiva pages 1-2) | Curate as central process edge for filament-shaped scope | | Polarisome architecture | Scy | stabilizes/supports | apical polarisome / normal branching pattern | mutant evidence indicates strong effects on morphology and branching; some evidence indirect in retrieved set (sen2024adispensablesepiva pages 10-12) | Curate, but mark taxon-specific to Streptomyces and seek direct Scy mutant primary citation | | Cytoskeletal support | FilP | supports | apical growth / hyphal morphology | mutant and localization evidence weaker than for Scy; often contextual or interaction-based (sen2024adispensablesepiva pages 10-12) | Curate as contributing factor, not sole required cause; mark moderate confidence | | Cell-wall glycopolymer ligation | CglA | attaches/ligates | cell-wall glycopolymers to peptidoglycan | strong 2024 perturbation evidence with wall-mass reduction and enlarged hyphae/FtsZ defects (bhowmick2024cellshapeand pages 8-10, bhowmick2024cellshapeand pages 1-2) | High-priority curation as direct causal module for maintaining normal filament shape | | Shape maintenance | cell-wall glycopolymer decoration | maintains | normal hyphal width/shape | strong phenotype evidence from cglA mutant (bhowmick2024cellshapeand pages 8-10, bhowmick2024cellshapeand pages 1-2) | Curate as direct morphology-maintenance edge | | Stress-adaptive tip organization | StlP | organizes | tip membrane microdomain / local membrane fluidity under hyperosmotic stress | 2024 preprint; mechanistically rich but not peer-reviewed; branching and wall defects reported (claessen2024thestomatinlikeprotein pages 27-28, claessen2024thestomatinlikeprotein pages 20-27) | Curate only as uncertain/contextual edge or hold until peer-reviewed publication | | Stress phenotype | loss of StlP | causes | hyperbranching, diffuse wall synthesis, wall-deficient cell extrusion | preprint-only perturbation evidence (claessen2024thestomatinlikeprotein pages 27-28, claessen2024thestomatinlikeprotein pages 20-27) | Do not use as core universal edge yet; retain in warning list | | Sporogenic branching control | SflA/SflB | restrict | ectopic DivIVA/FtsZ persistence and branching in sporogenic aerial hyphae | mutant phenotype plus localization/correlation; developmental stage-specific (zhang2020branchingofsporogenic pages 27-41) | Keep as contextual/boundary module, not core vegetative filament-shape mechanism | | Sporulation septation | SsgB | recruits/positions | FtsZ at sporulation septum sites | strong for sporulation-specific septation, not vegetative filament maintenance (zhang2020branchingofsporogenic pages 27-41) | Boundary/context only; avoid using as direct cause of filament-shaped trait | | Sporulation coordination | SepG | ensures localization of | SsgB/FtsZ complex during sporulation | strong but sporulation-specific context (zhang2020branchingofsporogenic pages 27-41) | Boundary/context only | | Developmental division scaffold | FtsZ | forms | sporulation septa / Z-ladders | strong developmental evidence, but pertains to hypha-to-spore transition (zhang2020branchingofsporogenic pages 27-41) | Exclude from core trait graph except as boundary relation | | Polar-growth-associated but dispensable factor | SepIVA | localizes to | growing hyphal tips / DivIVA-associated polar-growth zones | localization and interaction evidence, but deletion shows no detectable filament-growth defect (sen2024adispensablesepiva pages 10-12, sen2024adispensablesepiva pages 1-2) | Do not curate as required cause of filament-shaped morphology | | Negative causal claim | sepIVA deletion | does not measurably alter | hyphal growth pattern, tip extension, branching, or wall composition | strong 2024 negative evidence (sen2024adispensablesepiva pages 10-12) | Record as anti-edge/warning; prevents overcuration of SepIVA | | Boundary case outside Streptomyces trait core | transient division-inhibition filamentation | differs from | sustained hypha-like polar growth | scope distinction supported by contrast between Streptomyces vegetative growth and non-Streptomyces reversible filamentation literature in conversation; core retrieved context emphasizes separation of polar growth from sporulation/division modules (sen2024adispensablesepiva pages 10-12, sen2024adispensablesepiva pages 1-2) | Add as scope note only, not graph edge | *Table: This table prioritizes candidate mechanisms for curating METPO:1000674 in Streptomyces, separating core vegetative filament-growth edges from contextual sporulation and uncertain stress-specific modules. It is useful for deciding which nodes and edges should enter the first TraitMech graph versus remain as warnings or boundary annotations.* ## Candidate nodes grouped by type ### Trait, taxon, and anatomical nodes | Candidate node | Grounding recommendation | Comment | |---|---|---| | filament-shaped morphology | **METPO:1000674** | Target trait; quote CURIE exactly in YAML. | | Streptomyces | **NCBITaxon:1883** | Appropriate genus-level taxon restriction. | | Streptomyces venezuelae | Use a verified NCBITaxon record at implementation | Main organism in the 2024 CglA and SepIVA studies; do not insert an unchecked numeric CURIE. | | Streptomyces coelicolor | Use a verified strain-specific NCBITaxon record | Many foundational morphogenesis results are strain-specific. | | vegetative hypha | Label-only candidate | Distinguish from aerial/sporogenic hypha. |
Curation history
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SEEDED_FROM_METPO · seed_from_metpo
imported from data/raw/metpo.owl (CLASS)
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CURATED_WITH_LITERATURE · codex
Added DOI-backed definition and causal graph for DivIVA, Scy, apical polarisome, apical peptidoglycan synthesis, and hyphal tip extension.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (biolink:located_in×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007400×1).
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RENAME_PREDICATE_LABELS · claude
Renamed 1 causal-edge predicate label(s) to align with existing groundings: drives → regulates ×1.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002211×1).
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GROUND_CAUSAL_NODES · claude
Grounded 2 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:Q1IYG2×1, UniProtKB:A0A191V3Q4×1).
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RENAME_PREDICATE_LABELS · claude
Renamed 1 causal-edge predicate label(s) to align with existing groundings: organizes → enables ×1.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002327×1).
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ENRICH_CAUSAL_GRAPH · claude
Added 7 evidence-backed generic edges (7 new nodes) from the deep-research report.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 6 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002211×2, RO:0002327×2, RO:0002212×1, RO:0002213×1).
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GROUND_CAUSAL_NODES · claude
Grounded 2 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:H8YHZ0×1, UniProtKB:A0A0C1K447×1).
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RETRACT_DEAD_UNIPROT_GROUNDINGS · claude
Retracted 1 UniProtKB grounding(s) whose accessions are deleted from UniProt; nodes demoted to label-only pending re-grounding (docs/GROUNDING_POLICY.md)
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REGROUND_CAUSAL_EDGE · claude
Edge scy -> apical_polarisome in graph filament_shaped_streptomyces_polar_growth: re-grounded it from enables/RO:0002327 to part of/biolink:part_of. Issue 334. biolink declares enables range 'biological process or activity', which of CausalNodeTypeEnum only BIOLOGICAL_PROCESS, PATHWAY and MOLECULAR_FUNCTION satisfy, so this edge entailed a false type on its object. 'Scy is a COMPONENT of the tip-organizing center.' Mereology, not causation. The corpus already uses `part of` this way (flii_atpase_complex part of ft3ss_export_system).