CellStructureMech

Spirostomum myoneme fishnet

cellstructuremech:spirostomum_myoneme_fishnet · Cytoskeleton · Other · Proposed

A mesh-like cortical myoneme characterized in Spirostomum, containing intersecting centrin/spasmin-rich fibrillar bundles and giant Sfi1-like scaffold proteins. The extended network shortens during calcium-triggered cell contraction and is distinct from adjacent microtubule bundles and from an isolated scaffold-centrin protein complex. [DOI:10.1126/sciadv.add6550]

Image (not hosted — CC_BY_NC_4_0): PMC9946354.1 F5

Spirostomum minus myoneme mesh in Figure 5B/C. B compares centrin signal (red) with anti-GSBP2 signal (green) using merged optical layers. C compares anti-GSBP1 (red) with anti-GSBP2 (green) in a single optical layer and includes Western insets. Anti-GSBP2 recognizes both GSBP proteins. Panel A is a predicted partial protein complex, not a native mesh reconstruction. FLUORESCENCE · Spirostomum minus (NCBITaxon:402029) · Jing Zhang, Weiwei Qin, Che Hu, Siyu Gu, Xiaocui Chai, Mingkun Yang, Fang Zhou, Xueyan Wang, Kai Chen, Guanxiong Yan, Guangying Wang, Chuanqi Jiang, Alan Warren, Jie Xiong and Wei Miao; Copyright 2023 The Authors, exclusive licensee American Association for the Advancement of Science; CC BY-NC 4.0; Figure 5 of Giant proteins in a giant cell, Science Advances, doi:10.1126/sciadv.add6550, via PubMed Central. Link only; no repository copy or adaptation. · CC_BY_NC_4_0 · source: PMC PMC9946354.1 F5 · DOI:10.1126/sciadv.add6550

Synonyms: Spirostomum mesh-like contractile fibrillar system; myoneme

Part of: GO:0030863 — cortical cytoskeleton (no local record)

UniProt location names: UniProt Consortium, CC BY 4.0. Reference label and route sources.

Components

ComponentTypePart of / acts onGroundingGenesStoichiometryEssentialRole
Myonemal centrin-family proteinsProteinpart ofReviewed label only (reviewed name; no accession asserted)UNKNOWNCalcium-binding centrin/spasmin constituents of the contractile bundles, exemplified by Spasmin 1 and 2 in S. minus. Localization and proteomics do not establish an exhaustive paralogue inventory or individual assembly requirements.
  • DOI:10.1126/sciadv.add6550 Results on spasmin identification combine whole-cell MS with centrin, GSBP1 and GSBP2 immunoprecipitation-MS. Figure 5 uses anti-centrin staining, not antibodies distinguishing Spasmin 1 from Spasmin 2.
  • DOI:10.1073/pnas.2601408123 Published abstract reports centrin localization by immunofluorescence and immunogold electron microscopy in S. ambiguum. Full journal methods were not accessible; no exact paralogue or quantitative result is imported.
Giant Sfi1-like myoneme scaffold proteinsProteinpart ofReviewed label only (reviewed name; no accession asserted)UNKNOWNRepeat-rich centrin/spasmin-binding scaffold class, exemplified by GSBP1 and GSBP2 in S. minus. Evidence supports mesh membership, but limited RNAi phenotypes do not establish each paralogue's universal assembly requirement.
  • DOI:10.1126/sciadv.add6550 Sequence, transcript, MS, immunoprecipitation, Western and localization Results support GSBP1/GSBP2. Anti-GSBP1 is specific in the reported Western, whereas anti-GSBP2 recognizes both proteins; its fluorescence is not an isoform-specific GSBP2 map. GSBP2 is abundant in GSBP1 immunoprecipitates.
  • DOI:10.1073/pnas.2601408123 Published abstract reports Sfi1-homolog localization and calcium-dependent compaction/self-association of a reconstituted centrin-Sfi1 repeat complex. That assay is not reconstitution of the complete native fishnet.

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Source: data/structures/cytoskeleton/spirostomum_myoneme_fishnet.yaml