# Assembly and mother centriole recruitment of IFT-B subcomplexes to form IFT-B holocomplex

**Authors:** Koshi Tasaki, Yohei Katoh, Hye-Won Shin, Kazuhisa Nakayama

PMC · DOI: 10.1247/csf.25027 · Cell Structure and Function · 2025-06-24

## TL;DR

This study explores how the IFT-B complex assembles and localizes to the mother centriole to support cilia formation.

## Contribution

The paper reveals the specific roles of IFT-B subcomplexes in centriole recruitment and ciliogenesis.

## Key findings

- IFT-B2 is essential for the localization of IFT-B1b and IFT-B1a to the mother centriole.
- IFT-B1b is crucial for bridging IFT-B2 and IFT-B1a and their centriole localization.
- All IFT-B components are necessary for ciliogenesis, but not for initial centriole recruitment.

## Abstract

For the biogenesis and maintenance of cilia, bidirectional protein trafficking within cilia is crucial, and is conducted by intraflagellar transport (IFT) trains containing the IFT-A and IFT-B complexes that are powered by dynein-2 and kinesin-II motors. We have recently shown that before the assembly of anterograde IFT trains, the IFT-A, IFT-B, and dynein-2 complexes are independently recruited to the mother centriole/basal body. The IFT-B complex, which consists of 16 subunits, can be divided into the IFT-B1 and IFT-B2 subcomplexes, and IFT-B1 can be further divided into the IFT-B1a and IFT-B1b subgroups. Here we investigated how the IFT-B complex is assembled and recruited to the mother centriole for ciliogenesis. Analyses using cells with knockouts of individual IFT-B subunits, and analyses of proteins coimmunoprecipitated with EGFP-fused IFT-B2, IFT-B1b, and IFT-B1a subunits expressed in these knockout cells demonstrated the following: (i) although IFT-B2 is dispensable for the linkage between IFT-B1b and IFT-B1a, it is essential for their localization to the mother centriole; (ii) IFT-B1b is essential both for bridging IFT-B2 and IFT-B1a, and for their localization to the mother centriole; (iii) IFT-B1a is not required for the linkage between IFT-B2 and IFT-B1b nor for their localization to the mother centriole; and (iv) all IFT-B components (IFT-B2, IFT-B1b, and IFT-B1a) are essential for ciliogenesis. Thus, although ciliogenesis is not a prerequisite for the recruitment of the IFT-B complex to the mother centriole, the linkage between IFT-B2 and IFT-B1b is crucial for the mother centriole localization of the IFT-B complex for ciliogenesis.

## Linked entities

- **Proteins:** IFTA (intraflagellar transport associated protein), klc1.S (kinesin light chain 1 S homeolog)

## Full-text entities

- **Genes:** IFT122 (intraflagellar transport 122) [NCBI Gene 55764] {aka CED, CED1, CFAP80, FAP80, SPG, WDR10}, IFT56 (intraflagellar transport 56) [NCBI Gene 79989] {aka BRENS, DYF13, TTC26, dyf-13}, IFT70B (intraflagellar transport 70B) [NCBI Gene 150737] {aka IFT70, TTC30B, fleer}, CEP83 (centrosomal protein 83) [NCBI Gene 51134] {aka CCDC41, NPHP18, NY-REN-58}, AP1G1 (adaptor related protein complex 1 subunit gamma 1) [NCBI Gene 164] {aka ADTG, CLAPG1, USRISD}, GPR161 (G protein-coupled receptor 161) [NCBI Gene 23432] {aka RE2}, GSTK1 (glutathione S-transferase kappa 1) [NCBI Gene 373156] {aka GST, GST 13-13, GST13, GST13-13, GSTK1-1, hGSTK1}, IFT46 (intraflagellar transport 46) [NCBI Gene 56912] {aka C11orf2, C11orf60, CFAP32, FAP32}, IFT81 (intraflagellar transport 81) [NCBI Gene 28981] {aka CDV-1, CDV-1R, CDV1, CDV1R, DV1, SRTD19}, IFT172 (intraflagellar transport 172) [NCBI Gene 26160] {aka BBS20, NPHP17, RP71, SLB, SRTD10, osm-1}, IFT27 (intraflagellar transport 27) [NCBI Gene 11020] {aka BBS19, CFAP156, FAP156, RABL4, RAYL}, WDR19 (WD repeat domain 19) [NCBI Gene 57728] {aka ATD5, CED4, CFAP66, DYF-2, FAP66, IFT144}, TERT (telomerase reverse transcriptase) [NCBI Gene 7015] {aka CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1}, TUBA1B (tubulin alpha 1b) [NCBI Gene 10376] {aka K-ALPHA-1}, ANKRD26 (ankyrin repeat domain 26) [NCBI Gene 22852] {aka THC2, bA145E8.1}, IFT74 (intraflagellar transport 74) [NCBI Gene 80173] {aka BBS22, CCDC2, CMG-1, CMG1, JBTS40, SPGF58}, TTBK2 (tau tubulin kinase 2) [NCBI Gene 146057] {aka SCA11, TTBK}, IFT80 (intraflagellar transport 80) [NCBI Gene 57560] {aka ATD2, CFAP167, FAP167, SRTD2, WDR56}, NCS1 (neuronal calcium sensor 1) [NCBI Gene 23413] {aka FLUP, FREQ}, IFT20 (intraflagellar transport 20) [NCBI Gene 90410], KIF3B (kinesin family member 3B) [NCBI Gene 9371] {aka FLA8, HH0048, KLP-11, OTSC12, RP89}, IFT38 (intraflagellar transport 38) [NCBI Gene 23059] {aka CFAP22, CLUAP1, FAP22}, FBF1 (Fas binding factor 1) [NCBI Gene 85302] {aka Alb, FBF-1}, IFT57 (intraflagellar transport 57) [NCBI Gene 55081] {aka ESRRBL1, HIPPI, MHS4R2, OFD18}, IFT52 (intraflagellar transport 52) [NCBI Gene 51098] {aka C20orf9, CGI-53, NGD2, NGD5}, IFT25 (intraflagellar transport 25) [NCBI Gene 51668] {aka C1orf41, CFAP232, FAP232, HSPB11, HSPCO34, PP25}, IFT22 (intraflagellar transport 22) [NCBI Gene 64792] {aka CFAP9, FAP9, RABL5}, CEP164 (centrosomal protein 164) [NCBI Gene 22897] {aka NPHP15}, PIDD1 (p53-induced death domain protein 1) [NCBI Gene 55367] {aka LRDD, MRT75, PIDD, altPIDD1}, IFT88 (intraflagellar transport 88) [NCBI Gene 8100] {aka D13S1056E, DAF19, TG737, TTC10, hTg737}, TULP3 (TUB like protein 3) [NCBI Gene 7289] {aka HRCDF, TUBL3}, CEP43 (centrosomal protein 43) [NCBI Gene 11116] {aka FGFR1OP, FOP}, IFT54 (intraflagellar transport 54) [NCBI Gene 26146] {aka CFAP116, FAP116, MIP-T3, MIPT3, SLSN9, TRAF3IP1}, BBS2 (Bardet-Biedl syndrome 2) [NCBI Gene 583] {aka BBS, RP74}
- **Diseases:** Bardet-Biedl syndrome (MESH:D020788)
- **Chemicals:** CO2 (MESH:D002245), glutathione (MESH:D005978), KOH (MESH:C029943), Sepharose (MESH:D012685), paraformaldehyde (MESH:C003043), KCl (MESH:D011189), glucose (MESH:D005947), sodium bicarbonate (MESH:D017693), DAP (-), glycerol (MESH:D005990), HEPES (MESH:D006531), SDS (MESH:D012967), dithiothreitol (MESH:D004229), methanol (MESH:D000432), NaCl (MESH:D012965), MgCl2 (MESH:D015636), Zeocin (MESH:C105427), blasticidin S (MESH:C004500), Polyethylenimine (MESH:D011094), EDTA (MESH:D004492), Triton X-100 (MESH:D017830)
- **Species:** Homo sapiens (human, species) [taxon 9606], Chlamydomonas (genus) [taxon 3052]
- **Cell lines:** RPE1 — Homo sapiens (Human), Telomerase immortalized cell line (CVCL_4388), hTERT-RPE1 — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0145), S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232), HEK293T — Homo sapiens (Human), Transformed cell line (CVCL_0063)

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## Figures

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## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC12967509/full.md

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Source: https://tomesphere.com/paper/PMC12967509