The DOI matches its Crossref record, with a small difference in title or year; 5 of the 5 references it cites were found in a registry or an index.
The chromokinesin Kid (KIF22) forms a homodimer, moves processively along microtubules, and transports double-stranded DNA
Open accessPublished version of a preprint
Abstract
During prometaphase in mitosis, chromosomes are pushed toward the spindle equator. The chromokinesin Kid, also known as KIF22, moves chromosomes along spindle microtubules during prometaphase. Kid has long been considered a monomeric and nonprocessive motor, different from typical kinesins. In this study, we demonstrate that the full-length Kid forms a homodimer and moves processively along microtubules. A conserved coiled-coil domain within the stalk region of Kid is sufficient for homodimer formation and is required for the processivity of Kid. Furthermore, the neck linker and coiled-coil domains of Kid could add processive activity to the motor domain of KIF1A, suggesting that Kid contains a functional neck linker and dimerization capability, a prerequisite for the processivity of kinesin motor domains. The full-length Kid, containing a helix–hairpin–helix domain, can transport double-stranded DNA along microtubules in vitro. AlphaFold3 prediction suggests that the dimerization of Kid stabilizes the association with DNA. These findings collectively suggest the reclassification of Kid as a processive and dimeric motor that transports DNA along microtubules.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764
Intramolecular Strain Coordinates Kinesin Stepping Behavior along Microtubules
Yildiz, A., Tomishige, M., Gennerich, A., & Vale, R. D. (2008) · Cell · doi:10.1016/j.cell.2008.07.018 · Cited by 313
Funabiki, H., & Murray, A. W. (2000) · Cell · doi:10.1016/s0092-8674(00)00047-7 · Cited by 305
Highly processive microtubule-stimulated ATP hydrolysis by dimeric kinesin head domains
Hackney, D. D. (1995) · Nature · doi:10.1038/377448a0 · Cited by 177
Cdc2-mediated phosphorylation of Kid controls its distribution to spindle and chromosomes
Ohsugi, M., Tokai‐Nishizumi, N., Shiroguchi, K., Toyoshima, Y. Y., Inoue, J., & Yamamoto, T. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg208 · Cited by 65
Flagged first, then by citations
Research works printed but not linked: 47
- Afshar, 1995, DNA binding and meiotic chromosomal localization of the Drosophila nod kinesin-like protein, Cell, 81, 129, 10.1016/0092-8674(95)90377-1 · DOI
- Al-Bassam, 2014, Reconstituting dynamic microtubule polymerization regulation by TOG domain proteins, Methods in Enzymology, 540, 131, 10.1016/B978-0-12-397924-7.00008-X · DOI
- Anazawa, 2022, De novo mutations in KIF1A-associated neuronal disorder (KAND) dominant-negatively inhibit motor activity and axonal transport of synaptic vesicle precursors, PNAS, 119, 10.1073/pnas.2113795119 · DOI
- Antonio, 2000, Xkid, a chromokinesin required for chromosome alignment on the metaphase plate, Cell, 102, 425, 10.1016/s0092-8674(00)00048-9 · DOI
- Bieling, 2010, Microtubule motility on reconstituted meiotic chromatin, Current Biology, 20, 763, 10.1016/j.cub.2010.02.067 · DOI
- Brouhard, 2005, Microtubule movements on the arms of mitotic chromosomes: polar ejection forces quantified in vitro, PNAS, 102, 13903, 10.1073/pnas.0506017102 · DOI
- Case, 2000, Role of the kinesin neck linker and catalytic core in microtubule-based motility, Current Biology, 10, 157, 10.1016/s0960-9822(00)00316-x · DOI
- Castoldi, 2003, Purification of brain tubulin through two cycles of polymerization-depolymerization in a high-molarity buffer, Protein Expression and Purification, 32, 83, 10.1016/S1046-5928(03)00218-3 · DOI
- Chiba, 2019, Disease-associated mutations hyperactivate KIF1A motility and anterograde axonal transport of synaptic vesicle precursors, PNAS, 116, 18429, 10.1073/pnas.1905690116 · DOI
- Chiba, 2022, Synergistic autoinhibition and activation mechanisms control kinesin-1 motor activity, Cell Reports, 39, 10.1016/j.celrep.2022.110900 · DOI
- Chiba, 2023, Insight into the regulation of axonal transport from the study of KIF1A-associated neurological disorder, Journal of Cell Science, 136, 10.1242/jcs.260742 · DOI
- Chiba, 2024, Autoinhibition and activation of kinesin-1 and their involvement in amyotrophic lateral sclerosis, Current Opinion in Cell Biology, 86, 10.1016/j.ceb.2023.102301 · DOI
- Doherty, 1996, The helix-hairpin-helix DNA-binding motif: a structural basis for non-sequence-specific recognition of DNA, Nucleic Acids Research, 24, 2488, 10.1093/nar/24.13.2488 · DOI
- Fan, 2022, Control of motor landing and processivity by the CAP-Gly domain in the KIF13B tail, Nature Communications, 14, 10.1038/s41467-023-40425-4 · DOI
- Gibson, 2009, Enzymatic assembly of DNA molecules up to several hundred kilobases, Nature Methods, 6, 343, 10.1038/nmeth.1318 · DOI
- Hancock, 1998, Processivity of the motor protein kinesin requires two heads, The Journal of Cell Biology, 140, 1395, 10.1083/jcb.140.6.1395 · DOI
- Hoeprich, 2014, Kinesin’s neck-linker determines its ability to navigate obstacles on the microtubule surface, Biophysical Journal, 106, 1691, 10.1016/j.bpj.2014.02.034 · DOI
- Iemura, 2015, Chromokinesin Kid and kinetochore kinesin CENP-E differentially support chromosome congression without end-on attachment to microtubules, Nature Communications, 6, 10.1038/ncomms7447 · DOI
- Isojima, 2010, Optimal size of the neck linker is important for the coordinated processive movement of Kinesin-1, Biophysical Journal, 98, 10.1016/j.bpj.2009.12.1995 · DOI
- Kita, 2024, Comparative analysis of two Caenorhabditis elegans kinesins KLP-6 and UNC-104 reveals a common and distinct activation mechanism in kinesin-3, eLife, 12, 10.7554/eLife.89040 · DOI
- Levesque, 2001, The chromokinesin Kid is necessary for chromosome arm orientation and oscillation, but not congression, on mitotic spindles, The Journal of Cell Biology, 154, 1135, 10.1083/jcb.200106093 · DOI
- Li, 2016, NuSAP governs chromosome oscillation by facilitating the Kid-generated polar ejection force, Nature Communications, 7, 10.1038/ncomms10597 · DOI
- Malaby, 2019, KIF18A’s neck linker permits navigation of microtubule-bound obstacles within the mitotic spindle, Life Science Alliance, 2, 10.26508/lsa.201800169 · DOI
- Matthies, 2001, Orphan kinesin NOD lacks motile properties but does possess a microtubule-stimulated ATPase activity, Molecular Biology of the Cell, 12, 4000, 10.1091/mbc.12.12.4000 · DOI
- Mirdita, 2022, ColabFold: making protein folding accessible to all, Nature Methods, 19, 679, 10.1038/s41592-022-01488-1 · DOI · Paper page
- Okada, 2003, Processivity of the single-headed kinesin KIF1A through biased binding to tubulin, Nature, 424, 574, 10.1038/nature01804 · DOI
- Pike, 2018, KIF22 coordinates CAR and EGFR dynamics to promote cancer cell proliferation, Science Signaling, 11, 10.1126/scisignal.aaq1060 · DOI
- Rieder, 1986, Oscillatory movements of monooriented chromosomes and their position relative to the spindle pole result from the ejection properties of the aster and half-spindle, The Journal of Cell Biology, 103, 581, 10.1083/jcb.103.2.581 · DOI
- Shastry, 2010, Neck linker length determines the degree of processivity in kinesin-1 and kinesin-2 motors, Current Biology, 20, 939, 10.1016/j.cub.2010.03.065 · DOI
- Shastry, 2011, Interhead tension determines processivity across diverse N-terminal kinesins, PNAS, 108, 16253, 10.1073/pnas.1102628108 · DOI
- Shiroguchi, 2003, The second microtubule-binding site of monomeric kid enhances the microtubule affinity, The Journal of Biological Chemistry, 278, 22460, 10.1074/jbc.M212274200 · DOI
- Soeda, 2016, The microtubule-binding and coiled-coil domains of Kid are required to turn off the polar ejection force at anaphase, Journal of Cell Science, 129, 3609, 10.1242/jcs.189969 · DOI
- Sonn-Segev, 2020, Quantifying the heterogeneity of macromolecular machines by mass photometry, Nature Communications, 11, 10.1038/s41467-020-15642-w · DOI
- Soppina, 2014, Dimerization of mammalian kinesin-3 motors results in superprocessive motion, PNAS, 111, 5562, 10.1073/pnas.1400759111 · DOI
- Stumpff, 2012, Kif18A and chromokinesins confine centromere movements via microtubule growth suppression and spatial control of kinetochore tension, Developmental Cell, 22, 1017, 10.1016/j.devcel.2012.02.013 · DOI
- Takagi, 2013, Chromosome position at the spindle equator is regulated by chromokinesin and a bipolar microtubule array, Scientific Reports, 3, 10.1038/srep02808 · DOI
- Tan, 2023, Autoinhibited kinesin-1 adopts a hierarchical folding pattern, eLife, 12, 10.7554/eLife.86776 · DOI · Paper page
- Thompson, 2022, Pathogenic mutations in the chromokinesin KIF22 disrupt anaphase chromosome segregation, eLife, 11, 10.7554/eLife.78653 · DOI
- Tokai, 1996, Kid, a novel kinesin-like DNA binding protein, is localized to chromosomes and the mitotic spindle, The EMBO Journal, 15, 457, 10.1002/j.1460-2075.1996.tb00378.x · DOI
- Tomishige, 2002, Conversion of Unc104/KIF1A kinesin into a processive motor after dimerization, Science, 297, 2263, 10.1126/science.1073386 · DOI
- Walker, 2019, Chromokinesins NOD and KID use distinct ATPase mechanisms and microtubule interactions to perform a similar function, Biochemistry, 58, 2326, 10.1021/acs.biochem.9b00011 · DOI
- Wandke, 2012, Human chromokinesins promote chromosome congression and spindle microtubule dynamics during mitosis, The Journal of Cell Biology, 198, 847, 10.1083/jcb.201110060 · DOI
- Wang, 2022, The architecture of kinesin-3 KLP-6 reveals a multilevel-lockdown mechanism for autoinhibition, Nature Communications, 13, 10.1038/s41467-022-32048-y · DOI
- Weijman, 2022, Molecular architecture of the autoinhibited kinesin-1 lambda particle, Science Advances, 8, 10.1126/sciadv.abp9660 · DOI · Paper page
- Wordeman, 2010, How kinesin motor proteins drive mitotic spindle function: Lessons from molecular assays, Seminars in Cell & Developmental Biology, 21, 260, 10.1016/j.semcdb.2010.01.018 · DOI
- Yajima, 2003, The human chromokinesin Kid is a plus end-directed microtubule-based motor, The EMBO Journal, 22, 1067, 10.1093/emboj/cdg102 · DOI
- Ye, 2018, NOD is a plus end-directed motor that binds EB1 via a new microtubule tip localization sequence, The Journal of Cell Biology, 217, 3007, 10.1083/jcb.201708109 · DOI
Metadata
- Authors
- Niwa, S., Furusaki, N., Kita, T., Suzuki, Y., & Chiba, K.
- Affiliations
- Tohoku University (JP)
- Mie University (JP)
- Corresponding author
- Niwa, Shinsuke
- Chiba, Kyoko
- Venue
- eLife
- Publisher
- eLife Sciences Publications, Ltd
- Published
- 2026-09-16
- Volume
- 13
- ISSN
- 2050-084X (ISSN-L)
- PMC
- PMC13581288
- OpenAlex
- W4404523437
- Cited by
- 0
- References
- 5
- Type
- posted content
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- eLife (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- Japan Society for the Promotion of Science (JP23H02472, JP23KJ0168, JP22K15053)
- Uehara Memorial Foundation
- Naito Foundation
- Takeda Science Foundation (2024036450)
- Astellas Foundation for Research on Metabolic Disorders (2024a1048)
- Brain Science Foundation
- MEXT Leading Initiative for Excellent Researchers (JPMXS0320200156)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
- Keywords
- KIF22, chromokinesin, homodimerization, microtubule motility, coiled-coil domain, neck linker, DNA transport, double-stranded DNA, mitotic spindle
- MeSH terms
- Protein Domains, Animals, DNA, DNA-Binding Proteins, Humans, Microtubules, Kinesins, Protein Multimerization
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review