| 2000 |
KIF20A (Rab6-KIFL) was identified as a Rab6-binding kinesin via two-hybrid screen; it localizes to the spindle midzone in anaphase and to the cleavage furrow and midbody in telophase, and microinjection of anti-Rab6-KIFL antibodies causes binucleation due to failure of cleavage furrow formation, establishing a direct role in cytokinesis. |
Yeast two-hybrid screen, microinjection of inhibitory antibodies, time-lapse microscopy, immunofluorescence localization |
The EMBO journal |
High |
11060022
|
| 2004 |
MKlp2 (KIF20A) is required for relocation of the Aurora B–INCENP chromosome passenger complex (CPC) from centromeres to the central spindle at the metaphase-to-anaphase transition; MKlp2 physically binds Aurora B and also binds the phosphatase Cdc14A, which can dephosphorylate INCENP to facilitate CPC relocation. |
siRNA depletion, co-immunoprecipitation, immunofluorescence microscopy |
The Journal of cell biology |
High |
15263015
|
| 2005 |
KIF20A (RAB6KIFL) transports the scaffolding protein DLG5 as cargo; proteomics with anti-RAB6KIFL antibody identified DLG5 as a KIF20A cargo, and KIF20A knockdown displaced DLG5 from cytoplasmic membranes to the cytoplasm, demonstrating a membrane-trafficking function. |
Proteomics/pull-down with anti-RAB6KIFL antibody, siRNA knockdown, subcellular fractionation/immunolocalization |
Cancer research |
Medium |
15665285
|
| 2005 |
KIF20A ATPase activity and microtubule-binding can be studied biochemically using recombinant protein from insect cells; Polo-like kinase 1 (Plk1) interaction with KIF20A was established using recombinant proteins in vitro. |
In vitro biochemical assays (microtubule binding, ATPase), recombinant protein expression in insect cells, in vitro Plk1 binding assay |
Methods in enzymology |
Medium |
16473625
|
| 2010 |
Mad2 binds MKlp2 (KIF20A) via a consensus Mad2-binding motif on MKlp2, preventing its loading onto the mitotic spindle and blocking CPC relocation from centromeres; an MKlp2 mutant refractory to Mad2 binding prematurely loads onto the spindle and mislocalizes Aurora B from the midbody, causing cytokinesis failure. |
Co-immunoprecipitation, site-directed mutagenesis of Mad2-binding motif, live-cell imaging, siRNA rescue experiments |
The Journal of cell biology |
High |
21149564
|
| 2013 |
MKlp2 requires myosin-II for its own localization to the equatorial cortex; this event is required to recruit Aurora B to the equatorial cortex, which in turn promotes focused RhoA accumulation and stable cleavage furrow ingression. An MKlp2 mutant defective in myosin-II binding fails to recruit Aurora B to the cortex and fails to maintain the ingressing furrow. |
Drug-induced monopolar cytokinesis assay, dominant-negative myosin-II, MKlp2 binding-mutant expression, immunofluorescence, live-cell imaging |
PloS one |
High |
23750214
|
| 2014 |
Cdk1/cyclin B1 phosphorylates multiple sites in the MKlp2 stalk and C-terminal tail, inhibiting microtubule binding, bundling, oligomerization, and chromosome targeting of MKlp2 during early mitosis. Reversal of Cdk1 phosphorylation at anaphase onset promotes MKlp2–CPC complex formation and CPC relocation from chromosomes to the central spindle for cytokinesis. |
Identification of Cdk1 phosphorylation sites by mass spectrometry and mutagenesis, in vitro kinase assays, microtubule-binding/bundling assays, immunofluorescence, cell cycle analysis |
Cell reports |
High |
24656812
|
| 2014 |
KIF20A promotes motility and invasiveness of pancreatic cancer cells by transporting the RNA-binding protein IGF2BP3 and its bound transcripts (including ARF6 and ARHGEF4 mRNAs) toward cell protrusions along microtubules; KIF20A knockdown inhibits IGF2BP3-containing stress granule accumulation in protrusions and suppresses local protein expression from these transcripts. |
siRNA knockdown, immunofluorescence, time-lapse microscopy, cell invasion/migration assays |
Neoplasia (New York, N.Y.) |
Medium |
25499221
|
| 2015 |
FOXM1 directly transcriptionally regulates KIF20A expression through a Forkhead response element (FHRE) in the KIF20A promoter; FOXM1 depletion reduces KIF20A expression, causes abnormal mitotic spindle morphology and chromosome alignment, and sensitizes breast cancer cells to paclitaxel-induced mitotic catastrophe. |
ChIP assay, promoter-luciferase reporter, siRNA knockdown, cell viability/senescence assays, spindle morphology by immunofluorescence |
Oncogene |
High |
25961928
|
| 2016 |
Aurora B phosphorylates MKlp2 at S878 within a lipid-association motif (LAM) in the C-terminal tail, acting as an inhibitory signal for abscission; B56-bound PP2A dephosphorylates MKlp2 S878 to promote abscission. A phospho-resistant S878A mutant of MKlp2 overrides Aurora B–mediated abscission blockade. |
Phospho-site mutagenesis (S878A), Aurora B kinase assay, PP2A phosphatase assay, live-cell imaging, abscission timing assays |
Current biology : CB |
High |
27939310
|
| 2018 |
KIF20A/MKLP2 interacts with RGS3 at the intercellular bridge of dividing neural progenitor cells (NPCs); KIF20A knockdown/knockout causes dislocation of RGS3 from the intercellular bridge, impairs Ephrin-B–RGS cell fate signaling, and shifts NPCs from proliferative to differentiative divisions, resulting in thinner cortex and ventriculomegaly without substantial cytokinesis defect. |
Co-immunoprecipitation, immunofluorescence, in utero electroporation knockdown, germline and inducible conditional KO mice, live imaging |
Nature communications |
High |
30006548
|
| 2018 |
Loss of function of KIF20A (R182W ATPase-defective mutation identified in congenital cardiomyopathy patients) prevents efficient transport of Aurora B as part of the CPC: Aurora B remains trapped on chromatin and fails to translocate to the spindle midzone during cytokinesis. |
Patient compound heterozygous mutations, functional ATPase assay, immunofluorescence of Aurora B localization in patient-derived cells, zebrafish translational-blocking morpholino model |
PLoS genetics |
High |
29357359
|
| 2020 |
MKLP2 (KIF20A) is a processive, plus-end-directed motor that can transport the CPC along microtubules in vitro; strong suppression of MKLP2 motor activity via a P-loop mutant disrupts CPC accumulation at both the spindle midzone and equatorial cortex, whereas partial inhibition with Paprotrain mainly affects equatorial cortex localization. |
In vitro single-molecule motility assays with purified MKLP2 and CPC, P-loop ATPase mutant expression, Paprotrain inhibitor, live-cell imaging |
Current biology : CB |
High |
32502404
|
| 2020 |
The INCENP RRKKRR motif is required for both centromeric CPC localization in metaphase and MKLP2-dependent CPC transport in anaphase; MKLP2 and DNA bind competitively to this motif, and INCENP T59 phosphorylation acts as a switch that prevents MKLP2 binding in metaphase. CPC binding to MKLP2 promotes the microtubule-dependent ATPase activity of MKLP2 in anaphase. |
Crystal structure of survivin–H3pT3 complex, mutagenesis of INCENP RRKKRR motif, ATPase assays, immunofluorescence, competitive binding assays |
The Journal of cell biology |
High |
32356865
|
| 2020 |
SEPT7 interacts with KIF20A at the intercellular bridge of dividing NPCs; SEPT7 knockdown displaces KIF20A from the midbody, causing early neuronal differentiation. NPC-specific inducible knockout of Sept7 causes early cell cycle exit and precocious differentiation without noticeable cytokinesis defect. |
Co-immunoprecipitation, immunofluorescence, in utero electroporation knockdown, inducible conditional KO mice |
Cerebral cortex (New York, N.Y. : 1991) |
High |
31813992
|
| 2022 |
MKLP2 facilitates chromosome congression in prometaphase by promoting error correction of syntelic kinetochore-microtubule attachments; MKLP2 inhibition results in elevated Aurora kinase activity, phosphorylation of HEC1-Ser55, and aneuploidy. |
Live imaging with fluorescent histones, MKLP2 small-molecule inhibitor (MKLP2i), siRNA, flow cytometry for aneuploidy |
Journal of cell science |
Medium |
35638575
|
| 2022 |
KIF20A promotes castration-resistant prostate cancer (CRPC) progression through its role in Golgi-driven secretory vesicle fission and trafficking; KIF20A expression causes secretion of autocrine factors that activate androgen receptor signaling, and pharmacologic disruption of vesicle biogenesis blocks KIF20A-driven castration-resistant proliferation. |
Stable KIF20A overexpression, conditioned media transfer assays, Paprotrain inhibitor, androgen receptor reporter assays, in vivo xenograft, vesicle biogenesis inhibitors |
Oncogene |
Medium |
35418689
|
| 2022 |
The C-terminal tail of MKlp2 (CTM peptides) selectively binds PI(3)P-containing membranes over other negatively charged lipids, and this interaction depends critically on residue S21; this selective phosphoinositide binding provides a mechanism for MKlp2 tethering to the plasma membrane at the intercellular bridge during abscission. |
Quartz crystal microbalance-dissipation (QCM-D), atomic force microscopy force spectroscopy, synthetic peptide mutagenesis on model lipid membranes |
The journal of physical chemistry. B |
Medium |
35316051
|
| 2023 |
High-resolution crystal and cryo-EM structures of the KIF20A motor domain reveal an unusually long L6 insertion that integrates into the core of the motor domain, dramatically affecting allostery and ATPase activity. The neck linker is four times longer than in kinesin-1, and the extended neck linker is required for motor activity. These structural features explain the low processivity/motility of KIF20A compared to other kinesins. |
X-ray crystallography (nucleotide-free motor domain), cryo-EM (microtubule-bound structure), ATPase activity assays, mutagenesis of L6 insertion and neck linker |
Open biology |
High |
37726093
|
| 2023 |
KIF20A physically interacts with BTRC (β-TrCP1), a substrate recognition subunit of SCFβ-TrCP E3 ubiquitin ligase; via this interaction, KIF20A reduces BTRC-mediated CDC25A poly-ubiquitination and enhances CDC25A protein stability. |
GST pull-down, co-immunoprecipitation, in vitro ubiquitination assay, cycloheximide chase assay |
Journal of ginseng research |
Medium |
38223825
|
| 2024 |
KIF20A inhibits FBXW7-mediated ubiquitination and degradation of c-Myc by competitively inhibiting the FBXW7–c-Myc interaction; KIF20A overexpression thereby stabilizes c-Myc, promotes glycolysis, and enhances tumor proliferation. KIF20A downregulation reduces c-Myc levels and suppresses MMR expression. |
KIF20A liver-specific knockout mouse, co-immunoprecipitation, c-Myc splicing mutant constructs, ubiquitination assays, immunohistochemistry of patient cohort |
Cancer letters |
Medium |
38971490
|
| 2024 |
KIF20A inhibits DHX9 proteasomal degradation by blocking TRIM21-mediated K48-linked polyubiquitination at DHX9-K755; elevated DHX9 stabilizes SOX2 mRNA, upregulating SOX2 to promote cancer stem cell maintenance and ferroptosis resistance in OSCC. |
Co-immunoprecipitation, ubiquitination assay (K48-linkage specific), co-localization, SOX2 mRNA stability assay, loss-of-function/gain-of-function in vitro and in vivo |
Cell death & disease |
Medium |
41672965
|
| 2025 |
KIF20A maximal enrichment at antiparallel microtubule overlaps of the spindle midzone requires PRC1-crosslinked microtubules and cooperation with KIF4A: KIF20A delivers the CPC from non-overlapping microtubules to the midzone, while KIF4A retains the CPC at PRC1-crosslinked overlaps. Conditional depletion of KIF4A confirms it is required for CPC localization at the spindle midzone in anaphase. |
In vitro reconstitution with purified proteins, conditional KIF4A depletion in mitotic cells, live-cell imaging, immunofluorescence |
bioRxivpreprint |
Medium |
|
| 2025 |
KIF20A cooperates with Myosin II to regulate actomyosin and branched actin dynamics, facilitating fission of transport intermediates at early endosomes; KIF20A inhibition causes enlargement of early and late endosomes, impairs Transferrin trafficking, and mislocalizes β1-Integrin from the plasma membrane. |
KIF20A inhibitor (Paprotrain), live-cell endosome imaging, Transferrin trafficking assay, β1-Integrin localization, Myosin II co-localization and functional assays |
bioRxivpreprint |
Low |
|
| 2026 |
SYMPK interacts with KIF20A and NUMA1 during meiotic metaphase I in oocytes, as revealed by immunoprecipitation-mass spectrometry; SYMPK is required for proper localization of KIF20A and NUMA1 to the acentrosomal spindle, and SYMPK-deficient oocytes show disorganized spindle architecture and metaphase I arrest. |
Oocyte-specific Sympk knockout mice, immunoprecipitation-mass spectrometry, immunofluorescence, chromosome spread analysis |
Journal of genetics and genomics |
Medium |
41520922
|
| 2019 |
KIF20A localizes to microtubules in spermatogenic cells and co-localizes with the spindle midzone and midbody; KIF20A inhibition (Paprotrain) leads to defects in central spindle assembly and cytokinetic abscission in male meiosis, increased aneuploidy, and impaired acrosome formation and maturation during spermatogenesis. |
Immunofluorescence localization, Paprotrain inhibitor treatment, flow cytometry for ploidy, acrosome staining |
Biochimica et biophysica acta. Molecular cell research |
Medium |
31884069
|
| 2020 |
Transcription factor GATA2 directly binds the KIF20A promoter and transcriptionally activates KIF20A in HBV-related hepatocellular carcinoma; HBx protein indirectly upregulates KIF20A via GATA2. GATA2 overexpression promotes HepG2.2.15 cell growth and inhibits apoptosis via KIF20A. |
ChIP assay, luciferase reporter assay, siRNA knockdown, overexpression, CCK-8 and flow cytometry |
Frontiers in cellular and infection microbiology |
Medium |
39624268
|
| 2026 |
Lactate-driven histone H3K18 lactylation (H3K18la) directly activates transcription of KIF20A; KIF20A in turn stabilizes c-Myc protein, enhancing PD-L1 expression and suppressing cytotoxic T cell function, constituting a metabolic-epigenetic immune evasion axis. Glycolysis inhibition reduces H3K18la-driven KIF20A upregulation and synergizes with anti-PD-1 therapy. |
ChIP-sequencing, ChIP-PCR, dual-luciferase reporter, HCC-CD8+ T cell co-cultures, gene knockdown/overexpression, mouse xenograft and orthotopic models, pan-lysine and H3K18la immunohistochemistry in patient cohorts |
Cancer biology & medicine |
Medium |
41937416
|
| 2022 |
Auxin-inducible acute degradation of endogenous Mklp2 in MDCK cells causes delayed relocation of CPC component Aurora-B to the spindle midzone during anaphase and leads to cytokinesis failure and binucleation; these phenotypes are rescued by re-expression of Mklp2, confirming specificity. |
AID (auxin-inducible degron) tag on endogenous MKLP2, live-cell imaging, immunofluorescence, rescue by re-expression |
Biology of the cell |
Medium |
40490973
|
| 2026 |
KIF20A physically interacts with DEPDC1 in liposarcoma cells as shown by co-immunoprecipitation; KIF20A knockdown partially reverses DEPDC1-driven proliferation, migration, and invasion, and attenuates PI3K/AKT/mTOR signaling activation. |
Co-immunoprecipitation, siRNA knockdown, CCK-8/invasion assays, western blot of PI3K/AKT/mTOR pathway |
Frontiers in endocrinology |
Low |
40600015
|
| 2026 |
KIF20A physically interacts with CLIP1 and enhances its protein stability in cervical cancer cells; CLIP1 silencing reverses the oncogenic effects of KIF20A overexpression. |
Co-immunoprecipitation, siRNA knockdown, protein stability assays, proliferation/migration/invasion functional assays, in vivo xenograft |
Scientific reports |
Low |
41776329
|
| 2026 |
Transcription factor ATF2 binds directly to the KIF20A promoter and activates its transcription in prostate cancer, as validated by ChIP and dual-luciferase reporter assays. |
ChIP assay, dual-luciferase reporter, qRT-PCR, western blot, KIF20A knockdown functional assays |
Frontiers in bioscience (Landmark edition) |
Medium |
42216528
|