Kinesin-like protein KIF23 is a
protein that in humans is encoded by the KIF23gene.[5][6]
Function
In cell division
KIF23 (also known as Kinesin-6, CHO1/MKLP1,
C. elegans ZEN-4 and
Drosophila Pavarotti) is a member of kinesin-like protein family. This family includes microtubule-dependent molecular motors that transport
organelles within cells and move chromosomes during
cell division. This protein has been shown to cross-bridge antiparallel
microtubules and drive microtubule movement in vitro. Alternate
splicing of this gene results in two transcript variants encoding two different
isoforms, better known as CHO1, the larger isoform and MKLP1, the smaller isoform.[6] KIF23 is a plus-end directed motor protein expressed in
mitosis, involved in the formation of the cleavage furrow in late
anaphase and in
cytokinesis.[5][7][8] KIF23 is part of the
centralspindlin complex that includes
PRC1,
Aurora B and
14-3-3 which cluster together at the
spindle midzone to enable anaphase in dividing cells.[9][10][11]
In neurons
In neuronal development KIF23 is involved in the transport of minus-end distal microtubules into
dendrites and is expressed exclusively in cell bodies and dendrites.[12][13][14][15][16] Knockdown of KIF23 by antisense oligonucleotides and by siRNA both cause a significant increase in axon length and a decrease in dendritic phenotype in neuroblastoma cells and in rat neurons.[14][15][17] In differentiating neurons, KIF23 restricts the movement of short microtubules into axons by acting as a "brake" against the driving forces of cytoplasmic dynein. As neurons mature, KIF23 drives minus-end distal microtubules into nascent dendrites contributing to the multi-polar orientation of dendritic microtubules and the formation of their short, fat, tapering morphology.[17]
Model for co-regulation of microtubule polarity in axons and dendrites by different mitotic kinesins. During axonal differentiation, forces generated by cytoplasmic dynein drive plus-end-distal microtubules into the axon and nascent dendrites (not shown). (A) Forces generated by kinesin-6 at the cell body oppose the forces generated by cytoplasmic dynein, restricting the transport of plus-end-distal microtubules into the axon. As the neuron matures, kinesin-6 fuels the transport of short microtubules with their minus-end distal into all of the processes except the one designated to remain the axon, thus causing the other processes to differentiate into dendrites. (B) Forces generated by kinesin-12 behave similarly to kinesin-6 with regard to introducing minus-end-distal microtubules into the dendrite, but kinesin-12 is also present in the axon and growth cone, pushing plus-end-distal microtubules back toward the cell body. As a result, kinesin-12 behaves like kinesin-6 with regard to dendrites but produces effects more like kinesin-5 with regard to the axon.
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^
abNislow C, Lombillo VA, Kuriyama R, McIntosh JR (Nov 1992). "A plus-end-directed motor enzyme that moves antiparallel microtubules in vitro localizes to the interzone of mitotic spindles". Nature. 359 (6395): 543–7.
Bibcode:
1992Natur.359..543N.
doi:
10.1038/359543a0.
PMID1406973.
S2CID4361579.
^Sharp DJ, Kuriyama R, Essner R, Baas PW (October 1997). "Expression of a minus-end-directed motor protein induces Sf9 cells to form axon-like processes with uniform microtubule polarity orientation". J. Cell Sci. 110 (19): 2373–80.
doi:
10.1242/jcs.110.19.2373.
PMID9410876.
^Xu X, He C, Zhang Z, Chen Y (February 2006). "MKLP1 requires specific domains for its dendritic targeting". J. Cell Sci. 119 (Pt 3): 452–8.
doi:
10.1242/jcs.02750.
PMID16418225.
S2CID29919060.
^Takahashi S, Fusaki N, Ohta S, Iwahori Y, Iizuka Y, Inagawa K, Kawakami Y, Yoshida K, Toda M (February 2012). "Downregulation of KIF23 suppresses glioma proliferation". J. Neurooncol. 106 (3): 519–29.
doi:
10.1007/s11060-011-0706-2.
PMID21904957.
S2CID33089132.
Deavours BE, Walker RA (July 1999). "Nuclear localization of C-terminal domains of the kinesin-like protein MKLP-1". Biochem. Biophys. Res. Commun. 260 (3): 605–8.
doi:
10.1006/bbrc.1999.0952.
PMID10403813.
Rush J, Moritz A, Lee KA, Guo A, Goss VL, Spek EJ, Zhang H, Zha XM, Polakiewicz RD, Comb MJ (January 2005). "Immunoaffinity profiling of tyrosine phosphorylation in cancer cells". Nat. Biotechnol. 23 (1): 94–101.
doi:
10.1038/nbt1046.
PMID15592455.
S2CID7200157.
Kinesin-like protein KIF23 is a
protein that in humans is encoded by the KIF23gene.[5][6]
Function
In cell division
KIF23 (also known as Kinesin-6, CHO1/MKLP1,
C. elegans ZEN-4 and
Drosophila Pavarotti) is a member of kinesin-like protein family. This family includes microtubule-dependent molecular motors that transport
organelles within cells and move chromosomes during
cell division. This protein has been shown to cross-bridge antiparallel
microtubules and drive microtubule movement in vitro. Alternate
splicing of this gene results in two transcript variants encoding two different
isoforms, better known as CHO1, the larger isoform and MKLP1, the smaller isoform.[6] KIF23 is a plus-end directed motor protein expressed in
mitosis, involved in the formation of the cleavage furrow in late
anaphase and in
cytokinesis.[5][7][8] KIF23 is part of the
centralspindlin complex that includes
PRC1,
Aurora B and
14-3-3 which cluster together at the
spindle midzone to enable anaphase in dividing cells.[9][10][11]
In neurons
In neuronal development KIF23 is involved in the transport of minus-end distal microtubules into
dendrites and is expressed exclusively in cell bodies and dendrites.[12][13][14][15][16] Knockdown of KIF23 by antisense oligonucleotides and by siRNA both cause a significant increase in axon length and a decrease in dendritic phenotype in neuroblastoma cells and in rat neurons.[14][15][17] In differentiating neurons, KIF23 restricts the movement of short microtubules into axons by acting as a "brake" against the driving forces of cytoplasmic dynein. As neurons mature, KIF23 drives minus-end distal microtubules into nascent dendrites contributing to the multi-polar orientation of dendritic microtubules and the formation of their short, fat, tapering morphology.[17]
Model for co-regulation of microtubule polarity in axons and dendrites by different mitotic kinesins. During axonal differentiation, forces generated by cytoplasmic dynein drive plus-end-distal microtubules into the axon and nascent dendrites (not shown). (A) Forces generated by kinesin-6 at the cell body oppose the forces generated by cytoplasmic dynein, restricting the transport of plus-end-distal microtubules into the axon. As the neuron matures, kinesin-6 fuels the transport of short microtubules with their minus-end distal into all of the processes except the one designated to remain the axon, thus causing the other processes to differentiate into dendrites. (B) Forces generated by kinesin-12 behave similarly to kinesin-6 with regard to introducing minus-end-distal microtubules into the dendrite, but kinesin-12 is also present in the axon and growth cone, pushing plus-end-distal microtubules back toward the cell body. As a result, kinesin-12 behaves like kinesin-6 with regard to dendrites but produces effects more like kinesin-5 with regard to the axon.
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^
abNislow C, Lombillo VA, Kuriyama R, McIntosh JR (Nov 1992). "A plus-end-directed motor enzyme that moves antiparallel microtubules in vitro localizes to the interzone of mitotic spindles". Nature. 359 (6395): 543–7.
Bibcode:
1992Natur.359..543N.
doi:
10.1038/359543a0.
PMID1406973.
S2CID4361579.
^Sharp DJ, Kuriyama R, Essner R, Baas PW (October 1997). "Expression of a minus-end-directed motor protein induces Sf9 cells to form axon-like processes with uniform microtubule polarity orientation". J. Cell Sci. 110 (19): 2373–80.
doi:
10.1242/jcs.110.19.2373.
PMID9410876.
^Xu X, He C, Zhang Z, Chen Y (February 2006). "MKLP1 requires specific domains for its dendritic targeting". J. Cell Sci. 119 (Pt 3): 452–8.
doi:
10.1242/jcs.02750.
PMID16418225.
S2CID29919060.
^Takahashi S, Fusaki N, Ohta S, Iwahori Y, Iizuka Y, Inagawa K, Kawakami Y, Yoshida K, Toda M (February 2012). "Downregulation of KIF23 suppresses glioma proliferation". J. Neurooncol. 106 (3): 519–29.
doi:
10.1007/s11060-011-0706-2.
PMID21904957.
S2CID33089132.
Deavours BE, Walker RA (July 1999). "Nuclear localization of C-terminal domains of the kinesin-like protein MKLP-1". Biochem. Biophys. Res. Commun. 260 (3): 605–8.
doi:
10.1006/bbrc.1999.0952.
PMID10403813.
Rush J, Moritz A, Lee KA, Guo A, Goss VL, Spek EJ, Zhang H, Zha XM, Polakiewicz RD, Comb MJ (January 2005). "Immunoaffinity profiling of tyrosine phosphorylation in cancer cells". Nat. Biotechnol. 23 (1): 94–101.
doi:
10.1038/nbt1046.
PMID15592455.
S2CID7200157.