The Kinesin-3 Motor UNC-104/KIF1A Is Degraded upon Loss of Specific Binding to Cargo
UNC-104/KIF1A is a Kinesin-3 motor that transports synaptic vesicles from the cell body towards the synapse by binding to PI(4,5)P2 through its PH domain. The fate of the motor upon reaching the synapse is not known. We found that wild-type UNC-104 is degraded at synaptic regions through the ubiquitin pathway and is not retrogradely transported back to the cell body. As a possible means to regulate the motor, we tested the effect of cargo binding on UNC-104 levels. The unc-104(e1265) allele carries a point mutation (D1497N) in the PI(4,5)P2 binding pocket of the PH domain, resulting in greatly reduced preferential binding to PI(4,5)P2 in vitro and presence of very few motors on pre-synaptic vesicles in vivo. unc-104(e1265) animals have poor locomotion irrespective of in vivo PI(4,5)P2 levels due to reduced anterograde transport. Moreover, they show highly reduced levels of UNC-104 in vivo. To confirm that loss of cargo binding specificity reduces motor levels, we isolated two intragenic suppressors with compensatory mutations within the PH domain. These show partial restoration of in vitro preferential PI(4,5)P2 binding and presence of more motors on pre-synaptic vesicles in vivo. These animals show improved locomotion dependent on in vivo PI(4,5)P2 levels, increased anterograde transport, and partial restoration of UNC-104 protein levels in vivo. For further proof, we mutated a conserved residue in one suppressor background. The PH domain in this triple mutant lacked in vitro PI(4,5)P2 binding specificity, and the animals again showed locomotory defects and reduced motor levels. All allelic variants show increased UNC-104 levels upon blocking the ubiquitin pathway. These data show that inability to bind cargo can target motors for degradation. In view of the observed degradation of the motor in synaptic regions, this further suggests that UNC-104 may get degraded at synapses upon release of cargo.
Vyšlo v časopise:
The Kinesin-3 Motor UNC-104/KIF1A Is Degraded upon Loss of Specific Binding to Cargo. PLoS Genet 6(11): e32767. doi:10.1371/journal.pgen.1001200
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1001200
Souhrn
UNC-104/KIF1A is a Kinesin-3 motor that transports synaptic vesicles from the cell body towards the synapse by binding to PI(4,5)P2 through its PH domain. The fate of the motor upon reaching the synapse is not known. We found that wild-type UNC-104 is degraded at synaptic regions through the ubiquitin pathway and is not retrogradely transported back to the cell body. As a possible means to regulate the motor, we tested the effect of cargo binding on UNC-104 levels. The unc-104(e1265) allele carries a point mutation (D1497N) in the PI(4,5)P2 binding pocket of the PH domain, resulting in greatly reduced preferential binding to PI(4,5)P2 in vitro and presence of very few motors on pre-synaptic vesicles in vivo. unc-104(e1265) animals have poor locomotion irrespective of in vivo PI(4,5)P2 levels due to reduced anterograde transport. Moreover, they show highly reduced levels of UNC-104 in vivo. To confirm that loss of cargo binding specificity reduces motor levels, we isolated two intragenic suppressors with compensatory mutations within the PH domain. These show partial restoration of in vitro preferential PI(4,5)P2 binding and presence of more motors on pre-synaptic vesicles in vivo. These animals show improved locomotion dependent on in vivo PI(4,5)P2 levels, increased anterograde transport, and partial restoration of UNC-104 protein levels in vivo. For further proof, we mutated a conserved residue in one suppressor background. The PH domain in this triple mutant lacked in vitro PI(4,5)P2 binding specificity, and the animals again showed locomotory defects and reduced motor levels. All allelic variants show increased UNC-104 levels upon blocking the ubiquitin pathway. These data show that inability to bind cargo can target motors for degradation. In view of the observed degradation of the motor in synaptic regions, this further suggests that UNC-104 may get degraded at synapses upon release of cargo.
Zdroje
1. HirokawaN
TakemuraR
2005 Molecular motors and mechanisms of directional transport in neurons. Nat Rev Neurosci 6 201 214
2. GoldsteinAY
WangX
SchwarzTL
2008 Axonal transport and the delivery of pre-synaptic components. Curr Opin Neurobiol 18 495 503
3. HallDH
HedgecockEM
1991 Kinesin-related gene unc-104 is required for axonal transport of synaptic vesicles in C. elegans. Cell 65 837 847
4. Pack-ChungE
KurshanPT
DickmanDK
SchwarzTL
2007 A Drosophila kinesin required for synaptic bouton formation and synaptic vesicle transport. Nat Neurosci 10 980 989
5. BarkusRV
KlyachkoO
HoriuchiD
DicksonBJ
SaxtonWM
2008 Identification of an axonal kinesin-3 motor for fast anterograde vesicle transport that facilitates retrograde transport of neuropeptides. Mol Biol Cell 19 274 283
6. OkadaY
YamazakiH
Sekine-AizawaY
HirokawaN
1995 The neuron-specific kinesin superfamily protein KIF1A is a unique monomeric motor for anterograde axonal transport of synaptic vesicle precursors. Cell 81 769 780
7. OtsukaAJ
JeyaprakashA
Garcia-AnoverosJ
TangLZ
FiskG
1991 The C. elegans unc-104 gene encodes a putative kinesin heavy chain-like protein. Neuron 6 113 122
8. GongTW
WinnickiRS
KohrmanDC
LomaxMI
1999 A novel mouse kinesin of the UNC-104/KIF1 subfamily encoded by the Kif1b gene. Gene 239 117 127
9. ZhaoC
TakitaJ
TanakaY
SetouM
NakagawaT
2001 Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta. Cell 105 587 597
10. NguyenM
AlfonsoA
JohnsonCD
RandJB
1995 Caenorhabditis elegans mutants resistant to inhibitors of acetylcholinesterase. Genetics 140 527 535
11. GoldsteinLS
YangZ
2000 Microtubule-based transport systems in neurons: the roles of kinesins and dyneins. Annu Rev Neurosci 23 39 71
12. KlopfensteinDR
ValeRD
2004 The lipid binding pleckstrin homology domain in UNC-104 kinesin is necessary for synaptic vesicle transport in Caenorhabditis elegans. Mol Biol Cell 15 3729 3739
13. NiwaS
TanakaY
HirokawaN
2008 KIF1Bbeta- and KIF1A-mediated axonal transport of presynaptic regulator Rab3 occurs in a GTP-dependent manner through DENN/MADD. Nat Cell Biol 10 1269 1279
14. KlopfensteinDR
TomishigeM
StuurmanN
ValeRD
2002 Role of phosphatidylinositol(4,5)bisphosphate organization in membrane transport by the Unc104 kinesin motor. Cell 109 347 358
15. TomishigeM
KlopfensteinDR
ValeRD
2002 Conversion of Unc104/KIF1A kinesin into a processive motor after dimerization. Science 297 2263 2267
16. LeeJR
ShinH
ChoiJ
KoJ
KimS
2004 An intramolecular interaction between the FHA domain and a coiled coil negatively regulates the kinesin motor KIF1A. EMBO J 23 1506 1515
17. HammondJW
CaiD
BlasiusTL
LiZ
JiangY
2009 Mammalian Kinesin-3 motors are dimeric in vivo and move by processive motility upon release of autoinhibition. PLoS Biol 7 e72 doi:10.1371/journal.pbio.1000072
18. VerheyKJ
LizotteDL
AbramsonT
BarenboimL
SchnappBJ
1998 Light chain-dependent regulation of Kinesin's interaction with microtubules. J Cell Biol 143 1053 1066
19. BlasiusTL
CaiD
JihGT
ToretCP
VerheyKJ
2007 Two binding partners cooperate to activate the molecular motor Kinesin-1. J Cell Biol 176 11 17
20. AllyS
JollyAL
GelfandVI
2008 Motor-cargo release: CaMKII as a traffic cop. Nat Cell Biol 10 3 5
21. HirokawaN
Sato-YoshitakeR
KobayashiN
PfisterKK
BloomGS
1991 Kinesin associates with anterogradely transported membranous organelles in vivo. J Cell Biol 114 295 302
22. YamazakiH
NakataT
OkadaY
HirokawaN
1995 KIF3A/B: a heterodimeric kinesin superfamily protein that works as a microtubule plus end-directed motor for membrane organelle transport. J Cell Biol 130 1387 1399
23. LiJY
PfisterKK
BradyS
DahlstromA
1999 Axonal transport and distribution of immunologically distinct kinesin heavy chains in rat neurons. J Neurosci Res 58 226 241
24. NonetML
1999 Visualization of synaptic specializations in live C. elegans with synaptic vesicle protein-GFP fusions. J Neurosci Methods 89 33 40
25. ZhouHM
Brust-MascherI
ScholeyJM
2001 Direct visualization of the movement of the monomeric axonal transport motor UNC-104 along neuronal processes in living Caenorhabditis elegans. J Neurosci 21 3749 3755
26. KulkarniM
SmithHE
2008 E1 ubiquitin-activating enzyme UBA-1 plays multiple roles throughout C. elegans development. PLoS Genet 4 e1000131 doi:10.1371/journal.pgen.1000131
27. MahoneyTR
LiuQ
ItohT
LuoS
HadwigerG
2006 Regulation of synaptic transmission by RAB-3 and RAB-27 in Caenorhabditis elegans. Mol Biol Cell 17 2617 2625
28. BounoutasA
ZhengQ
NonetML
ChalfieM
2009 mec-15 encodes an F-box protein required for touch receptor neuron mechanosensation, synapse formation and development. Genetics 183 607-617, 601SI 604SI
29. ClarkSG
ChiuC
2003 C. elegans ZAG-1, a Zn-finger-homeodomain protein, regulates axonal development and neuronal differentiation. Development 130 3781 3794
30. SchaeferAM
HadwigerGD
NonetML
2000 rpm-1, a conserved neuronal gene that regulates targeting and synaptogenesis in C. elegans. Neuron 26 345 356
31. RaoGN
KulkarniSS
KoushikaSP
RauKR
2008 In vivo nanosecond laser axotomy: cavitation dynamics and vesicle transport. Opt Express 16 9884 9894
32. DowlerS
CurrieRA
DownesCP
AlessiDR
1999 DAPP1: a dual adaptor for phosphotyrosine and 3-phosphoinositides. Biochem J 342 (Pt1) 7 12
33. FergusonKM
KavranJM
SankaranVG
FournierE
IsakoffSJ
2000 Structural basis for discrimination of 3-phosphoinositides by pleckstrin homology domains. Mol Cell 6 373 384
34. VakserIA
1995 Protein docking for low-resolution structures. Protein Eng 8 371 377
35. WeinkoveD
BastianiM
ChessaTA
JoshiD
HauthL
2008 Overexpression of PPK-1, the Caenorhabditis elegans Type I PIP kinase, inhibits growth cone collapse in the developing nervous system and causes axonal degeneration in adults. Dev Biol 313 384 397
36. MahoneyTR
LuoS
NonetML
2006 Analysis of synaptic transmission in Caenorhabditis elegans using an aldicarb-sensitivity assay. Nat Protoc 1 1772 1777
37. HallamSJ
JinY
1998 lin-14 regulates the timing of synaptic remodelling in Caenorhabditis elegans. Nature 395 78 82
38. DixonSJ
RoyPJ
2005 Muscle arm development in Caenorhabditis elegans. Development 132 3079 3092
39. AlamSL
LangelierC
WhitbyFG
KoiralaS
RobinsonH
2006 Structural basis for ubiquitin recognition by the human ESCRT-II EAP45 GLUE domain. Nat Struct Mol Biol 13 1029 1030
40. GordonDM
RoofDM
2001 Degradation of the kinesin Kip1p at anaphase onset is mediated by the anaphase-promoting complex and Cdc20p. Proc Natl Acad Sci U S A 98 12515 12520
41. HoepfnerS
SeverinF
CabezasA
HabermannB
RungeA
2005 Modulation of receptor recycling and degradation by the endosomal kinesin KIF16B. Cell 121 437 450
42. OkadaY
HirokawaN
1999 A processive single-headed motor: kinesin superfamily protein KIF1A. Science 283 1152 1157
43. FiserA
SaliA
2003 Modeller: generation and refinement of homology-based protein structure models. Methods Enzymol 374 461 491
44. NonetML
SaifeeO
ZhaoH
RandJB
WeiL
1998 Synaptic transmission deficits in Caenorhabditis elegans synaptobrevin mutants. J Neurosci 18 70 80
45. PraitisV
2006 Creation of transgenic lines using microparticle bombardment methods. Methods Mol Biol 351 93 107
46. DittmanJS
KaplanJM
2006 Factors regulating the abundance and localization of synaptobrevin in the plasma membrane. Proc Natl Acad Sci U S A 103 11399 11404
47. SaifeeO
WeiL
NonetML
1998 The Caenorhabditis elegans unc-64 locus encodes a syntaxin that interacts genetically with synaptobrevin. Mol Biol Cell 9 1235 1252
Štítky
Genetika Reprodukčná medicínaČlánok vyšiel v časopise
PLOS Genetics
2010 Číslo 11
- Je „freeze-all“ pro všechny? Odborníci na fertilitu diskutovali na virtuálním summitu
- Gynekologové a odborníci na reprodukční medicínu se sejdou na prvním virtuálním summitu
Najčítanejšie v tomto čísle
- Genome-Wide Association Study Identifies Two Novel Regions at 11p15.5-p13 and 1p31 with Major Impact on Acute-Phase Serum Amyloid A
- Analysis of the 10q11 Cancer Risk Locus Implicates and in Human Prostate Tumorigenesis
- The Parental Non-Equivalence of Imprinting Control Regions during Mammalian Development and Evolution
- A Functional Genomics Approach Identifies Candidate Effectors from the Aphid Species (Green Peach Aphid)