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Unconventional myosin-VI

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MYO6
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

2N11, 2N13, 2N0Z, 2N10, 2N12

Identifiers
AliasesMYO6, DFNA22, DFNB37, myosin VI, Myo6-008, Myo6-007
External IDsOMIM: 600970; MGI: 104785; HomoloGene: 56417; GeneCards: MYO6; OMA:MYO6 - orthologs
Gene location (Human)
Chromosome 6 (human)
Chr.Chromosome 6 (human)
Chromosome 6 (human)Genomic location for MYO6Genomic location for MYO6
Band6q14.1Start75,749,201 bp
End75,919,537 bp
Gene location (Mouse)
Chromosome 9 (mouse)
Chr.Chromosome 9 (mouse)
Chromosome 9 (mouse)Genomic location for MYO6Genomic location for MYO6
Band9 E1|9 43.98 cMStart80,072,313 bp
End80,219,011 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • amniotic fluid

  • internal globus pallidus

  • corpus callosum

  • sural nerve

  • external globus pallidus

  • pancreatic ductal cell

  • inferior ganglion of vagus nerve

  • pars reticulata

  • subthalamic nucleus

  • renal medulla
Top expressed in
  • olfactory epithelium

  • neural layer of retina

  • yolk sac

  • right kidney

  • human kidney

  • utricle

  • epithelium of small intestine

  • ileum

  • Ileal epithelium

  • vestibular sensory epithelium
More reference expression data
BioGPS




More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

4646

17920

Ensembl

ENSG00000196586

ENSMUSG00000033577

UniProt

Q9UM54

Q64331

RefSeq (mRNA)
NM_001300899
NM_004999
NM_001368136
NM_001368137
NM_001368138

NM_001368139
NM_001368140
NM_001368865
NM_001368866

NM_001039546
NM_008662

RefSeq (protein)
NP_001287828
NP_004990
NP_001355065
NP_001355066
NP_001355067

NP_001355068
NP_001355069
NP_001355794
NP_001355795

n/a

Location (UCSC)Chr 6: 75.75 – 75.92 MbChr 9: 80.07 – 80.22 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Unconventional myosin-VI, is a protein that in humans is coded for by MYO6. Unconventional myosin-VI is a myosin molecular motor involved in intracellular vesicle and organelle transport.

Structure

Human myosin-VI contains a N-terminal myosin head domain (residues 59–759), two coiled coil motifs (residues 902–984 and 986–1009 respectively), and a C-terminal myosin VI cargo binding domain (residues 1177–1267).

Function

Unconventional myosin-VI is unique because it travels in the opposite direction of other myosins, towards the negative end of actin filaments. Myosin-VI follows the same structure as other myosin but with two unique "inserts" allowing for its diversified properties. One insert is called the "reverse gear" and is responsible for its movement towards the negative end of actin filaments. The reverse gear is located on the neck region of the myosin and acts as a reorienting device for the lever arm to move backwards after myosin movement. The second insert assists in regulating ATP enzyme activity located in the motor head domain.

There are 3 amino acid binding sites essential for myosin-VI's interactions, Arg-Arg-Leu and Trp-Trp-Tyr in the tail region and Met-Ile-Sec in the helix. The Arg-Arg-Leu amino acid segment (abbreviated RRL) takes part in ubiquitin interactions while Trp-Trp-Tyr (abbreviated WWY) assists in interactions with DAB2. Myosin-VI's Met-Ile-Sec bonding interactions are limited to the myosin-VI long isoform but interact with clathrin in endocytosis.

Myosin-VI long isoform is formed by the inclusion of exon 31, adding an addition alpha-helix, restriction RRL interactions. Myosin-VI long struggles to interact with ubiquitin chains and GIPC1 due to this structural formation, however, increases attractivity to clathrin. Myosin-VI's structural flexibility provides a great width in interaction ability with its environment and interactors.

Interactions

MYO6 has been shown to interact with GIPC1, DAB2., ubiquitin, and clathrin. Myosin VI, being a motor protein, focuses its interactions by moving along actin filaments. This however does not limit its functions, because MYO6 is heavily involved in cytokinesis, creation of membrane compartments, and the regulation and organization of actin filaments.

Clinical significance

Mutations in the MYO6 gene are associated with hearing loss. MYO6 has also been found to be involved in many events in spermiogenesis in numerous different creatures. In common fruit flies (Drosophila), the myosin-VI ortholog controls the sterility of males by organization of actin involved in spermatid individualization. This same ortholog in roundworms (C. elegans) regulates the separation of cytosol in spermatid formation due to its influence in cytokinesis. In mice, this ortholog will control specialization and membrane compartment creation.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000196586Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000033577Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "MYO6 - Unconventional myosin-VI - Homo sapiens (Human) - MYO6 gene & protein". www.uniprot.org. Retrieved 7 April 2022.
  6. "Entrez Gene: MYO6 myosin VI".
  7. "Protein: MYO6_HUMAN (Q9UM54)". Pfam. European Molecular Biology Laboratory.
  8. Zakrzewski P, Lenartowska M, Buss F (March 2021). "Diverse functions of myosin VI in spermiogenesis". Histochemistry and Cell Biology. 155 (3): 323–340. doi:10.1007/s00418-020-01954-x. PMC 8021524. PMID 33386429.
  9. Magistrati E, Polo S (April 2021). "Myomics: myosin VI structural and functional plasticity". Current Opinion in Structural Biology. 67: 33–40. doi:10.1016/j.sbi.2020.09.005. hdl:2434/801699. PMID 33053464. S2CID 222421080.
  10. Ewing RM, Chu P, Elisma F, Li H, Taylor P, Climie S, et al. (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry". Molecular Systems Biology. 3 (1): 89. doi:10.1038/msb4100134. PMC 1847948. PMID 17353931.
  11. Aschenbrenner L, Lee T, Hasson T (July 2003). "Myo6 facilitates the translocation of endocytic vesicles from cell peripheries". Molecular Biology of the Cell. 14 (7): 2728–2743. doi:10.1091/mbc.E02-11-0767. PMC 165672. PMID 12857860.
  12. Morris SM, Arden SD, Roberts RC, Kendrick-Jones J, Cooper JA, Luzio JP, Buss F (May 2002). "Myosin VI binds to and localises with Dab2, potentially linking receptor-mediated endocytosis and the actin cytoskeleton". Traffic. 3 (5): 331–341. doi:10.1034/j.1600-0854.2002.30503.x. PMID 11967127. S2CID 25079713.
  13. Inoue A, Sato O, Homma K, Ikebe M (March 2002). "DOC-2/DAB2 is the binding partner of myosin VI". Biochemical and Biophysical Research Communications. 292 (2): 300–307. doi:10.1006/bbrc.2002.6636. PMID 11906161.
  14. He F, Wollscheid HP, Nowicka U, Biancospino M, Valentini E, Ehlinger A, et al. (March 2016). "Myosin VI Contains a Compact Structural Motif that Binds to Ubiquitin Chains". Cell Reports. 14 (11): 2683–2694. doi:10.1016/j.celrep.2016.01.079. PMC 4805485. PMID 26971995.
  15. Biancospino M, Buel GR, Niño CA, Maspero E, Scotto di Perrotolo R, Raimondi A, et al. (October 2019). "Clathrin light chain A drives selective myosin VI recruitment to clathrin-coated pits under membrane tension". Nature Communications. 10 (1): 4974. Bibcode:2019NatCo..10.4974B. doi:10.1038/s41467-019-12855-6. PMC 6823378. PMID 31672988.
  16. ^ Sweeney HL, Houdusse A (February 2007). "What can myosin VI do in cells?". Current Opinion in Cell Biology. 19 (1): 57–66. doi:10.1016/j.ceb.2006.12.005. PMID 17175153.
  17. Friedman TB, Belyantseva IA, Frolenkov GI (2020). "Myosins and Hearing". Myosins. Advances in Experimental Medicine and Biology. Vol. 1239. pp. 317–330. doi:10.1007/978-3-030-38062-5_13. ISBN 978-3-030-38061-8. PMID 32451864. S2CID 218894008.

Further reading

External links

  • Overview of all the structural information available in the PDB for UniProt: Q9UM54 (Unconventional myosin-VI) at the PDBe-KB.
PDB gallery
  • 2bkh: MYOSIN VI NUCLEOTIDE-FREE (MDINSERT2) CRYSTAL STRUCTURE 2bkh: MYOSIN VI NUCLEOTIDE-FREE (MDINSERT2) CRYSTAL STRUCTURE
  • 2bki: MYOSIN VI NUCLEOTIDE-FREE (MDINSERT2-IQ) CRYSTAL STRUCTURE 2bki: MYOSIN VI NUCLEOTIDE-FREE (MDINSERT2-IQ) CRYSTAL STRUCTURE
Proteins of the cytoskeleton
Human
Microfilaments
and ABPs
Myofilament
Actins
Myosins
Other
Other
Intermediate
filaments
Type 1/2
(Keratin,
Cytokeratin)
Epithelial keratins
(soft alpha-keratins)
Hair keratins
(hard alpha-keratins)
Ungrouped alpha
Not alpha
Type 3
Type 4
Type 5
Microtubules
and MAPs
Tubulins
MAPs
Kinesins
Dyneins
Microtubule organising proteins
Microtubule severing proteins
Other
Catenins
Membrane
Other
Nonhuman
See also: cytoskeletal defects
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