Myelin protein zero: Difference between revisions

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{{Use dmy dates|date=October 2012}}
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{{Infobox_gene}}
'''Myelin protein zero''' ('''P0''', '''MPZ''') is a single membrane [[glycoprotein]]<ref>{{cite journal | vauthors = Magnaghi V, Cavarretta I, Galbiati M, Martini L, Melcangi RC | title = Neuroactive steroids and peripheral myelin proteins | journal = Brain Research. Brain Research Reviews | volume = 37 | issue = 1-3 | pages = 360–71 | date = November 2001 | pmid = 11744100 | doi = 10.1016/s0165-0173(01)00140-0 }}</ref> which in humans is encoded by the ''MPZ'' gene.  P0 is a major structural component of the [[myelin sheath]] in the [[peripheral nervous system|peripheral nervous system (PNS)]].<ref name="Shy_2006">{{cite journal | vauthors = Shy ME | title = Peripheral neuropathies caused by mutations in the myelin protein zero | journal = Journal of the Neurological Sciences | volume = 242 | issue = 1-2 | pages = 55–66 | date = March 2006 | pmid = 16414078 | doi = 10.1016/j.jns.2005.11.015 }}</ref> Myelin protein zero is expressed by [[Schwann cell]]s and accounts for over 50% of all proteins in the peripheral nervous system, making it the most common protein expressed in the PNS.<ref name="Shy_2006" /> Mutations in myelin protein zero can cause myelin deficiency and are associated with [[Peripheral neuropathy|neuropathies]] like [[Charcot–Marie–Tooth disease]] and [[Dejerine–Sottas disease]].<ref name="Shy_2004">{{cite journal | vauthors = Shy ME, Jáni A, Krajewski K, Grandis M, Lewis RA, Li J, Shy RR, Balsamo J, Lilien J, Garbern JY, Kamholz J | title = Phenotypic clustering in MPZ mutations | journal = Brain | volume = 127 | issue = Pt 2 | pages = 371–84 | date = February 2004 | pmid = 14711881 | doi = 10.1093/brain/awh048 }}</ref>
== Structure ==
{{Infobox protein family
{{Infobox protein family
| Symbol = Myelin-PO_C
| Symbol = Myelin-PO_C
| Name = Myelin-PO_C
| Name = Myelin-PO_C
| image =  
| image = Structure of Extracellular domain of Myelin Protein Zero with Labelled BetaSheets .png
| width =
| width =
| caption =
| caption = Structure of myelin protein zero's extracellular domain with labelled beta strands.  Strands D, E, B, and A make up one beta sheet, Strands A<nowiki>', G, F, C, C', C''</nowiki> make up the other beta sheet.
| Pfam = PF10570
| Pfam = PF10570
| Pfam_clan =
| Pfam_clan =
Line 14: Line 19:
| SCOP =
| SCOP =
| TCDB =
| TCDB =
| OPM family = 230
| OPM family = 193
| OPM protein = 3oai
| OPM protein = 3oai
| CAZy =
| CAZy =
| CDD =
| CDD =
| Membranome family = 213
| align = left
}}
}}
{{Infobox_gene}}
In humans, the gene that encodes myelin protein zero is located on [[chromosome 1]] near the [[Duffy antigen system|Duffy Locus]] or the Duffy Antigen/Chemokine Receptor. The gene is about 7,000 bases long and is divided into 6 exons. In total, myelin protein zero is 219 amino acids long<ref name="Shy_2006" /> and has many basic amino acid residues.<ref name="Shapiro_1996">{{cite journal | vauthors = Shapiro L, Doyle JP, Hensley P, Colman DR, Hendrickson WA | title = Crystal structure of the extracellular domain from P0, the major structural protein of peripheral nerve myelin | journal = Neuron | volume = 17 | issue = 3 | pages = 435–49 | date = September 1996 | pmid = 8816707 | doi = 10.1016/s0896-6273(00)80176-2 }}</ref>
 
Myelin protein zero consists of an [[extracellular]] N-terminal domain (amino acids 1-124), a single [[Protein kinase#Receptor tyrosine kinases|transmembrane]] region (125-150), and a smaller positively charged [[intracellular]] region (151-219).<ref name="Shy_2006" /><ref name="pmid2578885" /><ref name=":4">{{cite journal | vauthors = Lemke G, Lamar E, Patterson J | title = Isolation and analysis of the gene encoding peripheral myelin protein zero | journal = Neuron | volume = 1 | issue = 1 | pages = 73–83 | date = March 1988 | pmid = 2483091 | doi = 10.1016/0896-6273(88)90211-5 }}</ref> Its cytoplasmic domain is highly positively charged but presumably does not fold into a globular structure.<ref name="Jan_2013" /> The extracellular domain is structurally similar to the [[immunoglobin|immunoglobulin]] domain<ref name="Shapiro_1996" /> and therefore the protein is considered as belonging to [[immunoglobulin superfamily]]<ref name="Kamholz_2007">{{Citation|last=Kamholz|first=John A. | name-list-format = vanc |title=Myelin Protein Zero and CMT1B: A Tale of Two Phenotypes|date=2007 | last2 = Brucal | first2 = Michelle | last3=Li|first3=Jun|last4=Shy|first4=Michael |work=Molecular Neurology|pages=463–474|publisher=Elsevier|doi=10.1016/b978-012369509-3.50031-7|isbn=9780123695093 }}</ref>
 
Besides existing as a monomer, myelin protein zero is also known to form dimers and tetramers with other myelin protein zero molecules in vertebrates.<ref>{{cite journal | vauthors = Thompson AJ, Cronin MS, Kirschner DA | title = Myelin protein zero exists as dimers and tetramers in native membranes of Xenopus laevis peripheral nerve | journal = Journal of Neuroscience Research | volume = 67 | issue = 6 | pages = 766–71 | date = March 2002 | pmid = 11891790 | doi = 10.1002/jnr.10167 }}</ref>{{clear|left}}
 
== Function ==
The [[myelin sheath]] is a multi-layered membrane, unique to the nervous system, that functions as an insulator to greatly increase the velocity of axonal impulse conduction. Myelin protein zero, absent in the central nervous system,<ref name="pmid2435734">{{cite journal | vauthors = Sakamoto Y, Kitamura K, Yoshimura K, Nishijima T, Uyemura K | title = Complete amino acid sequence of PO protein in bovine peripheral nerve myelin | journal = The Journal of Biological Chemistry | volume = 262 | issue = 9 | pages = 4208–14 | date = March 1987 | pmid = 2435734 | doi = }}</ref> is a major component of the [[myelin]] sheath in [[peripheral nervous system|peripheral]] [[nerve]]s. Mutations that disrupt the function of myelin protein zero can lead to less expression of myelin and degeneration of myelin sheath in the peripheral nervous system.<ref>{{cite journal | vauthors = Kirschner DA, Inouye H, Saavedra RA | title = Membrane adhesion in peripheral myelin: good and bad wraps with protein P0 | journal = Structure | volume = 4 | issue = 11 | pages = 1239–44 | date = November 1996 | pmid = 8939762 | doi = 10.1016/s0969-2126(96)00132-3 }}</ref> Currently, myelin protein zero expression is postulated to be produced by signals from the axon. However, more details about the regulation of myelin protein zero are unknown.<ref name="Shy_2006" />


'''Myelin protein zero''' ('''P0''', '''MPZ''') is a [[glycoprotein]] which in humans is encoded by the ''MPZ'' gene. P0 is a major structural component of the [[myelin sheath]], and its deficiency due to various [[mutation]]s in the ''MPZ'' gene is associated with [[Charcot–Marie–Tooth disease]] and [[Dejerine–Sottas disease]].
It is postulated that myelin protein zero is a [[Cis-regulatory element|structural element]] in the formation and stabilization of peripheral nerve myelin.<ref name="pmid2578885">{{cite journal | vauthors = Lemke G, Axel R | title = Isolation and sequence of a cDNA encoding the major structural protein of peripheral myelin | journal = Cell | volume = 40 | issue = 3 | pages = 501–8 | date = March 1985 | pmid = 2578885 | doi = 10.1016/0092-8674(85)90198-9 }}</ref> Myelin protein zero is also hypothesized to serve as a cell adhesion molecule, holding multiple layers of myelin together.<ref name=":4" /> When a myelinating cell wraps its membrane around an axon multiple times, generating multiple layers of myelin,  myelin protein zero helps keep these sheets compact by serving as a "glue" that keeps the layers of myelin together.<ref name="Jan_2013">{{cite journal | vauthors = Han H, Myllykoski M, Ruskamo S, Wang C, Kursula P | title = Myelin-specific proteins: a structurally diverse group of membrane-interacting molecules | journal = BioFactors | volume = 39 | issue = 3 | pages = 233–41 | date = January 2013 | pmid = 23780694 | doi = 10.1002/biof.1076 }}</ref> It does so by holding its characteristic coil [[secondary structure|structure]] together by the electrostatic interactions<ref name="Shapiro_1996" /> of its positively charged intracellular domain with [[acidic]] [[lipids]] in the [[cytoplasm]]ic face of the opposite bilayer.<ref name="pmid2435734" /> and by interaction between [[hydrophobic]] globular 'heads' of adjacent extracellular [[protein domain|domains]].<ref name="pmid2435734" />


==Function==
Myelin protein zero's function is similar to the function of other proteins with immunoglobin domains like polyimmunoglobin and T4 protein. These proteins function as binding and adhesion molecules and participate in homotypic interactions, or interactions that involve two similar proteins.<ref name="pmid2578885" /> Myelin protein zero holds together the myelin sheath by participating in homotypic interactions with other myelin protein zero proteins. Myelin protein zero's extracellular domain binds to the myelin [[sphingolipid]] membrane and holds together myelin layers using homotypic interactions with other myelin protein zero extracellular domains,<ref name="Shy_2004" /> and with extracellular tryptophan residues interacting with the membrane.<ref name="Shapiro_1996" />
The [[myelin sheath]] is a multi-layered membrane, unique to the nervous system, that functions as an insulator to greatly increase the velocity of axonal impulse conduction. The P0 glycoprotein, absent in the central nervous system,<ref name="pmid2435734">{{cite journal |vauthors=Sakamoto Y, Kitamura K, Yoshimura K, Nishijima T, Uyemura K | title = Complete amino acid sequence of P0 protein in bovine peripheral nerve myelin | journal = J. Biol. Chem. | volume = 262 | issue = 9 | pages = 4208–14 |date=March 1987 | pmid = 2435734 | doi = | url = }}</ref> is a major component of the [[myelin]] sheath in [[peripheral nervous system|peripheral]] [[nerve]]s. It comprises a large [[extracellular]] N-terminal domain, a single [[Protein kinase#Receptor tyrosine kinases|transmembrane]] region, and a smaller positively charged [[intracellular]] [[Domain (biology)|domain]]. It is postulated that P0 is a [[Cis-regulatory element|structural element]] in the formation and stabilisation of peripheral nerve myelin,<ref name="pmid2578885">{{cite journal |vauthors=Lemke G, Axel R | title = Isolation and sequence of a cDNA encoding the major structural protein of peripheral myelin | journal = Cell | volume = 40 | issue = 3 | pages = 501–8 |date=March 1985 | pmid = 2578885 | doi = 10.1016/0092-8674(85)90198-9| url = }}</ref> holding its characteristic coil [[secondary structure|structure]] together by the interaction of its positively charged domain with [[acidic]] [[lipids]] in the [[cytoplasm]]ic face of the opposed bilayer, and by interaction between [[hydrophobic]] globular `heads' of adjacent extracellular [[protein domain|domains]].<ref name="pmid2435734" />


==Interactions==
Myelin protein zero has also been demonstrated to [[Protein–protein interaction|interact]] with other proteins like [[peripheral myelin protein 22]].<ref name="pmid10212299">{{cite journal|vauthors=D'Urso D, Ehrhardt P, Müller HW|date=May 1999|title=Peripheral myelin protein 22 and protein zero: a novel association in peripheral nervous system myelin|url=http://www.jneurosci.org/content/19/9/3396.full.pdf|journal=The Journal of Neuroscience|volume=19|issue=9|pages=3396–403|pmid=10212299}}</ref> However, at this point the purpose of these interactions has not yet been determined.<ref name="pmid10212299" />
Myelin protein zero has been shown to [[Protein–protein interaction|interact]] with [[peripheral myelin protein 22]].<ref name=pmid10212299>{{cite journal |last=D'Urso |first=D |authorlink= |author2=Ehrhardt P |author3=Müller H W  |date=May 1999 |title=Peripheral myelin protein 22 and protein zero: a novel association in peripheral nervous system myelin |journal=J. Neurosci. |volume=19 |issue=9 |pages=3396–403 |publisher = Society for Neuroscience |location = United States| issn = 1529-2401| pmid = 10212299 | bibcode = | oclc =| id = | url = http://www.jneurosci.org/content/19/9/3396.full.pdf | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = }}</ref>


==See also==
== Associations with neuropathy ==
* [[myelin]]
Mutations in myelin protein zero are known to cause myelin degeneration and [[Peripheral neuropathy|neuropathy]].<ref name="Shy_2004" /> Mutations that reduce myelin protein zero's adhesion function or it's ability to participate in homeotypic interactions with other myelin protein zero proteins are thought to cause neuropathy.<ref>{{Citation|last=Pareyson|first=Davide|title=Dominant Charcot–Marie–Tooth syndrome and cognate disorders|date=2013|url=https://doi.org/10.1016/B978-0-444-52902-2.00047-3|last2=Marchesi|first2=Chiara|last3=Salsano|first3=Ettore|work=Handbook of Clinical Neurology|pages=817–845|publisher=Elsevier|doi=10.1016/b978-0-444-52902-2.00047-3|isbn=9780444529022|access-date=2018-06-15}}</ref> Mutations to myelin protein zero can lead to issues with the development of myelin early on in life or myelin degeneration on the axon later on in life.<ref name="Kamholz_2007" />  Some mutations can cause neuropathy in infancy like [[Dejerine–Sottas disease|Derjerine-Sottas disease]] while other mutations can cause neuropathy within the first two decades of life like [[Charcot–Marie–Tooth disease|Charcot-Marie-Tooth disease]].<ref name="Shy_2004" />  Adding a charged amino acid or changing a cysteine residue in the extracellular membrane can lead to neuropathy onset early on. Truncating the cytoplasmic domain or changing the tertiary structure of myelin protein zero can also result in neuropathy<ref name="Shy_2004" /> because the cytoplasmic domain has been demonstrated to be necessary for homotypic interactions.<ref name="Kamholz_2007" />


==References==
== References ==
{{reflist}}
{{reflist}}


==Further reading==
== Further reading ==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading
* {{cite journal | vauthors = Patel PI, Lupski JR | title = Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease | journal = Trends in Genetics | volume = 10 | issue = 4 | pages = 128–33 | date = April 1994 | pmid = 7518101 | doi = 10.1016/0168-9525(94)90214-3 }}
| citations =
* {{cite journal | vauthors = Roa BB, Lupski JR | title = Molecular genetics of Charcot-Marie-Tooth neuropathy | journal = Advances in Human Genetics | volume = 22 | issue =  | pages = 117–52 | year = 1995 | pmid = 7762451 | doi = 10.1007/978-1-4757-9062-7_3 }}
*{{cite journal |vauthors=Patel PI, Lupski JR |title=Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease. |journal=Trends Genet. |volume=10 |issue= 4 |pages= 128–33 |year= 1994 |pmid= 7518101 |doi=10.1016/0168-9525(94)90214-3 }}
* {{cite journal | vauthors = Nelis E, Haites N, Van Broeckhoven C | title = Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies | journal = Human Mutation | volume = 13 | issue = 1 | pages = 11–28 | year = 1999 | pmid = 9888385 | doi = 10.1002/(SICI)1098-1004(1999)13:1<11::AID-HUMU2>3.0.CO;2-A }}
*{{cite journal |vauthors=Roa BB, Lupski JR |title=Molecular genetics of Charcot-Marie-Tooth neuropathy. |journal=Adv. Hum. Genet. |volume=22 |issue=  |pages= 117–52 |year= 1995 |pmid= 7762451 |doi= 10.1007/978-1-4757-9062-7_3}}
* {{cite journal | vauthors = Watanabe M, Yamamoto N, Ohkoshi N, Nagata H, Kohno Y, Hayashi A, Tamaoka A, Shoji S | title = Corticosteroid- responsive asymmetric neuropathy with a myelin protein zero gene mutation | journal = Neurology | volume = 59 | issue = 5 | pages = 767–9 | date = September 2002 | pmid = 12221176 | doi = 10.1212/wnl.59.5.767 }}
*{{cite journal |vauthors=Nelis E, Haites N, Van Broeckhoven C |title=Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies. |journal=Hum. Mutat. |volume=13 |issue= 1 |pages= 11–28 |year= 1999 |pmid= 9888385 |doi= 10.1002/(SICI)1098-1004(1999)13:1<11::AID-HUMU2>3.0.CO;2-A }}
* {{cite journal | vauthors = Hattori N, Yamamoto M, Yoshihara T, Koike H, Nakagawa M, Yoshikawa H, Ohnishi A, Hayasaka K, Onodera O, Baba M, Yasuda H, Saito T, Nakashima K, Kira J, Kaji R, Oka N, Sobue G | title = Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients | journal = Brain | volume = 126 | issue = Pt 1 | pages = 134–51 | date = January 2003 | pmid = 12477701 | doi = 10.1093/brain/awg012 }}
*{{cite journal   |vauthors=Watanabe M, Yamamoto N, Ohkoshi N, etal |title=Corticosteroid- responsive asymmetric neuropathy with a myelin protein zero gene mutation. |journal=Neurology |volume=59 |issue= 5 |pages= 767–9 |year= 2002 |pmid= 12221176 |doi= 10.1212/wnl.59.5.767}}
* {{cite journal | vauthors = Shy ME | title = Peripheral neuropathies caused by mutations in the myelin protein zero | journal = Journal of the Neurological Sciences | volume = 242 | issue = 1-2 | pages = 55–66 | date = March 2006 | pmid = 16414078 | doi = 10.1016/j.jns.2005.11.015 }}
*{{cite journal   |vauthors=Hattori N, Yamamoto M, Yoshihara T, etal |title=Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients. |journal=Brain |volume=126 |issue= Pt 1 |pages= 134–51 |year= 2003 |pmid= 12477701 |doi=10.1093/brain/awg012 }}
* {{cite journal | vauthors = Hayasaka K, Nanao K, Tahara M, Sato W, Takada G, Miura M, Uyemura K | title = Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin | journal = Biochemical and Biophysical Research Communications | volume = 180 | issue = 2 | pages = 515–8 | date = October 1991 | pmid = 1719967 | doi = 10.1016/S0006-291X(05)81094-0 }}
*{{cite journal | author=Shy ME |title=Peripheral neuropathies caused by mutations in the myelin protein zero. |journal=J. Neurol. Sci. |volume=242 |issue= 1–2 |pages= 55–66 |year= 2006 |pmid= 16414078 |doi= 10.1016/j.jns.2005.11.015 }}
* {{cite journal | vauthors = Ouvrier RA, McLeod JG, Conchin TE | title = The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood | journal = Brain | volume = 110 ( Pt 1) | issue = 1 | pages = 121–48 | date = February 1987 | pmid = 3467805 | doi = 10.1093/brain/110.1.121 }}
*{{cite journal   |vauthors=Hayasaka K, Nanao K, Tahara M, etal |title=Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin. |journal=Biochem. Biophys. Res. Commun. |volume=180 |issue= 2 |pages= 515–8 |year= 1991 |pmid= 1719967 |doi=10.1016/S0006-291X(05)81094-0 }}
* {{cite journal | vauthors = Tachi N, Ishikawa Y, Minami R | title = Two cases of congenital hypomyelination neuropathy | journal = Brain & Development | volume = 6 | issue = 6 | pages = 560–5 | year = 1985 | pmid = 6099985 | doi = 10.1016/s0387-7604(84)80101-1 }}
*{{cite journal |vauthors=Ouvrier RA, McLeod JG, Conchin TE |title=The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood. |journal=Brain |volume=110 |issue= 1|pages= 121–48 |year= 1987 |pmid= 3467805 |doi= 10.1093/brain/110.1.121}}
* {{cite journal | vauthors = Hayasaka K, Himoro M, Wang Y, Takata M, Minoshima S, Shimizu N, Miura M, Uyemura K, Takada G | title = Structure and chromosomal localization of the gene encoding the human myelin protein zero (MPZ) | journal = Genomics | volume = 17 | issue = 3 | pages = 755–8 | date = September 1993 | pmid = 7503936 | doi = 10.1006/geno.1993.1400 }}
*{{cite journal |vauthors=Tachi N, Ishikawa Y, Minami R |title=Two cases of congenital hypomyelination neuropathy. |journal=Brain Dev. |volume=6 |issue= 6 |pages= 560–5 |year= 1985 |pmid= 6099985 |doi= 10.1016/s0387-7604(84)80101-1}}
* {{cite journal | vauthors = Su Y, Brooks DG, Li L, Lepercq J, Trofatter JA, Ravetch JV, Lebo RV | title = Myelin protein zero gene mutated in Charcot-Marie-tooth type 1B patients | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 90 | issue = 22 | pages = 10856–60 | date = November 1993 | pmid = 7504284 | pmc = 47877 | doi = 10.1073/pnas.90.22.10856 }}
*{{cite journal   |vauthors=Hayasaka K, Himoro M, Wang Y, etal |title=Structure and chromosomal localization of the gene encoding the human myelin protein zero (MPZ). |journal=Genomics |volume=17 |issue= 3 |pages= 755–8 |year= 1993 |pmid= 7503936 |doi= 10.1006/geno.1993.1400 }}
* {{cite journal | vauthors = Himoro M, Yoshikawa H, Matsui T, Mitsui Y, Takahashi M, Kaido M, Nishimura T, Sawaishi Y, Takada G, Hayasaka K | title = New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1 | journal = Biochemistry and Molecular Biology International | volume = 31 | issue = 1 | pages = 169–73 | date = September 1993 | pmid = 7505151 | doi =  }}
*{{cite journal   |vauthors=Su Y, Brooks DG, Li L, etal |title=Myelin protein zero gene mutated in Charcot-Marie-tooth type 1B patients. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=90 |issue= 22 |pages= 10856–60 |year= 1993 |pmid= 7504284 |doi=10.1073/pnas.90.22.10856 | pmc=47877  }}
* {{cite journal | vauthors = Hayasaka K, Himoro M, Sawaishi Y, Nanao K, Takahashi T, Takada G, Nicholson GA, Ouvrier RA, Tachi N | title = De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III) | journal = Nature Genetics | volume = 5 | issue = 3 | pages = 266–8 | date = November 1993 | pmid = 7506095 | doi = 10.1038/ng1193-266 }}
*{{cite journal   |vauthors=Himoro M, Yoshikawa H, Matsui T, etal |title=New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1. |journal=Biochem. Mol. Biol. Int. |volume=31 |issue= 1 |pages= 169–73 |year= 1994 |pmid= 7505151 |doi=  }}
* {{cite journal | vauthors = Pham-Dinh D, Fourbil Y, Blanquet F, Mattéi MG, Roeckel N, Latour P, Chazot G, Vandenberghe A, Dautigny A | title = The major peripheral myelin protein zero gene: structure and localization in the cluster of Fc gamma receptor genes on human chromosome 1q21.3-q23 | journal = Human Molecular Genetics | volume = 2 | issue = 12 | pages = 2051–4 | date = December 1993 | pmid = 7509228 | doi = 10.1093/hmg/2.12.2051 }}
*{{cite journal   |vauthors=Hayasaka K, Himoro M, Sawaishi Y, etal |title=De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III). |journal=Nat. Genet. |volume=5 |issue= 3 |pages= 266–8 |year= 1994 |pmid= 7506095 |doi= 10.1038/ng1193-266 }}
* {{cite journal | vauthors = Thomas FP, Lebo RV, Rosoklija G, Ding XS, Lovelace RE, Latov N, Hays AP | title = Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome | journal = Acta Neuropathologica | volume = 87 | issue = 1 | pages = 91–7 | year = 1994 | pmid = 7511317 | doi = 10.1007/BF00386259 }}
*{{cite journal   |vauthors=Pham-Dinh D, Fourbil Y, Blanquet F, etal |title=The major peripheral myelin protein zero gene: structure and localization in the cluster of Fc gamma receptor genes on human chromosome 1q21.3-q23. |journal=Hum. Mol. Genet. |volume=2 |issue= 12 |pages= 2051–4 |year= 1994 |pmid= 7509228 |doi=10.1093/hmg/2.12.2051 }}
* {{cite journal | vauthors = Nelis E, Timmerman V, De Jonghe P, Vandenberghe A, Pham-Dinh D, Dautigny A, Martin JJ, Van Broeckhoven C | title = Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene | journal = Human Genetics | volume = 94 | issue = 6 | pages = 653–7 | date = December 1994 | pmid = 7527371 | doi = 10.1007/bf00206959 }}
*{{cite journal   |vauthors=Thomas FP, Lebo RV, Rosoklija G, etal |title=Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome. |journal=Acta Neuropathol. |volume=87 |issue= 1 |pages= 91–7 |year= 1994 |pmid= 7511317 |doi=10.1007/BF00386259 }}
* {{cite journal | vauthors = Hilmi S, Fournier M, Valeins H, Gandar JC, Bonnet J | title = Myelin P0 glycoprotein: identification of the site phosphorylated in vitro and in vivo by endogenous protein kinases | journal = Journal of Neurochemistry | volume = 64 | issue = 2 | pages = 902–7 | date = February 1995 | pmid = 7530295 | doi = 10.1046/j.1471-4159.1995.64020902.x }}
*{{cite journal   |vauthors=Nelis E, Timmerman V, De Jonghe P, etal |title=Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene. |journal=Hum. Genet. |volume=94 |issue= 6 |pages= 653–7 |year= 1995 |pmid= 7527371 |doi= 10.1007/bf00206959}}
* {{cite journal | vauthors = Rautenstrauss B, Nelis E, Grehl H, Pfeiffer RA, Van Broeckhoven C | title = Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotype | journal = Human Molecular Genetics | volume = 3 | issue = 9 | pages = 1701–2 | date = September 1994 | pmid = 7530550 | doi = 10.1093/hmg/3.9.1701 }}
*{{cite journal   |vauthors=Hilmi S, Fournier M, Valeins H, etal |title=Myelin P0 glycoprotein: identification of the site phosphorylated in vitro and in vivo by endogenous protein kinases. |journal=J. Neurochem. |volume=64 |issue= 2 |pages= 902–7 |year= 1995 |pmid= 7530295 |doi=10.1046/j.1471-4159.1995.64020902.x }}
* {{cite journal | vauthors = Latour P, Blanquet F, Nelis E, Bonnebouche C, Chapon F, Diraison P, Ollagnon E, Dautigny A, Pham-Dinh D, Chazot G | title = Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B | journal = Human Mutation | volume = 6 | issue = 1 | pages = 50–4 | year = 1995 | pmid = 7550231 | doi = 10.1002/humu.1380060110 }}
*{{cite journal   |vauthors=Rautenstrauss B, Nelis E, Grehl H, etal |title=Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotype. |journal=Hum. Mol. Genet. |volume=3 |issue= 9 |pages= 1701–2 |year= 1995 |pmid= 7530550 |doi=10.1093/hmg/3.9.1701 }}
*{{cite journal  |vauthors=Latour P, Blanquet F, Nelis E, etal |title=Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B. |journal=Hum. Mutat. |volume=6 |issue= 1 |pages= 50–4 |year= 1995 |pmid= 7550231 |doi= 10.1002/humu.1380060110 }}
}}
{{refend}}
{{refend}}
{{PDB Gallery|geneid=4359}}


==External links==
== External links ==
{{Wiktionary|myelin protein zero}}
{{Wiktionary|myelin protein zero}}
* [https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=cmt1  GeneReviews/NCBI/NIH/UW entry on Charcot-Marie-Tooth Neuropathy Type 1]
* [https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=cmt1  GeneReviews/NCBI/NIH/UW entry on Charcot-Marie-Tooth Neuropathy Type 1]
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* {{MeshName|Myelin+protein+zero}}
* {{MeshName|Myelin+protein+zero}}


{{PDB Gallery|geneid=4359}}
{{Glycoproteins}}
{{Glycoproteins}}
{{Cell adhesion molecules}}
{{Cell adhesion molecules}}
{{Cell membrane proteins}}
{{Cell membrane proteins}}
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{{InterPro content|IPR019566}}
{{InterPro content|IPR019566}}


[[Category:Human proteins]]
[[Category:Human proteins]]
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Latest revision as of 16:50, 21 September 2018

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
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Myelin protein zero (P0, MPZ) is a single membrane glycoprotein[1] which in humans is encoded by the MPZ gene. P0 is a major structural component of the myelin sheath in the peripheral nervous system (PNS).[2] Myelin protein zero is expressed by Schwann cells and accounts for over 50% of all proteins in the peripheral nervous system, making it the most common protein expressed in the PNS.[2] Mutations in myelin protein zero can cause myelin deficiency and are associated with neuropathies like Charcot–Marie–Tooth disease and Dejerine–Sottas disease.[3]

Structure

Myelin-PO_C
File:Structure of Extracellular domain of Myelin Protein Zero with Labelled BetaSheets .png
Structure of myelin protein zero's extracellular domain with labelled beta strands. Strands D, E, B, and A make up one beta sheet, Strands A', G, F, C, C', C'' make up the other beta sheet.
Identifiers
SymbolMyelin-PO_C
PfamPF10570
InterProIPR019566
OPM superfamily193
OPM protein3oai
Membranome213

In humans, the gene that encodes myelin protein zero is located on chromosome 1 near the Duffy Locus or the Duffy Antigen/Chemokine Receptor. The gene is about 7,000 bases long and is divided into 6 exons. In total, myelin protein zero is 219 amino acids long[2] and has many basic amino acid residues.[4]

Myelin protein zero consists of an extracellular N-terminal domain (amino acids 1-124), a single transmembrane region (125-150), and a smaller positively charged intracellular region (151-219).[2][5][6] Its cytoplasmic domain is highly positively charged but presumably does not fold into a globular structure.[7] The extracellular domain is structurally similar to the immunoglobulin domain[4] and therefore the protein is considered as belonging to immunoglobulin superfamily[8]

Besides existing as a monomer, myelin protein zero is also known to form dimers and tetramers with other myelin protein zero molecules in vertebrates.[9]

Function

The myelin sheath is a multi-layered membrane, unique to the nervous system, that functions as an insulator to greatly increase the velocity of axonal impulse conduction. Myelin protein zero, absent in the central nervous system,[10] is a major component of the myelin sheath in peripheral nerves. Mutations that disrupt the function of myelin protein zero can lead to less expression of myelin and degeneration of myelin sheath in the peripheral nervous system.[11] Currently, myelin protein zero expression is postulated to be produced by signals from the axon. However, more details about the regulation of myelin protein zero are unknown.[2]

It is postulated that myelin protein zero is a structural element in the formation and stabilization of peripheral nerve myelin.[5] Myelin protein zero is also hypothesized to serve as a cell adhesion molecule, holding multiple layers of myelin together.[6] When a myelinating cell wraps its membrane around an axon multiple times, generating multiple layers of myelin, myelin protein zero helps keep these sheets compact by serving as a "glue" that keeps the layers of myelin together.[7] It does so by holding its characteristic coil structure together by the electrostatic interactions[4] of its positively charged intracellular domain with acidic lipids in the cytoplasmic face of the opposite bilayer.[10] and by interaction between hydrophobic globular 'heads' of adjacent extracellular domains.[10]

Myelin protein zero's function is similar to the function of other proteins with immunoglobin domains like polyimmunoglobin and T4 protein. These proteins function as binding and adhesion molecules and participate in homotypic interactions, or interactions that involve two similar proteins.[5] Myelin protein zero holds together the myelin sheath by participating in homotypic interactions with other myelin protein zero proteins. Myelin protein zero's extracellular domain binds to the myelin sphingolipid membrane and holds together myelin layers using homotypic interactions with other myelin protein zero extracellular domains,[3] and with extracellular tryptophan residues interacting with the membrane.[4]

Myelin protein zero has also been demonstrated to interact with other proteins like peripheral myelin protein 22.[12] However, at this point the purpose of these interactions has not yet been determined.[12]

Associations with neuropathy

Mutations in myelin protein zero are known to cause myelin degeneration and neuropathy.[3] Mutations that reduce myelin protein zero's adhesion function or it's ability to participate in homeotypic interactions with other myelin protein zero proteins are thought to cause neuropathy.[13] Mutations to myelin protein zero can lead to issues with the development of myelin early on in life or myelin degeneration on the axon later on in life.[8] Some mutations can cause neuropathy in infancy like Derjerine-Sottas disease while other mutations can cause neuropathy within the first two decades of life like Charcot-Marie-Tooth disease.[3] Adding a charged amino acid or changing a cysteine residue in the extracellular membrane can lead to neuropathy onset early on. Truncating the cytoplasmic domain or changing the tertiary structure of myelin protein zero can also result in neuropathy[3] because the cytoplasmic domain has been demonstrated to be necessary for homotypic interactions.[8]

References

  1. ↑ Magnaghi V, Cavarretta I, Galbiati M, Martini L, Melcangi RC (November 2001). "Neuroactive steroids and peripheral myelin proteins". Brain Research. Brain Research Reviews. 37 (1–3): 360–71. doi:10.1016/s0165-0173(01)00140-0. PMID 11744100.
  2. ↑ 2.0 2.1 2.2 2.3 2.4 Shy ME (March 2006). "Peripheral neuropathies caused by mutations in the myelin protein zero". Journal of the Neurological Sciences. 242 (1–2): 55–66. doi:10.1016/j.jns.2005.11.015. PMID 16414078.
  3. ↑ 3.0 3.1 3.2 3.3 3.4 Shy ME, Jáni A, Krajewski K, Grandis M, Lewis RA, Li J, Shy RR, Balsamo J, Lilien J, Garbern JY, Kamholz J (February 2004). "Phenotypic clustering in MPZ mutations". Brain. 127 (Pt 2): 371–84. doi:10.1093/brain/awh048. PMID 14711881.
  4. ↑ 4.0 4.1 4.2 4.3 Shapiro L, Doyle JP, Hensley P, Colman DR, Hendrickson WA (September 1996). "Crystal structure of the extracellular domain from P0, the major structural protein of peripheral nerve myelin". Neuron. 17 (3): 435–49. doi:10.1016/s0896-6273(00)80176-2. PMID 8816707.
  5. ↑ 5.0 5.1 5.2 Lemke G, Axel R (March 1985). "Isolation and sequence of a cDNA encoding the major structural protein of peripheral myelin". Cell. 40 (3): 501–8. doi:10.1016/0092-8674(85)90198-9. PMID 2578885.
  6. ↑ 6.0 6.1 Lemke G, Lamar E, Patterson J (March 1988). "Isolation and analysis of the gene encoding peripheral myelin protein zero". Neuron. 1 (1): 73–83. doi:10.1016/0896-6273(88)90211-5. PMID 2483091.
  7. ↑ 7.0 7.1 Han H, Myllykoski M, Ruskamo S, Wang C, Kursula P (January 2013). "Myelin-specific proteins: a structurally diverse group of membrane-interacting molecules". BioFactors. 39 (3): 233–41. doi:10.1002/biof.1076. PMID 23780694.
  8. ↑ 8.0 8.1 8.2 Kamholz JA, Brucal M, Li J, Shy M (2007), "Myelin Protein Zero and CMT1B: A Tale of Two Phenotypes", Molecular Neurology, Elsevier, pp. 463–474, doi:10.1016/b978-012369509-3.50031-7, ISBN 9780123695093
  9. ↑ Thompson AJ, Cronin MS, Kirschner DA (March 2002). "Myelin protein zero exists as dimers and tetramers in native membranes of Xenopus laevis peripheral nerve". Journal of Neuroscience Research. 67 (6): 766–71. doi:10.1002/jnr.10167. PMID 11891790.
  10. ↑ 10.0 10.1 10.2 Sakamoto Y, Kitamura K, Yoshimura K, Nishijima T, Uyemura K (March 1987). "Complete amino acid sequence of PO protein in bovine peripheral nerve myelin". The Journal of Biological Chemistry. 262 (9): 4208–14. PMID 2435734.
  11. ↑ Kirschner DA, Inouye H, Saavedra RA (November 1996). "Membrane adhesion in peripheral myelin: good and bad wraps with protein P0". Structure. 4 (11): 1239–44. doi:10.1016/s0969-2126(96)00132-3. PMID 8939762.
  12. ↑ 12.0 12.1 D'Urso D, Ehrhardt P, Müller HW (May 1999). "Peripheral myelin protein 22 and protein zero: a novel association in peripheral nervous system myelin" (PDF). The Journal of Neuroscience. 19 (9): 3396–403. PMID 10212299.
  13. ↑ Pareyson, Davide; Marchesi, Chiara; Salsano, Ettore (2013), "Dominant Charcot–Marie–Tooth syndrome and cognate disorders", Handbook of Clinical Neurology, Elsevier, pp. 817–845, doi:10.1016/b978-0-444-52902-2.00047-3, ISBN 9780444529022, retrieved 2018-06-15

Further reading

  • Patel PI, Lupski JR (April 1994). "Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease". Trends in Genetics. 10 (4): 128–33. doi:10.1016/0168-9525(94)90214-3. PMID 7518101.
  • Roa BB, Lupski JR (1995). "Molecular genetics of Charcot-Marie-Tooth neuropathy". Advances in Human Genetics. 22: 117–52. doi:10.1007/978-1-4757-9062-7_3. PMID 7762451.
  • Nelis E, Haites N, Van Broeckhoven C (1999). "Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies". Human Mutation. 13 (1): 11–28. doi:10.1002/(SICI)1098-1004(1999)13:1<11::AID-HUMU2>3.0.CO;2-A. PMID 9888385.
  • Watanabe M, Yamamoto N, Ohkoshi N, Nagata H, Kohno Y, Hayashi A, Tamaoka A, Shoji S (September 2002). "Corticosteroid- responsive asymmetric neuropathy with a myelin protein zero gene mutation". Neurology. 59 (5): 767–9. doi:10.1212/wnl.59.5.767. PMID 12221176.
  • Hattori N, Yamamoto M, Yoshihara T, Koike H, Nakagawa M, Yoshikawa H, Ohnishi A, Hayasaka K, Onodera O, Baba M, Yasuda H, Saito T, Nakashima K, Kira J, Kaji R, Oka N, Sobue G (January 2003). "Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients". Brain. 126 (Pt 1): 134–51. doi:10.1093/brain/awg012. PMID 12477701.
  • Shy ME (March 2006). "Peripheral neuropathies caused by mutations in the myelin protein zero". Journal of the Neurological Sciences. 242 (1–2): 55–66. doi:10.1016/j.jns.2005.11.015. PMID 16414078.
  • Hayasaka K, Nanao K, Tahara M, Sato W, Takada G, Miura M, Uyemura K (October 1991). "Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin". Biochemical and Biophysical Research Communications. 180 (2): 515–8. doi:10.1016/S0006-291X(05)81094-0. PMID 1719967.
  • Ouvrier RA, McLeod JG, Conchin TE (February 1987). "The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood". Brain. 110 ( Pt 1) (1): 121–48. doi:10.1093/brain/110.1.121. PMID 3467805.
  • Tachi N, Ishikawa Y, Minami R (1985). "Two cases of congenital hypomyelination neuropathy". Brain & Development. 6 (6): 560–5. doi:10.1016/s0387-7604(84)80101-1. PMID 6099985.
  • Hayasaka K, Himoro M, Wang Y, Takata M, Minoshima S, Shimizu N, Miura M, Uyemura K, Takada G (September 1993). "Structure and chromosomal localization of the gene encoding the human myelin protein zero (MPZ)". Genomics. 17 (3): 755–8. doi:10.1006/geno.1993.1400. PMID 7503936.
  • Su Y, Brooks DG, Li L, Lepercq J, Trofatter JA, Ravetch JV, Lebo RV (November 1993). "Myelin protein zero gene mutated in Charcot-Marie-tooth type 1B patients". Proceedings of the National Academy of Sciences of the United States of America. 90 (22): 10856–60. doi:10.1073/pnas.90.22.10856. PMC 47877. PMID 7504284.
  • Himoro M, Yoshikawa H, Matsui T, Mitsui Y, Takahashi M, Kaido M, Nishimura T, Sawaishi Y, Takada G, Hayasaka K (September 1993). "New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1". Biochemistry and Molecular Biology International. 31 (1): 169–73. PMID 7505151.
  • Hayasaka K, Himoro M, Sawaishi Y, Nanao K, Takahashi T, Takada G, Nicholson GA, Ouvrier RA, Tachi N (November 1993). "De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)". Nature Genetics. 5 (3): 266–8. doi:10.1038/ng1193-266. PMID 7506095.
  • Pham-Dinh D, Fourbil Y, Blanquet F, Mattéi MG, Roeckel N, Latour P, Chazot G, Vandenberghe A, Dautigny A (December 1993). "The major peripheral myelin protein zero gene: structure and localization in the cluster of Fc gamma receptor genes on human chromosome 1q21.3-q23". Human Molecular Genetics. 2 (12): 2051–4. doi:10.1093/hmg/2.12.2051. PMID 7509228.
  • Thomas FP, Lebo RV, Rosoklija G, Ding XS, Lovelace RE, Latov N, Hays AP (1994). "Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome". Acta Neuropathologica. 87 (1): 91–7. doi:10.1007/BF00386259. PMID 7511317.
  • Nelis E, Timmerman V, De Jonghe P, Vandenberghe A, Pham-Dinh D, Dautigny A, Martin JJ, Van Broeckhoven C (December 1994). "Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene". Human Genetics. 94 (6): 653–7. doi:10.1007/bf00206959. PMID 7527371.
  • Hilmi S, Fournier M, Valeins H, Gandar JC, Bonnet J (February 1995). "Myelin P0 glycoprotein: identification of the site phosphorylated in vitro and in vivo by endogenous protein kinases". Journal of Neurochemistry. 64 (2): 902–7. doi:10.1046/j.1471-4159.1995.64020902.x. PMID 7530295.
  • Rautenstrauss B, Nelis E, Grehl H, Pfeiffer RA, Van Broeckhoven C (September 1994). "Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotype". Human Molecular Genetics. 3 (9): 1701–2. doi:10.1093/hmg/3.9.1701. PMID 7530550.
  • Latour P, Blanquet F, Nelis E, Bonnebouche C, Chapon F, Diraison P, Ollagnon E, Dautigny A, Pham-Dinh D, Chazot G (1995). "Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B". Human Mutation. 6 (1): 50–4. doi:10.1002/humu.1380060110. PMID 7550231.

External links

This article incorporates text from the public domain Pfam and InterPro: IPR019566
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