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词条 Merlin (protein)
释义

  1. Gene

  2. Structure

  3. Function

  4. Interactions

  5. References

  6. External links

{{Infobox_gene}}

Merlin (also called Neurofibromin 2 or schwannomin) is a cytoskeletal protein. In humans, it is a tumor suppressor protein involved in Neurofibromatosis type II.[1][2] Sequence data reveal its similarity to the ERM protein family.

The name "merlin" is an acronym for "Moesin-Ezrin-Radixin-Like Protein".

Gene

Human merlin is coded by the gene NF2 in Chromosome 22. Mouse merlin gene is located on chromosome 11[3] and rat merlin gene on chromosome 17. Fruit fly merlin gene (symbol Mer) is located on chromosome 1 and shares 58% similarity to its human homologue.

Other merlin-like genes are known from a wide range of animals, and the derivation of merlin is thought to be in early metazoa. Merlin is a member of the ERM family of proteins including ezrin, moesin, and radixin, which are in the protein 4.1 superfamily of proteins. Merlin is also known as schwannomin, a name derived from the most common type of tumor in the NF2 patient phenotype, the schwannoma.

Structure

Vertebrate merlin is a 70-kDa protein. There are 10 known isoforms of human merlin molecule (the full molecule being 595 amino acids in length). The two most common of these are also found in the mouse and are called type 1 and type 2, differing by the absence or presence of exon 16 or 17, respectively). All the known varieties have a conserved N-terminal part, which contains a FERM domain (a domain found in most cytoskeletal-membrane organizing proteins). The FERM domain is followed by an alpha-helical domain and a hydrophilic tail.[4][5] Merlin can dimerize with itself and heterodimerize with other ERM family proteins.

Function

Merlin is a membrane-cytoskeleton scaffolding protein, i.e. linking actin filaments to cell membrane or membrane glycoproteins.[6] Human merlin is predominantly found in nervous tissue, but also in several other fetal tissues, and is mainly located in adherens junctions.[7] Its tumor suppressor properties are probably associated with contact-mediated growth inhibition. Drosophila merlin is expressed in embryonic hindgut, salivary glands, and imaginal discs, and has apparently a slightly different role than in vertebrates.[8]

The phosphorylation of serine 518 is known to alter the functional state of merlin.[9] The signaling pathway of merlin is proposed to include several salient cell growth controlling molecules, including eIF3c, CD44, protein kinase A, and p21 activated kinases.

Work in Drosophila identified Merlin as an upstream regulator of the Hippo tumor suppressor pathway,[10] a function that is conserved in mammals.[11] The Hippo pathway is a well conserved signalling pathway that coordinately regulates cell proliferation and apoptosis.[12]

Mutations of the NF2 gene cause a human autosomal dominant disease called neurofibromatosis type 2. It is characterized by the development of tumors of the nervous system, most commonly of bilateral vestibular schwannomas (also called acoustic neuromas). NF2 belongs to the tumor suppressor group of genes.[13]

Interactions

Merlin (protein) has been shown to interact with:

{{div col|colwidth=20em}}
  • CUL4A,[14]
  • DDB1,[14]
  • EZR,[15]
  • HGS,[16][17]
  • MED28,[18]
  • RIT1,[14]
  • SDCBP,[19]
  • SPTBN1,[20] and
  • VPRBP.[14]
{{Div col end}}

References

1. ^{{cite journal | vauthors = Rouleau GA, Merel P, Lutchman M, Sanson M, Zucman J, Marineau C, Hoang-Xuan K, Demczuk S, Desmaze C, Plougastel B | title = Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2 | journal = Nature | volume = 363 | issue = 6429 | pages = 515–21 | year = 1993 | pmid = 8379998 | doi = 10.1038/363515a0 }}
2. ^{{cite journal | vauthors = Golovnina K, Blinov A, Akhmametyeva EM, Omelyanchuk LV, Chang LS | title = Evolution and origin of merlin, the product of the Neurofibromatosis type 2 (NF2) tumor-suppressor gene | journal = BMC Evol. Biol. | volume = 5 | pages = 69 | year = 2005 | pmid = 16324214 | pmc = 1315344 | doi = 10.1186/1471-2148-5-69 }}
3. ^{{cite journal | vauthors = Haase VH, Trofatter JA, MacCollin M, Tarttelin E, Gusella JF, Ramesh V | title = The murine NF2 homologue encodes a highly conserved merlin protein with alternative forms | journal = Hum. Mol. Genet. | volume = 3 | issue = 3 | pages = 407–11 | year = 1994 | pmid = 8012352 | doi = 10.1093/hmg/3.3.407 }}
4. ^{{cite journal | vauthors = Shimizu T, Seto A, Maita N, Hamada K, Tsukita S, Tsukita S, Hakoshima T | title = Structural basis for neurofibromatosis type 2. Crystal structure of the merlin FERM domain | journal = J. Biol. Chem. | volume = 277 | issue = 12 | pages = 10332–6 | year = 2002 | pmid = 11756419 | doi = 10.1074/jbc.M109979200 }}
5. ^{{Cite journal| pmid = 24882693| year = 2014| author1 = Ali Khajeh| first1 = J| title = Molecular conformation of the full-length tumor suppressor NF2/Merlin--a small-angle neutron scattering study.| journal = Journal of Molecular Biology| volume = 426| issue = 15| pages = 2755–68| last2 = Ju| first2 = JH| last3 = Atchiba| first3 = M| doi = 10.1016/j.jmb.2014.05.011| pmc=4407695}}
6. ^{{cite journal | vauthors = McClatchey AI, Giovannini M | title = Membrane organization and tumorigenesis--the NF2 tumor suppressor, Merlin | journal = Genes Dev. | volume = 19 | issue = 19 | pages = 2265–77 | year = 2005 | pmid = 16204178 | doi = 10.1101/gad.1335605 }}
7. ^{{cite journal | vauthors = den Bakker MA, Vissers KJ, Molijn AC, Kros JM, Zwarthoff EC, van der Kwast TH | title = Expression of the neurofibromatosis type 2 gene in human tissues | journal = J. Histochem. Cytochem. | volume = 47 | issue = 11 | pages = 1471–80 | year = 1999 | pmid = 10544220 | doi = 10.1177/002215549904701113 | url = http://www.jhc.org/cgi/content/abstract/47/11/1471 | deadurl = yes | archiveurl = https://web.archive.org/web/20080518194148/http://www.jhc.org/cgi/content/abstract/47/11/1471 | archivedate = 2008-05-18 | df = }}
8. ^{{cite journal | vauthors = LaJeunesse DR, McCartney BM, Fehon RG | title = Structural Analysis of Drosophila Merlin Reveals Functional Domains Important for Growth Control and Subcellular Localization | journal = J. Cell Biol. | volume = 141 | issue = 7 | pages = 1589–99 | year = 1998 | pmid = 9647651 | pmc = 2133006 | doi = 10.1083/jcb.141.7.1589 }}
9. ^{{cite journal | vauthors = Alfthan K, Heiska L, Grönholm M, Renkema GH, Carpén O | title = Cyclic AMP-dependent protein kinase phosphorylates merlin at serine 518 independently of p21-activated kinase and promotes merlin-ezrin heterodimerization | journal = J. Biol. Chem. | volume = 279 | issue = 18 | pages = 18559–66 | year = 2004 | pmid = 14981079 | doi = 10.1074/jbc.M313916200 }}
10. ^{{cite journal|title=The tumour-suppressor genes NF2/Merlin and Expanded act through Hippo signalling to regulate cell proliferation and apoptosis.|journal=Nature Cell Biology|date=2006|pmid=16341207|doi=10.1038/ncb1339|volume=8|issue=1|pages=27–36|vauthors=Hamaratoglu F, Willecke M, Kango-Singh M et al.}}
11. ^{{cite journal|title=The Merlin/NF2 tumor suppressor functions through the YAP oncoprotein to regulate tissue homeostasis in mammals.|journal=Developmental Cell|date=2010|pmid=20643348|doi=10.1016/j.devcel.2010.06.015|volume=19|issue=1|pmc=2925178|pages=27–38|vauthors=Zhang N, Bai H, David KK, Dong J, Zheng Y, Cai J, Giovannini M, Liu P, Anders RA, Pan D}}
12. ^{{cite journal|title=The hippo signaling pathway in development and cancer.|journal=Developmental Cell|pmid=20951342 | doi=10.1016/j.devcel.2010.09.011|pmc=3124840|volume=19|issue=4|date=October 2010|pages=491–505|vauthors=Pan D}}
13. ^{{cite journal | vauthors = Scoles DR, Yong WH, Qin Y, Wawrowsky K, Pulst SM | title = Schwannomin inhibits tumorigenesis through direct interaction with the eukaryotic initiation factor subunit c (eIF3c) | journal = Hum. Mol. Genet. | volume = 15 | issue = 7 | pages = 1059–70 | year = 2006 | pmid = 16497727 | doi = 10.1093/hmg/ddl021 }}
14. ^1 2 3 {{cite journal | vauthors = Huang J, Chen J | title = VprBP targets Merlin to the Roc1-Cul4A-DDB1 E3 ligase complex for degradation | journal = Oncogene | volume = 27 | issue = 29 | pages = 4056–64 | date = July 2008 | pmid = 18332868 | doi = 10.1038/onc.2008.44 }}
15. ^{{cite journal | vauthors = Grönholm M, Sainio M, Zhao F, Heiska L, Vaheri A, Carpén O | title = Homotypic and heterotypic interaction of the neurofibromatosis 2 tumor suppressor protein merlin and the ERM protein ezrin | journal = J. Cell Sci. | volume = 112 | issue = 6| pages = 895–904 | date = March 1999 | pmid = 10036239 | doi = }}
16. ^{{cite journal | vauthors = Gutmann DH, Haipek CA, Burke SP, Sun CX, Scoles DR, Pulst SM | title = The NF2 interactor, hepatocyte growth factor-regulated tyrosine kinase substrate (HRS), associates with merlin in the "open" conformation and suppresses cell growth and motility | journal = Hum. Mol. Genet. | volume = 10 | issue = 8 | pages = 825–34 | date = April 2001 | pmid = 11285248 | doi = 10.1093/hmg/10.8.825}}
17. ^{{cite journal | vauthors = Scoles DR, Huynh DP, Chen MS, Burke SP, Gutmann DH, Pulst SM | title = The neurofibromatosis 2 tumor suppressor protein interacts with hepatocyte growth factor-regulated tyrosine kinase substrate | journal = Hum. Mol. Genet. | volume = 9 | issue = 11 | pages = 1567–74 | date = July 2000 | pmid = 10861283 | doi = 10.1093/hmg/9.11.1567}}
18. ^{{cite journal | vauthors = Wiederhold T, Lee MF, James M, Neujahr R, Smith N, Murthy A, Hartwig J, Gusella JF, Ramesh V | title = Magicin, a novel cytoskeletal protein associates with the NF2 tumor suppressor merlin and Grb2 | journal = Oncogene | volume = 23 | issue = 54 | pages = 8815–25 | date = November 2004 | pmid = 15467741 | doi = 10.1038/sj.onc.1208110 }}
19. ^{{cite journal | vauthors = Jannatipour M, Dion P, Khan S, Jindal H, Fan X, Laganière J, Chishti AH, Rouleau GA | title = Schwannomin isoform-1 interacts with syntenin via PDZ domains | journal = J. Biol. Chem. | volume = 276 | issue = 35 | pages = 33093–100 | date = August 2001 | pmid = 11432873 | doi = 10.1074/jbc.M105792200 }}
20. ^{{cite journal | vauthors = Neill GW, Crompton MR | title = Binding of the merlin-I product of the neurofibromatosis type 2 tumour suppressor gene to a novel site in beta-fodrin is regulated by association between merlin domains | journal = Biochem. J. | volume = 358 | issue = Pt 3 | pages = 727–35 | date = September 2001 | pmid = 11535133 | pmc = 1222106 | doi = 10.1042/0264-6021:3580727}}

External links

  • [https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=nf2 GeneReviews/NCBI/NIH/UW entry on Neurofibromatosis 2]
  • FlyBase synopsis of gene Mer
{{Tumor suppressor genes}}{{Membrane proteins}}{{Hippo signaling pathway}}{{PDB_Gallery|geneid=4771}}

3 : Cytoskeleton|Peripheral membrane proteins|Human proteins
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