Skip to main content
Advertisement

Main menu

  • Home
  • Articles
    • Accepted manuscripts
    • Issue in progress
    • Latest complete issue
    • Issue archive
    • Archive by article type
    • Special issues
    • Subject collections
    • Cell Scientists to Watch
    • First Person
    • Sign up for alerts
  • About us
    • About JCS
    • Editors and Board
    • Editor biographies
    • Travelling Fellowships
    • Grants and funding
    • Journal Meetings
    • Workshops
    • The Company of Biologists
    • Journal news
  • For authors
    • Submit a manuscript
    • Aims and scope
    • Presubmission enquiries
    • Fast-track manuscripts
    • Article types
    • Manuscript preparation
    • Cover suggestions
    • Editorial process
    • Promoting your paper
    • Open Access
    • JCS Prize
    • Manuscript transfer network
    • Biology Open transfer
  • Journal info
    • Journal policies
    • Rights and permissions
    • Media policies
    • Reviewer guide
    • Sign up for alerts
  • Contacts
    • Contact JCS
    • Subscriptions
    • Advertising
    • Feedback
    • For library administrators
  • COB
    • About The Company of Biologists
    • Development
    • Journal of Cell Science
    • Journal of Experimental Biology
    • Disease Models & Mechanisms
    • Biology Open

User menu

  • Log in
  • Log out

Search

  • Advanced search
Journal of Cell Science
  • COB
    • About The Company of Biologists
    • Development
    • Journal of Cell Science
    • Journal of Experimental Biology
    • Disease Models & Mechanisms
    • Biology Open

supporting biologistsinspiring biology

Journal of Cell Science

  • Log in
Advanced search

RSS   Twitter  Facebook   YouTube  

  • Home
  • Articles
    • Accepted manuscripts
    • Issue in progress
    • Latest complete issue
    • Issue archive
    • Archive by article type
    • Special issues
    • Subject collections
    • Cell Scientists to Watch
    • First Person
    • Sign up for alerts
  • About us
    • About JCS
    • Editors and Board
    • Editor biographies
    • Travelling Fellowships
    • Grants and funding
    • Journal Meetings
    • Workshops
    • The Company of Biologists
    • Journal news
  • For authors
    • Submit a manuscript
    • Aims and scope
    • Presubmission enquiries
    • Fast-track manuscripts
    • Article types
    • Manuscript preparation
    • Cover suggestions
    • Editorial process
    • Promoting your paper
    • Open Access
    • JCS Prize
    • Manuscript transfer network
    • Biology Open transfer
  • Journal info
    • Journal policies
    • Rights and permissions
    • Media policies
    • Reviewer guide
    • Sign up for alerts
  • Contacts
    • Contact JCS
    • Subscriptions
    • Advertising
    • Feedback
    • For library administrators
Journal Articles
The Emery-Dreifuss muscular dystrophy phenotype arises from aberrant targeting and binding of emerin at the inner nuclear membrane
E.A. Fairley, J. Kendrick-Jones, J.A. Ellis
Journal of Cell Science 1999 112: 2571-2582;
E.A. Fairley
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
J. Kendrick-Jones
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
J.A. Ellis
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Info & metrics
  • PDF
Loading

Summary

The product of the X-linked Emery-Dreifuss muscular dystrophy gene is a single-membrane-spanning protein called emerin, which is localized to the inner nuclear membrane of all tissues studied. To examine whether a number of the mutant forms of emerin expressed in patients are mislocalized, we transfected GFP-emerin cDNA constructs reflecting these mutations into undifferentiated C2C12 myoblasts and showed that both wild type and all the mutant emerins are targeted to the nuclear membrane, but the mutants to a lesser extent. Mutant Del236-241 (deletion in transmembrane region) was mainly expressed as cytoplasmic aggregates, with only trace amounts at the nuclear envelope. Complete removal of the transmembrane region and C-terminal tail relocated emerin to the nucleoplasm. Mutations in emerin's N-terminal domain had a less severe effect on disrupting nuclear envelope targeting. This data suggests that emerin contains multiple non-overlapping nuclear-membrane-targeting determinants. Analysis of material immunoisolated using emerin antibodies, from either undifferentiated C2C12 myoblasts or purified hepatocyte nuclei, demonstrated that both A- and B-type lamins and nuclear actin interact with emerin. This is the first report of proteins interacting with emerin. The EDMD phenotype can thus arise by either the absence or a reduction in emerin at the nuclear envelope, and both of these disrupt its interactions with that of structural components of the nucleus. We propose that an emerin-nuclear protein complex exists at the nuclear envelope and that one of its primary roles is to stabilize the nuclear membrane against the mechanical stresses that are generated in muscle cells during contraction.

  • © 1999 by Company of Biologists

REFERENCES

    1. Alsheimer M.,
    2. Fecher E. and
    3. Benavente R.
    (1998). Nuclear envelope remodelling during rat spermatogenesis: distribution and expression pattern of LAP2. J. Cell Sci 111, 2227–2234
    OpenUrlAbstract/FREE Full Text
    1. Ansorge W.
    (1985). Fast and sensitive detection of protein and DNA bands by treatment with potassium permanganate. J. Biochem. Biophys. Meth 11, 13–20
    OpenUrlCrossRefPubMed
    1. Bione S.,
    2. Maestrini E.,
    3. Rivella S.,
    4. Mancini M.,
    5. Regis S.,
    6. Romeo G. and
    7. Toniolo D.
    (1994). Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy. Nature Genet 8, 323–327
    OpenUrlCrossRefPubMedWeb of Science
    1. Bonne G.,
    2. Di Barletta M. R.,
    3. Varnous S.,
    4. Becane H.-M.,
    5. Hammouda E.-H.,
    6. Merlini L.,
    7. Muntoni F.,
    8. Greenberg C. R.,
    9. Gary F.,
    10. Urtizbera J.-A.,
    11. Doboc D.,
    12. Fardeau M.,
    13. Toniolo D. and
    14. Schwartz K.
    (1999). Mutations in the gene encoding lamin A/C cause autosomal dominant EDMD. Nature Genet 21, 285–288
    OpenUrlCrossRefPubMedWeb of Science
    1. Burnette W. N.
    (1981). ‘Western blotting’ Electrophoretic transfer of proteins from SDS-PAGE gels to unmodified nitrocellulose and radiographic detection with antibodies and radioiodinated protein A. Anal. Biochem 112, 195–303
    OpenUrlCrossRefPubMedWeb of Science
    1. Cartegni L.,
    2. Raffaele de Barletta M.,
    3. Barresi R.,
    4. Sqarzoni S.,
    5. Sabatelli P.,
    6. Maraldi N.,
    7. Mora M.,
    8. Di Dlasi C.,
    9. Cornelio F.,
    10. Merlino L.,
    11. Villa A.,
    12. Cobianchi F. and
    13. Toniolo D.
    (1997). Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy. Hum. Mol. Genet 6, 2257–2264
    OpenUrlAbstract/FREE Full Text
    1. Ellis J. A.,
    2. Craxton M.,
    3. Yates J. R. W. and
    4. Kendrick-Jones J.
    (1998). Aberrant intracellular targeting and cell cycle-dependent phosphorylation of emerin contribute to the EMD phenotype. J. Cell Sci 111, 781–792
    OpenUrlAbstract/FREE Full Text
    1. Ellis J. A.,
    2. Tilley L. D.,
    3. Yates J. R. W.,
    4. Kendrick-Jones J. and
    5. Brown C. B.
    (1999). Changes at P183 of emerin weaken its protein-protein interactions resulting in X-linked EDMD. Hum. Genet 104, 262–268
    OpenUrlCrossRefPubMed
    1. Emery A. E. H.
    (1989). Emery-Dreifuss syndrome. J. Med. Genet 26, 637–641
    OpenUrlAbstract/FREE Full Text
    1. Foisner R. and
    2. Gerace L.
    (1993). Integral membrane proteins of the nuclear envelope interact with lamins and chromosomes, and binding is modulated by mitotic phosphorylation. Cell 73, 1267–1279
    OpenUrlCrossRefPubMedWeb of Science
    1. Furukawa K.,
    2. Pane N.,
    3. Aebi U. and
    4. Gerace L.
    (1995). Cloning of a cDNA for lamina-associated polypeptide 2 (LAP2) and identification of regions that specify targeting to the nuclear envelope. EMBO J 14, 1626–1636
    OpenUrlPubMedWeb of Science
    1. Furukawa K.,
    2. Fritze C. E. and
    3. Gerace L.
    (1998). The major nuclear envelope targeting domain of LAP2 coincides with its lamin binding region but is distinct from its chromatin interaction domain. J. Biol. Chem 273, 4213–4219
    OpenUrlAbstract/FREE Full Text
    1. Furukawa K. and
    2. Kondo T.
    (1998). Identification of the lamina-associated-polypeptide-2-binding domain of B-type lamin. Eur. J. Biochem 251, 729–733
    OpenUrlPubMedWeb of Science
    1. Georgatos S. P.,
    2. Meier J. and
    3. Simos G.
    (1994). Lamins and lamin-associated proteins. Curr. Opin. Cell Biol 6, 347–353
    OpenUrlCrossRefPubMedWeb of Science
    1. Harris C. A.,
    2. Andryuk P. J.,
    3. Cline S. W.,
    4. Mathew S.,
    5. Siekierka J. J. and
    6. Goldstein G.
    (1995). Structure and mapping of the human thymopoietin (TMPO) gene and relationship of the human TMPO-to rat lamina-associated polypeptide 2. Genomics 28, 198–205
    OpenUrlCrossRefPubMedWeb of Science
    1. Laemmli U. K.
    (1970). Cleavage of structural proteins during assembly of the head of bacteriophage T4. Nature 227, 680–685
    OpenUrlCrossRefPubMedWeb of Science
    1. Lorim D. and
    2. Lin J. J.-C.
    (1989). Expression of nuclear lamin A and muscle-specific proteins in differentiating muscle cells in ovo and in vitro. J. Cell Biol 109, 495–504
    OpenUrlAbstract/FREE Full Text
    1. Maison C.,
    2. Pyrpasopoulou A.,
    3. Theodoropoulos P. A. and
    4. Georgatos S. D.
    (1997). The inner nuclear membrane protein LAP1 forms a native complex with B-type lamins and partitions with spindle-associated mitotic vesicles. EMBO J 16, 4839–4850
    OpenUrlCrossRefPubMedWeb of Science
    1. Manilal S.,
    2. Nguyen thi Man ,
    3. Sewry C. A. and
    4. Morris G. E.
    (1996). The Emery-Dreifuss muscular dystrophy protein, emerin, is a nuclear protein. Hum. Mol. Genet 5, 801–808
    OpenUrlAbstract/FREE Full Text
    1. Manilal S.,
    2. Sewry C. A.,
    3. Nguyen thi Man ,
    4. Muntoni F. and
    5. Morris G. E.
    (1997). Diagnosis of Emery-Dreifuss muscular dystrophy by protein analysis of leucocytes with monocloncal antibodies. Neuromusc. Disorders 7, 63–66
    OpenUrlCrossRefPubMedWeb of Science
    1. Manilal S.,
    2. Recan D.,
    3. Sewry C. A.,
    4. Hoeltzenbein M.,
    5. Llense S.,
    6. Leturcq F.,
    7. Deburgrave N.,
    8. Barbot J.-C.,
    9. Nguyen thi Man ,
    10. Muntoni F.,
    11. Wehnert M.,
    12. Kaplan J.-C. and
    13. Morris G. E.
    (1998). Mutations in Emery-Dreifuss muscular dystrophy and their effects on emerin protein expression. Hum. Mol. Genet 7, 855–864
    OpenUrlAbstract/FREE Full Text
    1. Manilal S.,
    2. Nguyen thi and
    3. Man Morris G. E.
    (1998). Co-localization of emerin and lamins in interphase nuclei and changes in mitosis. Biochem. Biophys. Res. Commun 249, 643–647
    OpenUrlCrossRefPubMedWeb of Science
    1. Manilal S.,
    2. Sewry C. A.,
    3. Pereboev A.,
    4. Nguyen thi man ,
    5. Gobbi P.,
    6. Hawkes S.,
    7. Love D. R. and
    8. Morris G. E.
    (1999). Distribution of emerin and lamins in the heart and implications for EDMD. Hum. Mol. Genet 8, 353–359
    OpenUrlAbstract/FREE Full Text
    1. Maniotis A. J.,
    2. Chen C. S. and
    3. Ingber D. E.
    (1997). Demonstration of mechanical connections between integrins, cytoskeletal filaments and nucleoplasm that stabilize nuclear structure. Proc. Natl. Acad. Sci.USA 94, 849–854
    OpenUrlAbstract/FREE Full Text
    1. Martin L.,
    2. Crimaudo C. and
    3. Gerace L.
    (1995). cDNA cloning and characterization of lamina-associated polypeptide 1C (LAP1C), an integral protein of the inner nuclear membrane. J. Biol. Chem 270, 8822–8828
    OpenUrlAbstract/FREE Full Text
    1. McKeon F. D.,
    2. Kirschner M. W. and
    3. Caput D.
    (1986). Homologies in both primary and secondary structure between nuclear envelope and intermediate filament proteins. Nature 319, 463–468
    OpenUrlCrossRefPubMed
    1. Moir R. D.,
    2. Montag-Lowy M. and
    3. Goldman R. D.
    (1994). Intrinsicproperties of nuclear lamins: lamin B is associated with sites of DNA replication. J. Cell Biol 125, 1201–1212
    OpenUrlAbstract/FREE Full Text
    1. Mora M.,
    2. Carregni L.,
    3. Di Dlasi C.,
    4. Barresi R.,
    5. Bione S.,
    6. Raffaele di Barletta M.,
    7. Morandi L.,
    8. Merlini L.,
    9. Nigro V.,
    10. Politano L.,
    11. Donati M. A.,
    12. Cornelio F.,
    13. Cobianchi F. and
    14. Toniolo D.
    (1997). X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample. Ann. Neurol 42, 249–253
    OpenUrlCrossRefPubMedWeb of Science
    1. Nagano A.,
    2. Koga R.,
    3. Ogawa M.,
    4. Kurano Y.,
    5. Kawada J.,
    6. Okada R.,
    7. Hayashi Y. K.,
    8. Tsukahara T. and
    9. Arahata K.
    (1996). Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy. Nature Genet 2, 254–259
    OpenUrl
    1. Nikolakaki E.,
    2. Simos G.,
    3. Georgatos S. D. and
    4. Giannakouros T.
    (1996). A nuclear envelope-associated kinase phosphorylates arginine-serine motifs and modulates interactions between the lamin B receptor and other nuclear proteins. J. Biol. Chem 271, 8365–8372
    OpenUrlAbstract/FREE Full Text
    1. Paine P. L.
    (1975). Nucleocytoplasmic movement of fluorescent tracers microinjected into living salivary gland cells. J. Cell Biol 66, 652–657
    OpenUrlAbstract/FREE Full Text
    1. Pardee J. D. and
    2. Spudich J. A.
    (1982). Purification of muscle actin. Meth. Enzymol 85, 164–181
    OpenUrlCrossRefPubMedWeb of Science
    1. Parfenov V. N.,
    2. Davis D. S.,
    3. Pochukalina G. N.,
    4. Sample C. E.,
    5. Bugaeva E. A. and
    6. Muriti K. G.
    (1995). Nuclear filaments and their topological changes in frog oocytes. Exp. Cell Res 217, 385–394
    OpenUrlCrossRefPubMed
    1. Roberts R.G.
    (1995). Dystrophin, its gene and the dystrophinopathies. Adv. Gen, 33, 177–231
    OpenUrlPubMedWeb of Science
    1. Sasseville A. M.-J. and
    2. Langelier Y.
    (1998). In vitro interaction of the carboxy-terminal domain of lamin A with actin. FEBS Lett 425, 485–489
    OpenUrlCrossRefPubMedWeb of Science
    1. Simos G. and
    2. Georgatos S. D.
    (1992). The inner nuclear membrane protein p58 associates in vivo with a p58 kinase and nuclear lamins. EMBO. J 11, 4027–4036
    OpenUrlPubMedWeb of Science
    1. Smith S. and
    2. Blobel G.
    (1993). The first membrane spanning region of the LBR is sufficient for sorting to the inner nuclear membrane. J. Cell Biol 120, 631–637
    OpenUrlAbstract/FREE Full Text
    1. Soullam B. and
    2. Worman G.
    (1993). The amino-terminal domain of the lamin-B receptor is a nuclear-envelope targeting signal. J. Cell Biol 120, 1093–1100
    OpenUrlAbstract/FREE Full Text
    1. Soullam B. and
    2. Worman G.
    (1995). Signals and structural features involved in integral membrane targeting to the inner nuclear membrane. J. Cell Biol 130, 15–27
    OpenUrlAbstract/FREE Full Text
    1. Squarzoni S.,
    2. Sabatelli P.,
    3. Ognibene A.,
    4. Toniolo D.,
    5. Cartegni L.,
    6. Cobianchi F.,
    7. Petrini S.,
    8. Merlini L. and
    9. Maraldi N. M.
    (1998). Immunocytochemical detection of emerin within the nuclear matrix. Neuromusc. Disorders 8, 338–344
    OpenUrlCrossRefPubMed
    1. Yang L.,
    2. Guan T. and
    3. Gerace L.
    (1997). Integral membrane proteins of the nuclear envelope are dispersed throughout the ER during mitosis. J. Cell Biol 137, 1199–1210
    OpenUrlAbstract/FREE Full Text
    1. Yang L.,
    2. Guan T. and
    3. Gerace L.
    (1997). Lamin-binding fragment of LAP2 inhibits increase in nuclear volume during the cell cycle and progression into S-phase. J. Cell Biol 139, 1077–1087
    OpenUrlAbstract/FREE Full Text
    1. Yates J. R. W.,
    2. Bagshaw J.,
    3. Aksmanovic V. M. A.,
    4. Coomber E.,
    5. McMahon R.,
    6. Whittaker J. L.,
    7. Morrison P. J.,
    8. Kendrick-Jones J. and
    9. Ellis J. A.
    (1999). Genotype-phenotype analysis in X-linked Emery-Dreifuss muscular dystrophy and identification of a missense mutation associated with a milder phenotype. Neuromusc. Disorders 9, 159–165
    OpenUrlCrossRefPubMed
    1. Ye Q. and
    2. Worman H. J.
    (1994). Primary structure analysis and DNA binding of human LBR, an integral protein of the nuclear envelope inner membrane. J. Biol. Chem 269, 11306–11311
    OpenUrlAbstract/FREE Full Text
Previous ArticleNext Article
Back to top
Previous ArticleNext Article

This Issue

 Download PDF

Email

Thank you for your interest in spreading the word on Journal of Cell Science.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
The Emery-Dreifuss muscular dystrophy phenotype arises from aberrant targeting and binding of emerin at the inner nuclear membrane
(Your Name) has sent you a message from Journal of Cell Science
(Your Name) thought you would like to see the Journal of Cell Science web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Share
Journal Articles
The Emery-Dreifuss muscular dystrophy phenotype arises from aberrant targeting and binding of emerin at the inner nuclear membrane
E.A. Fairley, J. Kendrick-Jones, J.A. Ellis
Journal of Cell Science 1999 112: 2571-2582;
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
Citation Tools
Journal Articles
The Emery-Dreifuss muscular dystrophy phenotype arises from aberrant targeting and binding of emerin at the inner nuclear membrane
E.A. Fairley, J. Kendrick-Jones, J.A. Ellis
Journal of Cell Science 1999 112: 2571-2582;

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Alerts

Please log in to add an alert for this article.

Sign in to email alerts with your email address

Article navigation

  • Top
  • Article
  • Info & metrics
  • PDF

Related articles

Cited by...

More in this TOC section

  • Involvement of actin filaments and integrins in the binding step in collagen phagocytosis by human fibroblasts
  • University administration
  • The cytoplasmic domain of the interleukin-6 receptor gp80 mediates its basolateral sorting in polarized madin-darby canine kidney cells
Show more Journal Articles

Similar articles

Other journals from The Company of Biologists

Development

Journal of Experimental Biology

Disease Models & Mechanisms

Biology Open

Advertisement

Cell scientist to watch: Janet Iwasa

Read our interview with molecular animator Janet Iwasa, where she talks about her transition from the wet lab, explains how animation can facilitate research and discusses the challenges of the field.


New funding scheme supports sustainable events

As part of our Sustainable Conferencing Initiative, we are pleased to announce funding for organisers that seek to reduce the environmental footprint of their event. The next deadline to apply for a Scientific Meeting grant is 26 March 2021.


Mole – The Corona files

“Despite everything, it's just incredible that we get to do science.”

Mole continues to offer his wise words to researchers on how to manage during the COVID-19 pandemic.


JCS and COVID-19

For more information on measures Journal of Cell Science is taking to support the community during the COVID-19 pandemic, please see here.

If you have any questions or concerns, please do not hestiate to contact the Editorial Office.

Articles

  • Accepted manuscripts
  • Issue in progress
  • Latest complete issue
  • Issue archive
  • Archive by article type
  • Special issues
  • Subject collections
  • Interviews
  • Sign up for alerts

About us

  • About Journal of Cell Science
  • Editors and Board
  • Editor biographies
  • Travelling Fellowships
  • Grants and funding
  • Journal Meetings
  • Workshops
  • The Company of Biologists

For Authors

  • Submit a manuscript
  • Aims and scope
  • Presubmission enquiries
  • Fast-track manuscripts
  • Article types
  • Manuscript preparation
  • Cover suggestions
  • Editorial process
  • Promoting your paper
  • Open Access
  • JCS Prize
  • Manuscript transfer network
  • Biology Open transfer

Journal Info

  • Journal policies
  • Rights and permissions
  • Media policies
  • Reviewer guide
  • Sign up for alerts

Contacts

  • Contact JCS
  • Subscriptions
  • Advertising
  • Feedback

Twitter   YouTube   LinkedIn

© 2021   The Company of Biologists Ltd   Registered Charity 277992