Chapter 6. Identification of Novel Integral Membrane Proteins of the Nuclear Envelope with Potential Disease Links Using Subtractive Proteomics

  1. Derek J. Chadwick Organizer,
  2. Jamie Goode
  1. Eric C. Schirmer1,
  2. Laurence Florens1,
  3. Tinglu Guan1,
  4. John R. Yates III1,
  5. Larry Gerace2,*

Published Online: 7 OCT 2008

DOI: 10.1002/0470093765.ch6

Nuclear Organization in Development and Disease: Novartis Foundation Symposium 264

Nuclear Organization in Development and Disease: Novartis Foundation Symposium 264

How to Cite

Schirmer, E. C., Florens, L., Guan, T., Yates, J. R. and Gerace, L. (2008) Identification of Novel Integral Membrane Proteins of the Nuclear Envelope with Potential Disease Links Using Subtractive Proteomics, in Nuclear Organization in Development and Disease: Novartis Foundation Symposium 264 (eds D. J. Chadwick and J. Goode), John Wiley & Sons, Ltd, Chichester, UK. doi: 10.1002/0470093765.ch6

Author Information

  1. 1

    Department of Cell Biology, The Scripps Research Institute, La Jolla CA, USA 92037, USA

  2. 2

    Departments of Cell and Molecular Biology, The Scripps Research Institute, 10550 N.Torrey Pines Road, La Jolla, CA 92037, USA

*Departments of Cell and Molecular Biology, The Scripps Research Institute, 10550 N.Torrey Pines Road, La Jolla, CA 92037, USA

Publication History

  1. Published Online: 7 OCT 2008
  2. Published Print: 14 JAN 2005

Book Series:

  1. Novartis Foundation Symposia

Book Series Editors:

  1. Novartis Foundation

ISBN Information

Print ISBN: 9780470093733

Online ISBN: 9780470093764

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Keywords:

  • integral membrane proteins;
  • Multidimensional Protein Identification Technology (MudPIT);
  • subtractive proteomics approach;
  • microsomal membrane (MM) fraction;
  • nuclear envelope transmembrane proteins (NETs);
  • candidate dystrophy genes;
  • novel putative NETs;
  • laminopathies

Summary

Lamin A and some integral membrane proteins of the nuclear envelope (NE) have been linked to human diseases, mostly dystrophies. To comprehensively identify integral membrane proteins specific to the nuclear envelope, we have carried out a subtractive proteomics analysis of NEs isolated from rodent liver using Multidimensional Protein Identification Technology (MudPIT). An NE fraction and a nucleus-depleted membrane fraction were separately analyzed by MudPIT and proteins appearing in both fractions were ‘subtracted’ from the NE fraction. This identified 67 novel putative NE transmembrane proteins in addition to the 13 that had been previously characterized. Most or all of the new proteins we identified are likely to be bona fideNETransmembrane proteins (NETs), since all eight of the first group of proteins we tested in a cell transfection assay target to the NE. Moreover, five of the eight NETs remained associated with the nuclear periphery after extraction with Triton-X100, suggesting an association with the nuclear lamin polymer. 27 of the proteins occur in chromosomal regions where 18 different human dystrophies have been mapped, making these proteins disease candidates. We have analysed the expression of these proteins using transcriptome databases, providing direction for future functional analysis of these novel proteins.