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PMID: 12958361 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Nuclear membrane proteins with potential disease links found by subtractive proteomics.

Science (New York, N.Y.) ·Vol. 301 ·No. 5638 ·2003-09-05 ·Pages 1380-2

Schirmer EC, Florens L, Guan T, Yates JR, Gerace L

Abstract

To comprehensively identify integral membrane proteins of the nuclear envelope (NE), we prepared separately NEs and organelles known to cofractionate with them from liver. Proteins detected by multidimensional protein identification technology in the cofractionating organelles were subtracted from the NE data set. In addition to all 13 known NE integral proteins, 67 uncharacterized open reading frames with predicted membrane-spanning regions were identified. All of the eight proteins tested targeted to the NE, indicating that there are substantially more integral proteins of the NE than previously thought. Furthermore, 23 of these mapped within chromosome regions linked to a variety of dystrophies.

MeSH Terms
Algorithms Animals Cell Fractionation Chromosome Mapping DNA, Complementary Genetic Diseases, Inborn/genetics Genetic Linkage Humans Liver/chemistry,ultrastructure Membrane Proteins/analysis,genetics,isolation & purification Mice Mice, Inbred Strains Nuclear Envelope/chemistry Nuclear Proteins/analysis,genetics,isolation & purification Open Reading Frames Protein Structure, Tertiary Proteomics Rats Rats, Sprague-Dawley
Chemicals
DNA, Complementary Membrane Proteins Nuclear Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Schirmer Eric C
Department of Cell Biology, Scripps Research Institute, La Jolla, CA 92037, USA.
Florens Laurence
Guan Tinglu
Yates John R
Gerace Larry
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
1095-9203
Published
2003-09-05
Pages
1380-2
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIGMS NIH HHS · F32 GM19085 · United States
NIGMS NIH HHS · GM28521 · United States
NCRR NIH HHS · RR11823 · United States
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