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Nucleus. 2010 Nov-Dec;1(6):513-25. doi: 10.4161/nucl.1.6.13512. Epub 2010 Sep 3.

Identification of differential protein interactors of lamin A and progerin.

Author information

1
Center for Heart Failure Research, Cardiovascular Research Institute Maastricht, The Netherlands.

Abstract

The nuclear lamina is an interconnected meshwork of intermediate filament proteins underlying the nuclear envelope. The lamina is an important regulator of nuclear structural integrity as well as nuclear processes, including transcription, DNA replication and chromatin remodeling. The major components of the lamina are A- and B-type lamins. Mutations in lamins impair lamina functions and cause a set of highly tissue-specific diseases collectively referred to as laminopathies. The phenotypic diversity amongst laminopathies is hypothesized to be caused by mutations affecting specific protein interactions, possibly in a tissue-specific manner. Current technologies to identify interaction partners of lamin A and its mutants are hampered by the insoluble nature of lamina components. To overcome the limitations of current technologies, we developed and applied a novel, unbiased approach to identify lamin A-interacting proteins. This approach involves expression of the high-affinity OneSTrEP-tag, precipitation of lamin-protein complexes after reversible protein cross-linking and subsequent protein identification by mass spectrometry. We used this approach to identify in mouse embryonic fibroblasts and cardiac myocyte NklTAg cell lines proteins that interact with lamin A and its mutant isoform progerin, which causes the premature aging disorder Hutchinson-Gilford progeria syndrome (HGPS). We identified a total of 313 lamina-interacting proteins, including several novel lamin A interactors, and we characterize a set of 35 proteins which preferentially interact with lamin A or progerin.

KEYWORDS:

Hutchinson-Gilford progeria syndrome; lamin A; laminopathies; mass spectrometry; oneSTrEP pull-down; progerin; protein interactions

PMID:
21327095
PMCID:
PMC3027055
DOI:
10.4161/nucl.1.6.13512
[Indexed for MEDLINE]
Free PMC Article

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