Association of progerin-interactive partner proteins with lamina proteins: Mel18 is associated with emerin in HGPS.

WN Ju, WT Brown, N Zhong - Beijing da xue xue bao. Yi xue ban …, 2009 - europepmc.org
Beijing da xue xue bao. Yi xue ban= Journal of Peking University …, 2009europepmc.org
Objective The Hutchinson-Gilford progeria syndrome (HGPS or progeria) is a childhood
disorder with features of premature aging and is caused by mutations in the lamin A gene
resulting in the production of an abnormal protein, termed progerin. To investigate the
underlying pathogenic mechanism, we studied the nuclear co-localization and association
of progerin interactive partner proteins (PIPPs) with lamina proteins. Methods Both wild-type
(WT) and progeria fibroblasts were studied by various methods including confocal …
Objective
The Hutchinson-Gilford progeria syndrome (HGPS or progeria) is a childhood disorder with features of premature aging and is caused by mutations in the lamin A gene resulting in the production of an abnormal protein, termed progerin. To investigate the underlying pathogenic mechanism, we studied the nuclear co-localization and association of progerin interactive partner proteins (PIPPs) with lamina proteins.
Methods
Both wild-type (WT) and progeria fibroblasts were studied by various methods including confocal microscopy, immunoprecipitation and Western blot.
Results
All PIPPs discovered so-far co-localized with lamin A/C. In addition, the PIPPs were selectively associated with lamina proteins. An increased immunofluorescent staining signal was found for Mel18 in HGPS as compared to WT cells. An association of Mel18 with emerin was observed in HGPS, but not in WT cells.
Conclusion
Based on these findings, we propose that PIPPs, along with associated lamina proteins may form a pathogenic progerin-containing protein complex.
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