Journal article
An accumulation of non-farnesylated prelamin A causes cardiomyopathy but not progeria
Human molecular genetics, Vol.19(13), pp.2682-2694
07/01/2010
DOI: 10.1093/hmg/ddq158
PMCID: PMC2883346
PMID: 20421363
Abstract
Lamin A is formed from prelamin A by four post-translational processing steps—farnesylation, release of the last three amino acids of the protein, methylation of the farnesylcysteine and the endoproteolytic release of the C-terminal 15 amino acids (including the farnesylcysteine methyl ester). When the final processing step does not occur, a farnesylated and methylated prelamin A accumulates in cells, causing a severe progeroid disease, restrictive dermopathy (RD). Whether RD is caused by the retention of farnesyl lipid on prelamin A, or by the retention of the last 15 amino acids of the protein, is unknown. To address this issue, we created knock-in mice harboring a mutant
Lmna
allele (
Lmna
nPLAO
) that yields exclusively non-farnesylated prelamin A (and no lamin C). These mice had no evidence of progeria but succumbed to cardiomyopathy. We suspected that the non-farnesylated prelamin A in the tissues of these mice would be strikingly mislocalized to the nucleoplasm, but this was not the case; most was at the nuclear rim (indistinguishable from the lamin A in wild-type mice). The cardiomyopathy could not be ascribed to an absence of lamin C because mice expressing an otherwise identical knock-in allele yielding only wild-type prelamin A appeared normal. We conclude that lamin C synthesis is dispensable in mice and that the failure to convert prelamin A to mature lamin A causes cardiomyopathy (at least in the absence of lamin C). The latter finding is potentially relevant to the long-term use of protein farnesyltransferase inhibitors, which lead to an accumulation of non-farnesylated prelamin A.
Details
- Title: Subtitle
- An accumulation of non-farnesylated prelamin A causes cardiomyopathy but not progeria
- Creators
- Brandon S.J Davies - ,Richard H Barnes II - ,Yiping Tu - ,Shuxun Ren - andDouglas A Andres - University of KentuckyH. Peter Spielmann - University of KentuckyJan Lammerding - Brigham and Women's Hospital/Harvard Medical SchoolYibin Wang - ,Stephen G Young - David Geffen School of Medicine, University of CaliforniaLoren G Fong - ,
- Resource Type
- Journal article
- Publication Details
- Human molecular genetics, Vol.19(13), pp.2682-2694
- Publisher
- Oxford University Press
- DOI
- 10.1093/hmg/ddq158
- PMID
- 20421363
- PMCID
- PMC2883346
- ISSN
- 0964-6906
- eISSN
- 1460-2083
- Language
- English
- Date published
- 07/01/2010
- Academic Unit
- Fraternal Order of Eagles Diabetes Research Center; Biochemistry and Molecular Biology
- Record Identifier
- 9984024559702771
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