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The LMNA gene encodes lamin A and lamin C, structural components of the nuclear lamina. The nuclear lamina of nuclear envelope (NE) is a scaffold, which provides structural and mechanical stability for the NE; it consists primarily of type V intermediate filament proteins (A-type and B-type lamins) and many inner nuclear membrane proteins.1 ,2 Interaction of lamins with heterochromatin and with transcriptional regulators suggests their important role in the maintenance of chromatin organisation and ingene expression.3 At the NE periphery, lamin precursors undergo a series of post-translational modifications. B-type lamins are permanently isoprenylated, whereas prelamin A loses its modification after incorporation into the lamina by lamin A-specific processing steps involving Zmpste24 endoprotease.4 ,5
The LMNA gene is located on chromosome 1q21.2–q21.3.6 Its coding region spans approximately 24 kb and contains 12 exons; alternative splicing within exon 10 gives rise to two different mRNAs that code for prelamin A and lamin C.7 Different diseases have been ascribed to mutations in this gene including these affecting skin, cardiac and/or skeletal muscles, nerves, fat tissue and bones.8 One of the diseases associated with the LMNA mutations is Hutchinson–Gilford progeria syndrome (HGPS), usually arising due to the de novo heterozygous single base change (GGC>GGT) in exon 11 creating an abnormal splice donor site and resulting in the production of truncated protein, progerin.9–12 HGPS is a very rare, fatal disorder characterised by postnatal growth retardation, midface hypoplasia, premature atherosclerosis, absence of subcutaneous fat, alopecia and generalised osteodysplasia with osteolysis and pathological fractures.9 ,10 ,13 The skin of children with HGPS has atrophic epidermis, dermal fibrosis (scleroderma-like with thickening, disorganisation and hyalinisation of collagen bundles), thin or absent hypodermis and a complete loss of skin appendages or decrease in number of sebaceous glands and hair …
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