Molecular Neurobiology

, Volume 47, Issue 1, pp 290–301

Nuclear Lamins in the Brain — New Insights into Function and Regulation


DOI: 10.1007/s12035-012-8350-1

Cite this article as:
Jung, HJ., Lee, J.M., Yang, S.H. et al. Mol Neurobiol (2013) 47: 290. doi:10.1007/s12035-012-8350-1


The nuclear lamina is an intermediate filament meshwork composed largely of four nuclear lamins — lamins A and C (A-type lamins) and lamins B1 and B2 (B-type lamins). Located immediately adjacent to the inner nuclear membrane, the nuclear lamina provides a structural scaffolding for the cell nucleus. It also interacts with both nuclear membrane proteins and the chromatin and is thought to participate in many important functions within the cell nucleus. Defects in A-type lamins cause cardiomyopathy, muscular dystrophy, peripheral neuropathy, lipodystrophy, and progeroid disorders. In contrast, the only bona fide link between the B-type lamins and human disease is a rare demyelinating disease of the central nervous system — adult-onset autosomal-dominant leukoencephalopathy, caused by a duplication of the gene for lamin B1. However, this leukoencephalopathy is not the only association between the brain and B-type nuclear lamins. Studies of conventional and tissue-specific knockout mice have demonstrated that B-type lamins play essential roles in neuronal migration in the developing brain and in neuronal survival. The importance of A-type lamin expression in the brain is unclear, but it is intriguing that the adult brain preferentially expresses lamin C rather than lamin A, very likely due to microRNA-mediated removal of prelamin A transcripts. Here, we review recent studies on nuclear lamins, focusing on the function and regulation of the nuclear lamins in the central nervous system.


Nuclear lamina Brain development A-type lamins B-type lamins Differential gene expression 

Copyright information

© Springer Science+Business Media New York 2012

Authors and Affiliations

  1. 1.Molecular Biology InstituteUniversity of California–Los AngelesLos AngelesUSA
  2. 2.Department of Medicine, David Geffen School of MedicineUniversity of California–Los AngelesLos AngelesUSA
  3. 3.Department of Human Genetics, David Geffen School of MedicineUniversity of California–Los AngelesLos AngelesUSA
  4. 4.Los AngelesUSA

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