The nuclear lamina and its functions in the nucleus

Yosef Gruenbaum*, Robert D. Goldman, Ronit Meyuhas, Erez Mills, Ayelet Margalit, Alexandra Fridkin, Yaron Dayani, Miron Prokocimer, Avital Enosh

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

199 Scopus citations

Abstract

The nuclear lamina is a structure near the inner nuclear membrane and the peripheral chromatin. It is composed of lamins, which are also present in the nuclear interior, and lamin-associated proteins. The increasing number of proteins that interact with lamins and the compound interactions between these proteins and chromatin-associated proteins make the nuclear lamina a highly complex but also a very exciting structure. The nuclear lamina is an essential component of metazoan cells. It is involved in most nuclear activities including DNA replication, RNA transcription, nuclear and chromatin organization, cell cycle regulation, cell development and differentiation, nuclear migration, and apoptosis. Specific mutations in nuclear lamina genes cause a wide range of heritable human diseases. These diseases include Emery-Dreifuss muscular dystrophy, limb girdle muscular dystrophy, dilated cardiomyopathy (DCM) with conduction system disease, familial partial lipodystrophy (FPLD), autosomal recessive axonal neuropathy (Charcot-Marie-Tooth disorder type 2, CMT2), mandibuloacral dysplasia (MAD), Hutchison Gilford Progeria syndrome (HGS), Greenberg Skeletal Dysplasia, and Pelger-Huet anomaly (PHA). Genetic analyses in Caenorhabditis elegans, Drosophila, and mice show new insights into the functions of the nuclear lamina, and recent structural analyses have begun to unravel the molecular structure and assembly of lamins and their associated proteins.

Original languageAmerican English
Pages (from-to)1-62
Number of pages62
JournalInternational Review of Cytology
Volume226
DOIs
StatePublished - 2003

Bibliographical note

Funding Information:
We thank the Israel Science Foundation, Binational USA–Israel Binational Science Foundation, the National Austrian Bank, the Gruss Lipper Foundation Fellowship, and the Marine Biological Laboratory, Woods Hole, MA, for grant support (Y. Gruenbaum). We also thank the National Cancer Institute (number CA31760 to R. D. Goldman) for grant support.

Keywords

  • Apoptosis
  • DNA replication
  • Heterochromatin
  • Laminopathies
  • Lamins
  • Nuclear envelope
  • Nuclear lamina
  • Transcriptional regulation

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