Lamin A/C and polymeric actin in genome organization.

Mol Cells

Laboratory of Molecular Cytology and Cytometry, Institute of Biophysics, Academy of Sciences of the Czech Republic, Kralovopolska, Brno, Czech Republic.

Published: October 2008

In this work, we have studied the structural and functional linkage between lamin A/C, nuclear actin, and organization of chromosome territories (CTs) in mammary carcinoma MCF-7 cells. Selective down-regulation of lamin A/C expression led to disruption of the lamin A/C perinuclear layer and disorganization of lamin-bound emerin complexes at the inner nuclear membrane. The silencing of lamin A/C expression resulted in a decrease in the volume and surface area of chromosome territories, especially in chromosomes with high heterochromatin content. Inhibition of actin polymerization led to relaxation of the structure of chromosome territories, and an increase in the volumes and surface areas of the chromosome territories of human chromosomes 1, 2 and 13. The results show an important role of polymeric actin in the organization of the nuclei and the chromosome territories.

Download full-text PDF

Source

Publication Analysis

Top Keywords

lamin a/c
20
chromosome territories
20
polymeric actin
8
actin organization
8
a/c expression
8
lamin
5
chromosome
5
territories
5
a/c polymeric
4
actin
4

Similar Publications

The Dual Roles of Lamin A/C in Macrophage Mechanotransduction.

Cell Prolif

December 2024

Department of Orthodontics, Faculty of Medicine, Justus Liebig University, Giessen, Germany.

Cellular mechanotransduction is a complex physiological process that integrates alterations in the external environment with cellular behaviours. In recent years, the role of the nucleus in mechanotransduction has gathered increased attention. Our research investigated the involvement of lamin A/C, a component of the nuclear envelope, in the mechanotransduction of macrophages under compressive force.

View Article and Find Full Text PDF

Case Report: Concurrent pathogenic variants in the gene as a cause of sporadic partial lipodystrophy.

Front Genet

November 2024

Department of Nutrition, Diabetes and Metabolism, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.

Introduction: Inherited lipodystrophies are a group of rare diseases defined by severe reduction in adipose tissue mass and classified as generalized or partial. We report a non-familial (sporadic) case of partial lipodystrophy caused by a novel genetic mechanism involving closely linked pathogenic variants in the gene.

Methods: A female adult with partial lipodystrophy and her parents were evaluated for gene variants across the exome under different mendelian inheritance models (autosomal dominant, recessive, compound heterozygous, and X-linked) to find pathogenic variants.

View Article and Find Full Text PDF

Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare genetic condition characterized by features of accelerated aging, and individuals with HGPS seldom live beyond their mid-teens. The syndrome is commonly caused by a point mutation in the LMNA gene which codes for lamin A and its splice variant lamin C, components of the nuclear lamina. The mutation causing HGPS leads to production of a truncated, farnesylated form of lamin A referred to as "progerin.

View Article and Find Full Text PDF

Phosphorylation of Lamin A/C regulates the structural integrity of the nuclear envelope.

J Biol Chem

November 2024

MOE Key Laboratory for Cellular Dynamics, Center for Advanced Interdisciplinary Science and Biomedicine of IHM, Hefei National Research Center for Interdisciplinary Sciences at the Microscale, University of Science and Technology of China, Hefei, China; Anhui Key Laboratory of Cellular Dynamics and Chemical Biology, University of Science and Technology of China, Hefei, China. Electronic address:

Article Synopsis
  • Dynamic disassembly and reconstruction of the nuclear lamina are crucial for cell division, with CDK1 phosphorylation playing a key role in this process.
  • Mass spectrometry identified specific phosphorylation sites on Lamin A/C during mitosis, with mutations altering phosphorylation status affecting lamina structure and function.
  • Disruption of Lamin A phosphorylation led to nuclear abnormalities, highlighting its importance for nuclear envelope dynamics and maintaining genomic stability during the cell cycle.
View Article and Find Full Text PDF

The term limb-girdle muscular dystrophy (LGMD) refers to a variety of genetic neuromuscular disorders that typically affect the proximal muscles surrounding the hip and shoulder girdles. Despite having multiple genetic subtypes, these share similar clinical and imaging findings. Autosomal dominant forms are grouped under type 1, and autosomal recessive forms are grouped under type 2.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!