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The nuclear lamina consists of two components, lamins and nuclear lamin-associated membrane proteins. The lamins are type V intermediate filaments which can be categorized as either A-type (lamin A, C) or B-type (lamin B 1, B 2) according to homology of their DNA sequences, biochemical properties and cellular localization during the cell cycle.
The nuclear envelope is made up of two lipid bilayer membranes, an inner nuclear membrane and an outer nuclear membrane. These membranes are connected to each other by nuclear pores. Two sets of intermediate filaments provide support for the nuclear envelope. An internal network forms the nuclear lamina on the inner nuclear membrane. [7]
Nuclear lamins interact with inner nuclear membrane proteins to form the nuclear lamina on the interior of the nuclear envelope. Lamins have elastic and mechanosensitive properties, and can alter gene regulation in a feedback response to mechanical cues. [1] Lamins are present in all animals but are not found in microorganisms, plants or fungi.
The nuclear lamina consist of a two-dimensional matrix of proteins located next to the inner nuclear membrane. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated.
The nuclear pore complex (NPC), is a large protein complex giving rise to the nuclear pore. Nuclear pores are found in the nuclear envelope that surrounds the cell nucleus in eukaryotic cells . The nuclear envelope is studded by a great number of nuclear pores that give access to various molecules, to and from the nucleoplasm and the cytoplasm.
Laminin-1 EHS laminin α1β1γ1 Laminin-111: Laminin-2 Merosin α2β1γ1 Laminin-211 Laminin-3 S-laminin α1β2γ1 Laminin-121 Laminin-4 S-merosin α2β2γ1 Laminin-221 Laminin-5 / Laminin-5A Kalinin, epiligrin, nicein, ladsin α3Aβ3γ2 Laminin-332 / Laminin-3A32 Laminin-5B α3Bβ3γ2 Laminin-3B32 Laminin-6 / Laminin-6A K-laminin α3Aβ1γ1
[1] [5] Animal intermediate filaments are subcategorized into six types based on similarities in amino acid sequence and protein structure. [6] Most types are cytoplasmic, but one type, Type V is a nuclear lamin. Unlike microtubules, IF distribution in cells shows no good correlation with the distribution of either mitochondria or endoplasmic ...
In this model, proteins diffuse freely from the ER to the inner nuclear membrane, where association with nuclear lamina or chromatin immobilizes them. [9] A nuclear localisation signal is not sufficient to target a protein to the INM, and the N-terminal domain of LBR cannot translocate into the nuclear lumen if its size is increased from 22 to ...