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Nuclear envelope encloses a viscous, amorphous mass of material. Nucleoli are irregularly shaped electron-dense structures that function in the synthesis of ribosomal RNA. Nuclear matrix is the network of fibres found throughout a cell nucleus. It is somewhat analogous to the cell cytoskeleton. Nuclear lamina provides mechanical support to the nuclear envelope. It also serves as a site of attachment for chromatin fibres at the nuclear
Nuclear envelope encloses a viscous, amorphous mass of material. Nucleoli are irregularly shaped electron-dense structures that function in the synthesis of ribosomal RNA. Nuclear matrix is the network of fibres found throughout a cell nucleus. It is somewhat analogous to the cell cytoskeleton. Nuclear lamina provides mechanical support to the nuclear envelope. It also serves as a site of attachment for chromatin fibres at the nuclear
Nuclear envelope encloses a viscous, amorphous mass of material. Nucleoli are irregularly shaped electron-dense structures that function in the synthesis of ribosomal RNA. Nuclear matrix is the network of fibres found throughout a cell nucleus. It is somewhat analogous to the cell cytoskeleton. Nuclear lamina provides mechanical support to the nuclear envelope. It also serves as a site of attachment for chromatin fibres at the nuclear
2. Robert brown (1831) 3. Genetic material 4. Uninucleate or multinucleate 5. Spherical , multi lobed (polymorph nuclear leukocyte) 6. Mostly central position 7. Five components i) Nuclear envelope encloses a viscous, amorphous mass of material and forms a boundary between the nucleus and cytoplasm. ii) Nucleolus/ nucleoli - which are irregularly shaped electron-dense structures that function in the synthesis of ribosomal RNA and the assembly of ribosomes. iii) Chromosomes which are present as highly extended nucleoprotein fibres, termed chromatin; iv) Nucleoplasm - the fluid substance in which the solutes of the nucleus are dissolved v) Nuclear matrix- the nuclear matrix is the network of fibres found throughout the inside of a cell nucleus and is somewhat analogous to the cell cytoskeleton
The Nuclear Envelope
The separation of a cells genetic material from the surrounding cytoplasm Double concentric membrane, arranged parallel to one another and separated by 10 to 50 nm space (perinuclear space) These membranes contain upwards of 60 distinct transmembrane proteins, including a number of species that link the outer nuclear membrane with elements of the cytoskeleton. Each layer is a phospholipid bilayer, permeable to small non polar compounds. Inner and outer nuclear membranes are fused at sites forming circular pores that contain complex assemblies of proteins. The outer membrane is generally studded with ribosomes and is continuous with the membrane of the rough endoplasmic reticulum. Perinuclear space is continuous with the ER lumen The inner surface is bound by specific integral membrane proteins to a thin filamentous meshwork nuclear lamina Nuclear lamina provides mechanical support to the nuclear envelope, serves as a site of attachment for chromatin fibres at the nuclear periphery and has a poorly understood role in DNA replication and transcription. The filaments of the nuclear lamina are approximately 10 nm in diameter and composed of polypeptides, called lamins. Lamins are members of the same superfamily of polypeptides that assemble into the 10-nm intermediate filaments of the cytoplasm The disassembly of the nuclear lamina prior to mitosis is induced by phosphorylation of the lamins. The Nuclear Pore Complex and Its Role in Nucleocytoplasmic Trafficking
Nuclear pores contain a doughnut-shaped structure called the nuclear pore
complex (NPC) that straddles the nuclear envelope, projecting into both the cytoplasm and nucleoplasm. The NPC is a huge, supramolecular complex15 to 30 times the mass of a ribosomethat exhibits octagonal symmetry due to the eightfold repetition of a number of structures. (Eight spokes surrounding a central channel) Both membranes fuse at nuclear pore NPCs contain only about 30 (50-100) different proteins, called nucleoporins. Each nucleoporin is present in multiple copies8, 16, or 32 in numberin keeping with the octagonal symmetry of the structure. At the heart of the NPC is a central channel, which is surrounded by a ring of nucleoporins whose rearrangements can change the diameter of the opening from about 20 to 40 nm. The NPC is not a static structure - many of its component proteins are replaced with new copies over a time period of seconds to minutes. Recent studies suggest that this dynamic exchange of nucleoporins may play a role in activating the transcription of chromatin that is associated with the NPC.