Nucleus and Endomembrane System Notes
3.4 Nucleus and Endomembrane System
Learning Outcomes
Describe the structure of the nucleus and explain its role as the storage place of genetic information.
Summarize the functions of the organelles of the endomembrane system.
Explain the role and location of the ribosomes.
Nucleus
Contains genetic instructions necessary for the production of proteins involved in most cellular functions.
Presence of a nucleus is a defining characteristic of eukaryotic cells (Fig. 3.13).
Function: stores genetic information as long chains of DNA.
Chromatin
Combination of DNA molecules and proteins.
Surrounded by nucleoplasm, a semifluid medium with different pH and composition from the cytoplasm.
During cell division, chromatin coils tightly to form visible, long, linear structures called chromosomes.
Uncoiled, individual chromosomes cannot be distinguished.
Appears grainy in electron micrographs.
Chromosomes are responsible for transmitting genetic information from one generation to the next (Section 19.1).
Genes: segments of DNA that contain information for the production of specific proteins.
Proteins determine a cell's specificity.
Every cell contains the same genes, but cells vary in which genes are turned on and off.
Nucleolus
Dark region of chromatin within the nucleus.
Site of ribosomal RNA (rRNA) production.
rRNA joins with proteins to form the subunits of ribosomes.
Nuclear Envelope
Double membrane separating the nucleus from the cytoplasm.
Continuous with the endoplasmic reticulum.
Nuclear pores allow passage of ribosomal subunits out of the nucleus and proteins into the nucleus.
Ribosomes
Organelles composed of proteins and RNA.
Site of protein synthesis.
Attached to the endoplasmic reticulum or free within the cytoplasm (singly or in groups called polyribosomes).
Proteins synthesized at ribosomes attached to the endoplasmic reticulum have different destinations than those manufactured by free ribosomes.
Endomembrane System
Consists of the nuclear envelope, endoplasmic reticulum, Golgi apparatus, lysosomes, and vesicles (tiny membranous sacs; Fig. 3.14).
Compartmentalizes the cell, restricting chemical reactions to specific regions.
Vesicles transport molecules from one part of the system to another.
Endoplasmic Reticulum (ER)
Two portions:
Rough ER: Studded with ribosomes on the side of the membrane facing the cytoplasm (Fig. 3.13).
Proteins synthesized at these ribosomes enter the interior of the ER.
Some proteins are incorporated into the plasma membrane (e.g., channel proteins).
Others are packed into vesicles and sent to the Golgi apparatus for additional processing and modifications.
Smooth ER: Continuous with the rough ER, but without attached ribosomes.
Synthesizes phospholipids and other lipids that occur in membranes.
Performs various other functions depending on the cell type.
Example: Produces testosterone in the testes.
Example: Detoxifies compounds (e.g., drugs) in the liver.
Forms transport vesicles in which large molecules are transported to other parts of the cell.
Vesicles often travel to the plasma membrane or the Golgi apparatus.
Golgi Apparatus
Named for Camilo Golgi, who discovered it in the late 19th century.
Consists of a stack of slightly curved saccules (resembling a stack of pancakes).
Proteins and lipids received from the ER are modified.
A chain of sugars (carbohydrates) may be added, forming glycoproteins and glycolipids.
These are incorporated into the plasma membrane to serve in cellular identification.
Vesicles leaving the Golgi apparatus move to other parts of the cell.
Some vesicles proceed to the plasma membrane, where they discharge their contents.
Functions: processing, packaging, and secretion.
Lysosomes
Membranous sacs produced by the Golgi apparatus that contain hydrolytic enzymes.
Found in all cells but particularly numerous in white blood cells.
When a lysosome fuses with an endocytic vesicle, its contents are digested by hydrolytic enzymes into simpler subunits, which then enter the cytoplasm.
Autodigestion: parts of a cell may be broken down by the lysosomes.
Some human diseases are caused by the lack of a particular enzyme in the lysosome.
Tay-Sachs disease: caused by an inactive enzyme in the lysosomes, leading to undigested lipids collecting in nerve cells, causing developmental problems and death in early childhood.