The centrosome, with its constituent centrioles, constitutes the microtubule-organizing center of the cell. The main purpose of this center is to anchor the microtubules at one end, and prevent this end from depolymerizing. The centrosome serves to provide direction for microtubules and is a control center for many intracellular movement and shuttling processes. For a vesicle of neurotransmitter to move across the soma, down the axon, and to the synapse, the centrosome must coordinate the assembly of the microtubule structure that carries the vesicle.

The nucleus contains the genetic code of each individual, and the mitochondria is a semiautonomous organelle that contains mitochondrial DNA (passed through the maternal line). mDNA codes specifically for the proteins involved in the electron transport chain, allowing for their implantation in the inner mitochondrial membrane without having to be synthesized elsewhere in the cell.

The nucleolus, which is located in the nucleus, is directly involved in the production of rRNA. The rRNA composes the ribosome structure, and is directly involved in synthesis of protein.

The nucleolus is a structure within the nucleus, and is the site of rRNA synthesis. The individual subunits of the ribosome assemble in the nucleus, are exported through the nuclear pores, and are finally brought together into function units in the cytosol.

The nucleus contains DNA, the lysosome has enzymes that break down molecules, and the mitochondria are the site of ATP production. The rough endoplasmic reticulum has a surface that is studded with ribosomes, and works in coordination with these ribosomes to modify proteins after synthesis.

The nucleolus is a special structure within the nucleus that is responsible for the transcription of rRNA genes and the formation of ribosomal subunits. Transcription of mRNA, tRNA, and miRNA occurs in other regions of the nucleus. Nuclear pores are highly regulated structures that allow for import and export of materials in the nucleus.

The nucleolus is located inside of the eukaryotic nucleus. It is responsible for the creation of the ribosomal subunits, as well as the rRNA that will be incorporated into the ribosomes. Ribosomal subunits are synthesized in the nucleolus and exported to the cytoplasm, where they can be assembled into functional translation complexes.

The rough endoplasmic reticulum contains ribosomes embedded in its membrane and is responsible for synthesizing certain proteins. The smooth endoplasmic reticulum is responsible for metabolizing toxins and synthesizing lipids. The Golgi apparatus plays a key role in protein sorting, packaging, and transport within vesicles.

The only option that cannot pass the nuclear envelope from the nucleus is mitochondria. Mitochondria range from 0.5-1.0 micrometers, while nuclear pore complexes are about 120 nanometers in diameter. That being said, mitochondria are too large to fit through a nuclear pore complex.

Ribosomes, pre-mRNA, and proteins (such as transcription factors) are all perfectly capable of moving through the nuclear pore complexes, given the appropriate environment.

Ribosomal subunits are synthesized in the nucleolus, which is located inside the nucleus. The nucleus is surrounded by two membranes, known as the nuclear envelope, studded with large nuclear pore complexes. Import and export of substances through the pore complexes is highly regulated. Nuclei are supported by what is known as a nuclear lamina. This nuclear lamina is composed of intermediate filaments that provide support and structure for the nucleus.

It has recently been shown that chromosomes are not randomly distributed through the nucleus. Chromosomes occupy specific regions of the nucleus, which are currently referred to as "nuclear territories". 

Lamins are intermediate filaments found inside the nucleus. Lamins attach to nuclear proteins and form a layer underneath the nuclear envelope (nuclear membrane) called the nuclear lamina. The nuclear lamina functions to position nuclear pores to let molecules pass between the cytoplasm and the nucleoplasm. It also functions to break and resynthesize the nuclear envelope during mitosis. Recall that the nuclear envelope is broken down during the prophase of mitosis; therefore, lack of lamins will directly affect this phase of mitosis.

In addition to the aforementioned functions, lamins are also involved in maintaining the integrity of chromosomes. Lack of lamins will decrease the stability of chromosomes. Cholesterol and most other lipids are synthesized in the smooth endoplasmic reticulum; therefore, lamins are irrelevant to cholesterol synthesis. Since they are involved in positioning nuclear pores, lamins are important for exchanging molecules between the nucleus and cytoplasm. Lack of lamins will decrease this trafficking.

The central dogma of molecular biology states that genetic information flows from DNA to RNA to protein. The first step is the replication of the genetic material, DNA, during the S phase of the cell cycle. The second step is the conversion of DNA to RNA. This process is called transcription and involves several enzymes that convert the DNA to mRNA. The final step is called translation, which involves the conversion of mRNA to protein.

DNA replication and transcription occur inside the nucleus because the enzymes required to carry out these processes are found in the nucleoplasm. Translation, on the other hand, occurs on ribosomes in the cytoplasm or on ribosomes on the rough endoplasmic reticulum.