Ядрышко

The nucleolus is the site of ribosomal RNA (rRNA) transcription, processing, and ribosome assembly, earning it the nickname 'ribosome producing factory.' As a membraneless organelle, it aggregates rRNA genes, small nucleolar ribonucleoproteins (snoRNPs), rRNA-processing enzymes, assembly factors, and partially assembled ribosomes to coordinate ribosome biogenesis.

Nucleolar organizer regions (NORs) are chromosomal regions containing clusters of rRNA genes that serve as the organizational foundation for nucleolus formation. In eukaryotes, three rRNA genes—18S, 5.8S, and 28S—are encoded by a single transcription unit that is tandemly repeated in arrays across one or several chromosomes, with NOR regions anchoring nucleolar assembly.

During interphase, the nucleolus exists as a single large entity reflecting high ribosome production. As cells enter mitosis, chromosomes condense and the nucleolus fragments into smaller nucleoli that gradually decrease in size and disappear. During telophase, tiny nucleoli emerge and progressively merge through nucleolar fusion, coalescing into a single large nucleolus as the cell re-enters interphase.

The nucleolus comprises three distinct regions: the fibrillar center containing rRNA genes transcribed at its boundary with the dense fibrillar component; the dense fibrillar component where rRNA processing begins; and the granular component where processed rRNAs assemble with ribosomal proteins and are exported to the cytoplasm as pre-ribosomal subunits.

Nucleolus size correlates with ribosome production demand and cellular differentiation. In aggressive breast cancer cells, the nucleolus enlarges by 30% during tumor progression due to heightened ribosomal synthesis. Conversely, in lymphocytes completing differentiation, ribosome synthesis terminates and nucleoli shrink to tiny fibrillar structures, allowing identification of cell differentiation states from nucleolar morphology.

Beyond rRNA genes, the nucleolus contains small nucleolar ribonucleoproteins (snoRNPs), rRNA-processing enzymes, assembly factors, and partially assembled ribosomes. These components work together to facilitate rRNA transcription, process precursor rRNAs into mature forms, and assemble them with ribosomal proteins into functional ribosomal subunits.

Protein synthesis requirements fluctuate dramatically as cells transition between interphase and mitosis. Synthesis is high during interphase when cells are actively growing and preparing for division, becomes low during most of M phase when cell division machinery takes priority, and increases again as cells re-enter interphase, directly driving changes in nucleolus size and ribosome production.