Transcription:
Definition: The process of synthesizing messenger RNA (mRNA) from a specific segment of DNA, which serves as a template.
Location: Takes place in the nucleus of eukaryotic cells.
Stages:
Initiation: A region called a promoter triggers the start of transcription.
Elongation: RNA polymerase unwinds the DNA and synthesizes mRNA by aligning complementary nucleotides (A, C, G, U) with the DNA template.
Termination: A terminator sequence signals the end of transcription, causing mRNA to fold and detach from the gene.
Post-Transcriptional Modifications: The pre-mRNA undergoes splicing where introns (non-coding regions) are removed and exons (coding regions) are joined together before exiting the nucleus.
Translation:
Definition: The process of interpreting the mRNA sequence into a specific amino acid chain (polypeptide), ultimately forming a protein.
Location: Takes place in the cytoplasm, primarily at ribosomes.
Stages:
Initiation: The ribosome subunits bind to the mRNA at the start codon, preparing for translation.
Elongation: Transfer RNA (tRNA) brings the appropriate amino acids based on the codons of mRNA, and ribosomes catalyze the formation of peptide bonds between amino acids.
Termination: A stop codon on the mRNA signals the end of translation, resulting in the release of the newly synthesized polypeptide chain.
Components Involved: Ribosomal RNA (rRNA) forms the structure of ribosomes, while tRNA delivers the respective amino acids matched to the codons on the mRNA.
Endocytosis: Process of a cell ingesting material by enveloping it in a portion of its cell membrane and pinching off to form an intracellular vesicle.
Vesicle: Membranous sac (spherical organelle) bounded by a lipid bilayer membrane.
Types of Endocytosis:
Phagocytosis (“cell eating”): Ingests large particles (e.g., immune cells phagocytizing pathogens).
Pinocytosis (“cell drinking”): Brings fluid with dissolved substances into the cell.
Receptor-mediated Endocytosis: Selective process where surface receptors bind specific ligands and endocytose them.
Example: Iron is endocytosed by red blood cells via transferrin receptors.
Exocytosis: Process of exporting material out of the cell using vesicular transport.
Involves packaging substances into membrane-bound vesicles within the cell.
When the vesicle membrane fuses with the cell membrane, it releases contents into interstitial fluid, becoming part of the cell membrane.
Examples: Secretion of digestive enzymes by stomach and pancreas cells; endocrine cells secrete hormones; certain immune cells secrete histamine.
Cell division is prevalent in body cells, except for some (e.g., gametes, red blood cells, neurons, muscle cells).
Somatic cells (body cells) divide regularly and have 2 copies of each chromosome (diploid).
Sequence of events from cell creation to division, generating two new cells.
Composed of two main phases:
Interphase: Non-dividing phase, most cells spend their time here.
Mitosis and Cytokinesis: Division of genetic material and cytoplasm.
G1 Phase (Gap 1):
Cell growth and normal metabolic functions.
S Phase (Synthesis):
DNA replication, doubling the amount of DNA.
G2 Phase (Gap 2):
Final preparations for mitosis; growth continues.
G0 Phase:
Resting phase; cells may stop dividing temporarily or permanently.
During S phase, DNA doubles; resulting chromosomes consist of sister chromatids.
Each chromosome has a centromere that bounds sister chromatids.
Mitosis lasts 1-2 hours and includes four stages:
Prophase:
Chromatin condenses into visible chromosomes.
Nucleolus disappears; nuclear envelope disassembles.
Metaphase:
Sister chromatids align along the metaphase plate.
Anaphase:
Sister chromatids separate and are pulled to opposite ends.
Telophase:
Two new nuclei form at each end; chromosomes de-condense.
Cytokinesis:
Division of cytoplasm and formation of two new cells; cleavage furrow forms.
Regulation of the cell cycle is crucial for health; deficiencies can lead to cancer.
Control systems use checkpoints to signal readiness for progression:
Cyclins and Cyclin-Dependent Kinases (CDKs) determine progression through checkpoints.
Specific checkpoints at G1, G2, and during mitosis ensure proper sequence of events and readiness.
Uncontrolled cell division can lead to tumors/cancer.
Tumors are classified as benign (non-threatening) or malignant (capable of damaging tissues).
Cancerous cells may go undetected but can proliferate and spread if regulation mechanisms fail.