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Cell Cycle, DNA Replication, and Protein Synthesis: Study Notes for Anatomy & Physiology

스터디 가이드 - 스마트 노트

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Cells: The Living Units

Cell Cycle

The cell cycle describes the series of events that cells undergo from their formation to their division. It is essential for growth, maintenance, and repair in multicellular organisms.

  • Interphase: The period between cell formation and cell division, where the cell grows and performs its functions. Nuclear material is called chromatin.

  • Mitotic Phase: The phase where the cell divides into two daughter cells.

Diagram of the cell cycle with phases and checkpoints

Interphase Subphases

  • G1 (Gap 1): Vigorous growth and metabolism. Cells that permanently cease dividing are said to be in the G0 phase.

  • S (Synthetic): DNA replication occurs.

  • G2 (Gap 2): Preparation for cell division.

Cell in interphase showing chromatin and centrosomes

DNA Replication

DNA replication is the process by which a cell copies its DNA before division, ensuring each daughter cell receives a complete set of genetic instructions.

  • Replication Bubbles: DNA helices are separated, forming bubbles with replication forks at each end.

  • DNA Polymerase: Adds nucleotides at the RNA primer, synthesizing one leading strand continuously and one lagging strand discontinuously.

  • DNA Ligase: Splices short segments of the lagging strand together.

  • Semiconservative Replication: Each new DNA molecule consists of one old and one new strand.

DNA replication showing leading and lagging strands

Cell Division

Cell division is crucial for growth, tissue repair, and reproduction. There are two main types:

  • Meiosis: Produces gametes (sperm and egg cells).

  • Mitotic Cell Division: Produces clones for body growth and tissue repair. Occurs continuously in some cells (e.g., skin, intestinal lining), but not in most mature nervous, skeletal, or cardiac muscle cells.

Events of Cell Division

  • Mitosis: Division of the nucleus, ensuring each cell receives a copy of replicated DNA. Four stages: Prophase, Metaphase, Anaphase, Telophase.

  • Cytokinesis: Division of cytoplasm by cleavage furrow.

Cell cycle diagram with mitosis stages

Mitosis Stages

  • Prophase: Chromosomes become visible, centrosomes migrate, mitotic spindles form, nuclear envelope fragments. Early prophase showing mitotic spindle and chromosomes Late prophase showing spindle and nuclear envelope fragments

  • Metaphase: Chromosomes align at the cell equator (metaphase plate). Metaphase showing chromosomes aligned at metaphase plate

  • Anaphase: Centromeres split, chromatids become chromosomes, pulled toward poles. Anaphase showing daughter chromosomes moving to poles

  • Telophase: Chromosomes uncoil to form chromatin, new nuclear membranes form, nucleoli reappear, spindle disappears. Telophase and cytokinesis showing nuclear envelope and cleavage furrow

Control of Cell Division

Cell division is tightly regulated by internal and external signals.

  • "Go" Signals: Critical cell volume, growth factors, hormones, and contact inhibition.

  • Cyclins and Cdks: Regulatory proteins that accumulate during interphase and activate enzymes for division.

  • Checkpoints: G1 checkpoint (restriction point) is most important; G2 checkpoint requires MPF (M-phase promoting factor).

  • Repressor Genes: Inhibit cell division (e.g., P53 gene).

Protein Synthesis

DNA and Genes

DNA is the master blueprint for protein synthesis. A gene is a segment of DNA coding for one polypeptide. DNA bases are A (adenine), G (guanine), T (thymine), and C (cytosine).

  • Triplets: Three sequential DNA bases specify the coding for amino acids.

  • Exons: Coding segments of genes.

  • Introns: Noncoding segments.

Role of RNA

  • Messenger RNA (mRNA): Carries instructions from DNA to ribosomes.

  • Ribosomal RNA (rRNA): Structural component of ribosomes, helps translate mRNA.

  • Transfer RNA (tRNA): Binds amino acids and pairs with mRNA codons at ribosome.

Information flow from DNA gene to mRNA to protein structure

Steps of Protein Synthesis

  • Transcription: DNA information is coded in mRNA. Occurs in three phases:

    • Initiation: RNA polymerase binds to promoter, separates DNA strands.

    • Elongation: RNA polymerase adds complementary nucleotides.

    • Termination: RNA polymerase releases completed mRNA transcript.

  • Translation: mRNA is decoded to assemble polypeptides. Involves mRNAs, tRNAs, and rRNAs.

Stages of transcription: initiation, elongation, termination Transcription: RNA polymerase binding to promoter Transcription: initiation phase Transcription: elongation phase Transcription: termination phase

Genetic Code

The genetic code is based on three-base sequences (codons) on mRNA, each specifying an amino acid. Some amino acids are represented by more than one codon.

Genetic code table showing codons and corresponding amino acids

Translation: Sequence of Events

  • Initiation: Small ribosomal subunit binds to initiator tRNA and mRNA, scans for start codon. Large subunit attaches, forming functional ribosome.

  • Elongation:

    • Codon Recognition: tRNA binds complementary codon in A site.

    • Peptide Bond Formation: Amino acid in P site is bonded to amino acid in A site.

    • Translocation: tRNAs move one position: A → P; P → E.

  • Termination: Stop codon enters A site, release factor binds, polypeptide released, ribosome subunits separate.

Translation: elongation, peptide bond formation, translocation, termination Translation: initiation phase Translation: codon recognition Translation: peptide bond formation Translation: termination phase Translation: release of polypeptide Translation: summary of steps

Polyribosomes

A polyribosome is a complex of multiple ribosomes reading a single mRNA strand, producing multiple copies of the same protein.

Polyribosome arrays showing multiple ribosomes on mRNA

Role of Rough ER in Protein Synthesis

The rough endoplasmic reticulum (ER) is involved in processing proteins synthesized by ribosomes. The mRNA–ribosome complex is directed to the rough ER by a signal-recognition particle (SRP), where the protein enters the ER, may be modified, and is enclosed in a vesicle for transport to the Golgi apparatus.

Rough ER processing of proteins: SRP, receptor, vesicle formation SRP directs mRNA-ribosome complex to rough ER Polypeptide enters ER membrane pore Signal sequence removed, sugar groups added Protein released and folds into 3-D conformation Protein enclosed in vesicle for transport to Golgi

Summary: From DNA to Proteins

  • Complementary base pairing directs transfer of genetic information from DNA to protein.

  • DNA triplets → mRNA codons → tRNA anticodons → amino acid sequence.

  • Anticodon sequence is identical to DNA sequence except uracil replaces thymine.

Information transfer from DNA to RNA to polypeptide

Other Roles of DNA and Cell Regulation

Noncoding DNA Functions

  • Antisense RNA: Prevents translation of protein-coding RNA.

  • MicroRNA: Silences mRNAs from certain exons.

  • Riboswitches: Folded RNAs acting as switches to regulate protein synthesis.

Cytosolic Protein Degradation

  • Autophagy: Degradation of cytoplasmic bits and organelles by lysosomes.

  • Ubiquitins: Tag damaged or unneeded proteins for digestion by proteasomes.

Extracellular Materials

  • Body Fluids: Interstitial fluid, blood plasma, cerebrospinal fluid.

  • Cellular Secretions: Intestinal and gastric fluids, saliva, mucus, serous fluids.

  • Extracellular Matrix: Jellylike mesh of proteins and polysaccharides acting as "glue" to hold cells together.

Developmental Aspects of Cells

  • All cells contain the same DNA, but chemical signals channel cells into specific developmental pathways (cell differentiation).

Apoptosis and Cell Division Rates

  • Apoptosis: Programmed cell death, important for eliminating excess cells during development.

  • Hyperplasia: Increase in cell numbers when needed.

  • Atrophy: Decrease in cell size due to loss of stimulation or use.

Theories of Cell Aging

  • Wear and Tear Theory: Chemical insults and free radicals accumulate over time.

  • Mitochondrial Theory: Free radicals in mitochondria reduce energy production.

  • Immune System Disorders: Autoimmune responses and weakened immunity contribute to aging.

  • Genetic Theory: Cessation of mitosis and cell aging programmed into genes. Telomeres may determine cell division limits; telomerase lengthens telomeres in germ cells.

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