Introduces the concept of cell cycle and cell division.
Understanding images related to cell division is encouraged.
Overview of cell division processes.
Understand why cells divide: \
The necessity of cell division in living organisms.
Compare cell division purposes: \
Differences in prokaryotic and eukaryotic cells.
Single-celled organisms:
Reproduction (e.g., amoeba divides to form new organisms).
Multicellular organisms:
Growth and development (e.g., sand dollar embryo).
Tissue renewal (e.g., new blood cells from dividing bone marrow).
Repair (not explicitly mentioned but also inferred).
Replacement of dead cells.
During cell division, cells:
Duplicate their DNA.
Divide into two daughter cells.
Importance: Ensures genetic fidelity except in meiosis.
Introduces prokaryotic cell cycle dynamics.
Describe prokaryotic cell cycle: \
Explain triggers for cell division: \
Summarize binary fission process.
Binary fission: the process of asexual reproduction in prokaryotes.
Three phases:
Growth phase
Cell mass increases.
Chromosomal replication phase.
Separation phase
DNA and physical division of the bacterial cell.
Prokaryotic cells reproduce asexually via binary fission.
Results in two genetically identical daughter cells.
No genetic variation occurs.
Varies by organism from < 1/2 hr to several days.
Influenced by:
Environmental conditions
Cellular mass (size).
Surface area must support the cell's volume.
Prepares to explore eukaryotic cell division processes.
Three stages of interphase: \
Cytokinesis process explanation: \
Define G0 phase and its significance.
Identify cell cycle checkpoints.
Interphase, Mitotic phase, Karyokinesis, Cytokinesis
G1 phase, S phase, G2 phase, G0 phase, Quiescent, Senescent, Differentiated.
Two major phases:
Interphase
Mitotic phase
Highly conserved across all eukaryotes.
Quiescent:
Reversible, preparatory state before entering the cell cycle.
Senescent:
Non-replicating due to damage but performs normal functions.
Differentiated:
Terminally differentiated cells fulfilling main functions indefinitely.
G1 Phase: Initial growth and cell function.
S Phase: DNA replication.
G2 Phase: Prepares for mitosis.
Note: Chromatin is not condensed during interphase.
Karyokinesis (Mitosis):
Division of the nucleus into daughter nuclei.
Five stages: Prophase, Prometaphase, Metaphase, Anaphase, Telophase.
Cytokinesis:
Division of cytoplasm and organelles.
Deep dive into mitosis and cellular behavior.
Discuss stages of mitotic phase and chromosome behavior.
Explain functions of key proteins.
Prophase, Prometaphase, Metaphase, Anaphase, Telophase, Cleavage, Spindle apparatus, Centrioles, Microtubules, Astral microtubules, Polar microtubules, Kinetochore.
Prophase: Chromosomes condense; mitotic spindle forms.
Prometaphase: Nuclear envelope breaks down; kinetochores develop.
Metaphase: Alignment along the metaphase plate.
Anaphase: Sister chromatids are pulled apart.
Telophase: Chromosomes reach poles, nuclear envelope re-forms.
Cytokinesis: Cell splits into daughter cells.
Centrosomes serve as microtubule organizing centers, critical during mitosis.
Composed of polar, astral, and kinetochore microtubules originating from the centrosomes.
Nuclear envelope breaks down; chromosomes condense with help from condensin proteins.
Nuclear envelope disintegrates.
Kinetochores manifest at centromeres; spindle microtubules attach.
Chromosomes align on the metaphase plate with sister chromatids attached by cohesion proteins.
Sister chromatids separate as cohesion proteins break down.
Separated chromatids pulled to opposite poles.
Chromosomes de-condense; nuclear envelopes reform around each set.
Mitotic spindle disassembles.
Description of centrosomes, chromatin, and early mitotic spindle appearance.
Overview of components undergoing changes during mitosis.
Cleavage furrow forms: Plasma membrane contracts, pinching the cell into two.
Cell plate formation: Golgi vesicles create a dividing plate against the cell's center.
Emphasizes regulation during the cell cycle.
Identify cell cycle checkpoints and their significance.
Understand cancer development mechanisms.
Cancer, Proto-oncogenes, Oncogenes, Tumor suppressor genes.
Checkpoints prevent progression until necessary conditions are met.
Types of signals: external triggers and internal factors.
G1 checkpoint: Assesses cell size, DNA integrity, nutrients, and growth signals.
G2 checkpoint: Verifies DNA replication and damage repair.
M checkpoint: Confirms chromosome alignment and attachment.
Mutation in DNA leads to abnormal protein production.
Accumulating mutations result in uncontrolled cell growth.
Growth of mutated cells surpass normal cell growth.
Genes that regulate cell cycle positively; mutations can lead to cancer.
Normal gene function prevents uncontrolled cell division; mutations inhibit this effect, leading to cancer.