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Genetic Control of Protein Synthesis, Cell Function, and Cell Reproduction PART 2.

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Presentation on theme: "Genetic Control of Protein Synthesis, Cell Function, and Cell Reproduction PART 2."— Presentation transcript:

1 Genetic Control of Protein Synthesis, Cell Function, and Cell Reproduction
PART 2

2 Cell Reproduction Mitosis is cell division Growth Cell repair
Not meiosis Goal is to make identical cells Cells do not divide all the time

3 Mitosis is a very short period
Most of the time is Interphase

4 Cells that cease division S phase (DNA synthesis)
Genetic Control of Cell Reproduction Life Cycle of the Cell: M phase: mitosis cytokinesis Cells that cease division M (mitosis) G1 (Gap 1) G2 (Gap 2) S phase (DNA synthesis) EUKARYOTIC CELL CYCLE Interphase (>95%): G1 phase S phase (DNA synthesis) G2 phase

5 DNA Replication: S phase
switched on by the cytoplasmic S-phase activator Replication is initiated at replication origin and proceeds in both directions. Entire genome is replicated once - further replication is blocked involves DNA polymerase and other proteins that function to unwind and stabilize the DNA and “prime” DNA replication of the “lagging” strand.

6 DNA Replication: S phase
nucleotides are always added to the 3’ end (DNA and RNA) formation of Okazaki fragments on lagging strand “new” DNA is proofread by DNA polymerase repairs are made and gaps filled by DNA ligase

7 DNA Repair, “Proofreading,” and “Mutations”
Following replication and prior to mitosis, DNA polymerase “proofreads” the “new” DNA, and cuts out mismatches DNA ligase replaces the mismatches with complementary nucleotides A “mistake” during transcription results in a mutation causing the formation of an abnormal protein Approximately 10 DNA mutations are passed to the next generation, however two copies of each chromosome almost always ensures the presence of a functional gene

8 Chromosomes and Their Replication
“New” DNA helices associate with histones to form chromosomes The two chromosomes remain temporarily attached at the centromere. Together, these chromosomes are called chromatids.

9 Mitosis Remember PMAT Prophase Metaphase Anaphase Telophase

10 Interphase Technically not part of mitosis DNA is copied (duplicated)
Centrosomes are duplicated

11 Prophase Chromosomes thicken Microtubules – mitotic spindle forming
Nuclear envelope is fragmenting (prometaphase) Microtubules are attaching to kinetochore

12 Metaphase For middle They line up in the middle, lining up in the metaphase plate

13 Anaphase ”away” Chromosomes move to opposite side of the cell
They have spindles Chromatids separate Equal numbers of DNA in each of the daughter cells

14 Telophase For two Telophase & cytokinesis Cell elongation
Cleavage furrrow Daughter nuclei form

15 Stages of Cell Reproduction
Mitosis: M phase 1. Assembly of the mitotic apparatus 2. Prophase (A,B,C) 3. Prometaphase (D) 4. Metaphase (E) 5. Anaphase (F) 6. Telophase (G, H) Figure 3-13

16 FILM

17 Cell Differentiation Different from reproduction ...
changes in physical and functional properties of cells as they proliferate results not from the loss of genes but from the selective repression/expression of specific genes development occurs in large part as a result of “inductions,” one part of the body affecting another

18 The cell cycle & cancer Growing of cells out of control

19 Not all mutations lead to cancer!
Dysregulation of cell growth Caused in all or almost all cases by the mutation or abnormal activation of genes that encode proteins that control cell growth and/or mitosis Proto-oncogenes: the “normal” genes Oncogenes: the “abnormal” gene Antioncogenes: genes whose product suppress the activation of oncogenes Not all mutations lead to cancer!

20 What causes these mutations?
Ionizing radiation: disrupts DNA strands Chemicals: “carcinogens” Physical irritants: e.g., abrasion of the intestinal lining Hereditary “tendencies”: e.g., some breast cancer Viruses: so-called “tumor viruses” (particularly retroviruses)

21 Q: Why does cancer kill? A: Cancer cells compete successfully with normal cells for limited nutrients


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