Biology Module 11: The Different Phases of Cell Cycle Meiosis PDF
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Harvard University
2024
Necy Luz Español Villamor Dinolan Ayag Lubo
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Summary
These notes detail the different phases of the cell cycle meiosis, including meiosis I and meiosis II. It explains the purpose and process of meiosis, focusing on reducing chromosome numbers and creating genetic diversity. The document also compares mitosis and meiosis.
Full Transcript
OWNED BY: Necy Luz Español Villamor Dinolan Ayag Lubo DATE: August 22, 2024 LESSON TITLE: THE DIFFERENT PHASES OF CELL CYCLE: MEIOSIS MODULE NUMBER: MODULE 11 LESSON OBJECTIVES: Identify the different phases of the meiotic cell division. Describe the events happening in the different phases of...
OWNED BY: Necy Luz Español Villamor Dinolan Ayag Lubo DATE: August 22, 2024 LESSON TITLE: THE DIFFERENT PHASES OF CELL CYCLE: MEIOSIS MODULE NUMBER: MODULE 11 LESSON OBJECTIVES: Identify the different phases of the meiotic cell division. Describe the events happening in the different phases of the meiotic cell division. MEIOSIS - type of cell division that reduces the chromosome number by half - from Diploid (2n = 46 chromosomes) to Haploid (n = 23 chromosomes). - Only in reproductive cells in sexually reproducing organisms. - Ensures genetic variability and maintains the chromosome number across generations. PHASES OF MEIOSIS (MEIOSIS I & MEIOSIS II) 1. MEIOSIS I (REDUCTIONAL DIVISION): - Reduces chromosome number from diploid (46) to haploid (23). ~ PHASES OF MEIOSIS I: A.) PROPHASE I: Leptonema: Chromosomes become visible after coiling. Zygonema: Homologous chromosomes pair in a process called synapsis, forming a bivalent (two homologous chromosomes consisting of four chromatids). Pachynema: Chromosomes thicken, and crossing-over occurs (exchange of chromosome segments between homologous chromosomes), ensuring genetic variability. Diplonema: Homologous chromosomes begin to separate, and chiasmata (points of crossing-over) are visible. Diakinesis: Chromosomes fully condense; chiasmata move to the ends, and the nuclear envelope breaks down, allowing spindle fibers to form. B.) METAPHASE I - Homologous chromosomes align on the metaphase plate. Spindle fibers attach to chromosomes from opposite poles. C.) ANAPHASE I - Homologous chromosomes separate and move to opposite poles. Unlike in mitosis, sister chromatids remain attached at the centromere. D.) TELOPHASE I: - Homologous chromosomes complete their migration to the poles. The nuclear envelope reforms, and cytokinesis occurs, producing two haploid daughter cells. OWNED BY: Necy Luz Español Villamor Dinolan Ayag Lubo 2. MEIOSIS II (EQUATIONAL DIVISION): - Similar to mitosis, meiosis II separates sister chromatids, maintaining the haploid number (23 chromosomes). ~ PHASES OF MEIOSIS II: A.) PROPHASE II - Spindle apparatus forms again; chromosomes condense and prepare for division. B.) METAPHASE II - Chromosomes align on the metaphase plate. The kinetochores of sister chromatids face opposite poles. C.) ANAPHASE II - Centromeres separate, and chromatids (now individual chromosomes) move to opposite poles. D.) TELOPHASE II: - Nuclear envelopes reform around the separated chromosomes. Cytokinesis occurs, producing four non-identical haploid daughter cells. KEY TERMS & DEFINITIONS: MEIOSIS: A type of cell division that reduces the chromosome number by half, creating four genetically diverse haploid cells from a diploid parent cell. DIPLOID (2n): A cell containing two complete sets of chromosomes (46 in humans). HAPLOID (n): A cell containing one complete set of chromosomes (23 in humans). HOMOLOGOUS CHROMOSOMES: Pairs of chromosomes (one from each parent) that are similar in shape, size, and genetic content. SYNAPSIS: The pairing of homologous chromosomes during meiosis. BIVALENT/TETRAD: A pair of homologous chromosomes (4 chromatids). CROSSING-OVER: The exchange of genetic material between homologous chromosomes, contributing to genetic diversity. CHIASMA: The point where two homologous non-sister chromatids exchange genetic material. OWNED BY: Necy Luz Español Villamor Dinolan Ayag Lubo NONDISJUNCTION: Failure of chromosomes or chromatids to separate properly during meiosis, leading to genetic disorders (Down Syndrome). CYTOKINESIS: - Division of the cytoplasm, completing cell division and resulting in four genetically distinct haploid cells. KEY POINTS TO REMEMBER: 1. Purpose of Meiosis: To reduce chromosome numbers and create genetic diversity through recombination (crossing-over). 2. Meiosis I Vs Meiosis II: - Meiosis I reduces the chromosome number from diploid to haploid. - Meiosis II separates sister chromatids, like mitosis, but in haploid cells. 3. Errors in Meiosis: Nondisjunction and other errors (translocation, deletion) can cause genetic disorders, impacting human health significantly. 4. Crossing-over & Genetic Variability: - Crossing-over during Prophase I is key to introducing genetic variation in offspring, which is a fundamental advantage of sexual reproduction. DIFFERENCES BETWEEN MITOSIS AND MEIOSIS: 1. NUMBER OF CELL DIVISIONS: - Mitosis: 1 - Meiosis: 2 2. NUMBER OF DAUGHTER CELLS: - Mitosis: 2 - Meiosis: 4 3. GENETIC IDENTITY: - Mitosis: Daughter cells are genetically identical to the parent cell. - Meiosis: Daughter cells are genetically different from the parent cell due to crossing-over and independent assortment. 4. CHROMOSOME NUMBER: - Mitosis: Same as parent cell (diploid, 46 chromosomes). - Meiosis: Half of parent cell (haploid, 23 chromosomes). 5. WHERE: - Mitosis: Somatic cells. - Meiosis: Gametes (sex cells). 6. WHEN: - Mitosis: Throughout life for growth and repair. - Meiosis: During sexual maturity for reproduction. 7. ROLE: - Mitosis: Growth, repair, and asexual reproduction. - Meiosis: Sexual reproduction and genetic diversity. OWNED BY: Necy Luz Español Villamor Dinolan Ayag Lubo COMMON ERRORS IN MEIOSIS: NON-DISJUNCTION: Failure of homologous chromosomes or sister chromatids to separate, leading to genetic disorders like: - DOWN SYNDROME: Extra copy of chromosome 21. - KLINEFELTER SYNDROME: Additional X chromosome (XXY). - TURNER SYNDROME: Missing X chromosome in females (XO). OTHER ERRORS: - TRANSLOCATION: A chromosome fragment attaches to a non- homologous chromosome. - DELETION: Loss of a chromosome segment, affecting the genetic material.