Meiosis Review

Overview of Meiosis

Color coating

  • highlights: #c6ffa8

  • colored words: #089800

Purpose of Meiosis

Meiosis is a specialized form of cell division that occurs in sexually reproducing organisms. It plays a crucial role in generating genetic diversity and ensuring the stability of chromosome numbers across generations. The key purposes of meiosis include:

  • Reduction of Chromosome Number: Meiosis reduces the chromosome number by half, producing haploid gametes (sperm and egg). This is essential for maintaining the chromosome number when fertilization happens, the union of two haploid gametes (23 chromosomes, half n) restores the diploid state (46 chromosomes, 2n).

  • Introduction of Genetic Variation: Meiosis introduces genetic variation through mechanisms such as crossing-over and independent assortment, which contribute to the diversity of the offspring and enhance the adaptability of species to changing environments.

Types of Cells

  • Gametes: The sex cells involved in reproduction (sperm & eggs). They are haploid, containing only one set of chromosomes (crucial for fertilization).

  • Somatic Cells: The other body cells (such as skin, bone, heart, and muscle cells) that are diploid, containing two sets of chromosomes, one inherited from each parent. Somatic cells undergo mitosis for growth and repair.

Key Events in Meiosis

Stages of Meiosis

  1. Prophase I: Chromosomes condense, and homologous chromosomes pair up to form tetrads (groups of four chromatids). This stage features significant genetic exchange through crossing-over, where segments of DNA are exchanged between non-sister chromatids, leading to increased genetic variability.

  2. Metaphase I: Tetrads align at the metaphase plate. The orientation of each tetrad is random, which is essential for independent assortment.

  3. Anaphase I: Tetrads are pulled apart into individual homologous chromosomes, each consisting of two sister chromatids. The sister chromatids remain attached at their centromeres.

  4. Telophase I and Cytokinesis: The cell divides into two haploid cells. Each cell has half the original number of chromosomes, but each chromosome still consists of two sister chromatids.

  5. Meiosis II: The second meiotic division resembles mitosis. It includes Prophase II, Metaphase II, Anaphase II, and Telophase II, ultimately leading to four unique haploid gametes.

Genetic Variation Mechanisms

  • Crossing-over: This process allows homologous chromosomes to exchange genetic material, resulting in new combinations of alleles, which enhances genetic diversity.

  • Independent Assortment: The random distribution of maternal and paternal chromosomes into gametes occurs during Metaphase I, leading to various combinations of genes in the resulting gametes.

Gametogenesis: Spermatogenesis and Oogenesis

Spermatogenesis

  • Takes place in the male reproductive system within the seminiferous tubules and results in four viable sperm cells, each with 23 chromosomes. This process is continuous and can produce millions of sperm daily.

Oogenesis

  • Occurs in the female ovaries and involves the transformation of an oogonium into an ovum, with uneven division of cytoplasm. This process yields one large, viable egg cell and three smaller polar bodies that eventually degenerate. The primary follicle selection leads to the maturation of one egg per menstrual cycle.

Chromosomal Abnormalities

Non-disjunction

  • Non-disjunction can happen during Anaphase, where homologous chromosomes (in meiosis I) or sister chromatids (in meiosis II) fail to separate properly, resulting in gametes with abnormal chromosome numbers. This can lead to conditions such as:

    • Trisomy: An extra chromosome leads to three instances of a chromosome instead of the usual two; for example, Down Syndrome (trisomy 21) occurs with an extra copy of chromosome 21.

    • Monosomy: A missing chromosome (only one instance instead of two) can result in conditions such as Turner Syndrome, where a female has only one copy of the X chromosome (45 total chromosomes). Non-disjunction events significantly affect development and can lead to various genetic disorders.

robot