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Biol 114 Spring 2025 Week 2 (1/30) Cell Division and Heredity

Genetic Heritability

  • Heritability of phenotypes is key to understanding natural selection as "descent with modification".
  • Darwinian evolution requires heritability; without it, selected variants would be lost.
  • Darwin acknowledged a lack of understanding regarding variation and trait inheritance.
  • Phenotypes (measurable traits) are caused by genotypes (genes).
  • Genetic variation encodes for phenotypic variation, which allows the environment to select for or against members of a population.
  • Genes are "selfish" and aim to replicate themselves (Richard Dawkins, The Selfish Gene).
  • Phenotypes serve as a mechanism for genes to get to the next generation; "instinct" is genes using phenotypes for self-preservation.

Genes

Definitions:

  • Genome: All hereditary information within an individual (including non-gene DNA).
  • Gene pool: All alleles of all genes within a population.
  • Genotype: All alleles of all genes within an individual, or a specific set under study.
  • Genes: DNA sections on chromosomes encoding for a polypeptide, causing a trait (phenotype), and may regulate other genes.
  • Locus: The location of a gene on a chromosome.
  • Alleles: Particular versions of a gene at the same locus on homologous chromosomes.

Does Genotype Really Equal Phenotype?

  • Similar genotypes can result in different phenotypes due to environmental pressures.
    • Example: Identical plants in different light conditions.
    • Identical twins have slight differences due to developmental environments affecting regulator genes.
  • Similar phenotypes can result from different genotypes.
    • Example: Convergent evolution of gray wolf and Tasmanian wolf.
      • Tasmanian wolf (marsupial) and true wolves share similarities like sharp teeth, powerful jaws, raised heels, and body form, despite distant common ancestry.
  • Truly identical phenotypes require identical genotypes and homogeneous developmental conditions, nearly impossible outside of lab settings.

Variation in Eukaryotes

Characteristics:

  • Genes are carried on chromosomes (DNA and proteins).
  • Chromosomes occur in sets; species have multiple chromosomes within a set.
  • Eukaryotes may have multiple sets of chromosomes; ploidy refers to the number of sets.
  • Homologous pairs of chromosomes: one copy from each parent (maternal/paternal) in the same nucleus (2n = diploid).
    • They have the same genes but can differ in gene expression based on alleles.
  • Individuals may be haploid (1n) or diploid (2n).
    • Examples: ants, bees, and wasps (haploid males, diploid females); mosses (mostly haploid); organisms alternating between sexual (haploid) and asexual (diploid) generations (Alternation of Generations).
  • Dominance: one allele is expressed even with another (recessive) allele present.

Meiosis

  • Meiosis: production of gametes (egg and sperm) by halving chromosome number.
  • Haploid gametes join to create a diploid zygote, which develops into a reproductive individual.
  • Meiosis involves two cell divisions (Meiosis I and II) to increase variation.
    • Homologous pairs exchange genetic material during early meiosis I.
    • Pairs of chromosomes (sister chromatids) come together with homologues (one from each parent).
    • The mechanism of attraction is unknown.
    • Resulting tetrad consists of four chromatids: two sisters from the paternal homolog, and two sisters from the maternal homolog.
    • Chromatids from parental homologs (maternal and paternal) are referred to as non-sister chromatids.
  • Tetrad: structure formed when homologous chromosomes pair during Prophase I of meiosis.
    • Consists of 4 chromatids: 2 sister chromatids from the paternal chromosome, 2 sister chromatids from the maternal chromosome.
    • Homologous chromosomes align and undergo crossing over, exchanging DNA between non-sister chromatids.

Areas of Variation in Meiosis:

  1. Non-sister chromatids link at a chiasma and exchange genetic information via crossover.
  2. Tetrads migrate and align randomly along the center of the cell during meiosis I; daughter cells can have all paternal, all maternal, or a combination of homologs.
  3. Sister chromatids separate into gametes with a single copy of each gene during meiosis II; alignment before separation is random.
  4. Mate selection is another source of variation.

Other Sources of Variation:

  1. Mutations from nucleotide sequence changes.
    • Caused by environmental mutagens (radiation, chemicals).
    • Most mutations are not deleterious, occurring in junk DNA and not expressed; used to measure genetic relationships of taxa.
    • Expressed mutations are usually harmful and removed by natural selection.
  2. Mutations from replication errors occur and are expressed more frequently.
  3. Nondisjunction: cell ends up with both pairs of homologs of one chromosome (meiosis I) or both sister chromatids (meiosis II).
    • Results in gametes with an extra chromosome (n+1) or one too few (n-1).
      • Example: Down Syndrome is trisomy 21 (3 copies of chromosome 21).
        n-1 is monosomy.
    • Too many or too few chromosomes are referred to as aneuploidy.
    • Happens in 10% of meiotic divisions, but most end as fetal death.
  4. Unequal crossing over: one arm of a chromatid ends up longer than its sister.
    • Example: Huntington’s Disease

Asexually Reproducing Organisms

The Problem:

  • Asexual organisms (e.g., bacteria) reproduce by splitting (similar to mitosis).
  • Mature cells are haploid. They copy their genetic makeup and split.
  • Each generation would look the same, meaning sexual reproduction and different types of asexual reproduction would not have evolved.

Sources of Variation in Asexual Organisms:

  • Mutations can occur.

Transformation:

  • Bacterial cells take up DNA fragments from other cells and incorporate them into their own DNA or as a separate plasmid.
  • Used in the lab to create modified organisms (e.g., golden rice, oil-eating bacteria).

Transduction:

  • Viral capsids attach to bacterial cells and inject their DNA, fragmenting the host DNA.
  • Host cell lysis releases fragments into the environment.
  • Other bacterial cells encounter capsids with viral DNA, viral + bacterial DNA, or just bacterial DNA; new bacterial DNA replicates with the new host DNA.

Conjugation:

  • Cytoplasmic tube forms between cells; a plasmid is transferred from a cell with a plasmid to one without.
  • Sometimes just a fragment of the plasmid is transferred, introducing a new variant.