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:
Non-sister chromatids link at a chiasma and exchange genetic information via crossover.
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.
Sister chromatids separate into gametes with a single copy of each gene during meiosis II; alignment before separation is random.
Mate selection is another source of variation.
Other Sources of Variation:
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.
Mutations from replication errors occur and are expressed more frequently.
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.
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.