Unit 5: Heredity

  • Genetics - the study of Heredity

  • Foundation of genetics is that traits are produced by genes found on chromosomes

  • Diploid organisms carry two copies of every gene, one on each of two homologous chromosomes, one that came from their mother and one that came from their father

  • Homozygous - same alleles

  • Heterozygous - different alleles

  • Genes - genotype of an organism

    • Physical expression of the traits is the phenotype

  • The allele in heterozygous individuals that directs the phenotype is the dominant allele, and the one that doesn’t show is the recessive allele

  • Transformation - When a cell (typically when we ) takes in foreign genetic material and incorporates it, resulting in genetic alteration

  • Transduction - Specific to bacteriophages and how they use bacteria to reproduce

  • Some viruses have reverse transcriptase

    • Enzyme that defies the central dogma of biology

    • Takes mRNA and brings it back to DNA

  • Whenever the question says “wild type“ it means nonmutant DNA

🧪 Labs

  • pglo

    • Take a gene and insert it to e coli plasmid DNA

    • Chromosomal DNA (bacteria) - single loop of DNA

    • Plasmid DNA - can be single stranded or double stranded

      • Generally smaller than Chromosomal DNA

  • Gel Electrophoresis

    • Used to compare the DNA of two individuals

    • We take two samples (liquids) containing the DNA of the two individuals

      • Add restriction enzymes to cut up the DNA

    • put the samples in wells on one side (negative)

    • The DNA will go to the other side (positive) across the gel because DNA is negatively charged due to the Sugar-Phosphate backbone

    • Some DNA will be faster than others

      • Longer sections of DNA are slower, and will lag behind

    • The DNA will split into different “bands“ across the gel based on how fast they are

    • The “bands“ can be used to compare if the DNA is the same or different

🌱 Mendelian Genetics

  • Simple genetics with dominants and recessives was illuminated by Gregor Mendel

  • Three laws:

    • Law of Dominance

    • Law of Segregation

      • Each gamete gets only one of two copies

      • Gametes are haploid

    • Law of Independent Assortment

      • How one trait gets split up into gametes has no bearing on how the other trait gets split up

      • This is because chromosomes segregate independently, homologous chromosomes are split left or right during Meiosis I

      • Alleles of different genes can mix and match

      • Use Dihybrid cross punnet square (4×4 looking thing)

        • Memorize the phenotype ratios ex:

        • 9 tall and green

        • 3 tall and yellow

        • 3 short and green

        • 1 short and yellow

        • 9:3:3:1 only when two heterozygotes for two genes are crossed

        • 6:3:3:2:1:1 when there is incomplete dominance & complete dominance on a dihybrid cross

  • Monohybrid Cross - when two individuals are crossed and one gene is being studies

    • Use punnet squares

  • Humans have 23 pairs of homologous chromosomes for a total of 46

    • 22 pairs are autosomes and 2 pairs are sex chromosomes

      • Females have XX, males have XY

      • Because females have two X chromosomes, one is inactivated in each cell and condenses into a Barr body

    • Most sex-linked traits are on the X-chromosome “X-linked“

    • Barr bodies - one of the two X linked chromosomes in each female cell is inactivated, creating this

🩸 Blood types

  • 4 blood types:

    • Type A

    • Type B

    • Type AB

    • Type O

  • A and B are codominant

  • O is recessive

👁 Non-Mendelian Genetics

  • Non-Mendelian genetics refers to a situation in which traits do not follow the Mendelian laws

  • Can be due to being governed by more than one gene

  • If two genes are on the same chromosome and close together, they are linked

    • cannot segregate independently, violating the law of independent assortment

  • Completely linked alleles on the same chromosome are locked together and travel together during gamete formation

  • Crossing over can separate linked alleles, though unlikely

    • separation of linked alleles leads to more predictable inheritance patterns with minimal variability

  • Crossing over can also lead to recombination, allowing for new genetic combinations that seems like it wouldn’t be possible due to linked alleles

  • Recombination frequency - can be used to measure how far apart two genes are on a chromosome

    • can be calculated by adding up the recombinants and dividing by the total number of offpsring

      • Ex: two linked genes A and B recombine with frequency of 9/90 = 10%

      • Distance on a chromosome is measured in map units/centrimorgans

      • Ex above: A and B are 10 units apart

  • Offspring formed form recombination events (crossing over)

    • Ex of Non Mendelian Genetics:

      • incomplete dominance

        • Traits blend together to produce an intermediate phenotype

      • codominance

        • heterozygous alleles in a gene pair are simultaneously expressed

        • neither dominant nor recessive

      • polygenic inheritance

        • Traits controlled by many genes

          • Ex: our height is controlled by over 400 genes

👪 Pedigrees

  • Traits that appear more in one sex than the other are usually sex-linked

  • Traits that skip generations are usually recessive

🧬 Meiosis

  • AKA gametogenesis

    • If sperm is produced, it is called spermatogenesis (oogenesis if egg is produced)

    • 4 cells are produced for each diploid cell

  • Meiosis produced four genetically distinct haploid gametes (sperm or egg cells)

    • Involved two rounds

    • Meiosis I - homologous chromosomes separate, and cross over some DNA

      • Prophase I

        • Crossing over takes place

      • Metaphase I

        • Law of independent assortment takes place

      • Anaphase I

        • Law of segregation takes place

      • Telophase I

    • Meiosis II - sister chromatids separate

      • Prophase II

      • Metaphase II

      • Anaphase II

      • Telophase II

    • Mutations, such as nondisjunction events or whole chromosome translocations, can lead to genetic diseases

  • Meiotic errors

    • Nondisjunction - chromosomes failed to separate properly during meiosis, producing the wrong number of chromosomes

    • Translocation - segment of a chromosome moves to another non homologous chromosome

      • Occurs when crossing over (recombination) occurs incorrectly

Mitosis vs. Meiosis

  • Mitosis

    • Occurs in somatic (body) cells

    • Produces identical cells

    • Diploid cell → diploid cells

    • 1 cell becomes 2 cells

    • Number of divisions: 1

  • Meiosis

    • Occurs in germ (sex) cells

    • Produced gametes

    • Diploid cell → haploid cells

    • 1 cell becomes 4 cells

    • Number of divisions: 2