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Genetics Exam 1 Review: Chromosomes, Pedigrees, Probabilities, and Bacterial Genetics

Study Guide - Smart Notes

Tailored notes based on your materials, expanded with key definitions, examples, and context.

Chromosomes and Chromatids

Chromosome and Chromatid Counting

Understanding chromosome and chromatid numbers is fundamental in genetics, especially when analyzing cell division processes such as mitosis and meiosis.

  • Haploid (1n): A cell with one set of chromosomes. Example: If 1n = 12, then the diploid number (2n) is 24.

  • Diploid (2n): A cell with two sets of chromosomes.

  • Chromosome Number: Determined by counting centromeres.

  • Chromatid Number: Determined by counting the arms of chromosomes (each chromosome in X form has two chromatids).

Chromatids in Mitosis

During metaphase of mitosis in a diploid cell (1n = 6):

  • Diploid means 2n = 12 chromosomes.

  • In metaphase, chromosomes are in X form, so there are 24 chromatids.

Chromatids in Meiosis

Meiosis involves two divisions, resulting in haploid cells.

  • Start: Diploid cell (2n = 12 chromosomes, 24 chromatids).

  • After Meiosis I: Chromosome number halves (1n = 6 chromosomes, 12 chromatids).

  • After Meiosis II: Each cell has 6 chromosomes and 6 chromatids.

Pedigree Analysis

Identifying Inheritance Patterns

Pedigrees are diagrams that show the inheritance of traits across generations. They are used to determine whether traits are autosomal or sex-linked, and dominant or recessive.

  • Autosomal Recessive: Affected children can have unaffected parents.

  • X-linked Recessive: More males are affected; trait is often passed through females.

  • Incomplete Penetrance: Not all individuals with the genotype express the phenotype.

Example: Pedigree Analysis

Look for affected children with unaffected parents to identify recessive inheritance. X-linked recessive traits often show more affected males and are transmitted through carrier females.

Pedigree chart showing inheritance pattern Pedigree chart with multiple generations

Punnett Squares and Probability

X-linked Punnett Squares

Punnett squares are used to predict the outcome of genetic crosses. X-linked crosses require careful attention to sex chromosomes.

  • RR x rr: All offspring are Rr.

  • XRXR x XrY: All offspring show dominant phenotype.

  • Test Cross: Female test cross yields half males with recessive phenotype; male test cross yields all males recessive, all females dominant.

  • XrXr x XRY: All males are recessive, all females dominant.

Dihybrid Punnett Squares

Dihybrid crosses involve two genes and can be analyzed using Punnett squares.

  • Dihybrid TtPp x TtPp: Ratio is 9:3:3:1.

  • Dihybrid test cross TtPp x ttpp: Ratio is 1:1:1:1.

  • Monohybrid Tt x Tt: Ratio is 3:1.

  • Monohybrid Tt x tt: Ratio is 1:1.

Probability Calculations

Probability in genetics can be calculated using sum, product, and binomial rules.

  • SUM Rule: For mutually exclusive events.

  • PRODUCT Rule: For sequential events (e.g., first tall, then short).

  • BINOMIAL Rule: For unordered events (e.g., 4 out of 7).

Binomial Example: Cat Coat Patterns

Cross: Tt x Tt (mackerel tabby dominant, classic tabby recessive)

  • Expected: 75% mackerel, 25% classic.

  • Probability of 5 out of 8 classic tabby kittens:

Use the binomial formula:

  • n = 8, x = 5, p = 0.25 (classic), q = 0.75 (mackerel)

Chi Square Analysis

Chi Square Test

The chi square test is used to compare observed and expected results in genetic crosses.

  • Expected: Theoretical ratio from Punnett square.

  • Observed: Actual data from experiment.

Chi square formula:

  • O = observed value

  • E = expected value

Chromosome Mapping

Test Cross and Recombination Frequency

Chromosome mapping in eukaryotes uses test crosses to determine recombination frequency.

  • Test Cross: Ratio is 1:1:1:1.

  • Parentals: Offspring with parental genotype.

  • Nonparentals: Offspring with recombinant genotype.

  • Recombination Frequency:

  • Map Units (cM): 1% recombination = 1 cM.

Alternative equation:

Extensions of Mendelian Genetics

Lethal Alleles and Epistasis

Extensions include lethal alleles and gene interactions such as epistasis.

  • Lethal Alleles: Can result in a 2:1 ratio in offspring.

  • Epistasis: Interaction between two genes affects phenotype.

Complementation Groups

Gene Complementation

Complementation tests determine whether mutations are in the same gene or different genes.

  • Same gene: Mutations do not complement.

  • Different gene: Mutations complement.

Complementation group diagram

Bacterial Genetics

Bacterial Conjugation

Bacterial conjugation is a process of genetic exchange involving F factors.

  • F+: Donor cell with fertility plasmid.

  • F-: Recipient cell without plasmid.

  • Hfr: High frequency recombination cell.

  • F': Cell with F plasmid carrying additional genes.

  • Merozygote: Partial diploid cell formed during conjugation.

F+ F- conjugation diagram

Hfr Conjugation

Hfr cells transfer chromosomal genes to F- cells during conjugation, allowing mapping of bacterial genes.

Hfr conjugation process

Viral Life Cycles

Bacteriophage Genetics

Bacteriophages are viruses that infect bacteria and are used in genetic mapping and analysis.

  • Lytic Cycle: Virus replicates and lyses host cell.

  • Lysogenic Cycle: Viral DNA integrates into host genome.

Additional info: Viral life cycles are important for understanding genetic exchange and mapping in bacteria.

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