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Genetics and Meiosis Flashcards

Dec 10, 2025

Overview

  • Flashcards covering key concepts from biology chapters on genetics, meiosis, Mendelian inheritance, DNA structure, and DNA replication.
  • Focus on definitions, processes, examples, and problem-style questions with concise answers.

Genetics: Genome and Chromosomes

  • Genome: complete set of an organism's genes and other DNA sequences.
  • Homologous chromosomes: carry information for the same traits.
  • Diploid (2n) and haploid (n) numbers:
    • Example: quaking aspen gametes n = 19 → asexual stem cells have 2n = 38.
    • If an organism has 46 chromosomes, gametes have 23.
  • Chromosome composition after meiosis and mitosis:
    • After telophase I: cells are haploid; chromosomes composed of two chromatids.
    • Completion of meiosis vs. prophase I cells: gametes have half the chromosome number and one-fourth the DNA amount compared to prophase I.
    • For meiosis I duration each chromosome consists of two sister chromatids joined at centromere.

Meiosis: Key Events and Consequences

  • Purpose: reduce chromosome number to haploid and create genetic diversity.
  • Events unique to meiosis:
    • Synapsis of homologous chromosomes (prophase I).
    • Crossing over (exchange between corresponding segments of non-sister chromatids).
    • Separation of homologous chromosomes (conclusion of meiosis I).
  • Meiosis II vs. mitosis:
    • Meiosis II separates sister chromatids in haploid cells.
    • Mitosis separates sister chromatids in diploid or haploid cells, but typically in diploid somatic context.
  • Centromere behavior: centromeres split and sister chromatids migrate in anaphase II.
  • Chiasmata visible indicates prophase I.
  • If dnaB (helicase) mutated in E. coli → no replication fork formed.

Genetic Variation Mechanisms

  • Independent assortment: random orientation of homologous pairs at metaphase I.
    • Result: for n = 23 haploid number → ~8 million combinations from independent assortment.
  • Crossing over: recombines alleles by exchanging non-sister chromatid segments.
  • Combined sources of diversity: mutations, crossing over, independent assortment.
  • Ecological implication: sexually reproducing species better adapt to changing environments due to more genetic variation.

Mendelian Inheritance

  • Mendel's major conclusion: traits are inherited as discrete units (genes), not by blending.
  • Segregation of alleles corresponds to anaphase I of meiosis.
  • Independent assortment basis: alignment of tetrads at equator in meiosis I.
  • Dominance relationships:
    • Dominant allele masks recessive in heterozygote (e.g., Mendel's F1 phenotype).
    • Example crosses:
      • Black (dominant) × albino (recessive) producing all black indicates albino is recessive.
      • Heterozygote (Tt) × homozygous tall (TT) → probability short = 0.
      • Two true-breeding parents (red axial × white terminal) with independent assortment: probability white axial in F2 = 3/16.
  • Mendel continued F2/F3 to reveal recessive trait reappearance.

Extensions Of Mendelian Genetics

  • Pleiotropy: one allele influences multiple phenotypic traits (example: Marfan syndrome).
  • Polygenic inheritance: multiple genes contribute to a single trait (example: human skin pigmentation).
  • Environmental effects interact with genotype (example: hydrangea flower color affected by soil pH).
  • Epistasis: one gene masks effect of another (example: ee genotype prevents fur color in rabbits).
  • Incomplete dominance: heterozygote shows intermediate phenotype (example: red × white → purple in radish).
  • Codominance and multiple alleles: ABO blood group
    • Alleles: IA, IB (codominant), i (recessive).
    • AB × O parents → children can be type A or B.

Key Terms and Definitions

  • Genome: all genes and DNA sequences of an organism.
  • Homologous chromosomes: chromosome pairs carrying same trait loci.
  • Haploid (n): one set of chromosomes (gametes).
  • Diploid (2n): two sets of chromosomes (somatic cells).
  • Chiasma: cytological evidence of crossing over.
  • Synapsis: pairing of homologous chromosomes in prophase I.
  • Pleiotropy: single gene influences multiple traits.
  • Polygenic inheritance: multiple genes affect one trait.
  • Epistasis: interaction where one gene affects expression of another.
  • Incomplete dominance: heterozygote phenotype is intermediate.
  • Codominance: both alleles expressed in heterozygote.

DNA Structure and Evidence for Genetic Material

  • Chargaff's rules: A = T and G = C in double-stranded DNA.
    • Example calculation: if C = 42% → G = 42%, remaining 16% split A = T = 8% each.
  • Watson and Crick: DNA stores information in base sequence.
  • Hershey-Chase experiment: DNA (not protein) enters E. coli during T2 bacteriophage infection.
    • Reason experimental labels matter: DNA contains phosphorus; proteins do not.
    • Labeling nitrogen would fail because proteins also contain nitrogen.

DNA Replication: Mechanism and Enzymes

  • Antiparallel strands: one strand runs 5'→3', the other 3'→5'.
  • Semiconservative replication: each daughter DNA has one parental strand as template.
  • DNA polymerase synthesizes new strand in 5'→3' direction; requires free 3'-OH.
  • Leading vs. lagging strand:
    • Leading synthesized continuously in replication fork movement direction.
    • Lagging synthesized discontinuously as Okazaki fragments opposite fork direction.
    • DNA ligase joins Okazaki fragments.
  • Primase: synthesizes RNA primer (5–10 nucleotides) to start DNA synthesis.
    • If primase mutated → replication cannot initiate on leading or lagging strand.
  • Topoisomerase: relieves torsional strain ahead of replication fork.
  • Single-strand binding proteins: hold separated DNA strands during replication.
  • Prokaryote vs eukaryote replication origins:
    • Prokaryotes: single origin of replication.
    • Eukaryotes: multiple origins on linear chromosomes.

Formulas and Short Answers

  • Diploid chromosome pairs: 2n = 16 → 8 homologous pairs.
  • Gamete chromosome count: if karyotype 46 → gametes n = 23.
  • Number of gamete combinations from independent assortment: 2^n (e.g., n = 23 → ~8 million).
  • Base-pair percentage example: given C = 42% → T = 8%.

Action Items / Study Steps

  • Review meiosis phases and identify where segregation and independent assortment occur.
  • Practice Punnett squares for dominance, codominance, incomplete dominance, and epistasis.
  • Memorize DNA replication enzymes and their roles (helicase, primase, DNA pol, ligase, topoisomerase).
  • Solve chromosome-number problems converting between diploid and haploid contexts.
  • Work through Chargaff percentage calculations and understand base-pairing rules.