1. Identify the three areas of genetics.
  2. Explain why Drosophila and E. coli are the most commonly studied organisms in genetics.
  3. State and apply Mendel's principles of dominance, segregation and independent assortment.
  4. Define and utilize the following terms in the context of working genetics problems: dominant, recessive, incomplete dominance, codominance, homozygous, heterozygous, hemizygous, multiple alleles, sex-linked, epistasis, penetrance, monohybrid, dihybrid, gamete, genotype, phenotype, test cross, lethal gene, pleiotropy.
  5. State the connection between chromosomal behavior in meiosis and the inheritance of Mendelian traits, as well as describe the experiment by McClintock and Creighton that confirmed this association.
  6. State the stage in meiosis where crossing over occurs, and correctly identify the following terms: chiasmata, synaptonemial complex, prophase, metaphase, anaphase, telophase, cytokinesis.
  7. Be able to apply the following rules of probability in the context of genetics problems: sum rule, product rule, degrees of freedom and chi square analysis.
  8. Analyze genetics problems involving one or two traits, sex-linked traits, multiple alleles.
  9. Analyze pedigrees to determine mode of inheritance and predict probabilities of offspring inheriting traits under consideration.
  10. Identify the mode of inheritance of sex in humans, Drosophila and birds.
  11. Identify linked mutations in coupling and repulsion.
  12. Map bacterial chromosome using results of Hfr crosses.
  13. Map linked genes using data from two and three factor crosses.
  14. Differentiate among the three types of genetic exchange between bacteria.
  15. Describe the lytic and lysogenic cycles of bacteriophages.
  16. Define: deletion, tandem duplication, reverse duplication, paracentric inversion, pericentric inversion and translocation. Identify chromosomal aberrations using these terms.
  17. Define: aneuploidy and polyploidy.
  18. Analyze human karyotypes to determine sex as well as gross chromosomal aberrations.
  19. Explain the differences between plants and animals in terms of their ability to tolerate changes in chromosomal numbers, as well as the typical outcome of such changes.
  20. Utilize the following terms in describing the structure of DNA: double helix, base pairing, sugar-phosphate backbone, Chargaff's rule, 5' phosphate, 3' hydroxyl, antiparallel, pyrimidines, purines, semiconservative replication.
  21. Compare and contrast DNA replication, transcription and translation, including the major enzymes involved, as well as location of events in prokaryotes and eukaryotes.
  22. Describe three types of RNA processing in eukaryotes.
  23. Describe the genetic code, correctly using the terms: triplet, degenerate, nonoverlapping, comma free, universal, unambiguous, ordered, wobble hypothesis, colinearity.
  24. Describe the use of the following tools/techniques in recombinant DNA technology: restriction enzymes, cloning, Southern, Northern and Western blots, PCR, synthesizing DNA.
  25. Map the restriction fragments in a circular plasmid.
  26. Discuss applications of recombinant DNA technology in medicine, agriculture and industry.
  27. Describe the regulation of gene expression in prokaryotes and phages, including the following terms: operon, repressor, inducible, repressible, attenuation.
  28. Describe the regulation of the lac and trp operons.
  29. Identify the role of the following in gene expression: sigma factors, enhancers, silencer elements.
  30. Define transposable element and describe the structure of an insertion sequence.
  31. Identify the significance of transposons in terms of gene expression, map distances between genes, and antibiotic resistance in bacteria.
  32. Compare the packaging of DNA in prokaryotes and eukaryotes, including the structure of the nucleosome.
  33. Describe the structure of centromeres and telomeres, and explain how telomeric DNA is replicated.
  34. Compare and contrast the function of methylation in prokaryotes and eukaryotes.
  35. Describe the arrangement of immunoglobulin genes and explain how numerous antibodies are made from a relatively small region of DNA.
  36. Identify various types of mutations (silent, missense, nonsense, frameshift, transitions and transversions).
  37. Distinguish among back mutation, intergenic suppression and intragenic suppression.
  38. Describe methods of DNA repair (excision repair, photoreactivation, RecA induced repair, SOS repair).
  39. Recognize traits that are inherited in a non-Mendelian fashion (maternal effects, cytoplasmic inheritance) based on data supplied.
  40. Use Hardy-Weinberg equilibrium to calculate allelic frequencies given genotypic frequencies, or calculate genotypic frequencies given allelic frequencies.
  41. State the assumptions of Hardy-Weinberg equilibrium.
  42. Identify if a gene pool is in Hardy-Weinberg equilibrium.
  43. Describe the following in the context of Hardy-Weinberg equilibrium: sampling error, genetic drift, founder effect, bottleneck, mutational equilibrium, natural selection.
For questions, comments and additional information, contact  mfhicks@pstcc.edu
Last Updated: Ju;y 8, 2001
Site map: Margaret F. Hicks Home - Biology 2120 - Notes - Final Exam Study Guide


 
 









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