Genetics Worksheet Exam 3 Key, Exercises of Genetics

Prof. Paul Hardin, Biol 3301: Genetics practice questions with answers. Prepare for genetics exam with this worksheet.

Typology: Exercises

2020/2021

Uploaded on 04/20/2021

ekaashaah
ekaashaah 🇺🇸

4.4

(41)

273 documents

1 / 4

Toggle sidebar

This page cannot be seen from the preview

Don't miss anything!

bg1
1
Biol 3301: Genetics
Exam #3
Practice questions
1. (9) Match the word or phrase that best defines each statement:
h Mutation in which a purine is substituted by a pyrimidine a) Nonsense mutation
g Mutation caused by the addition of a base in a protein coding region b) Silent mutation
a A base change resulting in a stop codon c) Conditional mutation
e Type of mutation that causes mutant sectors to appear on a flower petal d) Auxotrophic
b A base change resulting in a codon specifying the same amino acid e) Somatic mutation
i Mutation in which a pyrimidine is substituted for a pyrimidine f) Lethal
c Mutation that causes a mutant phenotype only under restrictive conditions g) Frameshift
d A biochemical mutant that must be supplied with a certain nutrient for growth h) Transversion
f Mutation that causes death of the zygote i) Transition mutation
2. (3) What principle did the fluctuation test of Luria and Delbruck establish?
That mutations pre=exist within a population rather than being somehow induced by the
Selecting agent.
3. (3) What is the difference between mutation rate and mutation frequency?
Mutation rate is the number of mutations per unit of biological time (i.e. generation)
Mutation frequency is the number of mutations per unit of population.
4. (4) The rare enol form of thymine pairs with guanine. If a thymidine within the DNA helix shifts to the enol
form during replication, base pairing would change from a _____T-A______ base pair to a
______C-G_______ base pair.
5. (2) Tautomerization, depurination, deamination and oxidative damage are all sources of
___spontaneous____ mutations.
6. (2) In E. coli, a region flanked by two repeats of a sequence such as GTGGTGTAA is prone to
answer - a
a) Deletion b) Missense mutation c) Duplication d) Inversion e) Frameshift mutation
7. (2) The ionized form of 5-bromouracil will hydrogen bond to which base
answer - c
a) adenine b) cytosine c) guanine d) thymine e) uracil
pf3
pf4

Partial preview of the text

Download Genetics Worksheet Exam 3 Key and more Exercises Genetics in PDF only on Docsity!

Biol 3301: Genetics

Exam

Practice questions

  1. (9) Match the word or phrase that best defines each statement: h Mutation in which a purine is substituted by a pyrimidine a) Nonsense mutation g Mutation caused by the addition of a base in a protein coding region b) Silent mutation a A base change resulting in a stop codon c) Conditional mutation e Type of mutation that causes mutant sectors to appear on a flower petal d) Auxotrophic b A base change resulting in a codon specifying the same amino acid e) Somatic mutation i Mutation in which a pyrimidine is substituted for a pyrimidine f) Lethal c Mutation that causes a mutant phenotype only under restrictive conditions g) Frameshift d A biochemical mutant that must be supplied with a certain nutrient for growth h) Transversion f Mutation that causes death of the zygote i) Transition mutation
  2. (3) What principle did the fluctuation test of Luria and Delbruck establish? That mutations pre=exist within a population rather than being somehow induced by the Selecting agent.
  3. (3) What is the difference between mutation rate and mutation frequency?Mutation rate is the number of mutations per unit of biological time ( i.e. generation) Mutation frequency is the number of mutations per unit of population.
  4. (4) The rare enol form of thymine pairs with guanine. If a thymidine within the DNA helix shifts to the enol form during replication, base pairing would change from a _____T-A______ base pair to a ______C-G_______ base pair.
  5. (2) Tautomerization, depurination, deamination and oxidative damage are all sources of ___spontaneous____ mutations.
  6. (2) In E. coli, a region flanked by two repeats of a sequence such as GTGGTGTAA is prone toanswer - a a) Deletion b) Missense mutation c) Duplication d) Inversion e) Frameshift mutation
  7. (2) The ionized form of 5-bromouracil will hydrogen bond to which base answer - c a) adenine b) cytosine c) guanine d) thymine e) uracil
  1. (2) The Ames test determines whether a compound is mutagenic by measuring __reversion______ frequencies of two different types of auxotrophic histidine mutations.
  2. (3) Acridine orange is an intercalating agent that causes ____frameshift___ mutations by inserting between ___bases_________ within the DNA double helix.
  3. (3) How does the mismatch repair system tell the newly replicated strand from the template strand?By determining which strand is methylated. The old (template) strand will be methylated.
  4. (3) Once damaged bases are removed by ___DNA glycosylases____________, the resulting AP sites are repaired by ____base excision repair/AP repair__________.
  5. (3) Name two reasons why heterozygous deletions are often lethal.
    1. Because recessive lethal mutations will be uncovered on the non-deleted homolog.2) Because of an alteration of gene dosage in the region of the deletion.
  6. (2) Through what process are tandem duplications generated?
    1. Unequal crossing-over.
    2. Slippage of repeats on the template strand.
  7. (2) A wild-type chromosome can be represented as ABCDEFGH, and from this a chromosomal aberrationarises that can be represented as ABCDEGFH. This is known as a: (* = centromere) answer - d a) Deletion b) Duplication c) Translocation d) paracentric inversion e) pericentric inversion
  8. (2) A crossover within the inverted region of __paracentric____ inversion will give rise to an acentric fragment and a dicentric fragment.
  9. (2) In a translocation heterozygote, what type of segregation will give rise to two complete and viable chromosome complements?Alternate segregation
  10. (4) What is the difference between an allopolyploid and an autopolyploid? An autopolyploid contains additional copies of the entire genome from the same species. An allopolyploid contains additional copies of the genome from another species.
  11. (3) Monosomics and disomics are generated because ___non-disjuntion______ occurred during eithermeiosis I or meiosis II.
  12. (2) What effect does age of the mother have on the probability of having a child with Down syndrome? Older mothers will have a higher probability of having a child with Downs syndrome.
  13. (3) In a haploid cross of m x +, which of the following linear octads shows the occurrence of gene conversion? a) ++++ mmmm b) ++ mmmm ++ c) +++++ mmm d) mm ++++ mm e) mmmm answer - c++++
  1. (2) Which of the following violate the assumptions of Hardy-Weinberg equilibrium? a) Little or no migrationd) random mating b) No selectione) No mutation c) Small population size answer - c
  2. (2) In an human population, the genotype frequencies at one locus are 0.5 AA, 0.4 Aa, and 0.1 aa. The frequency of the A allele in this population isa) 0.20 b) 0.32 c) 0.50 d) 0.70 e) 0.90 answer - d
  3. A population of rats in a Houston restaurant is measured for resistance to ebola virus.R 1 = resistant^ R 2 = sensitive Genotypes R 1 R 1 R 1 R 2 R 2 R 2 PhenotypesObserved numbers (n = 100) (Probability of infection upon exposure to 10 6 virions) 020 0.5 45 1.0 35 (2) What are the genotype frequencies? (2) RWhat are the allele frequencies?^1 R^1 = 20/100 or 0.20, R^1 R^2 = 45/100 or 0.45, R^2 R^2 = 35/100 or 0.35. RR 1 ƒ = 0.20 + 0.5(0.45) = 0.425. 2 ƒ = 0.35 + 0.5(0.45) = 0. (3) What are the expected genotypic frequencies?R R^1 R^1 = (0.425)^2 = 0. R^12 R R^22 = 2(0.425)(0.575) = 0.489= (0.575)2 = 0. (2) Assuming that the population is in Hardy-Weinberg equilibrium if observed genotypic frequencies are within 15% of expected frequencies, is this population in Hardy-Weienberg equilibrium?Yes
  4. (2) What two forms of variability lead from strict determination of phenotype by genotype to continuousvariation?
    1. Genotypic variation
    2. environmental variation
  5. (3) Why is additive genetic variance the only type of variation relevant to selection?Beacause it predicts how well a phenotype passes from parent to offspring.
  6. (2) Narrow heritability (h^2 ) is a quantification of the proportion of total variance due to a) phenotypic variance b) total genetic variance c) additive genetic variance answer - c d) dominance variance e) environmental variance