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1. The specified karyotype has two X chromosomes and no Y chromosome, so the person is a female. The female carries three copies of chromosome 21, i.e. trisomy 21 or Down Syndrome. Ans: (c) female with Down Syndrome 2, Albinism is an autosomal recessive disorder- one copy of the wild type allele is sufficient for a wild type phenotype It also manifests as a morphological mutation, in that the mutant phenotype is detectable due to an absence of melanocytes in the skin. Ans (a) morphological 3. As discussed in class, chromosome 2 in humans looks like it represents a Robertsonian translocation relative to other primate chromosomes A close examination of the banding patterns on chromsomes 4 and 5 indicate that they look as if breaks occurred to either side of the centromere for both chromosomes- i.e. pericentric inversions. Ans: (d) all of the above. 4. Variegated position effects are caused when a gene in a euchromatic region of the chromosome is transferred into or near a heterochromatic block…see pp. 430-31 Ans: (b) inversion that moves a gene from euchromatin into or near heterochromatin 5. 1: 143 2: 152 3: 160 4: 155 5: 148 6: 98 Contain 3/2 (150%) of what is observed in diploid cells, i.e. are carrying an extra gene copy Contains only a diploid amount of enzyme… z+ Ans: (d) Band 3 x y The previous quiz had a similar problem using deletions to map gene location…pseudodominance. Make sure you review this topic as well (pp. 448-50). 6. A double crossover must occur between the same non-sister chromatids for an exchange to generate balanced gametes. Ans: (d) z Pseudodominance: phenotype of deletion heterozygote is mutant (-) for x and y; wild type (+) for z D C c d b B a e E A a d C b e A B c D E 7. Expected characteristics: a) F+ will transfer chromosomal gene markers at LOW frequency (L = low recombinants) only to F− cells b) Hfr will transfer chromosomal gene markers at HIGH frequency (M = many recombinants) only to F− cells c) F− cells will yield no recombinants if crossed to themselves, but could show either L or M colonies depending on whether they are crossed to F+ or Hfr strains… Using these criteria: Strains 2, 5 and 6 must be F- cells Strain 1 and 4 must be Hfrs Strains 3, 7 and 8 must be F+ cells Ans: (c) 8. Crosses 2 and 7 would represent a F- x F+ cross. In this cross, the F factor would be expected to be transferred to virtually every cell, making them all F+ and consequently expressing the genes required to produce pili. Ans: (a) true Cross Hfr A x F Hfr B x F Hfr C x F Hfr D x F Hfr E x F Entry time (in minutes) for Hfr wild type genes x+ gene y+ gene 15 75 45 5 65 5 10 50 65 25 9. The integration site for B is 30 minutes away from the integration site for A Ans: (d) 10. Both the A and B F factors have integrated into the bacterial chromosome in the same relative orientation and their respective Hfr’s donate in the clockwise direction. Ans: (a) true x C y B