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310    Chapter 8    Gene Expression: The Flow of Information from DNA to RNA to Protein


                17.  You identify a proflavin­generated allele of a gene   the electron microscope? Your figure should include
                  that produces a 110­amino acid polypeptide rather    hybridization involving both DNA strands (template
                  than the usual 157­amino acid protein. After subjecting   and RNA­like) as well as the mRNA.
                  this mutant allele to extensive proflavin mutagenesis,   23.  In studying normal and mutant forms of a particular
                  you are able to find a number of intragenic suppressors   human enzyme, a geneticist came across a particu­
                  located in the part of the gene between the sequences   larly interesting mutant form of the enzyme. The
                  encoding the N terminus of the protein and the original   normal enzyme is 227 amino acids long, but the
                  mutation, but no suppressors located in the region    mutant form was 312 amino acids long. The extra
                  between the original mutation and the sequences      85 amino acids occurred as a block in the middle
                  encoding the usual C terminus of the protein. Why    of the normal sequence. The inserted amino acids
                  do you think this is the case?                       do not correspond in any way to the normal protein
              18.  Using recombinant DNA techniques (which will        sequence. What are possible explanations for
                  be described in Chapter 9), it is possible to take the   this phenomenon? How would you distinguish
                  DNA of a gene from any source and place it on a      among them?
                  chromosome in the nucleus of a yeast cell. When    24.  The Drosophila gene Dscam1 encodes proteins on the
                  you take the DNA for a human gene and put it into a   surface of nerve cells (neurons) that govern neuronal
                  yeast cell chromosome, the altered yeast cell can    connections. Each neuron has on its surface a single
                  make the human protein. But when you remove the      Dscam1 protein of the tens of thousands that exist.
                  DNA for a gene normally present on yeast mitochon­   The particular Dscam1 protein a neuron expresses is
                  drial chromosomes and put it on a yeast chromosome in   thought to tag the cell uniquely to determine the paths
                  the nucleus, the yeast cell cannot synthesize the correct   of the axons and dendrites it will grow. Eukaryotic
                  protein, even though the gene comes from the same    genes are monocistronic. How then can a single
                  organism. Explain. What would you need to do to ensure   Dscam1 gene encode tens of thousands of different
                  that such a yeast cell could make the correct protein?  proteins?


              Section 8.2
                                                                   Section 8.3
              19.  Describe the steps in transcription that require com­
                  plementary base pairing.                         25.  Describe the steps in translation that require comple­
              20.  Chapters 6 and 7 explained that mistakes made by    mentary base pairing.
                  DNA polymerase are corrected either by proofread­  26.  Locate as accurately as possible the listed items that
                  ing mechanisms during DNA replication or by DNA      are shown on the following figure. Some items are not
                  repair systems that operate after replication is com­  shown. (a) 5′ end of DNA template strand; (b) 3′ end
                  plete. The overall rate of errors in DNA replication is   of mRNA; (c) ribosome; (d) promoter; (e) codon;
                  about 1 × 10 −10 , that is, one error in 10 million base   (f) an amino acid; (g) DNA polymerase; (h) 5′ UTR;
                  pairs. RNA polymerase also has some proofreading     (i) centromere; (j) intron; (k) anticodon; (l) N termi­
                  capability, but the overall error rate for transcription   nus; (m) 5′ end of charged tRNA; (n) RNA polymerase;
                                           −4
                  is significantly higher (1 × 10 , or one error in each   (o) 3′ end of uncharged tRNA; (p) a nucleotide;
                  10,000 nucleotides). Why can organisms tolerate      (q) mRNA cap; (r) peptide bond; (s) P site; (t) aminoacyl­
                  higher error rates for transcription than for DNA    tRNA synthetase; (u) hydrogen bond; (v) exon;
                  replication?                                         (w) 5′ AUG 3′; (x) potential wobble interaction.
              21.  The coding sequence for gene F is read from left to
                  right on the accompanying figure. The coding se­
                  quence for gene G is read from right to left. Which
                  strand of DNA (top or bottom) serves as the template
                  for transcription of each gene?
                                                                             A C C                     A U G
              5'                                              3'                       GGG    UA C         UA A
                        Gene F                  Gene G
               3'                                             5'
                                                                   27.  Concerning the figure for Problem 26:
              22.  If you mixed the mRNA of a human gene with the
                  genomic DNA for the same gene and allowed the        a.  Which process is being represented?
                  RNA and DNA to form a hybrid molecule by base        b. What is the next building block to be added to the
                  complementarity, what would you be likely to see in    growing chain in the figure? To what end of the
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