MIT Biology Department 7.012: Introductory Biology-Fall 2004 Instructors: Professor Eric Lander, Professor Robert A. Weinberg Dr Claudette Gardel Name Section 7.012 Problem set 4 Please print out this problem set and record your answers on the printed copy. Answers to this problem set are to be turned in at the box outside by 4: 10 Wednesday, October 8. Problem sets will not be accepted late Solutions will be posted on the web October 9, 2003. Question 1 Below is an electron micrograph of a single gene being transcribed. The DNA strand runs horizontally with RNa transcripts extending vertically outward Image removed due to copyright reasons. a)Draw an arrow indicating the direction that the Rna polymerases are transcribing.Why did you choose this direction? b) Below is a partial sequence of the above gene. Its orientation is the same as pictured above Which strand is the template strand the top or the bottom strand? Explain your choice ACTCGATGCTAG S TGAGCTACGATC c)What would be the mRNA sequence transcribed from the above sequence? Be sure to label the5′and3′ends 7012Fall2003
MIT Biology Department 7.012: Introductory Biology - Fall 2004 Instructors: Professor Eric Lander, Professor Robert A. Weinberg, Dr. Claudette Gardel Name:___________________________________ Section:_____ 7.012 Problem Set 4 Please print out this problem set and record your answers on the printed copy. Answers to this problem set are to be turned in at the box outside by 4:10 Wednesday, October 8. Problem sets will not be accepted late. Solutions will be posted on the web October 9, 2003. Question 1 Below is an electron micrograph of a single gene being transcribed. The DNA strand runs horizontally with RNA transcripts extending vertically outward. Image removed due to copyright reasons. a) Draw an arrow indicating the direction that the RNA polymerases are transcribing. Why did you choose this direction? b) Below is a partial sequence of the above gene. Its orientation is the same as pictured above. Which strand is the template strand, the top or the bottom strand? Explain your choice. 5’ACTCGATGCTAG3’ 3’TGAGCTACGATC5’ c) What would be the mRNA sequence transcribed from the above sequence? Be sure to label the 5’ and 3’ ends. 7.012 Fall 2003 1
Name ection: Question 2 A tRNa molecule(shown below)is composed of an Rna chain that folds into a 3-D shape like that shown below. At one end it has an anti-codon that base pairs with the appropriate codon on the mRna and at the other end it has an amino acid arm that binds to a specific amino acid Below are three anti-codon sequences for three tRNAs, fill in the corresponding amino acid on the blanks Amino acid arm Anticodon Figure by MIT OCW anticodon found on trna amino acid attached to trNA SAGU 3 5 5 b) You are studying a certain enzyme. You have two mutant versions, one that works just as well as the wild-type and another that doesn't work at all. When you sequence the genes that code for these two mutant enzymes you find the enzyme that works has a 9 base pair deletion, whereas the enzyme that does not work has only a single base pair deletion. Explain why the sequence with the 9 base pair deletion results in an active enzyme when the sequence with a single base pair deletion produces an inactive enzyme cThe first 17 nucleotides from an mRNa molecule are GAaUGGCaCUUagCaa Write out the first 5 amino acids encoded by this sequence 7012Fall2003
_____________________ _____________________ _____________________ Name:___________________________________ Section:_____ Question 2 A tRNA molecule (shown below) is composed of an RNA chain that folds into a 3-D shape like that shown below. At one end it has an anti-codon that base pairs with the appropriate codon on the mRNA and at the other end it has an amino acid arm that binds to a specific amino acid. Below are three anti-codon sequences for three tRNAs, fill in the corresponding amino acid on the blanks. Amino acid arm Anticodon Amino acid arm Anticodon Figure by MIT OCW. anticodon found on tRNA amino acid attached to tRNA 5’ AGU 3’ 5’ AUG 3’ 5’ CUG 3’ b) You are studying a certain enzyme. You have two mutant versions, one that works just as well as the wild-type and another that doesn’t work at all. When you sequence the genes that code for these two mutant enzymes you find the enzyme that works has a 9 base pair deletion, whereas the enzyme that does not work has only a single base pair deletion. Explain why the sequence with the 9 base pair deletion results in an active enzyme when the sequence with a single base pair deletion produces an inactive enzyme. c)The first 17 nucleotides from an mRNA molecule are 5’ GAAUGGCCACUUAGCAA…3’ Write out the first 5 amino acids encoded by this sequence. 7.012 Fall 2003 2
Name ection: Question 3 a)How does the structure of the lac operon ensure that the lac genes are coordinately controlled? Why would this be beneficial? b)Describe the regulation of the lac operon (inducible, uniducible, or constitutive)in the case of each of the following mutants. In all cases the concentration glucose is low. Explain your choice i)A mutation in the lac repressor such that it can't bind DNA ii)A mutation that makes lac permease nonfunctional i)A mutant promoter that has a high affinity for polymerase iv)A mutant lac repressor that doesn,'t bind lactose c) You have a cell where the expression of the lac operon is constitutive due to a mutation in normal regulation be restored? Explain. pletely wild-type version of the lac operon would the operator. If you add to that cell a cor 7012Fall2003
Name:___________________________________ Section:_____ Question 3 a) How does the structure of the lac operon ensure that the lac genes are coordinately controlled? Why would this be beneficial? b) Describe the regulation of the lac operon (inducible, uniducible, or constitutive) in the case of each of the following mutants. In all cases the concentration glucose is low. Explain your choice. i) A mutation in the lac repressor such that it can’t bind DNA ii) A mutation that makes lac permease nonfunctional iii) A mutant promoter that has a high affinity for polymerase iv) A mutant lac repressor that doesn’t bind lactose c) You have a cell where the expression of the lac operon is constitutive due to a mutation in the operator. If you add to that cell a completely wild-type version of the lac operon would normal regulation be restored? Explain. 7.012 Fall 2003 3
Name Section Question 4 Lambda phage is a virus that infects e. coli bacteria. After infecting the bacteria it can take one of two paths, lysis or lysogeny. In the lysis path, the phage makes many copies of itself, breaks out of the cell and infects new cells. In lysogeny, the phage incorporates its DNA into the bacterial DNA and lays dormant in the cell. The presence of a protein called lambda repressor influences which path is taken by inhibiting lysis. When lambda repressor is present it turns off or represses the genes that allow the virus to reproduce, thus no phage progeny are produced and no cell lysis occurs a) In studying this protein you find that lambda repressor binds DNa at a site that overlaps the promoter for the lysis genes. Propose a mecha pression based on this information b) Activators typically work by binding near a promoter site and recruiting RNa polymerase to the promoter by forming non-covalent bonds with it. This helps the polymerase attach to the promoter and increases transcription from that promoter Although lambda repressor turns off the transcription of the lysis genes it stimulates the expression of its own lambda repressor gene(acts as an activator). In studying lambda repressor you find that there are two amino acids, Asp and glu, which are essential to the activator function. based on this information what type of bonds do you expect Lambda repressor to make with Rna polymerase and what type of amino acids do you expect to find on polymerase participating in these bonds? 7012Fall2003
Name:___________________________________ Section:_____ Question 4 Lambda phage is a virus that infects E. coli bacteria. After infecting the bacteria it can take one of two paths, lysis or lysogeny. In the lysis path, the phage makes many copies of itself, breaks out of the cell and infects new cells. In lysogeny, the phage incorporates its DNA into the bacterial DNA and lays dormant in the cell. The presence of a protein called lambda repressor influences which path is taken by inhibiting lysis. When lambda repressor is present it turns off or represses the genes that allow the virus to reproduce, thus no phage progeny are produced and no cell lysis occurs. a) In studying this protein you find that lambda repressor binds DNA at a site that overlaps the promoter for the lysis genes. Propose a mechanism for repression based on this information. b) Activators typically work by binding near a promoter site and recruiting RNA polymerase to the promoter by forming non-covalent bonds with it. This helps the polymerase attach to the promoter and increases transcription from that promoter. Although Lambda repressor turns off the transcription of the lysis genes, it stimulates the expression of its own lambda repressor gene (acts as an activator). In studying lambda repressor you find that there are two amino acids, Asp and Glu, which are essential to the activator function. Based on this information what type of bonds do you expect Lambda repressor to make with RNA polymerase and what type of amino acids do you expect to find on polymerase participating in these bonds? 7.012 Fall 2003 4
