
Biochemistry
9th Edition
ISBN: 9781319114671
Author: Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher: W. H. Freeman
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Compare DNA polymerase and RNA polymerase from E. coli in regard to each of the following features: (a) activated precursors,
(b) direction of chain elongation,
(c) conservation of the template, and
(d) need for a primer.
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- and set up a series of four dideoxy reactions (the dideoxy nucleotides are labeled with radioactive P32 ). You then separate the products of the reactions by gel electrophoresis and obtain the following banding pattern: a) Write out the base sequence of the newly synthesized strand from reading the gel (include the 5’ and 3’; end) b) Write out the base sequence of the original fragment you were given (include the 5’ and 3’ end)arrow_forwarda. Propose three different mutations to prevent initiation, elongation, and termination of bacterial DNA replication, respectively. Explain how/why each mutation would prevent its respective step. (Hint: mutations can be in genes that encode proteins or regulatory DNA sequences) b. In the early 1900s, Avery, MacLeod, and McCarty performed an experiment in bacterial cells to determine whether DNA, RNA, or protein functions as the 'transforming molecule' (i.e. the genetic material). In your own words, how did their experiment (depicted in the figure below) help to answer that question?arrow_forwardPlease label the following: (A) INITIATION *Complementary strand *Template Strand *RNA polymerase *Initiation Site *Termination Site *Promoter *5' and 3' end on each DNA strand Initiation (A) FRA FORÆTSIST Elongation (B) (C) restorag Termination IND PLATIN RNA (B) ELONGATION *Exiting DNA *Exiting RNA Transcript *Template Strand *Nucleotides (ATP, UTP, CTP, GTP) *Direction of transcription PHILLI 13' DIDIarrow_forward
- You isolate a mouse Tau-gene-containing DNA fragment from the chicken and hybridize it to the freshly-made and isolated hnRNA (primary transcript) from the nucleus of the mouse cells transcribed from the Tau gene (immediately after it was produced), allowing no time for processing of the hnRNA. Describe what you see when you look at the DNA/RNA hybrid molecule under the electron microscope.arrow_forwardWhat type of repair would be used to fix a mutation that arises during replication and that escapes detection by polymerase proofreading mechanisms? What is the most likely reason that this mutation escaped correction during proofreading?arrow_forwardFor the experiment shown Fig. 6.30 and 6.31, what is the advantage to use a labeled incoming nucleotide (α-32P-UTP or α-32P-CTP), not labeled reagent 1 itself? Please draw a diagram to help explain your answer by contrasting the RNA polymerase labeled with α-32P-Reagent (Panel A) vs α-32P-UTP (Panel B).arrow_forward
- Suppose that you want to assay reverse transcriptase activity. If polyriboadenylate is the template in the assay, what should you use as the primer? Which radioactive nucleotide should you use to follow chain elongation?arrow_forwardCan you help solve this problem?arrow_forwardDNA polymerases cannot act as primers for replication, yet primase and other RNA polymerases can. Some geneticists have speculated that the inability of DNA polymerase to prime replication is a result of its proofreading function. This hypothesis argues that proofreading is essential for the faithful transmission of genetic information and that because DNA polymerases have evolved the ability to proofread, they cannot prime DNA synthesis. Explain why proofreading and priming functions in the same enzyme might be incompatible.arrow_forward
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