Chapter 11: Problem 3
Compare conservative, semiconservative, and dispersive modes of DNA replication.
Short Answer
Step by step solution
Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Chapter 11: Problem 3
Compare conservative, semiconservative, and dispersive modes of DNA replication.
These are the key concepts you need to understand to accurately answer the question.
All the tools & learning materials you need for study success - in one app.
Get started for freeSeveral temperature-sensitive mutant strains of \(E .\) coli display the following characteristics. Predict what enzyme or function is being affected by each mutation. (a) Newly synthesized DNA contains many mismatched base pairs. (b) Okazaki fragments accumulate, and DNA synthesis is never completed. (c) No initiation occurs. (d) Synthesis is very slow. (e) Supercoiled strands remain after replication, which is never completed.
In Kornberg's initial experiments, it was rumored that he grew E. coli in Anheuser-Busch beer vats. (Kornberg was working at Washington University in St. Louis.) Why do you think this might have been helpful to the experiment?
Many of the gene products involved in DNA synthesis were initially defined by studying mutant \(E\), coli strains that could not synthesize DNA. (a) The \(d n a E\) gene encodes the \(\alpha\) subunit of DNA polymerase III. What effect is expected from a mutation in this gene? How could the mutant strain be maintained? (b) The \(d n a Q\) gene encodes the \(\epsilon\) subunit of DNA polymerase. What effect is expected from a mutation in this gene?
In \(1994,\) telomerase activity was discovered in human cancer cell lines. Although telomerase is not active in human somatic tissue, human somatic cells do contain the genes for telomerase proteins and telomerase RNA. since inappropriate activation of telomerase may contribute to cancer, why do you think the genes coding for this enzyme have been maintained in the human genome throughout evolution? Are there any types of human body cells where telomerase activation would be advantageous or even necessary? Explain.
What are the requirements for in vitro synthesis of DNA under the direction of DNA polymerase I?
What do you think about this solution?
We value your feedback to improve our textbook solutions.