Chapter 12: Problem 10
Why doesn't polynucleotide phosphorylase (Ochoa's enzyme) synthesize RNA in vivo?
Short Answer
Step by step solution
Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Chapter 12: Problem 10
Why doesn't polynucleotide phosphorylase (Ochoa's enzyme) synthesize RNA in vivo?
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 freeReview the Chapter Concepts list on p. 231. These all center on how genetic information is stored in DNA and transferred to RNA prior to translation into proteins. Write a short essay that summarizes the key properties of the genetic code and the process by which RNA is transcribed on a DNA.
Alternative splicing is a common mechanism for eukaryotes to expand their repertoire of gene functions. Studies by Xu and colleagues (2002. Nuc. Acids Res. 30: 3754-3766) indicate that approximately 50 percent of human genes use alternative splicing, and approximately 15 percent of disease-causing mutations involve aberrant alternative splicing. Different tissues show remarkably different frequencies of alternative splicing, with the brain accounting for approximately 18 percent of such events. (a) Define alternative splicing and speculate on the evolutionary strategy alternative splicing offers to organisms. (b) Why might some tissues engage in more alternative splicing than others?
When the amino acid sequences of insulin isolated from different organisms were determined, some differences were noted. For example, alanine was substituted for threonine, serine was substituted for glycine, and valine was substituted for isoleucine at corresponding positions in the protein. List the single-base changes that could occur in triplets to produce these amino acid changes.
In studies of frameshift mutations, Crick, Barnett, Brenner, and Watts-Tobin found that either three nucleotide insertions or deletions restored the correct reading frame. (a) Assuming the code is a triplet, what effect would the addition or loss of six nucleotides have on the reading frame? (b) If the code were a sextuplet (consisting of six nucleotides), would the reading frame be restored by the addition or loss of three, six, or nine nucleotides?
"Breaking the genetic code" has been referred to as one of the most significant scientific achievements in modern times. Describe (in outline or brief statement form) the procedures used to break the code.
What do you think about this solution?
We value your feedback to improve our textbook solutions.