Chapter 12: Problem 17
Define the process of transcription. Where does this process fit into the central dogma of molecular genetics?
Chapter 12: Problem 17
Define the process of transcription. Where does this process fit into the central dogma of molecular genetics?
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Get started for freeOne form of posttranscriptional modification of most eukaryotic RNA transcripts is the addition of a poly-A tail at the \(3^{\prime}\) -end. The absence of a poly-A tail leads to rapid degradation of the transcript. Poly-A tails of various lengths are also added to many bacterial RNA transcripts where, instead of promoting stability, they enhance degradation. In both cases, RNA secondary structures, stabilizing proteins, or degrading enzymes interact with poly-A tails. Considering the activities of RNAs, what might be the general functions of \(3^{\prime}\) -polyadenylation??
Alternative splicing is a common mechanism for eukaryotes to expand their repertoire of gene functions. At least one estimate indicates that approximately 50 percent of human genes use alternative splicing, and approximately 15 percent of diseasecausing 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?
In this chapter, we focused on the genetic code and the transcription of genetic information stored in DNA into complementary RNA molecules. Along the way, we found many opportunities to consider the methods and reasoning by which much of this information was acquired. From the explanations given in the chapter, what answers would you propose to the following fundamental questions: (a) How did we determine the compositions of codons encoding specific amino acids? (b) How were the specific sequences of triplet codes determined experimentally? (c) How were the experimentally derived triplet codon assignments verified in studies using bacteriophage MS2? (d) How do we know that mRNA exists and serves as an intermediate between information encoded in DNA and its concomitant gene product? (e) How do we know that the initial transcript of a eukaryotic gene contains noncoding sequences that must be removed before accurate translation into proteins can occur?
Most proteins have more leucine than histidine residues but more histidine than tryptophan residues. Correlate the number of codons for these three amino acids with this information.
Describe the structure of RNA polymerase in bacteria. What is the core enzyme? What is the role of the \(\sigma\) factor?
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