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Review 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.

Short Answer

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Question: Explain the key properties of the genetic code and describe the process of RNA transcription on a DNA template. Answer: The genetic code is a set of rules defining how DNA or RNA sequences are translated into amino acid sequences in proteins. It has three main properties: 1) Triplet code - codons or groups of three nucleotides code for specific amino acids; 2) Degeneracy - most amino acids are coded by more than one codon, allowing mutation tolerance; 3) Universality - the same codons code for the same amino acids in almost all organisms. Transcription, the process of transferring genetic information from DNA to RNA, comprises three stages: Initiation - RNA polymerase binds to a DNA promoter, unwinding the double helix; Elongation - RNA polymerase moves along the DNA template, adding complementary RNA nucleotides; Termination - transcription ends upon encountering a DNA terminator sequence, releasing the RNA molecule.

Step by step solution

01

Introduction

Genetic information is stored in DNA and transferred to RNA, which is later translated into proteins, the functional molecules in cells. In this essay, the key properties of the genetic code and the process of RNA transcription on a DNA template will be summarized.
02

Key Properties of the Genetic Code

The genetic code is the set of rules that determine how the nucleotide sequence in DNA or RNA is translated into the amino acid sequence in proteins. There are three main properties of the genetic code: 1. Triplet code: The genetic code is a triplet code, with each group of three nucleotides (called a codon) coding for a specific amino acid. There are 64 possible codons (4^3 combinations of the four nucleotides), of which 61 code for the 20 amino acids and 3 function as stop codons, signaling the end of translation. 2. Degeneracy: The genetic code is degenerate, meaning that most amino acids are coded for by more than one codon. This redundancy allows for some tolerance of mutations, as a single nucleotide change may not necessarily result in a different amino acid. 3. Universality: The genetic code is largely universal, with few exceptions, meaning that the same codons code for the same amino acids in almost all organisms. This shared genetic language supports the concept of a common ancestor for all life on Earth.
03

RNA Transcription Process

Transcription is the process by which genetic information stored in DNA is transferred to a complementary RNA molecule. This process occurs in three main stages: 1. Initiation: Transcription begins when an enzyme called RNA polymerase binds to a specific sequence on the DNA (the promoter). This binding unwinds the DNA double helix, exposing the template strand that will be used for RNA synthesis. 2. Elongation: RNA polymerase moves along the template strand, "reading" the DNA sequence and adding complementary RNA nucleotides to the growing RNA chain. Adenine (A) in DNA binds to uracil (U) in RNA, whereas cytosine (C) and guanine (G) bind as they do in DNA. 3. Termination: Transcription ends when RNA polymerase encounters a specific DNA sequence (the terminator) that signals the end of the gene. At this point, the RNA molecule is released, and the DNA double helix reforms. In summary, the genetic code is a triplet, degenerate, and universal code that translates nucleotide sequences in DNA or RNA into amino acid sequences in proteins. The transcription process transfers genetic information from DNA to RNA, which later undergoes translation to produce functional proteins.

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Most popular questions from this chapter

Suppose that in the use of polynucleotide phosphorylase, nucleotides A and C are added in a ratio of 1A:5C. What is the probability that an AAA sequence will occur?

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.

Why doesn't polynucleotide phosphorylase (Ochoa's enzyme) synthesize RNA in vivo?

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?

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