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Most amino acids are coded for by a set of similar codons (see Figure17.6). Propose at least one evolutionary explanation to account for this pattern.

Short Answer

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The amino acids are coded with a similar set of codons. Codon is the three-nucleotide sequence that is present in the DNA that can produce an amino acid.

Three different types of theories that deal with the origin and evolution of the codon are stereochemical theory, coevolution theory, and error minimization theory.

Step by step solution

01

Amino acids

Amino acids are the basic building block of the protein encoded in the DNA. These amino acids are produced out of genetic code that corresponds to a particular amino acid.

02

Stereochemical theory

There exists physicochemical affinity between the amino acids’ codon and nucleotide triplets. The physical property is an essential reason for the repetitions of the amino acid codon that codes for a particular amino acid.

03

Coevolution theory

According to this theory, the amino acid biosynthesis pathway is responsible for the amino acids codon arrangement. The gene is another controlling factor that can determine the similar codon responsible for coding particular amino acids.

04

Error minimization theory

The genetic code can minimize transcriptional as well as translational error. It reduces the randomization of amino acids. After minimization of randomization, the genetic code transfers into amino acids.

According to this theory, the similarity between amino acid codons results from a reduction in randomization.

Hence, the codons corresponding to amino acids arise out of three major evolutionary theories: stereochemical, coevolution, and error minimization.

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Most popular questions from this chapter

Evolution accounts for the unity and diversity of life, and the continuity of life is based on heritable information in the form of DNA. In a short essay (100-150words), discuss how the fidelity with which DNA is inherited is related to the processes of evolution. (Review the discussion of proofreading and DNA repair in Concept 16.2)

The anticodon of a particular tRNA molecule is:

  1. complementary to the corresponding mRNA codon.

  2. complementary to the corresponding triplet in rRNA.

  3. the part of tRNA that bonds to a specific amino acid.

  4. catalytic, making the tRNA a ribozyme.

What happens when one nucleotide pair is lost from the middle of the coding sequence of a gene?

In the sequence logo (bottom, left), the horizontal axis shows the primary sequence of the DNA by nucleotide position. Letters for each base are stacked on top of each other according to their relative frequency at that position among the aligned sequences, with the most common base as largest letter at the top of the stack. The height of each letter represents the relative frequency of that base at that position. (a) In the sequence alignment, count the number of each base at position-9 and order them from the most to least frequent. Compare this to the size and placement of each base -9 in the logo. (b) Do the same for position 0 and 1.

Individuals heterozygous for the sickle-cell allele are generally healthy but show phenotypic effects of the allele under some circumstances (see Figure 14.17). Explain in terms of gene expression.

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