Chapter 9

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Chapter 9 Using the Genetic Code

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Chapter 9. Using the Genetic Code. 9.1Introduction. The sequence of a coding strand of DNA is read in the direction from 5′ to 3′. This corresponds to the amino acid sequence of a polypeptide read from N-terminus to C-terminus. 9.2Related Codons Represent Related Amino Acids. - PowerPoint PPT Presentation

Transcript of Chapter 9

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Chapter 9

Using the Genetic Code

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9.1 Introduction

The sequence of a coding strand of DNA is read in the direction from 5′ to 3′.

This corresponds to the amino acid sequence of a polypeptide read from N-terminus to C-terminus.

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9.2 Related Codons Represent Related Amino Acids

• Sixty-one of the sixty-four possible triplets code for twenty amino acids.

• Three codons do not represent amino acids and cause termination of translation.

Figure 9.01: The genetic code is triplet.

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9.2 Related Codons Represent Related Amino Acids

• The genetic code was frozen at an early stage of evolution and is universal.

• Most amino acids are represented by more than one codon.

• The multiple codons for an amino acid are usually related.

• Related amino acids often have related codons, minimizing the effects of mutation.

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Figure 9.02: The number of codons for each amino acid does not correlate closely with its frequency of use in proteins.

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9.3 Codon–Anticodon Recognition Involves Wobbling

• Multiple codons that represent the same amino acid most often differ at the third base position.

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9.3 Codon–Anticodon Recognition Involves

Wobbling

• The wobble in pairing between the first base of the anticodon and the third base of the codon results from the structure of the anticodon loop.

Figure 9.04: G-U pairs form at the third codon base.

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9.3 Codon–Anticodon Recognition Involves Wobbling

Figure 9.5 Codon-anticodon pairing involves wobbling at third position.

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9.4 tRNA Contains Modified Bases

• tRNAs contain >50 modified bases.

• Modification usually involves direct alteration of the primary bases in tRNA.– There are some exceptions in which a base is

removed and replaced by another base.

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9.4 tRNA Contains Modified Bases

Figure 9.06: Base modifications in tRNA vary in complexity.

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9.5 Modified Bases Affect Anticodon–Codon Pairing

Modifications in the anticodon affect the pattern of wobble pairing. They are important in determining tRNA specificity.

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9.5 Modified Bases Affect Anticodon–Codon Pairing

Figure 9.07: Inosine pairs with three bases.

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9.5 Modified Bases Affect Anticodon–Codon Pairing

Figure 9.8: Modification to 2-thiouracil restricts paring to A

alone because only one H-bond can form with G.

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9.6 There Are Sporadic Alterations of the Universal Code

• Changes in the universal genetic code have occurred in some species.

• These changes are more common in mitochondrial genomes, where a phylogenetic tree can be constructed for the changes.

• In nuclear genomes, the changes are sporadic and usually affect only termination codons.

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9.6 There Are Sporadic Alterations of the Universal Code

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9.6 There Are Sporadic Alterations of the Universal Code

Figure 9.10: Mitochondria have changes in the genetic code.

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9.7 Novel Amino Acids Can Be Inserted at Certain Stop Codons

• Changes in the reading of specific codons can occur in individual genes.

• The insertion of seleno-Cys-tRNA at certain UGA codons requires several proteins to modify the Cys-tRNA and insert it into the ribosome.

• Pyrrolysine can be inserted at certain UAG codons.

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9.7 Novel Amino Acids Can Be Inserted at Certain Stop Codons

SelB is an elongation factor specific for Seleno-Cys-tRNA.

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9.8 tRNAs Are Charged with Amino Acids by Synthetases

• Aminoacyl-tRNA synthetases are enzymes that charge tRNA with an amino acid to generate aminoacyl-tRNA in a two-stage reaction that uses energy from ATP.

• There are twenty aminoacyl-tRNA synthetases in each cell. Each charges all the tRNAs that represent a particular amino acid.

• Recognition of a tRNA is based on a small number of points of contact in the tRNA sequence.

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9.8 tRNAs Are Charged with Amino Acids by Synthetases

Figure 9.12: The charging reaction uses ATP.

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9.9 Aminoacyl-tRNA Synthetases Fall into Two Groups

Aminoacyl-tRNA synthetases are divided into the class I and class II groups by sequence and structural similarities.

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9.9 Aminoacyl-tRNA Synthetases Fall into Two Groups

Figure 9.13: Class I (Glu-tRNA synthetase) and Class II (Asp-tRNA synthetase).

Photo courtesy of Dino Moras, Institute of Genetics and Molecular and Cellular Biology

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9.10 Synthetases Use Proofreading to Improve Accuracy

Specificity of recognition of both amino acid and tRNA is controlled by aminoacyl-tRNA synthetases. They function through proofreading reactions that

reverse the catalytic reaction if the wrong component has been incorporated.

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9.10 Synthetases Use Proofreading to Improve

Figure 9.16: Synthetases use chemical proofreading.

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9.11 Suppressor tRNAs Have Mutated Anticodons That Read New Codons

• A suppressor tRNA typically has a mutation in the anticodon that changes the codons to which it responds.

• Each type of nonsense codon is suppressed by tRNAs with mutant anticodons.

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9.11 Suppressor tRNAs Have Mutated Anticodons That Read New Codons

• When the new anticodon corresponds to a termination codon, an amino acid is inserted and the polypeptide chain is extended beyond the termination codon. – This results in:

• nonsense suppression at a site of nonsense mutation, or • readthrough at a natural termination codon

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9.11 Suppressor tRNAs Have Mutated Anticodons That Read New Codons

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9.11 Suppressor tRNAs Have Mutated Anticodons That Read New Codons

Figure 9.20: Nonsense suppression causes readthrough.

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• Suppressor tRNAs compete with wild type tRNAs that have the same anticodon to read the corresponding codon(s).

• Efficient suppression is deleterious because it results in readthrough past normal termination codons.

9.11 Suppressor tRNAs Have Mutated Anticodons That Read New Codons

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9.11 Suppressor tRNAs Have Mutated Anticodons That Read New Codons

• Missense suppression occurs when the tRNA recognizes a different codon from usual, so that one amino acid is substituted for another.

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9.11 Suppressor tRNAs Have Mutated Anticodons That Read

New Codons

Figure 9.21: Missense suppressors compete with wild type.

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9.12 Recoding Changes Codon Meanings

• Changes in codon meaning can be caused by mutant tRNAs or by tRNAs with special properties.

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9.12 Recoding Changes Codon Meanings

Figure 9.22: Special or mutant tRNAs change meaning.

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9.12 Recoding Changes Codon Meanings

• The reading frame can be changed by frameshifting or bypassing, both of which depend on properties of the mRNA.

Figure 9.23: Frameshifts can suppress termination.

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9.12 Recoding Changes Codon Meanings

Figure 9.24: Bypassing skips between identical codons.

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9.13 Frameshifting Occurs at Slippery Sequences

• The reading frame may be influenced by the sequence of mRNA and the ribosomal environment.

• Slippery sequences allow a tRNA to shift by one base after it has paired with its anticodon, thereby changing the reading frame.

• Translation of some genes depends upon the regular occurrence of programmed frameshifting.

• Some mutant tRNA suppressors recognize a four base codon instead of normal three bases.

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9.13 Frameshifting Occurs at Slippery Sequences

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9.14 Bypassing Involves Ribosome Movement

A ribosome encounters a GGA codon adjacent to a stop codon in a specific stem-loop structure.

It moves directly to a specific GGA downstream without adding amino acids to the polypeptide.

Figure 9.26: A ribosome can bypass a sequence of

mRNA.