Chapter 10: Molecular Biology of Gene Expression Jones and Bartlett Publishers © 2005.

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Chapter 10: Molecular Biology of Gene Expression Jones and Bartlett Publishers © 2005

Transcript of Chapter 10: Molecular Biology of Gene Expression Jones and Bartlett Publishers © 2005.

Page 1: Chapter 10: Molecular Biology of Gene Expression Jones and Bartlett Publishers © 2005.

Chapter 10:

Molecular Biology of

Gene Expression

Jones and Bartlett Publishers © 2005

Page 2: Chapter 10: Molecular Biology of Gene Expression Jones and Bartlett Publishers © 2005.

Chapter 10.1- 10.3

• Details of the central dogma will be discussed in Chapter 10.

• For Exam 3, we will cover up through p. 408.

• Our main topic for the rest of this lecture will be transcription, but first we will review amino acids and polypeptide chains.

Page 3: Chapter 10: Molecular Biology of Gene Expression Jones and Bartlett Publishers © 2005.

Structure of an amino acid

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Structure of all 20 amino acids commonly found in proteins

Page 5: Chapter 10: Molecular Biology of Gene Expression Jones and Bartlett Publishers © 2005.

Joining of amino acids by peptide bonds to create polypeptides

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Three-dimensional structure of a monomeric protein

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Location of a number of mutants in the trpA gene and the resulting amino acid replacements

Colinearity – the sequence of base pairs in DNA determines the amino acid sequence in a colinear manner.

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Transcription

• Transcription is the synthesis of RNA from the DNA coding for the gene.

• (Remember the differences between DNA and RNA).– RNA uses the four ribonucleosides ATP, GTP

CTP and UTP.– RNA polymerase is used instead of DNA

polymerase.– A promoter is used for initiation of

transcription (not a primer, as with DNA).

Page 9: Chapter 10: Molecular Biology of Gene Expression Jones and Bartlett Publishers © 2005.

A ribonucleoside differs from a deoxyribonucleoside in 2 ways

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RNA is synthesized by the addition of new nucleotides to the 3’-OH end of a growing chain

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Types of RNA polymerases

• Bacterial cells use only one RNA polymerase, with six polypeptides.

• The RNA polymerase holoenzyme contacts the promoter, then 35 nt of DNA.

• Processivity can be 10,000 nt for prokaryotes and 1,000,000 for eukaryotes.

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Mechanism of transcription

1. Promoter recognition

2. Chain initiation

3. Chain elongation

4. Chain termination

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RNA synthesis creates a bubble in the double-stranded DNA template

Note the 5` triphosphate group, and that only one strand is the template.

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Comparison of a number of E. coli promoter sequences reveals two conserved sequences (at -10 and -35 nt)

The position in DNA where the RNA chain starts is called +1 site. DNA 5’ to the start site is called “upstream” sequence and DNA to

the 3’-side is called “downstream” sequence.

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Rho-independent site for transcription termination generates RNA that can form a stable hairpin

followed by a number of U residues

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During transcription, RNA is copied from only one DNA strand for any one gene