Michael Cummings Chapter 9 Gene Expression and Gene Regulation Part 1 David Reisman • University of South Carolina 9.1 The Link between Genes and Proteins 1902 Archibald Garrod published a paper on the condition of alkaptonuria – he proposed that abnormal phenotypes resulted from biochemical defects or “inborn errors of metabolism” 1941 George Beadle and Edward Tatum firmly established the link between genes, the proteins produced from those genes, and a visible phenotype (won the Nobel Prize in 1958) 9.3 Tracing the Flow of Genetic Information Production of protein from instructions on the DNA requires several steps - Transcription = Production of mRNA - Translation = Production of protein using mRNA, tRNA, and rRNA - Folding of the protein into the active 3-D form DNA Transcription pre-mRNA mRNA processing Cell Cytoplasm Nucleus mRNA Translation Polypeptide Fig. 9-2, p. 201 Adenine (A) Adenine (A) Guanine (G) Guanine (G) Cytosine (C) Cytosine (C) Thymine (T) Uracil (U) RNA DNA Fig. 8-7, p. 183 Nucleic Acids DNA 1. 2. 3. 4. 5. 6. Usually double-stranded Thymine as a bas Sugar is deoxyribose Contains protein coding info Does not act as an enzyme Permanent Table 10.2 RNA 1. 2. 3. 4. 5. 6. Usually single-stranded Uracil as a base Sugar is ribose Carries protein code info Can function as an enzyme Transient Ribose Ribose There are three major types of RNA - messenger RNA or mRNA - ribosomal RNA or rRNA - transfer RNA or tRNA Ribose Ribose Fig. 8-11, p. 187 9.4 Transcription Produces Genetic Messages Transcription begins when DNA unwinds and one strand is used as template to make a pre-mRNA molecule Initiation: Binding of transcription factors and RNA polymerase to promoter region in the DNA Elongation: RNA polymerase adds nucleotides in 5’ 3’ direction Termination: terminator sequence is reached Gene region 5’ Promoter region RNA polymerase, the enzyme that catalyzes transcription (a) RNA polymerase binds to a promoter in the DNA, along with regulatory proteins (initiation). The binding positions the polymerase near a gene in the DNA. Only one strand of DNA provides a template for transcription of mRNA. Fig. 9-3a, p. 200 Newly forming RNA transcript DNA template winding up DNA template unwinding (b) The polymerase begins to move along the DNA and unwind it. As it does, it links RNA nucleotides into a strand of RNA in the order specified by the base sequence of the DNA (elongation). The DNA double helix rewinds after the polymerase passes. The structure of the “opened” DNA molecule at the transcription site is called a transcription bubble, after its appearance. Fig. 9-3b, p. 200 Pre-mRNA must Undergo Modification and Splicing Transcription produces large mRNA precursor molecules called pre-mRNA Before leaving nucleus – mRNA is processed • 1. 5’ methyl cap added - Recognition site for protein synthesis • 2. 3’ poly A tail - Stabilizes the mRNA • 3. Removal of introns (intervening sequences- don’t code for protein) Unit of transcription in DNA strand Exon Intron Exon Intron Exon Transcription into pre-mRNA Cap Poly-A tail Snipped out Snipped out Mature mRNA transcript Fig. 9-4, p. 202 Alternative Splicing Mutations in Splicing Sites and Genetic Disorders Splicing defects cause several human genetic disorders One hemoglobin disorder, b-thalassemia, is due to mutations at the exon/intron region that results in lower splicing efficiency and lower b-globin protein DNA Transcription pre-mRNA mRNA processing Cell Cytoplasm Nucleus mRNA Translation Polypeptide Fig. 9-2, p. 201 9.5 Translation Requires the Interaction of Several Components Translation requires the interaction of mRNA, amino acids, ribosomes, tRNA molecules, and energy sources mRNA is read in groups of 3 amino acids called codons Codon Chart—20 different amino acids to make all the proteins in living organisms Genetic Code Triplet code (3 mRNA bases = 1 amino acid) Redundant – more than one codon can specify an amino acid Unambiguous – each codon codes for just one amino acid Universal – nearly all organisms use the same code - bacteria, plants, animals INITIATION (a) A mature mRNA leaves the nucleus and enters the cytoplasm, which has many free amino acids, tRNAs, and ribosomal subunits. An initiator tRNA carrying methionine binds to a small ribosomal subunit and the mRNA. mRNA Initiator Small tRNA ribosomal subunit Large ribosomal subunit Fig. 9-9a, p. 206 Transfer RNA (tRNA) (b) A large ribosomal subunit joins, and the cluster is now called an initiation complex. Fig. 9-9b, p. 206 ELONGATION A peptide bond forms between the first two amino acids (here, methionine and valine). (c) An initiator tRNA carries the amino acid methionine, so the first amino acid of the new polypeptide chain will be methionine. A second tRNA binds the second codon of the mRNA (here, that codon is GUG, so the tRNA that binds carries the amino acid valine). Fig. 9-9c, p. 207 A peptide bond forms between the second and third amino acids (here valine and leucine). (d) The first tRNA is released and the ribosome moves to the next codon in the mRNA. A third tRNA binds to the third codon of the mRNA (here, that codon is UUA, so the tRNA carries the amino acid leucine). Fig. 9-9d, p. 207 A peptide bond forms between the third and fourth amino acids (here, leucine and glycine). (e) The second tRNA is released and the ribosome moves to the next codon. A fourth tRNA binds the fourth mRNA codon (here, that codon is GGG, so the tRNA carries the amino acid glycine). Fig. 9-9e, p. 207 TERMINATION (f) Steps d and e are repeated over and over until the ribosome encounters a stop codon in the mRNA. The mRNA transcript and the new poypeptide chain are released from the ribosome. The two ribosomal subunits separate from each other. Translation is now complete. Either the polypeptide chain will join the pool of proteins in the cytoplasm, the nucleus, or will enter the rough ER of the endomembrane system (Section 4.9). Fig. 9-9f, p. 207 Polysomes Once a ribosome has started translation, new initiation complexes can form on an mRNA in order to produce many protein molecules. Template DNA: 3’TGTACGCGGTCAGCTTTATT5’ (red = introns) Mature mRNA: tRNA anticodons: Amino acids: 27 Template DNA: 3’TGTACGCGGTCAGCTTTATT5’ (red = introns) Mature mRNA: AUG AGU CGA UAA tRNA anticodons: Amino acids: 28 Template DNA: 3’TGTACGCGGTCAGCTTTATT5’ (red = introns) Mature mRNA: AUG AGU CGA UAA tRNA anticodons: UAC UCA GCU AUU Amino acids: 29 **Mature mRNA: AUG AGU CGA UAA** tRNA anticodons: UAC UCA GCU AUU Amino acids: Methionine, Serine, Arginine, Stop 30 H Amino group Carboxyl group R (a) Amino acid Fig. 9-6a, p. 203 Each amino acid has a specific R-group. 9.7 Polypeptides are Folded to Form Proteins After synthesis, polypeptides fold into a threedimensional shape, often assisted by other proteins, called chaperones Improper folding leads to incorrect protein structure and inability to perform function (Alzheimer, Huntington, Parkinson diseases) Four levels of protein structure are recognized Four Levels of Protein Structure Primary structure (1O) • The amino acid sequence in a polypeptide chain Secondary structure (2O) • The pleated or helical structure in a protein molecule resulting from the peptide bonds between amino acids Four Levels of Protein Structure Tertiary structure (3O) • The folding of the helical and pleated sheet structures due to interaction of the R-groups. Quaternary structure (4O) • The interaction of two or more polypeptide chains to form a functional protein Levels of Protein Structure 1O 2O 3O 4O Exploring Genetics: Antibiotics and Protein Synthesis Antibiotics are produced by microorganisms as a defense mechanism Many antibiotics affect one or more stages in protein synthesis. For example: • Tetracycline: initiation of transcription • Streptomycin: codon-anticodon interaction • Erythromycin: ribosome movement along mRNA Other topics in Chp 9 Part 2 Protein folding diseases Regulation of protein synthesis occurs at several levels: • • • • Timing of transcription The rate of translation The ways in which proteins are processed The rate of protein break-down