1. Chapter 17 From Gene to Protein

2. Overview: The Flow of Genetic Information The information content of DNA is in the form of specific sequences of nucleotides The DNA inherited by an organism leads to specific traits by dictating the synthesis of proteins Proteins are the links between genotype and phenotype Gene expression, the process by which DNA directs protein synthesis, includes two stages: transcription and translation Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

3. Fig. 17-1

4. Concept 17.1: Genes specify proteins via transcription and translation How was the fundamental relationship between genes and proteins discovered? Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

5. Evidence from the Study of Metabolic Defects In 1909, British physician Archibald Garrod first suggested that genes dictate phenotypes through enzymes that catalyze specific chemical reactions He thought symptoms of an inherited disease reflect an inability to synthesize a certain enzyme Linking genes to enzymes required understanding that cells synthesize and degrade molecules in a series of steps, a metabolic pathway Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

6. Nutritional Mutants in Neurospora: Scientific Inquiry George Beadle and Edward Tatum exposed bread mold to X-rays, creating mutants that were unable to survive on minimal medium as a result of inability to synthesize certain molecules Using crosses, they identified three classes of arginine-deficient mutants, each lacking a different enzyme necessary for synthesizing arginine They developed a one gene–one enzyme hypothesis, which states that each gene dictates production of a specific enzyme Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

7. Fig. 17-2a EXPERIMENT Growth: Wild-type cells growing and dividing No growth: Mutant cells cannot grow and divide Minimal medium

8. Fig. 17-2b RESULTS Classes of Neurospora crassa Wild type Class I mutantsClass II mutants Class III mutants Minimal medium (MM) (control) MM + ornithine MM + citrulline MM + arginine (control) Condition

9. Fig. 17-2c CONCLUSION Class I mutants (mutation in gene A) Class II mutants (mutation in gene B) Class III mutants (mutation in gene C) Wild type Precursor Enzyme A Ornithine Enzyme B Citrulline Enzyme C Arginine Gene A Gene B Gene C

10. The Products of Gene Expression: A Developing Story Some proteins aren’t enzymes, so researchers later revised the hypothesis: one gene–one protein Many proteins are composed of several polypeptides, each of which has its own gene Therefore, Beadle and Tatum’s hypothesis is now restated as the one gene–one polypeptide hypothesis Note that it is common to refer to gene products as proteins rather than polypeptides Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

11. Basic Principles of Transcription and Translation RNA is the intermediate between genes and the proteins for which they code Transcription is the synthesis of RNA under the direction of DNA Transcription produces messenger RNA (mRNA) Translation is the synthesis of a polypeptide, which occurs under the direction of mRNA Ribosomes are the sites of translation Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

12. In prokaryotes, mRNA produced by transcription is immediately translated without more processing In a eukaryotic cell, the nuclear envelope separates transcription from translation Eukaryotic RNA transcripts are modified through RNA processing to yield finished mRNA Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

13. A primary transcript is the initial RNA transcript from any gene The central dogma is the concept that cells are governed by a cellular chain of command: DNA  RNA  protein Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

14. Fig. 17-3a-1 TRANSCRIPTION DNA mRNA (a) Bacterial cell

15. Fig. 17-3a-2 (a) Bacterial cell TRANSCRIPTION DNA mRNA TRANSLATION Ribosome Polypeptide

16. Fig. 17-3b-1 (b) Eukaryotic cell TRANSCRIPTION Nuclear envelope DNA Pre-mRNA

17. Fig. 17-3b-2 (b) Eukaryotic cell TRANSCRIPTION Nuclear envelope DNA Pre-mRNA RNA PROCESSING mRNA

18. Fig. 17-3b-3 (b) Eukaryotic cell TRANSCRIPTION Nuclear envelope DNA Pre-mRNA RNA PROCESSING mRNA TRANSLATION Ribosome Polypeptide

19. The Genetic Code How are the instructions for assembling amino acids into proteins encoded into DNA? There are 20 amino acids, but there are only four nucleotide bases in DNA How many bases correspond to an amino acid? Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

20. Codons: Triplets of Bases The flow of information from gene to protein is based on a triplet code DNA template strand TRANSCRIPTION TRANSLATION mRNA Protein Codon Amino acid

21. Codons: RNA

22. Evolution of the Genetic Code The genetic code is nearly universal, shared by the simplest bacteria to the most complex animals

23. Fig. 17-6 (a) Tobacco plant expressing a firefly gene (b) Pig expressing a jellyfish gene

24. RNA

25. Contrasting RNA with DNA Single- stranded Ribose Bases Adenine Uracil Guanine Cytosine Double- stranded Deoxyribose Bases Adenine Thymine Guanine Cytosine RNA DNA

26. mRNA- copies DNA and directs protein synthesis rRNA- joins with ribosomal proteins to make ribosomes tRNA- transfers amino acids to ribosomes to make protein

27. Ribosome

28. tRNA

29. 1.Transcription-occurs in nucleus mRNA copies DNA nucleotide sequence 2. Translation nucleotide sequence in mRNA is uncoded mRNA binds to rRNA tRNA brings appropriate amino acid to mRNA Polypeptide is manufactured

30. Fig. 17-25 TRANSCRIPTION RNA PROCESSING DNA RNA transcript 3 5 RNA polymerase Poly-A RNA transcript (pre-mRNA) Intron Exon NUCLEUS Aminoacyl-tRNA synthetase AMINO ACID ACTIVATION Amino acid tRNA CYTOPLASM Poly-A Growing polypeptide 3 Activated amino acid mRNA TRANSLATION Cap Ribosomal subunits Cap 5 E P A A Anticodon Ribosome Codon E

31. Fig. 17-7a-1 Promoter Transcription unit DNA Start point RNA polymerase 5 5 3 3

32. Fig. 17-7a-2 Promoter Transcription unit DNA Start point RNA polymerase 5 5 3 3 Initiation 3 3 1 RNA transcript 5 5 Unwound DNA Template strand of DNA

33. Fig. 17-7a-3 Promoter Transcription unit DNA Start point RNA polymerase 5 5 3 3 Initiation 3 3 1 RNA transcript 5 5 Unwound DNA Template strand of DNA 2 Elongation Rewound DNA 5 5 5 3 3 3 RNA transcript

34. Fig. 17-7a-4 Promoter Transcription unit DNA Start point RNA polymerase 5 5 3 3 Initiation 3 3 1 RNA transcript 5 5 Unwound DNA Template strand of DNA 2 Elongation Rewound DNA 5 5 5 3 3 3 RNA transcript 3 Termination 5 5 5 3 3 3 Completed RNA transcript

35. Fig. 17-7b Elongation RNA polymerase Nontemplate strand of DNA RNA nucleotides 3 end Direction of transcription (“downstream”) Template strand of DNA Newly made RNA 3 5 5

36. Synthesis of an RNA Transcript The three stages of transcription: – Initiation – Elongation – Termination Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

37. RNA Polymerase Binding and Initiation of Transcription Promoters signal the initiation of RNA synthesis Transcription factors mediate the binding of RNA polymerase and the initiation of transcription The completed assembly of transcription factors and RNA polymerase II bound to a promoter is called a transcription initiation complex A promoter called a TATA box is crucial in forming the initiation complex in eukaryotes Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

38. Fig. 17-8 A eukaryotic promoter includes a TATA box 3 1 2 3 Promoter TATA box Start point Template DNA strand 5 3 5 Transcription factors Several transcription factors must bind to the DNA before RNA polymerase II can do so. 5 53 3 Additional transcription factors bind to the DNA along with RNA polymerase II, forming the transcription initiation complex. RNA polymerase II Transcription factors 5 5 5 3 3 RNA transcript Transcription initiation complex

39. Elongation of the RNA Strand As RNA polymerase moves along the DNA, it untwists the double helix, 10 to 20 bases at a time Transcription progresses at a rate of 40 nucleotides per second in eukaryotes A gene can be transcribed simultaneously by several RNA polymerases Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

40. Termination of Transcription The mechanisms of termination are different in bacteria and eukaryotes In bacteria, the polymerase stops transcription at the end of the terminator In eukaryotes, the polymerase continues transcription after the pre-mRNA is cleaved from the growing RNA chain; the polymerase eventually falls off the DNA Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

41. Concept 17.3: Eukaryotic cells modify RNA after transcription Enzymes in the eukaryotic nucleus modify pre- mRNA before the genetic messages are dispatched to the cytoplasm During RNA processing, both ends of the primary transcript are usually altered Also, usually some interior parts of the molecule are cut out, and the other parts spliced together Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

42. Alteration of mRNA Ends Each end of a pre-mRNA molecule is modified in a particular way: – The 5 end receives a modified nucleotide 5 cap – The 3 end gets a poly-A tail These modifications share several functions: – They seem to facilitate the export of mRNA – They protect mRNA from hydrolytic enzymes – They help ribosomes attach to the 5 end Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

43. Fig. 17-9 Protein-coding segment Polyadenylation signal 3 3 UTR5 UTR 5 5 Cap Start codon Stop codon Poly-A tail G PPPAAUAAA AAA …

44. Split Genes and RNA Splicing Most eukaryotic genes and their RNA transcripts have long noncoding stretches of nucleotides that lie between coding regions These noncoding regions are called intervening sequences, or introns The other regions are called exons because they are eventually expressed, usually translated into amino acid sequences RNA splicing removes introns and joins exons, creating an mRNA molecule with a continuous coding sequence Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

45. Fig. 17-10 Pre-mRNA mRNA Coding segment Introns cut out and exons spliced together 5 Cap Exon Intron 5 1 30 31104 ExonIntron 105 Exon 146 3 Poly-A tail 5 Cap 5 UTR3 UTR 1 146

46. In some cases, RNA splicing is carried out by spliceosomes Spliceosomes consist of a variety of proteins and several small nuclear ribonucleoproteins (snRNPs) that recognize the splice sites Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

47. Fig. 17-11-1 RNA transcript (pre-mRNA) Exon 1Exon 2Intron Protein snRNA snRNPs Other proteins 5

48. Fig. 17-11-2 RNA transcript (pre-mRNA) Exon 1Exon 2Intron Protein snRNA snRNPs Other proteins 5 5 Spliceosome

49. Fig. 17-11-3 RNA transcript (pre-mRNA) Exon 1Exon 2Intron Protein snRNA snRNPs Other proteins 5 5 Spliceosome components Cut-out intron mRNA Exon 1 Exon 2 5

50. Ribozymes Ribozymes are catalytic RNA molecules that function as enzymes and can splice RNA The discovery of ribozymes rendered obsolete the belief that all biological catalysts were proteins Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

51. Three properties of RNA enable it to function as an enzyme – It can form a three-dimensional structure because of its ability to base pair with itself – Some bases in RNA contain functional groups – RNA may hydrogen-bond with other nucleic acid molecules Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

52. The Functional and Evolutionary Importance of Introns Some genes can encode more than one kind of polypeptide, depending on which segments are treated as exons during RNA splicing Such variations are called alternative RNA splicing Because of alternative splicing, the number of different proteins an organism can produce is much greater than its number of genes Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

53. Proteins often have a modular architecture consisting of discrete regions called domains In many cases, different exons code for the different domains in a protein Exon shuffling may result in the evolution of new proteins Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

54. Fig. 17-12 Gene DNA Exon 1Exon 2 Exon 3 Intron Transcription RNA processing Translation Domain 2 Domain 3 Domain 1 Polypeptide

55. Concept 17.4: Translation is the RNA-directed synthesis of a polypeptide: a closer look The translation of mRNA to protein can be examined in more detail Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

56. Fig. 17-13 Polypeptide Ribosome Amino acids tRNA with amino acid attached tRNA Anticodon Trp Phe Gly Codons 3 5 mRNA

57. Fig. 17-14 Amino acid attachment site 3 5 Hydrogen bonds Anticodon (a) Two-dimensional structure Amino acid attachment site 5 3 Hydrogen bonds 3 5 Anticodon (c) Symbol used in this book (b) Three-dimensional structure

58. Fig. 17-14a Amino acid attachment site (a) Two-dimensional structure Hydrogen bonds Anticodon 3 5

59. Fig. 17-14b Amino acid attachment site 3 3 5 5 Hydrogen bonds Anticodon (b) Three-dimensional structure (c) Symbol used in this book

60. Accurate translation requires two steps: – First: a correct match between a tRNA and an amino acid, done by the enzyme aminoacyl- tRNA synthetase – Second: a correct match between the tRNA anticodon and an mRNA codon Flexible pairing at the third base of a codon is called wobble and allows some tRNAs to bind to more than one codon Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

61. Fig. 17-15-1 Amino acid Aminoacyl-tRNA synthetase (enzyme) ATP Adenosine PPP

62. Fig. 17-15-2 Amino acid Aminoacyl-tRNA synthetase (enzyme) ATP Adenosine PPP P P P i P P i i

63. Fig. 17-15-3 Amino acid Aminoacyl-tRNA synthetase (enzyme) ATP Adenosine PPP P P P i P P i i tRNA Aminoacyl-tRNA synthetase Computer model AMP Adenosine P

64. Fig. 17-15-4 Amino acid Aminoacyl-tRNA synthetase (enzyme) ATP Adenosine PPP P P P i P P i i tRNA Aminoacyl-tRNA synthetase Computer model AMP Adenosine P Aminoacyl-tRNA (“charged tRNA”)

65. Ribosomes Ribosomes facilitate specific coupling of tRNA anticodons with mRNA codons in protein synthesis The two ribosomal subunits (large and small) are made of proteins and ribosomal RNA (rRNA)

66. Fig. 17-16b P site (Peptidyl-tRNA binding site) A site (Aminoacyl- tRNA binding site) E site (Exit site) mRNA binding site Large subunit Small subunit (b) Schematic model showing binding sites Next amino acid to be added to polypeptide chain Amino end Growing polypeptide mRNA tRNA EP A E Codons (c) Schematic model with mRNA and tRNA 5 3

67. Building a Polypeptide The three stages of translation: – Initiation – Elongation – Termination All three stages require protein “factors” that aid in the translation process Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

68. Fig. 17-17 3 3 5 5 U U A A C G Met GTP GDP Initiator tRNA mRNA 5 3 Start codon mRNA binding site Small ribosomal subunit 5 P site Translation initiation complex 3 EA Met Large ribosomal subunit

69. Fig. 17-18-1 Amino end of polypeptide mRNA 5 3 E P site A site

70. Fig. 17-18-2 Amino end of polypeptide mRNA 5 3 E P site A site GTP GDP E P A

71. Fig. 17-18-3 Amino end of polypeptide mRNA 5 3 E P site A site GTP GDP E P A E PA

72. Fig. 17-18-4 Amino end of polypeptide mRNA 5 3 E P site A site GTP GDP E P A E PA GTP Ribosome ready for next aminoacyl tRNA E P A

73. Fig. 17-19-1 Release factor 3 5 Stop codon (UAG, UAA, or UGA) Termination of Translation

74. Fig. 17-19-2 Release factor 3 5 Stop codon (UAG, UAA, or UGA) 5 3 2 Free polypeptide 2 GDP GTP Termination of Translation

75. Fig. 17-19-3 Release factor 3 5 Stop codon (UAG, UAA, or UGA) 5 3 2 Free polypeptide 2 GDP GTP 5 3 Termination of Translation

76. Polyribosomes A number of ribosomes can translate a single mRNA simultaneously, forming a polyribosome (or polysome) Polyribosomes enable a cell to make many copies of a polypeptide very quickly Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

77. Fig. 17-20 Growing polypeptides Completed polypeptide Incoming ribosomal subunits Start of mRNA (5 end) Polyribosome End of mRNA (3 end) (a) Ribosomes mRNA (b) 0.1 µm

78. Completing and Targeting the Functional Protein Often translation is not sufficient to make a functional protein Polypeptide chains are modified after translation Completed proteins are targeted to specific sites in the cell Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

79. Fig. 17-21 Ribosome mRNA Signal peptide Signal- recognition particle (SRP) CYTOSOL Translocation complex SRP receptor protein ER LUMEN Signal peptide removed ER membrane Protein Protein Folding and Post- Translational Modifications

80. Concept 17.5: Point mutations can affect protein structure and function Mutations are changes in the genetic material of a cell or virus Point mutations are chemical changes in just one base pair of a gene The change of a single nucleotide in a DNA template strand can lead to the production of an abnormal protein Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

81. Fig. 17-22 Wild-type hemoglobin DNA mRNA Mutant hemoglobin DNA mRNA 3 3 3 3 3 3 5 5 5 5 5 5 CCTT T T G G A A A A AA A GG U Normal hemoglobinSickle-cell hemoglobin Glu Val

82. Types of Point Mutations Point mutations within a gene can be divided into two general categories – Base-pair substitutions – Base-pair insertions or deletions Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

83. Fig. 17-23a Wild type 3 DNA template strand 3 3 5 5 5 mRNA Protein Amino end Stop Carboxyl end A instead of G 3 3 3 U instead of C 5 5 5 Stop Silent (no effect on amino acid sequence)

84. Fig. 17-23b Wild type DNA template strand 3 5 mRNA Protein 5 Amino end Stop Carboxyl end 5 3 3 T instead of C A instead of G 3 3 3 5 5 5 Stop Missense

85. Fig. 17-23c Wild type DNA template strand 3 5 mRNA Protein 5 Amino end Stop Carboxyl end 5 3 3 A instead of T U instead of A 3 3 3 5 5 5 Stop Nonsense

86. Fig. 17-23d Wild type DNA template strand 3 5 mRNA Protein 5 Amino end Stop Carboxyl end 5 3 3 Extra A Extra U 3 3 3 5 5 5 Stop Frameshift causing immediate nonsense (1 base-pair insertion)

87. Fig. 17-23e Wild type DNA template strand 3 5 mRNA Protein 5 Amino end Stop Carboxyl end 5 3 3 missing 3 3 3 5 5 5 Frameshift causing extensive missense (1 base-pair deletion)

88. Fig. 17-23f Wild type DNA template strand 3 5 mRNA Protein 5 Amino end Stop Carboxyl end 5 3 3 missing 3 3 3 5 5 5 No frameshift, but one amino acid missing (3 base-pair deletion) Stop

89. Substitutions A base-pair substitution replaces one nucleotide and its partner with another pair of nucleotides Silent mutations have no effect on the amino acid produced by a codon because of redundancy in the genetic code Missense mutations still code for an amino acid, but not necessarily the right amino acid Nonsense mutations change an amino acid codon into a stop codon, nearly always leading to a nonfunctional protein Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

90. Insertions and Deletions Insertions and deletions are additions or losses of nucleotide pairs in a gene These mutations have a disastrous effect on the resulting protein more often than substitutions do Insertion or deletion of nucleotides may alter the reading frame, producing a frameshift mutation Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

91. Mutagens Spontaneous mutations can occur during DNA replication, recombination, or repair Mutagens are physical or chemical agents that can cause mutations Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings Xrays & UV rays Viruses & bacteria Heavy metals Chemicals e.g. benzene

92. Concept 17.6: While gene expression differs among the domains of life, the concept of a gene is universal Archaea are prokaryotes, but share many features of gene expression with eukaryotes Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

93. Comparing Gene Expression in Bacteria, Archaea, and Eukarya Bacteria and eukarya differ in their RNA polymerases, termination of transcription and ribosomes; archaea tend to resemble eukarya in these respects Bacteria can simultaneously transcribe and translate the same gene In eukarya, transcription and translation are separated by the nuclear envelope In archaea, transcription and translation are likely coupled Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

94. Fig. 17-24 RNA polymerase DNA Polyribosome mRNA 0.25 µm Direction of transcription DNA RNA polymerase Polyribosome Polypeptide (amino end) Ribosome mRNA (5 end)

95. You should now be able to: 1.Describe the contributions made by Garrod, Beadle, and Tatum to our understanding of the relationship between genes and enzymes 2.Briefly explain how information flows from gene to protein 3.Compare transcription and translation in bacteria and eukaryotes 4.Explain what it means to say that the genetic code is redundant and unambiguous Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings

96. 5.Include the following terms in a description of transcription: mRNA, RNA polymerase, the promoter, the terminator, the transcription unit, initiation, elongation, termination, and introns 6.Include the following terms in a description of translation: tRNA, wobble, ribosomes, initiation, elongation, and termination Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings