Chapter 17: From Gene to Protein PDF

LECTURE PRESENTATIONS For CAMPBELL BIOLOGY, NINTH EDITION Jane B. Reece, Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Robert B. Jackson Chapter 17 From Gene to Protein...

LECTURE PRESENTATIONS For CAMPBELL BIOLOGY, NINTH EDITION Jane B. Reece, Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Robert B. Jackson Chapter 17 From Gene to Protein Lectures by Erin Barley Kathleen Fitzpatrick © 2011 Pearson Education, Inc. 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 Concept 17.1: Genes specify proteins via transcription and translation How was the fundamental relationship between genes and proteins discovered? Evidence from the Study of Metabolic Defects In 1902, 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 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 media Using crosses, they and their coworkers 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 Figure 17.2 EXPERIMENT RESULTS Classes of Neurospora crassa Growth: No growth: Wild-type Mutant cells Wild type Class I mutants Class II mutants Class III mutants cells growing cannot grow Minimal and dividing and divide medium (MM) Minimal medium (control) MM + ornithine Condition MM + citrulline MM + arginine (control) Can grow with Can grow on Can grow only Require arginine Summary ornithine, or without any on citrulline or to grow of results citrulline, or supplements arginine arginine CONCLUSION Gene Class I mutants Class II mutants Class III mutants (codes for (mutation in (mutation in (mutation in enzyme) Wild type gene A) gene B) gene C) Precursor Precursor Precursor Precursor Gene A Enzyme A Enzyme A Enzyme A Enzyme A Ornithine Ornithine Ornithine Ornithine Gene B Enzyme B Enzyme B Enzyme B Enzyme B Citrulline Citrulline Citrulline Citrulline Gene C Enzyme C Enzyme C Enzyme C Enzyme C Arginine Arginine Arginine Arginine 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 Basic Principles of Transcription and Translation RNA is the bridge 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, using information in the mRNA Ribosomes are the sites of translation  In prokaryotes, translation of mRNA can begin before transcription has finished In a eukaryotic cell, the nuclear envelope separates transcription from translation Eukaryotic RNA transcripts are modified through RNA processing to yield finished mRNA  A primary transcript is the initial RNA transcript from any gene prior to processing The central dogma is the concept that cells are governed by a cellular chain of command: DNA → RNA → protein Figure 17.UN01 DNA RNA Protein Figure 17.3 Nuclear envelope TRANSCRIPTION DNA Pre-mRNA RNA PROCESSING mRNA DNA TRANSCRIPTION mRNA Ribosome TRANSLATION Ribosome TRANSLATION Polypeptide Polypeptide (a) Bacterial cell (b) Eukaryotic cell 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 nucleotides correspond to an amino acid? Codons: Triplets of Nucleotides The flow of information from gene to protein is based on a triplet code: a series of nonoverlapping, three-nucleotide words The words of a gene are transcribed into complementary nonoverlaping three-nucleotide words of mRNA These words are then translated into a chain of amino acids, forming a polypeptide Figure 17.4 DNA template 3 5 DNA strand A C C A A A C C G A G T molecule T G G T T T G G C T C A 3 Gene 1 5 TRANSCRIPTION Gene 2 U G G U U U G G C U C A mRNA 5 3 Codon TRANSLATION Protein Trp Phe Gly Ser Gene 3 Amino acid  During transcription, one of the two DNA strands, called the template strand, provides a template for ordering the sequence of complementary nucleotides in an RNA transcript The template strand is always the same strand for a given gene During translation, the mRNA base triplets, called codons, are read in the 5 to 3 direction  Codons along an mRNA molecule are read by translation machinery in the 5 to 3 direction Each codon specifies the amino acid (one of 20) to be placed at the corresponding position along a polypeptide Cracking the Code All 64 codons were deciphered by the mid-1960s Of the 64 triplets, 61 code for amino acids; 3 triplets are “stop” signals to end translation The genetic code is redundant (more than one codon may specify a particular amino acid) but not ambiguous; no codon specifies more than one amino acid Codons must be read in the correct reading frame (correct groupings) in order for the specified polypeptide to be produced Figure 17.5 Second mRNA base U C A G UUU UCU UAU UGU U Phe Tyr Cys UUC UCC UAC UGC C U Ser UUA UCA UAA Stop UGA Stop A Leu Third mRNA base (3 end of codon) First mRNA base (5 end of codon) UUG UCG UAG Stop UGG Trp G CUU CCU CAU CGU U His CUC CCC CAC CGC C C Leu Pro Arg CUA CCA CAA CGA A Gln CUG CCG CAG CGG G AUU ACU AAU AGU U Asn Ser AUC Ile ACC AAC AGC C A Thr AUA ACA AAA AGA A Lys Arg Met or AUG start ACG AAG AGG G GUU GCU GAU GGU U Asp GUC GCC GAC GGC C G Val Ala Gly GUA GCA GAA GGA A Glu GUG GCG GAG GGG G Evolution of the Genetic Code The genetic code is nearly universal, shared by the simplest bacteria to the most complex animals Genes can be transcribed and translated after being transplanted from one species to another Figure 17.6 (a) Tobacco plant expressing (b) Pig expressing a jellyfish a firefly gene gene Concept 17.2: Transcription is the DNA- directed synthesis of RNA: a closer look Transcription is the first stage of gene expression Molecular Components of Transcription RNA synthesis is catalyzed by RNA polymerase, which pries the DNA strands apart and hooks together the RNA nucleotides The RNA is complementary to the DNA template strand RNA synthesis follows the same base-pairing rules as DNA, except that uracil substitutes for thymine  The DNA sequence where RNA polymerase attaches is called the promoter; in bacteria, the sequence signaling the end of transcription is called the terminator The stretch of DNA that is transcribed is called a transcription unit Figure 17.7-4 Promoter Transcription unit 5 3 3 5 DNA Start point RNA polymerase 1 Initiation Nontemplate strand of DNA 5 3 3 5 Template strand of DNA RNA Unwound transcript DNA 2 Elongation Rewound DNA 5 3 3 3 5 5 RNA transcript 3 Termination 5 3 3 5 5 3 Completed RNA transcript Direction of transcription (“downstream”) Synthesis of an RNA Transcript The three stages of transcription – Initiation – Elongation – Termination © 2011 Pearson Education, Inc. RNA Polymerase Binding and Initiation of Transcription Promoters signal the transcriptional start point and usually extend several dozen nucleotide pairs upstream of the start point 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 © 2011 Pearson Education, Inc. Figure 17.8 1 A eukaryotic promoter Promoter Nontemplate strand DNA 5 T A T A A AA 3 3 A T AT T T T 5 TATA box Template strand Start point 2 Several transcription Transcription factors bind to DNA factors 5 3 3 5 3 Transcription initiation complex forms RNA polymerase II Transcription factors 5 3 3 3 5 5 RNA transcript Transcription initiation complex 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 Nucleotides are added to the 3 end of the growing RNA molecule © 2011 Pearson Education, Inc. Figure 17.9 Nontemplate strand of DNA RNA nucleotides RNA polymerase A T C C A A 3 5 C 3 end C A U C C A 5 3 T A G G T T 5 Direction of transcription Template strand of DNA Newly made RNA 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 and the mRNA can be translated without further modification In eukaryotes, RNA polymerase II transcribes the polyadenylation signal sequence; the RNA transcript is released 10–35 nucleotides past this polyadenylation sequence © 2011 Pearson Education, Inc. Concept 17.3: Eukaryotic cells modify RNA after transcription Enzymes in the eukaryotic nucleus modify pre- mRNA (RNA processing) 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 © 2011 Pearson Education, Inc. 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 © 2011 Pearson Education, Inc. Figure 17.10 Protein-coding Polyadenylation segment signal 5 3 G P P P AAUAAA AAA … AAA Start Stop 5 Cap 5 UTR 3 UTR Poly-A tail codon codon 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 Figure 17.11 5 Exon Intron Exon Intron Exon 3 Pre-mRNA 5 Cap Poly-A tail Codon 1−30 31−104 105− numbers 146 Introns cut out and exons spliced together mRNA 5 Cap Poly-A tail 1−146 5 UTR 3 UTR Coding segment  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 Figure 17.12-3 RNA transcript (pre-mRNA) 5 Exon 1 Intron Exon 2 Protein Other snRNA proteins snRNPs Spliceosome 5 Spliceosome components Cut-out mRNA intron 5 Exon 1 Exon 2 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  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 that may participate in catalysis – RNA may hydrogen-bond with other nucleic acid molecules The Functional and Evolutionary Importance of Introns Some introns contain sequences that may regulate gene expression Some genes can encode more than one kind of polypeptide, depending on which segments are treated as exons during splicing This is called alternative RNA splicing Consequently, the number of different proteins an organism can produce is much greater than its number of genes  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 Figure 17.13 Gene DNA Exon 1 Intron Exon 2 Intron Exon 3 Transcription RNA processing Translation Domain 3 Domain 2 Domain 1 Polypeptide Concept 17.4: Translation is the RNA- directed synthesis of a polypeptide: a closer look Genetic information flows from mRNA to protein through the process of translation Molecular Components of Translation A cell translates an mRNA message into protein with the help of transfer RNA (tRNA) tRNA transfer amino acids to the growing polypeptide in a ribosome Translation is a complex process in terms of its biochemistry and mechanics Figure 17.14 Amino Polypeptide acids tRNA with amino acid attached Ribosome tRNA C G Anticodon U G G U U U G G C 5 Codons 3 mRNA The Structure and Function of Transfer RNA Molecules of tRNA are not identical – Each carries a specific amino acid on one end – Each has an anticodon on the other end; the anticodon base-pairs with a complementary codon on mRNA  A tRNA molecule consists of a single RNA strand that is only about 80 nucleotides long Flattened into one plane to reveal its base pairing, a tRNA molecule looks like a cloverleaf Figure 17.15 3 Amino acid attachment site 5 Amino acid attachment 5 site 3 Hydrogen bonds Hydrogen bonds A A G 3 5 Anticodon Anticodon Anticodon (c) Symbol used (a) Two-dimensional structure (b) Three-dimensional structure in this book Figure 17.15a 3 Amino acid attachment site 5 Hydrogen bonds Anticodon (a) Two-dimensional structure Figure 17.15b Amino acid attachment 5 site 3 Hydrogen bonds A A G 3 5 Anticodon Anticodon (c) Symbol used (b) Three-dimensional structure in this book  Because of hydrogen bonds, tRNA actually twists and folds into a three-dimensional molecule tRNA is roughly L-shaped  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 Figure 17.16-4 Aminoacyl-tRNA synthetase (enzyme) Amino acid P Adenosine P P P Adenosine P Pi ATP Aminoacyl-tRNA Pi Pi tRNA synthetase tRNA Amino acid P Adenosine AMP Computer model Aminoacyl tRNA (“charged tRNA”) 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) Bacterial and eukaryotic ribosomes are somewhat similar but have significant differences: some antibiotic drugs specifically target bacterial ribosomes without harming eukaryotic ribosomes Figure 17.17 Growing polypeptide Exit tunnel tRNA molecules Large subunit E P A Small subunit 5 mRNA 3 (a) Computer model of functioning ribosome Growing polypeptide P site (Peptidyl-tRNA Amino end Exit tunnel Next amino binding site) acid to be added to A site (Aminoacyl- polypeptide tRNA binding site) chain E site (Exit site) E tRNA E P A Large mRNA 3 subunit mRNA binding site Small 5 Codons subunit (b) Schematic model showing binding sites (c) Schematic model with mRNA and tRNA Figure 17.17a Growing polypeptide Exit tunnel tRNA molecules Large subunit E P A Small subunit 5 mRNA 3 (a) Computer model of functioning ribosome Figure 17.17b P site (Peptidyl-tRNA Exit tunnel binding site) A site (Aminoacyl- tRNA binding site) E site (Exit site) E P A Large subunit mRNA binding site Small subunit (b) Schematic model showing binding sites Figure 17.17c Growing polypeptide Amino end Next amino acid to be added to polypeptide chain E tRNA mRNA 3 5 Codons (c) Schematic model with mRNA and tRNA  A ribosome has three binding sites for tRNA – The P site holds the tRNA that carries the growing polypeptide chain – The A site holds the tRNA that carries the next amino acid to be added to the chain – The E site is the exit site, where discharged tRNAs leave the ribosome Building a Polypeptide The three stages of translation – Initiation – Elongation – Termination All three stages require protein “factors” that aid in the translation process Ribosome Association and Initiation of Translation The initiation stage of translation brings together mRNA, a tRNA with the first amino acid, and the two ribosomal subunits First, a small ribosomal subunit binds with mRNA and a special initiator tRNA Then the small subunit moves along the mRNA until it reaches the start codon (AUG) Proteins called initiation factors bring in the large subunit that completes the translation initiation complex Figure 17.18 Large ribosomal subunit 3 U A C 5 P site 5 A U G 3 Pi Initiator + tRNA GTP GDP E A mRNA 5 5 3 3 Start codon Small mRNA binding site ribosomal Translation initiation complex subunit Elongation of the Polypeptide Chain During the elongation stage, amino acids are added one by one to the preceding amino acid at the C-terminus of the growing chain Each addition involves proteins called elongation factors and occurs in three steps: codon recognition, peptide bond formation, and translocation Translation proceeds along the mRNA in a 5′ to 3′ direction Figure 17.19-4 Amino end of polypeptide E mRNA 3 Ribosome ready for P A site site GTP next aminoacyl tRNA 5 GDP + P i E E P A P A GDP + P i GTP E P A Termination of Translation Termination occurs when a stop codon in the mRNA reaches the A site of the ribosome The A site accepts a protein called a release factor The release factor causes the addition of a water molecule instead of an amino acid This reaction releases the polypeptide, and the translation assembly then comes apart  Animation: Translation Right-click slide / select “Play” © 2011 Pearson Education, Inc. Figure 17.20-3 Release factor Free polypeptide 5 3 3 2 GTP 3 5 5 2 GDP + 2 P i Stop codon (UAG, UAA, or UGA) 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 Figure 17.21 Completed Growing polypeptide polypeptides Incoming ribosomal subunits Start of mRNA End of (5 end) mRNA (a) (3 end) Ribosomes mRNA (b) 0.1 m Completing and Targeting the Functional Protein Often translation is not sufficient to make a functional protein Polypeptide chains are modified after translation or targeted to specific sites in the cell Protein Folding and Post-Translational Modifications During and after synthesis, a polypeptide chain spontaneously coils and folds into its three- dimensional shape Proteins may also require post-translational modifications before doing their job Some polypeptides are activated by enzymes that cleave them Other polypeptides come together to form the subunits of a protein Targeting Polypeptides to Specific Locations Two populations of ribosomes are evident in cells: free ribsomes (in the cytosol) and bound ribosomes (attached to the ER) Free ribosomes mostly synthesize proteins that function in the cytosol Bound ribosomes make proteins of the endomembrane system and proteins that are secreted from the cell Ribosomes are identical and can switch from free to bound  Polypeptide synthesis always begins in the cytosol Synthesis finishes in the cytosol unless the polypeptide signals the ribosome to attach to the ER Polypeptides destined for the ER or for secretion are marked by a signal peptide  A signal-recognition particle (SRP) binds to the signal peptide The SRP brings the signal peptide and its ribosome to the ER Figure 17.22 1 Ribosome 5 mRNA 4 Signal ER peptide Signal membrane 3 peptide SRP Protein removed 6 SRP 2 receptor CYTOSOL protein ER LUMEN Translocation complex Concept 17.5: Mutations of one or a few nucleotides 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 Figure 17.23 Wild-type hemoglobin Sickle-cell hemoglobin Wild-type hemoglobin DNA Mutant hemoglobin DNA 3 C T T 5 3 C A T 5 5 G A A 3 5 G T A 3 mRNA mRNA 5 G A A 3 5 G U A 3 Normal hemoglobin Sickle-cell hemoglobin Glu Val Types of Small-Scale Mutations Point mutations within a gene can be divided into two general categories – Nucleotide-pair substitutions – One or more nucleotide-pair insertions or deletions Substitutions A nucleotide-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 the correct amino acid Nonsense mutations change an amino acid codon into a stop codon, nearly always leading to a nonfunctional protein Figure 17.24 Wild type DNA template strand 3 T A C T T C A A A C C G A T T 5 5 A T G A A G T T T G G C T A A 3  mRNA5 A U G A A G U U U G G C U A A 3 Protein Met Lys Phe Gly Stop Amino end Carboxyl end (a) Nucleotide-pair substitution (b) Nucleotide-pair insertion or deletion A instead of G Extra A 3 T A C T T C A A A C C A A T T 5 3 T A C A T T C A A A C C G A T T 5 5 A T G A A G T T T G G T T A A 3 5 A T G T A A G T T T G G C T A A 3 U instead of C Extra U 5 A U G A A G U U U G G U U A A 3 5 A U G U A A G U U U G G C U A A 3 Met Lys Phe Gly Met Stop Stop Silent (no effect on amino acid sequence) Frameshift causing immediate nonsense (1 nucleotide-pair insertion) T instead of C A missing 3 T A C T T C A A A T C G A T T 5 3 T A C T T C A A C C G A T T 5T 5 A T G A A G T T T A G C T A A 3  5 A T G A A G T T G G C T A A 3A A instead of G U missing 5 A U G A A G U U U A G C U A A 3 5 A U G A A G U U G G C U A A 3 Met Lys Phe Ser Stop Met Lys Leu Ala Missense Frameshift causing extensive missense (1 nucleotide-pair deletion) A instead of T T T C missing 3 T A C A T C A A A C C G A T T 5 3 T A C A A A C C G A T T 5 5 A T G T A G T T T G G C T A A 3 5 A T G T T T G G C T A A 3 U instead of A A A G missing 5 A U G U A G U U U G G C U A A 3  A A 5 A U G U U U G G C U A A 3U Met Stop Met Phe Gly Stop Nonsense No frameshift, but one amino acid missing (3 nucleotide-pair deletion) Figure 17.24a Wild type DNA template strand 3 T A C T T C A A A C C G A T T 5 5 A T G A A G T T T G G C T A A 3 mRNA5 A U G A A G U U U G G C U A A 3 Protein Met Lys Phe Gly Stop Amino end Carboxyl end (a) Nucleotide-pair substitution: silent A instead of G 3 T A C T T C A A A C C A A T T 5 5 A T G A A G T T T G G T T A A 3 U instead of C 5 A U G A A G U U U G G U U A A 3 Met Lys Phe Gly Stop Figure 17.24b Wild type DNA template strand 3 T A C T T C A A A C C G A T T 5 5 A T G A A G T T T G G C T A A 3 mRNA5 A U G A A G U U U G G C U A A 3 Protein Met Lys Phe Gly Stop Amino end Carboxyl end (a) Nucleotide-pair substitution: missense T instead of C 3 T A C T T C A A A T C G A T T 5 5 A T G A A G T T T A G C T A A 3 A instead of G 5 A U G A A G U U U A G C U A A 3 Met Lys Phe Ser Stop Figure 17.24c Wild type DNA template strand 3 T A C T T C A A A C C G A T T 5 5 A T G A A G T T T G G C T A A 3 mRNA5 A U G A A G U U U G G C U A A 3 Protein Met Lys Phe Gly Stop Amino end Carboxyl end (a) Nucleotide-pair substitution: nonsense A instead of T T instead of C 3 T A C A T C A A A C C G A T T 5 5 A T G T A G T T T G G C T A A 3 U instead of A 5 A U G U A G U U U G G C U A A 3 Met Stop 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 Figure 17.24d Wild type DNA template strand 3 T A C T T C A A A C C G A T T 5 5 A T G A A G T T T G G C T A A 3 mRNA5 A U G A A G U U U G G C U A A 3 Protein Met Lys Phe Gly Stop Amino end Carboxyl end (b) Nucleotide-pair insertion or deletion: frameshift causing immediate nonsense Extra A 3 T A C A T T C A A A C G G A T T 5 5 A T G T A A G T T T G G C T A A 3 Extra U 5 A U G U A A G U U U G G C U A A 3 Met Stop 1 nucleotide-pair insertion Figure 17.24e Wild type DNA template strand 3 T A C T T C A A A C C G A T T 5 5 A T G A A G T T T G G C T A A 3 mRNA5 A U G A A G U U U G G C U A A 3 Protein Met Lys Phe Gly Stop Amino end Carboxyl end (b) Nucleotide-pair insertion or deletion: frameshift causing extensive missense A missing 3 T A C T T C A A C C G A T T 5 5 A T G A A G T T G G C T A A 3 U missing 5 A U G A A G U U G G C U A A 3 Met Lys Leu Ala 1 nucleotide-pair deletion Figure 17.24f Wild type DNA template strand 3 T A C T T C A A A C C G A T T 5 5 A T G A A G T T T G G C T A A 3 mRNA5 A U G A A G U U U G G C U A A 3 Protein Met Lys Phe Gly Stop Amino end Carboxyl end (b) Nucleotide-pair insertion or deletion: no frameshift, but one amino acid missing T T C missing 3 T A C A A A C C G A T T 5 5 A T G T T T G G C T A A 3 A A G missing 5 A U G U U U G G C U A A 3 Met Phe Gly Stop 3 nucleotide-pair deletion Mutagens Spontaneous mutations can occur during DNA replication, recombination, or repair Mutagens are physical or chemical agents that can cause mutations 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 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 Figure 17.25 RNA polymerase DNA mRNA Polyribosome Direction of 0.25 m RNA transcription polymerase DNA Polyribosome Polypeptide (amino end) Ribosome mRNA (5 end) What Is a Gene? Revisiting the Question The idea of the gene has evolved through the history of genetics We have considered a gene as – A discrete unit of inheritance – A region of specific nucleotide sequence in a chromosome – A DNA sequence that codes for a specific polypeptide chain Figure 17.26 DNA TRANSCRIPTION 3 RNA 5 RNA polymerase transcript Exon RNA RNA transcript PROCESSING (pre-mRNA) Intron Aminoacyl- tRNA synthetase NUCLEUS Amino acid AMINO ACID CYTOPLASM tRNA ACTIVATION Growing mRNA polypeptide 3 A P Aminoacyl E (charged) Ribosomal tRNA subunits TRANSLATION E A Anticodon Codon Ribosome  In summary, a gene can be defined as a region of DNA that can be expressed to produce a final functional product, either a polypeptide or an RNA molecule