Chapter 8
Structure and Function of the Genetic Material
· 8-1 Define genetics, genome, chromosome, gene, genetic code,
· genotype, phenotype, and genomics.
· 8-2 Describe how DNA serves as genetic information.
· 8-3 Describe the process of DNA replication.
· 8-4 Describe protein synthesis, including transcription, RNA
· processing, and translation.
· 8-5 Compare protein synthesis in prokaryotes and eukaryotes.
- Genetics is the study of what genes are, how they carry information, how their information is expressed, and how they are replicated and passed to subsequent generations or other organisms.
- DNA in cells exists as a double-stranded helix; the two strands are held together by hydrogen bonds between specific nitrogenous base pairs: AT and CG.
- A gene is a sequence of nucleotides, that encodes a functional product, usually a protein.
- The DNA in a cell is duplicated before the cell divides, so each offspring cell receives the same genetic information.
Genotype and Phenotype
- Genotype is the genetic composition of an organism, its entire complement of DNA.
- Phenotype is the expression of the genes: the proteins of the cell and the properties they confer on the organism.
DNA and Chromosomes
- The DNA in a chromosome exists as one long double helix associated with various proteins that regulate genetic activity.
- Genomics is the molecular characterization of genomes.
The Flow of Genetic Information
- Following cell division, each offspring cell receives a chromosome that is virtually identical to the parent’s.
- Information contained in the DNA is transcribed into RNA and translated into proteins.
DNA Replication
- During DNA replication, the two strands of the double helix separate at the replication fork, and each strand is used as a template by DNA polymerases to synthesize two new strands of DNA according to the rules of complementary base pairing.
- The result of DNA replication is two new strands of DNA, each having a base sequence complementary to one of the original strands.
- Because each double-stranded DNA molecule contains one original and one new strand, the replication process is called semiconservative.
- DNA is synthesized in one direction designated 5’ S 3’. At the replication fork, the leading strand is synthesized continuously and the lagging strand discontinuously.
- DNA polymerase proofreads new molecules of DNA and removes mismatched bases before continuing DNA synthesis.
RNA and Protein Synthesis
- During transcription, the enzyme RNA polymerase synthesizes a strand of RNA from one strand of double-stranded DNA, which serves as a template.
- RNA is synthesized from nucleotides containing the bases A, C, G, and U, which pair with the bases of the DNA strand being transcribed.
- RNA polymerase binds the promoter; transcription begins at AUG; the region of DNA that is the end point of transcription is the terminator; RNA is synthesized in the 5’ S 3’ direction.
- Translation is the process in which the information in the nucleotide base sequence of mRNA is used to dictate the amino acid sequence of a protein.
- The mRNA associates with ribosomes, which consist of rRNA and protein. 21. Three-base codons of mRNA specify amino acids.
- The genetic code refers to the relationship among the nucleotide base sequence of DNA, the corresponding codons of mRNA, and the amino acids for which the codons code.
- Specific amino acids are attached to molecules of tRNA. Another portion of the tRNA has a base triplet called an anticodon.
- The base pairing of codon and anticodon at the ribosome results in specific amino acids being brought to the site of protein synthesis.
- The ribosome moves along the mRNA strand as amino acids are joined to form a growing polypeptide; mRNA is read in the 5’ S 3’ direction.
- Translation ends when the ribosome reaches a stop codon on the mRNA.
The Regulation of Bacterial Gene Expression
· 8-6 Define operon.
· 8-7 Explain pre-transcriptional regulation of gene expression in bacteria.
· 8-8 Explain post-transcriptional regulation of gene expression.
- Regulating protein synthesis at the gene level is energy-efficient because proteins are synthesized only as they are needed.
- Constitutive genes are expressed at a fixed rate. Examples are genes for the enzymes in glycolysis.
Pre-transcriptional Control
- In bacteria, a group of coordinately regulated structural genes with related metabolic functions, plus the promoter and operator sites that control their transcription, is called an operon.
- In the operon model for an inducible system, a regulatory gene codes for the repressor protein.
- When the inducer is absent, the repressor binds to the operator, and no mRNA is synthesized.
- When the inducer is present, it binds to the repressor so that it cannot bind to the operator; thus, mRNA is made, and enzyme synthesis is induced.
- In repressible systems, the repressor requires a corepressor in order to bind to the operator site; thus, the corepressor controls enzyme synthesis.
- Transcription of structural genes for catabolic enzymes (such as b-galactosidase) is induced by the absence of glucose. Cyclic AMP and CRP must bind to a promoter in the presence of an alternative carbohydrate.
- Methylated nucleotides are not transcribed in epigenetic control.
Post-transcriptional Control
- mRNA as a riboswitch regulates translation.
- MicroRNAs combine with mRNA; the resulting double-stranded RNA is destroyed.
Changes in Genetic Material
· 8-9 Classify mutations by type.
· 8-10 Describe two ways mutations can be repaired.
· 8-11 Describe the effect of mutagens on the mutation rate.
· 8-12 Outline the methods of direct and indirect selection of mutants.
· 8-13 Identify the purpose of and outline the procedure for the Ames test.
- Mutations and horizontal gene transfer can change a bacterium’s genotype.
Mutation
- A mutation is a change in the nitrogenous base sequence of DNA; that change causes a change in the product coded for by the mutated gene.
- Many mutations are neutral, some are disadvantageous, and others are beneficial.
Types of Mutations
- A base substitution occurs when one base pair in DNA is replaced with a different base pair.
- Alterations in DNA can result in missense mutations, frameshift, or nonsense mutations.
- Spontaneous mutations occur without the presence of any mutagen.
Mutagens
- Mutagens are agents in the environment that cause permanent changes in DNA.
- Ionizing radiation causes the formation of ions and free radicals that react with DNA; base substitutions or breakage of the sugarphosphate backbone results.
- Ultraviolet (UV) radiation is nonionizing; it causes bonding between adjacent thymines.
The Frequency of Mutation
- Mutation rate is the probability that a gene will mutate when a cell divides; the rate is expressed as 10 to a negative power.
- A low rate of spontaneous mutations is beneficial in providing the genetic diversity needed for evolution.
Identifying Mutants
- Mutants can be detected by selecting or testing for an altered phenotype.
- Positive selection involves the selection of mutant cells and the rejection of nonmutated cells.
- Replica plating is used for negative selection—to detect, for example, auxotrophs that have nutritional requirements not possessed by the parent (nonmutated) cell.
Identifying Chemical Carcinogens
- The Ames test is a relatively inexpensive and rapid test for identifying possible chemical carcinogens.
- The test assumes that a mutant cell can revert to a normal cell in the presence of a mutagen and that many mutagens are carcinogens.
Genetic Transfer and Recombination.
8-14 Describe the functions of plasmids and transposons.
8-15 Differentiate horizontal and vertical gene transfer.
8-16 Compare the mechanisms of genetic recombination in bacteria.
- Genetic recombination, the rearrangement of genes from separate groups of genes, usually involves DNA from different organisms; it contributes to genetic diversity.
- In crossing over, genes from two chromosomes are recombined into one chromosome containing some genes from each original chromosome.
- Vertical gene transfer occurs during reproduction when genes are passed from an organism to its offspring.
- Horizontal gene transfer in bacteria involves a portion of the cell’s DNA being transferred from donor to recipient.
- When some of the donor’s DNA has been integrated into the recipient’s DNA, the resultant cell is called a recombinant.
Plasmids and Transposons
- Plasmids are self-replicating circular molecules of DNA carrying genes that are not usually essential for the cell’s survival.
- There are several types of plasmids, including conjugative plasmids, dissimilation plasmids, plasmids carrying genes for toxins or bacteriocins, and resistance factors.
- Transposons are small segments of DNA that can move from one region to another region of the same chromosome or to a different chromosome or a plasmid.
- Complex transposons can carry any type of gene, including antibiotic-resistance genes, and are thus a natural mechanism for moving genes from one chromosome to another.
Transformation in Bacteria
- During this process, genes are transferred from one bacterium to another as “naked” DNA in solution.
Conjugation in Bacteria
- This process requires contact between living cells.
- One type of genetic donor cell is an F+; recipient cells are F-. F cells contain plasmids called F factors; these are transferred to the F cells during conjugation.
Transduction in Bacteria
- In this process, DNA is passed from one bacterium to another in a bacteriophage and is then incorporated into the recipient’s DNA.
- In generalized transduction, any bacterial genes can be transferred.
Genes and Evolution
8-17 Discuss how genetic mutation and recombination provide material for natural selection to act upon.
- Diversity is the precondition for evolution.
- Genetic mutation and recombination provide diversity of organisms, and the process of natural selection allows the growth of those best adapted to a given environment.