Professional Documents
Culture Documents
COURSE CONTENT
The course content is comprehensively covered in Chapters 10, 11, 14, 15, 17, 18, 13, 24
and 21 of the prescribed textbook.
Theoretical
At the end of the course the student should, with reference to the prescribed text,
understand, and be able to explain the following concepts:
• Characteristics of genetic material
• DNA as genetic material in prokaryotes and eukaryotes
• RNA as genetic material
• Chemical composition of nucleic acids
• DNA and RNA structure
• Analyses of nucleic acids
• Mechanisms of DNA replication
• DNA synthesis in microorganisms
• A model of DNA synthesis
• Genetic control of replication
• Synthesis of eukaryotic DNA
• Recombination of DNA
• Characteristics of the genetic code
• Early studies on the mechanism of the code
• Deciphering of the code and the code dictionary
• Overview of the expression of genetic information
• Transcription: RNA synthesis
• Transcription in eukaryotes
• Introns
• The elements involved in the translation process
• The process of translation
• The functional prokaryote ribosome
• Translation in eukaryotes
• The one-gene:one-enzyme hypothesis
• The one-gene:one-protein and one-gene:one polypeptide hypotheses
• Protein structure and function
• Post-translational modification
• Overview of gene regulation in prokaryotes
• Inducible regulation: lactose metabolism in E. coli
• Positive and negative control
• Repressible regulation: tryptophan metabolism in E. coli
• The arabinose operon
• Overview of gene regulation in eukaryotes
• Chromosome and chromatin influences on eukaryotic gene expression
• Transcriptional regulation at Cis-acting sites
• The role of transcription factors
• The role of activators and repressors
• A eukaryotic gene regulation model: inducible transcription of the yeast GAL genes
• Posttranscriptional regulation of gene expression
• RNA silencing controls gene expression
• Overview of recombinant DNA technology
• The role of restriction enzymes in the construction of recombinant DNA molecules
• Cloning vectors
• Cloning of DNA in E. coli
• Cloning in eukaryotic hosts
• Gene transfer in eukaryotic cells
• The polymerase chain reaction
• Construction of DNA libraries
• Identification and analysis of cloned DNA sequences
• DNA sequencing
• Mapping of genes
• Diagnosis and screening of genetic disorders
• Gene therapy
• DNA fingerprints
• Genome analysis
• Biotechnology
• Genomics: sequencing and assembling of entire genomes
• DNA sequence analysis: Bioinformatics tools and genome databases
• Functional Genomics: identification of genes and their function
• The human genome project
• The “Omics” revolution
• Prokaryotic and Eukaryotic genomes
• Comparative genomics
• Metagenomics
• Proteomics: identification and analysis of proteins expressed in a cell
• Systems Biology
Practical
A student should, with the aid of a relevant protocol, be able to demonstrate the following
practical skills:
• correct handling and accurate pipetting using micropipettes
• execution of basic biological calculations like molarities, percentages (v/v) and
(m/v), as well as densities
• execution of plasmid and genomic DNA extractions
• calculation of reaction volumes and execution of restriction enzyme digestions
• calculation of reaction volumes and execution of PCRs
• loading of horizontal agarose gels
• interpretation of gel electrophoresis results
General
The following general principles apply for the course and students are expected to
adhere to these:
• accept responsibility for own learning of the study material
• learn to understand the concepts and principles relevant to the course at all times
(i.e. see the big picture) and know where to find detailed information
• develop an understanding and appreciation for the nature of the experimentation-
based process of scientific discovery
• have the computer literacy to exploit the variety of electronic information sources
available (e.g. internet, CD-ROMs and WebCT)
• effective utilisation of the prescribed text
• have writing skills