Using genome projects Flashcards
What is the aim of genome projects?
- to map the DNA base sequences making up the
genes of an organism, to then map those onto the individual chromosomes of that organism.
What is a genome?
- complete map of the DNA in a cell/organism
What is a proteome?
- all the proteins produced in a given cell type (cellular proteome) or organism (complete proteome)
What do genome projects create?
- a genome and proteome at a given time, under specific conditions
How is genome projects done?
- Via Bioinformatics – using computer algorithms to collect, store and interpret biological data
Describe the method of genome project
- DNA is cut into many small sections and computer algorithms help align overlapping
segments to assemble the genome.
Knowledge of the proteome of organisms like bacteria has a number of applications, including the development of vaccines (through identification of antigens) & production of biofuels and pollutant ‘cleaners’ (through researching bacteria that withstand extreme
conditions). Suggest and explain why determining the proteome of simple organisms is relatively easy?
- Most prokaryotes have just one, circular piece of DNA that is not associated with histones
- There are no introns (non-coding portions) in the DNA, typical of eukaryotic cells, so it’s easier to predict the amino acid sequence of any protein
The Human Genome Project of 2003 is a testimony to what can be achieved in mapping DNA sequences. Explain why determining the genome and proteome of complex organisms
like humans, however, has been a relatively complex thing to do?
- The genome consists of much more DNA, much of which is non-coding. Introns need to be identified and removed from a base sequence
before predicting an amino acid sequence that will be formed. - Regulatory DNA, e.g., promoter regions need to be identified, as these can pinpoint the start of a gene. Different cells produce different
transcription factors, so working out which proteins will be produced in any given cell is difficult. - Question over which sample to use for mapping, as all individuals (except identical twins) will have different DNA base sequences