topic 6.1.3: manipulating genomes Flashcards
what is a genome
the genetic material of an organism
what are the ingredients of dna sequencing
dna polymerase, primer, excess of nucleotides, terminator bases, dna to be sequenced mixed in a thermocycler
what are the principles of dna sequencing
dna p adds comp bases to dna, creating new strand
terminator bases added at diff points, creating every possible length
each base labelled with fluorescent dye
gel electrophoresis separates according to size
what is high throughput sequencing
many fragments processed and sequenced simultaneously
what are the benefits of genome wide comparisons
identify sources of infections, identify resistant bac, track spread of pathogens
what is synthetic biology
creation of artificial organisms or devices, or redesign of natural systems eg genetic engineering, synthesis of genes
what is bioinformatics
use of software to analyse and store data
what is computational biology
use of computers to study biology eg modelling
what are introns made up of
variable number tandem repeats
what are vntrs
sequences where nucleotides are repeated a variable number of times, meaning they are different lengths in individuals
what are the 6 stages of dna profiling
extraction, digestion, separation, hybridisation, development, analysis
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what happens in the extraction stage of dna profiling
small fragment multiplied by pcr
what happens in the digestion stage of dna profiling
restriction endonucleases added to cut dna into smaller pieces
what happens in the separation stage of dna profiling
gel electrophoresis
what happens in the hybridisation stage of dna profiling
fluorescent or radioactive probes added in excess and bind to dna
what are probes
short complementary fragments
what happens in the development stage of dna profiling
southern blotting:
strands transferred to nylon membrane and exposed to x rays to visualise position of probes
what happens in the analysis stage of dna profiling
bands compared to identify relationships, presence of disease, or match unknown samples
what equipment is needed for a polymerase chain reaction
thermocycler, dna fragment, primers, taq polymerase, nucleotides
why is taq polymerase used
thermophilic bacteria thrive in hot conditions, work faster
what are the principles of pcr
95: h bonds broken, dna split
55: annealing
72: synthesis
describe the process of electrophoresis
samples loaded into agar plates, ph buffer added and voltage applied to cathode end
dna move to pos end
alkali added to denature strands
what are the 4 stages of genetic engineering
identification, removal, insertion, transformation
what happens in the identification stage of genetic engineering
desired gene selected in organism and plasmid