topic 7 : modern genetics Flashcards
what is a genome
all of the DNA of an organism including mitochondrial/chloroplast DNA
what is the PCR used for
amplify DNA sample. used for dna sequencing and dna profiling
what is DNA sequencing
determine nucleotide sequence
what is DNA profiling
identifies unique sections of DNA to identify an individual
How is PCR done
- Reaction mixture contains: DNA sample, primers (short section of complementary DNA, its used as a starting point for the free nucleotides to then continue making the complementary chain), free nucleotides, Taq DNA polymerase (taken from organisms living in extreme heat environments so that the enzyme does not denature at high temp)
- The mixture is heated 99C to break the H bonds between the complementary bases of the DNA (DNA unzips)
- The mixture is then cooled 55C to allow the primers to join to the complementary section of the DNA – annealing
- Mixture is heated again to 70C (optimum temp for Taq polymerase) for the phosphodiester bonds to form between the free nucleotides
- This is repeated several times to produce many molecules of the DNA sample
why is DNA sequencing used
used to predict the amino acid sequence and to determine the links between genetically connected individuals. This is done by gel electrophoresis
How is DNA sequencing done
- The sample of DNA is divided into four separate sequencing reactions. Each of the reactions contain the 4 standard nucleotides, DNA polymerase, primers and fluorescently labelled terminator nucleotides
- The primers initiate the formation of complementary strands
- Terminator nucleotides cause the replication to be terminated
- As a result, several fragments of complementary strands are produced which are all different in size
- Gel electrophoresis is used to separate the fragments
- Fragments are viewed under UV light to enable the base sequence to be read
what is DNA profiling used for
used for forensics to identify individuals and paternity testing
how is dna profiling done
- Fragments of DNA are cut by restriction enzymes
- The fragments are separated using gel electrophoresis
how is gel electrophoresis done
- Fragments of DNA are placed in agar, and they are dyed with ethidium bromide so they are visible under UV light
- DNA is negatively charged so it moves and is attracted towards the positive electrode at the end of the electrophoresis equipment
- Fragments of DNA have different masses, so the lighter fragments move quicker and the heavier fragments move slower
- This produces the appearance of various “bands” which can be analysed to identify the DNA sequence
what is gene expression
The process by which a gene gets turned on in a cell to make RNA and proteins.
what are transcription factors
proteins which bind to specific base sequences on DNA
- they sometimes initiate protein synthesis and other times they prevent protein synthesis
what are promotor sequences
- They are found upstream of the gene they act on
- Enable the binding of RNA polymerase and hence promotes transcription
what are enhancer sequences
- Regulate DNA structure by changing the structure of chromatin
- This allows/prevent RNA polymerase from binding
- Open: gene expression is active, Closed: gene expression is inactive
what is epigenetics
heritable and reversible modifications to the DNA that do not involve changes to the nucleotide sequence.
- Study of changes in organisms due to the changes in gene expression rather than the change in the actual DNA code