• Like
Dna profiling
Upcoming SlideShare
Loading in...5

Thanks for flagging this SlideShare!

Oops! An error has occurred.



Published in Technology , Education
  • Full Name Full Name Comment goes here.
    Are you sure you want to
    Your message goes here
    Be the first to comment
    Be the first to like this
No Downloads


Total Views
On SlideShare
From Embeds
Number of Embeds



Embeds 0

No embeds

Report content

Flagged as inappropriate Flag as inappropriate
Flag as inappropriate

Select your reason for flagging this presentation as inappropriate.

    No notes for slide


  • 1. DNA profiling
  • 2. It is highly unlikely that any two individuals have the exact same pattern of DNA, unless they are twins, of course! DNA  Introns – the regions of the chromosomes which are used in DNA profiling.  Mini-satellites – 20-50 base sequence repeated from 50 to several hundred times.  Micro-satellites – 2-4 bases repeated between 5 and 15 times.  The more closely related the two individuals, the more similar the DNA patterns are.
  • 3. The process  DNA is extracted from a blood or cell sample.  It is split into fragments using restriction endonucleases.  These cut the DNA at certain points in the intron sequences.  Each type cuts a DNA molecule into fragments at different recognition sites. Using restriction enzymes that cut either side of mini- and micro-satellite units leaves the repeated sequences intact, giving a mixture of DNA fragments made up largely of miniand micro-satellite sequences.
  • 4. A dye is also added to the DNA samples. It moves through the gel faster than the DNA so that the current can be turned off before all the samples run off at the end. Gel electrophoresis       The fragments are placed in wells in an agarose gel medium in a buffering solution, with known DNA fragments. The gel contains a dye which binds to the DNA fragments in the gel. A dye is also added to the DNA samples. An electric current is passed through the apparatus and the DNA fragments move towards the positive anode. The plate is placed under UV light. The DNA fluoresces so it can be identified.
  • 5. Southern blotting  An alkaline buffer solution is added to the gel after electrophoresis.  A nylon filter or (nitrocellulose paper) is placed over it.  Dry absorbent paper is used to draw the solution containing the fragments from the gel to the filter, leaving ‘blots’ on it.  The alkaline solution also denatures the fragments so the strands separate and the base sequences are exposed.
  • 6. Each probe is labelled, either with a radioactive element or with a fluorescent molecule. Gene probes     These are short DNA sequences that are complementary to specific sequences which are required. Hybridisation - large amounts of the probe are added to the filter and bind with the complementary DNA strands. Excess probes are washed away. X-ray pictures are taken of the filter or the filter is placed under UV light. In forensic science, they are used for picking out short tandem repeats – micro-satellite regions which are now widely used in DNA identification . The more micro-satellites are used to make up a profile the more accurate it will be.
  • 7. Polymerase chain reaction The reactants are placed in a vial in a PCR machine. The reactants: •DNA sample •DNA polymerase (enzyme) •Primers •The four nucleotide bases Mixture is heated to 90-95 C – which causes the DNA strands to separate as the hydrogen bonds between them break down. Mixture is cooled to 50-60 C – the primers bind (anneal) to the single DNA strands. Mixture is heated to 75 C – the optimum temperature for the enzyme to build the complementary strands of DNA.