2. How are the Genome Sequenced ?
• The most popular method is dideoxy method also termed as sanger’s method.
• Method developed by :- Fred Sanger and awarded Nobel prize in 1980.
Fred Sanger’s Method
Step1:- To denature the double stranded DNA into the Single Stranded DNA.
Step2:- In this method denatured DNA is mixed with the DNA polymerase and all four type of Bases and one of the
dNTP atom is radioactive.
DNA Sample
All four Types of dNTPs in which
one of the dNTP is radioactive
atom.
DNA polymerase
RNA polymerase as initiator
Types of dNTPs:-
1. dATPs
2. dCTPs
3. dGTPs
4. dTTPs
One of them is radioactive
+
+
+
3. Step3:- In this step the last mixture (DNA + dNTPs + DNA polymerase + RNA polymerase) is divided into the four aliquoted tubes.
This mixture is divided into the 4 aliquoted tubes
Tube 1
Tube 2
Tube 3
Tube 4
4. Step4:- Each tube is added a small dose of one of the four dideoxyribonucleotide triphosphate
(ddNTPs = ddGTPs, ddCTPs , ddATPs , ddTTPs.).
Aliquoted mixture is divided into 4 tubes and then treated with one
of the radioactive ddNTPs.
Tube 1 Tube 4Tube 3Tube 2
Tube 1
treated with
radioactive
ddGTPs
Tube 4
treated with
radioactive
ddTTPs
Tube 3
treated with
radioactive
ddATPs
Tube 2
treated with
radioactive
ddCTPs
• A ddNTPs lacks the 3’ hydroxyl group (-OH) found on normal deoxyribonucleotides.
• When DNA is being polymerized , the newest dNTP to be added to forms a covalent bond onto the protruding 3’ hydroxyl
group of the last successfully added dNTPs.
5. Step 5 :-
• The ddNTPs incorporated when the last dNTP is attached and there is non-availability of dNTPs in sample.
• The ddNTPs incorporated with the termination of elongation of DNA.
Each and every DNA
terminates the
elongation process by
incorporating with the
ddGTPs
Each and every DNA
terminates the
elongation process by
incorporating with the
ddTTPs
Each and every DNA
terminates the
elongation process by
incorporating with the
ddATPs
Each and every DNA
terminates the
elongation process by
incorporating with the
ddCTPs
• After incorporation of ddNTPs the reaction will stop and elongation will End.
6. Step 6:-
• The content of each of four types of tube is loaded into four different lenses of gel
• The different length of the DNA segment travels the different distance in the gel.
• Smallest size of DNA covers the maximum length in the gel.
7. • The DNA Sequencing gel is exposed to the X- ray and read from the bottom to top respective in 5’ to 3’ direction
• Radioactive sequencing worked well but seems to be labor intensive it could collect only 500 bases in 24 Hours to make, run
and expose to X-ray films.
A faster method of sequencing was developed by Caltech, Leroy Hood and members of
his lab innovate an Non-Radioactive method.
• They used ddNTPs and fluorescent dye with the Bases (There is no use or radioactive atom).
• The different ddNTPs labelled with the different color of fluorescent dye.
• With this innovation the time consumption in the X-ray film exposition and manual reading will be reduce.
• There is only tube of sample will needed to load into the Single lane of gel.
• Each band flashed it’s colour and indicates the presence of specific type of the ddNTPs.
• That data was recorded into the computer.
• In this method of sequencing there is replacement of the four bands into single band in the different colour flashing also
termed as chromatograms.