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DNA Sequencing: Two Main Methods

DNA sequencing is a method to determine the precise order of nucleotide bases (adenine, guanine, cytosine, thymine) that make up a DNA strand. There are two main methods: the Maxam-Gilbert method and the Sanger method. The Maxam-Gilbert method involves chemically modifying specific nucleotide bases in a radioactively labeled, single-stranded DNA fragment and then cleaving the DNA backbone at sites adjacent to the modified bases, generating fragments of different lengths that can be used to deduce the DNA sequence.

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56 views

DNA Sequencing: Two Main Methods

DNA sequencing is a method to determine the precise order of nucleotide bases (adenine, guanine, cytosine, thymine) that make up a DNA strand. There are two main methods: the Maxam-Gilbert method and the Sanger method. The Maxam-Gilbert method involves chemically modifying specific nucleotide bases in a radioactively labeled, single-stranded DNA fragment and then cleaving the DNA backbone at sites adjacent to the modified bases, generating fragments of different lengths that can be used to deduce the DNA sequence.

Uploaded by

Rooth Adajet
Copyright
© © All Rights Reserved
Available Formats
Download as DOCX, PDF, TXT or read online on Scribd
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DNA Sequencing

DNA sequencing is a method used to determine the precise order of the four
nucleotide bases adenine, guanine, cytosine and thymine - that make up a
strand of DNA.

Two Main Methods:


1. Maxam-Gilbert Sequencing Method
2. Sanger Sequencing Method

Maxam-Gilbert Sequencing Method


MaxamGilbert sequencing is a method of DNA sequencing developed
by Allan Maxam and Walter Gilbert in 19761977. This method is based
on nucleobase-specific partial chemical modification of DNA and
subsequent cleavage of the DNA backbone at sites adjacent to the
modified nucleotides.

Procedure

1. Denature a double-stranded DNA to single-stranded by increasing temperature.


2. Radioactively label one 5' end of the DNA fragment to be sequenced by a kinase reaction
using gamma-32P.
3. Cleave DNA strand at specific positions using chemical reactions. For example, we can use
one of two chemicals followed by piperdine. Dimethyl sulphate selectively attacks purine (A
and G), while hydrazine selectively attacks pyrimidines (C and T). The chemical treatments
outlined in Maxam-Gilbert's paper cleaved at G, A+G, C and C+T. A+G means that it cleaves
at A, but occasionally at G as well.
4. Now in four reaction tubes, we will have several differently sized DNA strands.
5. Fragments are electrophoresed in high-resolution acrylamide gels for size separation.
6. These gels are placed under X-ray film, which then yields a series of dark bands which show
the location of radiolabeled DNA molecules. The fragments are ordered by size and so we
can deduce the sequence of the DNA molecule.

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