How do we analyze dna
1 / 19

How do we analyze DNA? - PowerPoint PPT Presentation

  • Updated On :

How do we analyze DNA?. Gel electrophoresis Restriction digestion Sequencing. DNA analysis. How do we manipulate DNA to improve our crop? First we need to identify which genes in the DNA sequence are important for the trait we are trying to improve

I am the owner, or an agent authorized to act on behalf of the owner, of the copyrighted work described.
Download Presentation

PowerPoint Slideshow about 'How do we analyze DNA?' - amanda

An Image/Link below is provided (as is) to download presentation

Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author.While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server.

- - - - - - - - - - - - - - - - - - - - - - - - - - E N D - - - - - - - - - - - - - - - - - - - - - - - - - -
Presentation Transcript
How do we analyze dna l.jpg
How do we analyze DNA?

  • Gel electrophoresis

  • Restriction digestion

  • Sequencing

Dna analysis l.jpg
DNA analysis

  • How do we manipulate DNA to improve our crop?

  • First we need to identify which genes in the DNA sequence are important for the trait we are trying to improve

  • BUT - DNA from a single human cell can be over 2m in length! Some plants have genomes as large as 7.5 x 1010 base pairs (25 times the size of the human genome).

Gel electrophoresis l.jpg
Gel Electrophoresis

  • 1949 a team led by chemist Linus Pauling found two samples of hemoglobin from healthy and sickle-cell anemia sufferers migrated at different rates.

  • Today, gel electrophoresis is indispensable

  • Wide variety of applications includes determination of a gene's sequence, isolation of entire chromosomes, and separation and characterization of proteins

Uses outside the laboratory l.jpg
Uses outside the laboratory

  • DNA fingerprinting evidence

  • Men proving or disproving paternity via the technique

  • Hospitals replacing conventional heel prints with genetic fingerprints as a means of identifying newborns.

How does it work l.jpg
How does it work?

  • Agarose and polyacrylamide are the two media most commonly used in gel electrophoresis. Both substances create a porous matrix through which charged macromolecules migrate in response to an electric field.

  • Negatively charged DNA, for example, travels toward the positively charged electrode when current is applied.

Slide6 l.jpg

  • Pores in the matrix limit the migration of large molecules, while smaller molecules migrate more freely and travel farther toward the opposite pole. This molecular sieving separates molecules on the basis of size.

  • Agarose is used as the support matrix to separate nucleic acids and very large proteins or complexes.

  • Agarose is a natural polysaccharide derived from certain types of red seaweed. When heated and then cooled, agarose solidifies into a solid matrix with relatively large, nonrestrictive pores.

Slide7 l.jpg

  • Agarose gel electrophoresis (AGE) can be used to separate molecules by charge or by their molecular weight.

  • One of the most common applications of AGE is its use in separation of the fragments generated by cleaving DNA with restriction enzymes

  • Gel electrophoresis not only separates macromolecules, but also allows the researcher to actually use the nucleic acid or protein by transferring it to a support membrane made of nitrocellulose or nylon, and then probing it with radioisotope- or enzyme-labeled complementary DNA or antibodies

Slide8 l.jpg

DNA has to be cut into more manageable pieces before it can be analyzed

Restriction enzymes cut DNA in very specific places that are determined by the order of 4-8 base pairs of nucleotides

These smaller pieces can then be cloned into a plasmid or bacteriophage vector for amplification and further analysis

Restriction mapping l.jpg
Restriction Mapping be analyzed

  • A restriction map is a description of restriction endonuclease cleavage sites within a single piece of DNA

  • First step in characterizing an unknown DNA, and a prerequisite to manipulating it for other purposes

  • Restriction enzymes that cleave DNA infrequently (e.g. those with 6 bp recognition sites) and are relatively inexpensive are used to produce a map

Creating a map digestion with multiple restriction enzymes l.jpg
Creating a Map - Digestion with Multiple Restriction Enzymes be analyzed

Digestsamples of the plasmid with a set of individual enzymes, and with pairs of those enzymes

Digests are then "run out" on an agarose gel to determine sizes

Deduce where each enzyme cuts, which is what mapping is all about

E g plasmid with 3000 base pair bp fragment of unknown dna l.jpg
e.g. Plasmid with 3000 base pair (bp) fragment of unknown DNA

  • Digestion with Kpn I yields two fragments: 1000 bp and "big“

  • Digestion with BamH I yields 3 fragments: 600, 2200 and "big“

  • double digest yields fragments of 600, 1000 and 1200 bp (plus the "big" fragment)

Slide12 l.jpg

Dna sequencing l.jpg
DNA Sequencing set of enzymes, a much more complete map would result.

  • Short stretches of DNA can be sequenced using “primers” that are based on the known nucleotides where the restriction enzyme has cut the DNA

  • DNA heated to a critical temperature called the Tm will “denature” or separate into two single strands

  • These strands can be used to build new complementary strands, or can “reanneal” or stick back together when the temperature is reduced

Slide14 l.jpg

  • Polymerase Chain Reaction (PCR) set of enzymes, a much more complete map would result.

  • For each strand, we provide a primer, which is a short piece of DNA that sticks to one end of the strand.

  • Any single-stranded piece of DNA can only hybridize with another if their sequences are complementary. If we have just one strand, we can actually build another strand to match it.

  • DNA polymerase "reads" the bases on one strand and can attach the complementary base to the growing strand.

Slide15 l.jpg

  • DNA sequencing reactions set of enzymes, a much more complete map would result. are just like the PCR reactions for replicating DNA

  • The reaction mix includes the template DNA, free nucleotides, an enzyme (usually a variant of Taq polymerase) and a 'primer'

Slide16 l.jpg

Dna sequencing17 l.jpg
DNA Sequencing mixture is specially modified to form a dideoxynucleotide and is labeled with a unique fluorescent dye or tag

  • As the reaction proceeds to build a new DNA strand from the existing one the signal from each of the bases can be recognized and so we can work out in which order the bases were added

Slide18 l.jpg

  • A 'Scan' of one gel lane: The computer “reads” the lane for us! This is what the sequencer's computer shows us - a plot of the colors detected in one 'lane' of a gel (one sample), scanned from smallest fragments to largest. The computer even interprets the colors by printing the nucleotide sequence across the top of the plot

How do we use this information l.jpg
How do we use this information?

  • We can compare organisms to one another

  • DNA fingerprints allow for identification of each individual

  • Once genes have been identified we can begin to work with these areas of the genome in order to improve traits