Title: DNA Technology
1DNA Technology Genomics
2DNA Cloning (gene cloning)
- methods
- insert gene of interest into a bacterial plasmid
allow the recombinant bacterium to reproduce - PCR (polymerase chain reaction)
- uses
- make multiple copies of a particular gene for
use in basic research or insertion into another
organisms genome - harvest large quantities of the encoded protein
from bacterial cultures carrying the cloned gene
3Restriction Enzymes
- enzymes that cut DNA at specific locations
(restriction sites) yielding restriction
fragments - used to insert genes into bacterial plasmids
- the sticky ends of the restriction fragments can
base-pair with the sticky ends of a cut plasmid
then be sealed together by DNA ligase
4Genomic Libraries
- the process of DNA cloning usually results in
thousands of different types of recombinant
plasmids - the complete set of these recombinant plasmids is
called a genomic library - one method for identifying bacteria with the
recombinant plasmid containing the gene of
interest is nucleic acid probe hybridization
white colonies
5Nucleic Acid Hybridization
6Expressing Eukaryotic Genes in Prokaryotic Cells
- Problem 1 bacterial cell doesnt recognize the
eukaryotic genes promoter - solution link the gene of interest to a highly
active prokaryotic promoter that the bacterial
cell will recognize - this is accomplished by inserting the gene of
interest into a cloning vector (plasmid) that
contains a this promoter - Problem 2 eukaryotic genes contain introns
bacterial cells lack RNA-splicing machinery - solution insert the cDNA (complimentary DNA)
form of the gene
7Creating cDNA
- mRNA transcript of gene of interest is combined
with reverse transcriptase to create a
complimentary DNA strand - the mRNA strand is then degraded and the
complimentary, second strand of DNA is created by
adding DNA polymerase - the resulting cDNA molecule is modified by adding
sticky ends so that it can be inserted into a
cloning vector
8Eukaryotic Hosts for DNA Cloning
- yeast cells (which also contain plasmids) can be
used as hosts for DNA cloning to avoid
eukaryotic-prokaryotic incompatibility
9PCR (Polymerase Chain Reaction)
- alternative method for cloning a gene
- used primarily when the source of DNA is scanty
or impure - applications
- amplify fragments of ancient DNA
- amplify DNA from fingerprints or tiny amounts of
blood, tissue, or semen found at crime scenes - amplify DNA from embryonic cells to test for
genetic disorders
10Restriction Fragment Analysis
- the DNA fragments produced by restriction enzyme
digestion can be sorted by gel electrophoresis - uses a gel an electric field to separate
nucleic acids or proteins on the basis of size
and charge - the bands produced by gel electrophoresis can be
analyzed for a particular gene using nucleic acid
hybridization (this technique is called Southern
blotting)
11(No Transcript)
12Genome Mapping
- 3 stages
- linkage mapping
- physical mapping
- DNA sequencing
13Cytogenetic Maps
- the starting point for DNA mapping
- shows a chromosomes banding pattern and the
location of specific genes on the chromosome - the genes were located using a technique called
FISH (fluorescence in situ hybridization) in
which fluorescently labeled probes are allowed to
hybridize to an immobilized array of whole
chromosomes
14Linkage Maps
- a map of genetic markers based on recombination
frequencies - the markers can be
- genes
- RFLPs (restriction fragment length polymorphisms)
different restriction fragment patterns on
homologous chromosomes due to differences in
their restriction sites - simple sequence DNA sections of DNA that
contain repeated short sequences
15Physical Maps
- express the distance (number of base-pairs)
between markers - made by cutting the DNA of a chromosome into a
number of restriction fragments and then
determining the original order of the fragments
in the chromosome by looking for areas where the
fragments overlap
16DNA Sequencing
- determining the complete nucleotide sequence of
each chromosome - techniques for DNA sequencing include
- dideoxy chain-termination method
- shotgun approach developed by Celera Genomics
- skips the linkage physical mapping stages
- takes random DNA fragments uses computer
programs to sequence and order them
17shotgun approach
dideoxy chain- termination method
18Human Genome Project
- sequencing of the 22 autosomes and the sex
chromosomes (largely completed in 2003) - also involves mapping the genomes of other
species important to biological research - allows scientists to study whole sets of genes
their interactions
19Searching for Protein-Coding Genes
- scientists used software to scan DNA sequences
for - transcriptional translational start and stop
sequences - RNA-splicing sites
- short coding sequences (expressed sequence tags)
similar to those in known genes
20Determining Gene Function
- disable gene and observe the consequences
- in vitro mutagenesis a mutation is introduced
in a cloned gene then returned to the cell - RNA interference (RNAi) synthetic,
double-stranded RNA molecules matching the
sequence of a particular gene are used to trigger
the breakdown or block the translation of the
genes mRNA
21Studying Gene Expression
- to determine which genes are expressed in a
particular cell, scientists can use DNA
microarray assays - isolate all the mRNAs made in a particular cell
- use them to make fluorescently-labeled cDNAs by
reverse transcription - apply the cDNA to a microarray containing all
the organisms genes
22Comparing Genomes of Different Species
- allows scientists to determine evolutionary
relationships between species - helps scientists better understand the human
genome - provides scientists with a scaffold for
organizing the DNA sequences of closely related
species - makes it easier for scientists to correlate
phenotypic differences between species with
particular genetic differences - can be used to help study certain genetic diseases
23Future Areas of Research
- Proteomics studying the full protein sets
encoded by genomes - studying human evolution the history of human
populations through the identification of SNP
sites - SNPs (single nucleotide polymorphisms) are single
base-pair variations that account for the genetic
differences between individuals (which is only
about 0.1)
24Applications of DNA Technology
- Medicine
- Pharmaceuticals
- Forensics
- Environmental Cleanup
- Agriculture
25Medical Applications
- diagnosing diseases
- detecting susceptibility of diseases
- treating diseases
- gene therapy alteration of an afflicted
individuals genes
26Pharmaceutical Applications
- manufacture large quantities of human proteins
(ex insulin) - production of vaccines
- pharmacogenomics
27Forensic Applications
28Environmental Cleanup
- genetically engineered microbes are being used or
created to - remove heavy metals from the environment
- cleanup highly toxic mining wastes
- degrade chlorinated hydrocarbons in wastewater
- breakdown chemical released during oil spills
- breakdown toxic wastes in waste dumps
29Agricultural Applications
- make vaccines growth hormones for treating farm
animals - creating transgenic animals plants