Cloning:Recombinant DNA
Multistep Process
. Produce fragments of DNA using enzymes that cut DNA at specific base sequences. . Link these fragments to selfreplicating forms of DNA = vectors.
. Replicate the recombinant DNA molecule in the host organism (1000s of copies).
. Retrieve the cloned copies for use or modification. . Produce and purify gene product.
Some useful definitions
Restriction Enzymes
Enzymes
that recognize a specific base sequence in DNA and cleave at that site Isolated from bacteria that inactivated viruses via cutting their DNA Molecular scissors
Recognition sequence
Palindrome
- sequence is read the same on either strand, when read from 5 to 3 Creates either sticky ends or blunt ends
Eco R1
Vectors
A
self-replicating DNA molecule that is used to transfer foreign DNA fragments between cells.
Steps in Cloning
Steps in cloning - General
Isolate
vector DNA and gene of interest Cut both with the same restriction enzyme Mix DNAs and ligate = recombinant DNA
Transfer
recombinant molecule into host cell (transform) Grow/Select transformants
Types of Vectors and DNA delivery systems
Types of Vectors
Plasmid
Phage
(virus) Cosmid Yeast Artificial Chromosome (YAC)
Plasmids
Circular
extrachromosomal DNA molecules naturally found in bacteria Self-replicating Can insert pieces up to 10kb
Plasmid vectors need
origin
of replication selectable marker (antibiotic) unique restriction enzyme cleavage sites
Plasmid Placement in Cell
Phage vectors
Derivatives
Linear
of phage (lambda)
DNA Can insert up to 15 kb fragments
Phage Insertion
Cosmids
Dont
occur naturally Constructed using features of both plasmids and phage Can carry inserts up to 45 kb
YACs
YACs
YACs
Yeast
artificial chromosome Self-replicating elements Can insert segments up to 1 million base pairs Can replicate any inserted DNA via transfer to yeast cells
Essential elements for YACs
Tel
- telomeres Cen - centromere Ori - Origin of replication Selectable markers Restriction enzyme recognition sites
Particle Gun
Usually
using cell culture Shoot DNA coated objects into cells Tungsten pellets, Whiskers
We can insert the gene into cells Now what?
Selecting for transformed cells and amplifying the product
Basic Steps
Identify
the transformants Isolate transformed colonies Amplify the product
Identifying transformants
Vectors
containing antibiotic resistance genes can be used Those that took up the vector will now express antibiotic resistance Ability to metabolize substances included in media
Isolate Colonies of Interest
Amplify the Product
Use
bacteria (usually E. Coli) to amplify product Sometimes yeast cells, if the gene you are amplifying is a eukaryote specific gene
Genetic Libraries
Genetic library
Collection
of clones that contains all the genetic information of an individual = genomic library - gene bank Chromosomes, set of genes of single cell type etc.
cDNA
- mRNA population made into cDNA. Produce clones
Can
recover genes of interest from libraries for
Clinical studies
Evolutionary comparison Experimental studies Commercial use
Construction of...
DNA
isolated from an organism Digest into smaller segments which can be inserted within vectors (size limitations)
record
of genome or portion of Can be screened, hybridization