dna libraries ppt
DESCRIPTION
DNA Libraries are collection of fragments of DNA cloned to a vector so that researchers can easily identify and isolate a particular gene of interest for future use.TRANSCRIPT
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SRUTHY K . S11-BVP-216
VPB 321
DNA LIBRARIES
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DNA LIBRARY
The term "library" can refer to a population of organisms, each of which carries a DNA molecule inserted into a cloning vector, or alternatively to the collection of all of the cloned vector molecules.
Collection of DNA fragments that have been cloned into vectors so that researchers can identify and isolate the DNA fragments that interest them for further study.
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Genomic libraries
cDNA libraries
Gene library
(made from genomic DNA)
(made from cDNA- copy of mRNA)
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For the construction of DNA library
Size of the gene
Capacity of the vector
Molecular tools
Vectors
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Vector type Max. Insert size cloned DNA
(kb)
Approx.no: of cloned DNA required in a
library
Plasmid 20 >10^5
Lambda phage 20 5 x10^5
Cosmid 45 2 x 10^5
BAC >500 5 x 10^4
YAC 1Mb 1o^5
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Genomic DNA library: Contains the whole genome of an organism
Genome size is expressed in terms of number of base pairs.
Smallest genomic size is…………..????
For human the genomic size is………….????
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STEPS
1) Purification of genomic DNA
PROKARYOTES
EUKARYOTES
•Genomic libraries of prokaryotes are easier to make and contain all the genome sequences.
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2) Cleaving the genome into smaller fragments by restriction endonucleases.
• Parial digestion is used to getting longer DNA sequences.
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3) In cooperation of these fragments into a suitable vector.
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4) Introduction of vector into a suitable host like bacterium(Transformation)
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Multiplication
Screening
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Screening: The process of identifying one particular clone containing the gene of interest from amongthe very large number of others in the gene library .
Expression screening
Hybridisation technique
PCR
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Expression screening
Eg: Finding the gene for alanine production
Grow in alanine deficit medium
Then they are labelled in the petri plate indicates that gene for alanine production is stored in bacteria.
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Hybridisation technique
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cDNA Library
No cDNA library was made from prokaryotic mRNA…..???
cDNA libraries are very useful for eukaryotic gene analysis.
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mRNA isolation, purification
Check the RNA integrity
Synthesis of cDNA
Treatment of cDNA ends
Ligation to vector
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mRNA isolation
Most eukaryotic mRNAs are polyadenylated at their 3’ ends
• oligo (dT) can be bound to the poly(A) tail and used to recover the mRNA.
AAAAAAAAAAn5’ cap
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Check the mRNA integrity
Make sure that the mRNA is not degraded.
•Translating the mRNA
•Analysis the mRNAs by gel elctrophoresis
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Synthesis of cDNA
First stand synthesis: Reverse transcriptase ,primer( oligo(dT) or
hexanucleotides) and dNTPs.
Second strand synthesis: Best way of making full-length cdna is to
‘tail’ the 3’-end of the first strand and then use a complementary primer to make the second.
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5’ mRNA AAAAA-3’ HO-TTTTTP-5’
5’
Reverse transcriptaseFour dNTPs
AAAAA-3’TTTTTP-5’
mRNA
mRNA
cDNA
cDNA
cDNA
Duplex cDNA
AAAAA-3’
TTTTTP-5’
TTTTTP-5’
3’
3’-CCCCCCC
Terminal transferasedCTP
Alkali (hydrolyaes RNA)Purify DNA oligo(dG)
Klenow polymerase or reverseTranscriotase Four dNTPs
5’-pGGGG-OH
5’
3’-CCCCCCC
5’-pGGGG3’-CCCCCCC TTTTTP-5’
-3’
Angelia 09 22
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5’-pGGGG3’-CCCCCCC
HO-CCGAATTCGGGGGG 3’-GGCTTAAGCCCCCC
5’-pAATTCGGGGGG
TTTTTGGCTTAAGCC-OH CCGAATTCGG-3’
3’-CCCC
3’-CCCCCCC
3’-CCC 5’-pGGGG
5’-pGGGG
TTTTTp-5’ -3’
TTTTTp-5’
TTTTTp-5’
-3’
-3’
TTTTTGGCTTAAp-5’
HO-CCG/AATTCGG-3’ 3’-GGCTTAA/GCC-OH
CCG-3’
Duplex cDNA
Single strand-specific nuclease
Klenow polymerase
treat with E.coRI methylase
Add E.colRI linkers using T4 DNA ligase
E.colRI digestion
Ligate to vector and transfom
Fig2.1 Second strand synthesis23
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Treatment of cDNA ends
Blunt and ligation of large fragment is not efficient, so we have to use special acid linkers to create sticky ends for cloning.
Move protruding 3’-ends (strand-special nuclease)
Fill in missing 3’ nucleotide
Ligate the blunt-end and linkers(T4 DNA ligase)
Restriction enzyme digestion (E.coRI )
Tailing with terminal transferase or using adaptor molecules
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Ligation to vector
Any vectors with an EcoRI site would suitablefor cloning the cDNA.
Dephosphorylate the vector with alkalinephosphatase
Ligate vector and cDNA with T4 DNA ligase
(plasmid or λ phage vector)
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Uses of cDNA library
Used when reproducing eukaryotic genomes as the amount of information is reduced to remove the large number of non-coding regions from the library.
To express eukaryotic genes in prokaryotes.
Useful for subsequently isolating the gene that codes for that mRNA.
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THANK YOU