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Linker, Adaptor, Homopolymeric Tailing & Terminal Transferase
The document discusses techniques for constructing DNA molecules with sticky and blunt ends, highlighting methods such as linker and adaptor addition, and homopolymeric tailing using terminal transferase. Linkers and adaptors facilitate the efficient ligation of DNA fragments, while homopolymeric tailing provides a way to create complementary ends for DNA ligation. Terminal transferase, a template-independent enzyme, is also detailed for its ability to add nucleotides to DNA ends, contributing to various applications in genetic engineering.
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Discusses ligation efficiency depending on DNA ends: sticky (efficient) vs blunt (less efficient).
Explains methods to create sticky ends using linkers, adaptors, and homopolymeric tailing for DNA cloning. Defines linkers, their structure and use in creating sticky ends for effective DNA ligation and cloning.
Describes adaptors, their designs, and potential issues like self-ligation when creating compatible ends.
Outlines solutions to prevent adaptor self-ligation using enzymatic treatments and molar adjustments.
Describes the use of homopolymeric tails and the methods for their attachment to aid in DNA ligation.
Introduces TdT enzyme, its function in DNA synthesis, and regulation of its expression.
Gives structural details of TdT, its buffer requirements, and activity affected by ions.
Explores applications of TdT in DNA labeling, mutagenesis, and assays for gene research.
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Linker, Adaptor, Homopolymeric Tailing & Terminal Transferase
- 1. B Y U ts a R o y I C A R - C e n t r a l I n s t i t u t e O f F i s h e r i e s E d u c a t i o n M u m b a i Linker, Adaptor, Homopolymeric Tailing & Terminal Transferase
- 2. Introduction Ligation efficiencydepends on the ends of DNA in the reaction. Mainly two types of end. 1. “sticky” ends: Ligation is efficient annealing of complementary overhangs brings 5’P and 3’OH into close proximity. 2. “Blunt” ends: Ligation is less efficient need high concentrations of ligase and DNA
- 3. Blunt end ligation Mainly three methods can be used to put the correct sticky ends onto the DNA fragments- 1. Cloning foreign DNA by adding linkers 2. Cloning foreign DNA by adding adaptors 3. Homopolymeric tail adding by using Terminal transferase enzyme.
- 4. 1. Linker Linkersare the chemically synthesized double stranded DNA oligonucleotides containing on it one or more restriction sites for cleavage by restriction enzymes, e.g. Eco RI, Hind III, Bam HI, etc. Linkers are ligated to blunt end DNA by using DNA ligase. Both the vector and DNA are treated with restriction enzyme to develop sticky ends. The staggered cuts i.e. sticky ends are then ligated with T4 DNA ligase with very high efficiency to the termini of the vector and recombinant plasmid DNA molecules are produced.
- 5. Before cloning ofa particular sequence in PCR, a primer, associated with a linker is used. This type of primer is called as linker-primer. Now-a-days, two different linkers are used which has different RE sites with F/R primer. This strategy helps in directional cloning.
- 6. Limitations It maybe the case that the restriction enzyme used to generate the cohesive ends in the linker will also cut the foreign DNA at internal sites. Solution: CHOOSE ANOTHER RESTRICTION ENZYME But there may not be a suitable choice if the foreign DNA is large and has sites for several restriction enzymes. Methylation of internal restriction sites with the Appropriate modification methylase for example EcoRI methylase.
- 7. 2. Adaptors Theyare also short double stranded oligonucleotides that carry an internal RE sites and single stranded tails at one or both ends. This protruding sequences can be ligated to DNA fragments containing a complementary single stranded terminus. After ligation, the DNA can be cleaved with appropriate RE to create new protruding terminus.
- 8. Adaptors areavailable in two basic designs and a variety of specifications. 1. Some consists of a partial duplex formed between two oligonucleotides of different length; for example, the EcoR1-Not1 adaptor.
- 9. 2. Anotherclass of adaptor is supplied as an unphosphorylated single oligonucleotide whose sequence is partially self complementary. As an example- EcoR1-Pst1 adaptor.
- 10. Problems The stickyends of individual adaptors could base pair with themselves to form dimers and the new DNA molecule remains blunt-ended.
- 11. Solution For asolution to this problem, the 3'-OH terminus of the sticky end is kept unchanged, but the 5' terminus is modified from 5'-P to 5'-OH terminus. Therefore DNA ligase can't form a phosphodiester bond between 5'-OH and 3'-OH ends. Adaptors therefore can be ligated to a DNA molecule but not to themselves. Adaptor molecules alter their 5' terminus(From 5'-P to 5'-OH) by an enzymatic treatment of the enzyme Alkaline phosphatase to prevent self ligation. Afterwards, they can be treated with Polynucleotide kinases to restore it & ligate to vectors.
- 12. However, H-Bondscan form between the complimentary bases of 2 adaptor. The adaptor molecules can be heated at 90◦c for 3 minutes before use. 30X more adaptor is given (in terms of molar) in reaction than insert to ensure proper binding. This strategy eliminates the need of methylation of cDNA or to digest it with RE before insertion into vector.
- 13. 3. Homopolymeric tailing It is a technique by which sticky ends can be produced on a blunt-ended DNA molecule. In a homopolymer, all the subunits are same. A DNA strand made up entirely of deoxyguanosine is an example of homopolymer, and is referred to as polydeoxyguanosine or poly(dG). Tailing involves using the enzyme terminal deoxynucleotidyl transferase to add a series of nucleotides on to the 3'-OH termini of a double-stranded DNA molecule. The reaction when carried out in the presence of just one deoxynucleotide, then a homopolymer tail will be produced.
- 15. For ligationof two tailed molecules, the homopolymers must be complementary. Frequently poly(dc) tails are attached to the vector and poly(dg) to the DNA to be cloned.
- 16. Terminal transferase Terminaldeoxynucleotidyl transferase (TdT) is a template independent DNA polymerase. It is expressed in immature, pre-B, pre-T lymphoid cells, and acute lymphoblastic leukemia/lymphoma cells. In humans, terminal transferase is encoded by the DNTT gene.
- 17. Function TdT catalysesthe addition of nucleotides to the 3' terminus of a DNA molecule. Unlike most DNA polymerases, it does not require a template. The preferred substrate of this enzyme is a 3'- overhang but it can also add nucleotides to blunt or recessed 3' ends. Cobalt is a necessary cofactor, however the enzyme catalyzes reaction upon Mg and Mn administration in vitro.
- 18. Regulation TdT isexpressed mostly in the primary lymphoid organs, like the thymus and bone marrow. Regulation of its expression occurs via multiple pathways. These include protein-protein interactions, like those with TdIF1. TdIF1 is another protein that interacts with TdT to inhibit its function by masking the DNA binding region of the TdT polymerase
- 19. Structure Monomeric Mol.Wt.- 58000 Da Amino acids- 508 to529(depending upon source) A high degree of sequence homology(>80%)in TdT between different species
- 20. Reaction buffer Activityis strongly inhibited by the ammonium ion as well as chloride, iodide and phosphate anions. Potassium or sodium cacodylate(dimethyl arsenic acid) buffers are preferred- shown to be optimal for polypurine and polypyrimidine synthesis Certain drawbacks with cacodylate such as toxicity, contamination by metal etc
- 21. Divalent cation Polymerizationrequires presence of divalent cations. Order of efficiency for damp addition to oligonucleotide is as following Mg>Zn>Co>Mn For dGTP- Magnesium ion For pyrimidine- Cobalt ion
- 22. Heat Inactivation 75°Cfor 20 min 5' - 3' Exonuclease No 3' - 5' Exonuclease No Source An E. coli strain that carries the cloned Terminal Transferase gene from calf thymus.
- 23. Applications Addition ofhomopolymeric tails to plasmid DNA and to cDNA. Double- or single-stranded DNA 3´-termini labeling with radioactively labeled or non-radioactively labeled nucleotides. Addition of single nucleotides to the 3´ ends of DNA for in vitro mutagenesis. Production of synthetic homo- and heteropolymers. RACE (Rapid Amplification of cDNA Ends). TUNEL assay (in situ localization of apoptosis).