1. Section J Analysis and application of cloning DNA

2. Section J -Analysis and application of cloning DNA J1 CHARACTERIZATION OF CLONES J1 CHARACTERIZATION OF CLONES J2 NUCLEIC AND SEQUENCING J2 NUCLEIC AND SEQUENCING J3 POLYMERASE CHAIN REACTION J3 POLYMERASE CHAIN REACTION J4 ORGANIZATION OF CLONED GENES J4 ORGANIZATION OF CLONED GENES J5 MUTAGENESIS OF CLONED GENE J5 MUTAGENESIS OF CLONED GENE J6 APPLICATIONS OF CLONING J6 APPLICATIONS OF CLONING

3. J1 CHARACTERIZATION OF CLONES Characterization Determining various properties of recombinant DNA molecule, such as size, restriction map, orientation of any gene present and nucleotide sequence, constitutes the process of clone characterization. It requires a purified preparation of the cloned DNA. Characterization Determining various properties of recombinant DNA molecule, such as size, restriction map, orientation of any gene present and nucleotide sequence, constitutes the process of clone characterization. It requires a purified preparation of the cloned DNA. Restriction mapping Digesting recombinant DNA molecules with restriction enzymes, alone and in combination, allows the construction of a diagram(restriction map) of the molecules indicating the cleavage position and fragment sizes. Restriction mapping Digesting recombinant DNA molecules with restriction enzymes, alone and in combination, allows the construction of a diagram(restriction map) of the molecules indicating the cleavage position and fragment sizes. Partial digestion The partial digestion of end- labeled DNA fragments with restriction enzymes, and sizing of fragments produced, also enables a restriction map to be constructed. Partial digestion The partial digestion of end- labeled DNA fragments with restriction enzymes, and sizing of fragments produced, also enables a restriction map to be constructed.

4. Labelilg nucleic acid DNA and RNA can be end- labeled using polynucleotide kinase or terminal transferase. Uniform labeling requires polymerases to synthesize a complete labeled strand. Labelilg nucleic acid DNA and RNA can be end- labeled using polynucleotide kinase or terminal transferase. Uniform labeling requires polymerases to synthesize a complete labeled strand. Southern and Northern blotting The nucleic acid in lanes of a gel is transferred to a memebrane, bound and then hybridized with a labeled nucleic acid probe. Washing removes nonhybridized probe, and the membrane is then treated to reveal the bands produced. Specific RNA species are detected on Northern blots, whereas the DNA bands on Southern blots could be genes in genomic DNA or parts of cloned genes. Southern and Northern blotting The nucleic acid in lanes of a gel is transferred to a memebrane, bound and then hybridized with a labeled nucleic acid probe. Washing removes nonhybridized probe, and the membrane is then treated to reveal the bands produced. Specific RNA species are detected on Northern blots, whereas the DNA bands on Southern blots could be genes in genomic DNA or parts of cloned genes.

5. Fig. 1. Restriction mapping (a) using single and double digests to completion; (b) by partial digestion of an end-labeled molecule. * is the labeled end

6. Fig. 2. 5′-End labeling of a nucleic acid molecule.

7. Fig. 3. Southern blotting.

8. J2 NUCLEIC AND SEQUENCING DNA sequencing The two main methods of DNA sequencing are Maxam and Gilbert chemical method in which end-labeled DNA is subjected to base-specific cleave reaction prior to gel separation, and Snger’s enzymic method. The latter uses dideoxynucleotides as chain terminators to produce a ladder of molecules generated by polymerase extension of primer. DNA sequencing The two main methods of DNA sequencing are Maxam and Gilbert chemical method in which end-labeled DNA is subjected to base-specific cleave reaction prior to gel separation, and Snger’s enzymic method. The latter uses dideoxynucleotides as chain terminators to produce a ladder of molecules generated by polymerase extension of primer. RNA sequencing A set of four Rnase that cleave 3’ to specific nucleotides are used to produce a ladder of fragments from end-labeled RNA. Polyacrylamide gel electrophoresis analysis allows the sequence to be read. RNA sequencing A set of four Rnase that cleave 3’ to specific nucleotides are used to produce a ladder of fragments from end-labeled RNA. Polyacrylamide gel electrophoresis analysis allows the sequence to be read.

9. Sequence databases Newly determined DNA,RNA and protein sequences are entered into databases(EMBL and GeneBank). These collections of all known sequences are available for analysis by computer. Sequence databases Newly determined DNA,RNA and protein sequences are entered into databases(EMBL and GeneBank). These collections of all known sequences are available for analysis by computer. Analysis of sequences Special computer software is used to search nucleic acid and protein sequences for the presence of or similarities Analysis of sequences Special computer software is used to search nucleic acid and protein sequences for the presence of or similarities Genome sequencing projects The entire genome sequences of several organisms have been determined and those of other organisms are in progress. Often a genetic map is first produced to aid the project. Genome sequencing projects The entire genome sequences of several organisms have been determined and those of other organisms are in progress. Often a genetic map is first produced to aid the project.

10. Fig. 1. DNA sequencing. (a) An example of a Maxam and Gilbert sequencing gel; (b) Sanger sequencing.

11. J3 POLYMERASE CHAIN REACTION The PCR cycle The reaction cycle comprises a 95 ℃ step to denature the duplex DNA, an annealing step of around 55 ℃ to allow the primers to bind and a 72 ℃ polymerization step. Mg2+ and dNTP are required in addition to template, primers, buffer and enzyme. The PCR cycle The reaction cycle comprises a 95 ℃ step to denature the duplex DNA, an annealing step of around 55 ℃ to allow the primers to bind and a 72 ℃ polymerization step. Mg2+ and dNTP are required in addition to template, primers, buffer and enzyme. Template Almost any source that contains one or more intact target DNA molecule can, in theory, be amplified by PCR, providing appropriate primers can be designed. Template Almost any source that contains one or more intact target DNA molecule can, in theory, be amplified by PCR, providing appropriate primers can be designed. Primers A pair of oligonucleotides of about 18-30 nt with similar G+C content will serve as PCR primers as long as they direct DNA synthesis towards one another. Primers with some degeneracy can also be used if the target DNA sequence is not completely known. Primers A pair of oligonucleotides of about 18-30 nt with similar G+C content will serve as PCR primers as long as they direct DNA synthesis towards one another. Primers with some degeneracy can also be used if the target DNA sequence is not completely known.

12. Enzymes Thermostable DNA polymerases(e.g. Taq polymerase) are used in PCR as they survive the hot denaturation step. Some are more error-prone than others. Enzymes Thermostable DNA polymerases(e.g. Taq polymerase) are used in PCR as they survive the hot denaturation step. Some are more error-prone than others. PCR optimization It may be necessary to vary the annealing temperature and/or the Mg2+ concentration to obtain faithful amplification. From complex mixtures, a second pair of nested primers can improve specificity. PCR optimization It may be necessary to vary the annealing temperature and/or the Mg2+ concentration to obtain faithful amplification. From complex mixtures, a second pair of nested primers can improve specificity. PCR variation Variation on basic PCR include quantitative PCR, degenerate oligonucleotide primer PCR(DOP-PCR), inverse PCR, multiplex PCR, rapid amplification of cDNA ends(RACE) and PCR mutagenesis. PCR variation Variation on basic PCR include quantitative PCR, degenerate oligonucleotide primer PCR(DOP-PCR), inverse PCR, multiplex PCR, rapid amplification of cDNA ends(RACE) and PCR mutagenesis.

13. Fig. 1. The first three cycles of a polymerase chain reaction. Only after cycle 3 are there any duplex molecules which are the exact length of the region to be amplified (molecules 2 and 7). After a few more cycles these become the major product.

14. J4 ORGANIZATION OF CLONED GENES Organization The polarity of oligo(dT)-primed cDNA clones is often apparent from the location of the poly(A), and the coding region can thus be deduced. The presence and polarity of any gene in a genomic clone is not obvious, but can be determined by mapping and probing experiments. Organization The polarity of oligo(dT)-primed cDNA clones is often apparent from the location of the poly(A), and the coding region can thus be deduced. The presence and polarity of any gene in a genomic clone is not obvious, but can be determined by mapping and probing experiments. Mapping cDNA on genomic DNA Southern blotting, using probes from part of a cDNA clone, can show which parts of a genomic clone have corresponding sequences. Mapping cDNA on genomic DNA Southern blotting, using probes from part of a cDNA clone, can show which parts of a genomic clone have corresponding sequences. S1 nuclease mapping The 5’- or 3’- of a transcript can be identified by hybridizing a longer, end-labeled antisense fragment to the RNA. The hybrid is treated with nuclease S1 to remove single-stranded regions, and remaining fragment’s size is measured on a gel. S1 nuclease mapping The 5’- or 3’- of a transcript can be identified by hybridizing a longer, end-labeled antisense fragment to the RNA. The hybrid is treated with nuclease S1 to remove single-stranded regions, and remaining fragment’s size is measured on a gel. Primer extension A primer is extended by a polymerase until the end of the template is reached and the polymerase dissociates. The length of the extended product indicates the 5’-end of the template. Primer extension A primer is extended by a polymerase until the end of the template is reached and the polymerase dissociates. The length of the extended product indicates the 5’-end of the template.

15. Gel retardation Mixing a protein extract with a labeled DNA fragment and running the mixture on a native gel will show the presence of DNA-protein complexes as retarded bands on the gel. Gel retardation Mixing a protein extract with a labeled DNA fragment and running the mixture on a native gel will show the presence of DNA-protein complexes as retarded bands on the gel. Dnase I footprinting The ‘footprint’ of a protein bound specifically to a DNA sequence can be visualized by treating the mixture of end-labeled DNA plus protein with small amounts of Dnase I prior to running the mixture on a gel. The footprint is a region with few bands in a ladder of cleave products. Dnase I footprinting The ‘footprint’ of a protein bound specifically to a DNA sequence can be visualized by treating the mixture of end-labeled DNA plus protein with small amounts of Dnase I prior to running the mixture on a gel. The footprint is a region with few bands in a ladder of cleave products. Reporter genes To verify the function of promoter, it can be joined to the coding region of an easily detected gene(reporter gene) and the protein product assayed under condition when the promoter should be active. Reporter genes To verify the function of promoter, it can be joined to the coding region of an easily detected gene(reporter gene) and the protein product assayed under condition when the promoter should be active.

16. Fig. 1. S1 nuclease mapping the 5′-end of an RNA. * = position of end label. 3’ DNA 3’ RNA 5’ DNA 3’ Add S1 nuclease * 5’ 3’ 5’ PAGE Analysis RNA 5’

17. Fig. 2. Primer extension. * = position of end label.

18. J5 MUTAGENESIS OF CLONED GENE Deletion mutagenesis Progressively deleting DNA from one end is very useful for defining the important of particular sequences. Unidirectional deletion can be created using exonuclease III which removes one ztrand in a 3’ to 5’ direction from a recessed 3’-end. A single strand –specific nuclease then creates blunt end molecules for ligation, and transformation generates then deleted clones. Deletion mutagenesis Progressively deleting DNA from one end is very useful for defining the important of particular sequences. Unidirectional deletion can be created using exonuclease III which removes one ztrand in a 3’ to 5’ direction from a recessed 3’-end. A single strand –specific nuclease then creates blunt end molecules for ligation, and transformation generates then deleted clones. Site-directed mutagenesis Changing one or a few nucleotides at a particular site usually involves annealing a mutagenic primer to a template followed by complementary strand synthesis by a DNA polymerase. Formerly. Single-stranded templates prepared using M13 were used, but polymerase chain reaction(PCR) techniques are now preferred. Site-directed mutagenesis Changing one or a few nucleotides at a particular site usually involves annealing a mutagenic primer to a template followed by complementary strand synthesis by a DNA polymerase. Formerly. Single-stranded templates prepared using M13 were used, but polymerase chain reaction(PCR) techniques are now preferred. PCR mutagenesis By making forward and reverse mutagenic primers and using other primers that anneal to common vector sequences, two PCR reactions are carried out to amplify 5’- and 3’-portions of the DNA to be mutated. The two PCR products are mixed and used for another PCR using the outer primers only. Part of this product is then suncloned to replace the region to be mutated in the starting molecule. PCR mutagenesis By making forward and reverse mutagenic primers and using other primers that anneal to common vector sequences, two PCR reactions are carried out to amplify 5’- and 3’-portions of the DNA to be mutated. The two PCR products are mixed and used for another PCR using the outer primers only. Part of this product is then suncloned to replace the region to be mutated in the starting molecule.

19. Fig. 1. Unidirectional deletion mutagenesis

20. Fig. 2. PCR mutagenesis. X is the mutated site in the PCR product

21. J6 APPLICATIONS OF CLONING Applications The various applications of gene cloning incluse recombinant protein production, genetically modified organism, DNA fingerprinting, diagnostic kits and gene therapy. Applications The various applications of gene cloning incluse recombinant protein production, genetically modified organism, DNA fingerprinting, diagnostic kits and gene therapy. Recombinant protein By inserting the gene for a rare protein into a plasmid and expressing it in bacteria, large amounts of recombinant protein can be produced. If post-translational modifications are critical, the gene may have to be expressed in aeukaryotic cell. Recombinant protein By inserting the gene for a rare protein into a plasmid and expressing it in bacteria, large amounts of recombinant protein can be produced. If post-translational modifications are critical, the gene may have to be expressed in aeukaryotic cell.

22. Genetically modified organisms Imtroducting a foreign gene into an organism which can propagate creats a genetically modified organism. Transgenic sheep have been created to produce foreign proteins in their milk. Genetically modified organisms Imtroducting a foreign gene into an organism which can propagate creats a genetically modified organism. Transgenic sheep have been created to produce foreign proteins in their milk. DNA fingerprinting Hybridizing Southern blots of genomic DNA with probes that recognize simple nucleotide repeats gives a pattern that is unique to an individual and can be used as a fingerprint. This has applications in forensic science, animal and plant breeding and evolutionary studies. DNA fingerprinting Hybridizing Southern blots of genomic DNA with probes that recognize simple nucleotide repeats gives a pattern that is unique to an individual and can be used as a fingerprint. This has applications in forensic science, animal and plant breeding and evolutionary studies. Medical diagnosis The sequence information derived from cloning medically important genes has allowed the design of many diagnistic test kits which can help predict and confirm a wide range of disorders. Medical diagnosis The sequence information derived from cloning medically important genes has allowed the design of many diagnistic test kits which can help predict and confirm a wide range of disorders. Gene therapy Attempts to correct a genetic disorder by delivering a gene to patient are described as gene therapy. Gene therapy Attempts to correct a genetic disorder by delivering a gene to patient are described as gene therapy.

23. Fig. 1. DNA fingerprinting showing how two VNTR alleles might be inherited (see text). (a) Parental VNTR alleles. (b) Agarose gel analysis of VNTR alleles.