DNA & Genetics in Biotechnology

1. DNA & Genetics in Biotechnology

2. What is a DNA? • A nucleic acid that carries the genetic information in the cell and is capable of self-replication and synthesis of RNA. • DNA consists of two long chains of nucleotides twisted into a double helix and joined by hydrogen bonds between the complementary bases adenine and thymine or cytosine and guanine. • The sequence of nucleotides determines individual hereditary characteristics.

3. What is a Nucleotide? • A single molecule of DNA comprised of 2 basic parts made from 3 distinct molecules. • Sugar/Phosphate Backbone • Nitrogenous Base

4. Sugar/Phosphate Backbone • Comprised of deoxyribose sugar and a simple phosphate molecule • Forms a strong bond that creates the backbone of a DNA strand • EXACTLY THE SAME IN ALL DNA

5. Nitrogenous Base • Bond with complimentary bases in other nucleotides to form the rungs of the DNA ladder (zip DNA together) • Only 4 types in all DNA-Adenine, Cytosine, Guanine, and Thymine • Adenine and Thymine bond only with each other • Cytosine and Guanine bond only with each other

6. DNA form • DNA nucleotides combine in cells to form long strands in the shape of a double helix (looks like a twisted ladder)

7. DNA Form • Nucleotides bond at two spots • Sugar/Phosphate molecules form the backbone (outside rails) • Nitrogenous bases bond in the middle by hydrogen bonds (steps or rungs) • Hydrogen bonds between nitrogenous bases are MOST EASILY BROKEN • The order of the nucleotides is the determining factor in the expression of genes in organisms.

8. Characteristics of DNA

9. DNA • Accounts for all genetic variation between different individuals and organisms by the use of different: • Sequences of nitrogenous bases • Lengths of DNA segments • Numbers of Chromosomes and amounts of DNA in an organism • The amount of DNA in an organism DOES NOT relate to the size or complexity of an organism.

10. DNA Replication • The process through which cells copy DNA for transmission to daughter cells during cell division. • The double helix structure allows DNA to easily unzip down the center between nitrogenous bases. • Free floating nucleotides attach to each of the separated DNA strands forming 2 new strands of DNA, each an exact copy of the original.

11. DNA Replication

12. Mutations • A mutation is an unexpected change in a DNA sequence, usually occurring during the replication/cell division. • Mutations are common in most organisms (especially simple organisms) though only a small percentage produce noticeable changes in organisms.

13. Genetic Hierarchy

14. Genetic Hierarchy • A group of nucleotides=a gene/allele=45-150 base pairs • A group of genes=1 strand of DNA • Several condensed strands of DNA=1 chromosome • 2 chromosomes=1 chromatid pair • All possible gene forms in a population=Genome

15. Gene Mapping • Mapping the genome of a species allows scientists to identify beneficial and harmful genes in a population, and is the first step in determining the location of specific genes on chromosomes. • Changes in the genome of a species occur slowly in response to environmental changes.

16. Transferring of DNA • Polygenic traits are controlled by more genes and therefore it is more difficult to improve polygenic traits. • DNA is passed to offspring during sexual reproduction through single chromosomes.

17. Human Genetics • Almost all humans have 46 chromosomes. • Individuals with Down Syndrome have one extra chromosome. • Humans generally differ from each other by approximately 3 million nitrogenous base pairs, or 0.1% of the total gene sequence.

18. Genetic Disorders

19. Genetic Disorders • Diseases or other problems resulting from errors in the transmission of genetic information, or the expression of certain negative gene sequences.

20. Genetic Disorders • Most genetic disorders are recessive, and thus cannot be predicted without genetic analysis • Recessive disorders are transmitted by carriers-parents with one dominant gene (normal) and one recessive gene (disorder) • Example-Tt

21. Genetic Disorders • Certain disorders are more common in certain populations • Example: The occurrence of sickle cell in African Americans.

22. Common Genetic Disorders • Inherited Disorders • Examples: Tay-Sachs, Sickle Cell Anemia, Hemophilia • Mutations • Cancer-uncontrolled division of abnormal cells • Treatment must destroy mutated cells

23. Genetic Mutations • Sudden unexpected changes in the genetic code of an organism which appear most often during the process of replication

24. Genetic Mutations • Often result from increased levels of stress on cells just prior to or during cell division • Stresses include-radiation, UV rays, environmental, etc.

25. Genetic Mutations • Almost all mutated cells die immediately, or never impact living organisms • Most mutations in humans are harmful such as cancer • A small fraction of noticeable mutations are beneficial, such as Chimeras which are used to give us variegated plants.

26. Genetic Mutations • Most mutations occur in developed plants and animals, affecting isolated groups of cells. • Mutations are most devastating when the occur in the early development of organisms. (STEM CELL STAGE)

27. Types of Mutations • Point mutation • A mutation that changes DNA at a single point, substituting one nucleotide pair. • Frameshift • Nucleotides are inserted or deleted, altering the entire DNA sequence after the mutation

28. DNA Extraction and Analysis

29. DNA Extraction • The process of isolating nucleic acids (DNA) from organic material. • DNA can be extracted from almost any intact cellular tissue (more cells make it easier) • Skin, blood, saliva, semen, mucus, muscle tissue, bone marrow, etc. • DNA cannot be extracted from hair, unless skin is attached at the bottom • Mitochondrial DNA can often be extracted long after nuclear DNA has degraded.

30. Simple DNA Extraction • For observation only, not feasible for analyzing DNA • Works well with fruit (Example: Strawberries)

31. Simple DNA Extraction • Step 1 • Physically break apart plant material, usually fruits • Step 2 • Use a detergent to break apart the cell membrane • Step 3 • Treat with ethyl alcohol to isolate DNA from remaining proteins and sugars • Step 4 • Spool using a glass rod to view a large clump of nucleic acids (DNA)

32. Advanced DNA Extraction • The organism to be tested is chosen, and a sample is taken from which DNA can be extracted. • Detergents are used in simple DNA extraction procedures to break down cell membranes, blending the contents of the cell.

33. Advanced DNA Extraction • The DNA sample is treated with enzymes to isolate nucleic acids, usually both DNA and RNA • Enzymes dissolve proteins, sugars, and other materials • Examples: protease, amylase, etc (enzymes end with the suffix –ase) • A second enzyme may be applied to cut DNA into gene segments for analysis called restriction enzyme

34. Restriction Digests and Enzymes • Restriction enzymes are used to cut extracted DNA into smaller gene sequences. • Make analysis easier during the process of gel electrophoresis. • Enables scientists to isolate specific genes with specific enzymes for use in genetic engineering.

35. Restriction Digests and Enzymes • Cuts the gene from the chromosome making a sort of gene soup after the removal of proteins • Leaves the ends of gene segments “sticky” with usually 3 exposed nucleotides on one side of the double helix, so that ends may be rejoined later.

36. Methods of DNA Analysis • There are several simple methods used for analyzing DNA • Paternity Testing • Gel Electrophoresis • Advanced Methods • Polymer Chain Reaction (PCR) • Amniocentesis

37. Paternity Testing • Simple method of DNA analysis that compares the DNA of an offspring, plant or animal, with a known mother and suspected father.

38. Paternity Testing Process • DNA sample taken usually from saliva or blood in animals and leaf or callus tissue in plants. (Hair does not contain DNA, but the hair follicle does.) • DNA isolated in sample through the use of protein “eating” enzymes.

39. Paternity Testing Process • Sample run on gels or through a gene sequencer to indicate the presence of certain genes. • Comparison of genes-anything present in the child MUST BE PRESENT IN EITHER THE MOTHER OR THE FATHER. 13 genes present in the child that are not in the mother, but present in the father make a 99% match.

40. Polymer Chain Reaction (PCR) • Method used in forensic science to amplify genetic material for identification or analysis. • Newer technique used only in advanced laboratories. • Only a few cells are needed with this technique.

41. Amniocentesis • Method used to analyze the DNA of a mammal (occasionally other animals) prior to birth. • Used widely in humans to predict the expression of lethal genes or genetic disorders in high-risk pregnancies. • Gaining favor in high expense animal breeding (Ex. Race horses)

42. Gel Electrophoresis • Method used to analyze extracted DNA through the distribution of genetic markers on an agar media. • Smaller genes travel further distances on the gel. Samples extracted through the same process can be easily compared on a single gel.

43. Gel Electrophoresis Process • An agar gel is placed into a mold to dry, then placed into an electrophoresis chamber. • DNA extraction is placed in small wells at one end of the agar gel. Each well represents a different sample or individual.

44. Gel Electrophoresis Process • Low voltage direct current is run through a buffer solution surrounding the agar gel distributing DNA fragments across the gel • Fragments separated by the size of the gene segment; smaller move faster than larger • Negative charged DNA fragments are repelled away from the negatively charged wells to the positive charged end.

45. Gel Electrophoresis Process • Buffer solution provides a means of transmission for electrical current, but also keeps DNA samples in place in wells in the gel. • Buffer is heavier than DNA

46. Gel Electrophoresis Process • Strength of the electrical current determines the speed at which DNA moves across the gel. • Ethidium Bromide or another Bromine based solution is applied at the end of the electrophoresis process to stain DNA for better viewing under certain bands of light.