1. Restriction Nucleases Cut at specific recognition sequence Fragments with same cohesive ends can be joined

2. Gel Electrophoresis DNA molecules separated by size DNA detected by ethidium bromide staining or by prior incorporation of radioisotope

3. Nucleic Acid Hybridization Complementary strands of DNA or RNA can renature Labeled single stranded DNA probe often used to detect specific DNA or RNA molecules in a sample

4. Generating Labeled Probe Random primers annealed to DNA fragment DNA polymerase incorporates labeled nucleotides

5. At higher temperatures only identical sequences hybridize At lower temperatures related sequences also hybridize Stringency Of Hybridization

6. Southern And Northern Blotting Complex mixture of DNA or RNA separated by electrophoresis Transferred to membrane and hybridized with labeled probe

7. DNA Cloning In Bacteria Insert DNA fragment into bacterial plasmid Propagate recombinant plasmid in bacteria

8. DNA Library Collection of cloned DNA fragments Usually are set of recombinant plasmids contained in bacteria Each bacterial colony contains one cloned fragment

9. Genomic DNA Library Contains entire genome of a particular individual DNA fragments generated by restriction nuclease

10. cDNA Library Contains only DNA sequences that are transcribed into mRNA cDNA generated from mRNA using reverse transcriptase Different library generated from every cell type

11. cDNA Vs. Genomic DNA Clones cDNA clones useful for deducing protein sequences Genomic clones useful for obtaining noncoding and total genome sequences Library screening to select clones of interest

12. Polymerase Chain Reaction Oligonucleotides complementary to opposite ends of sequence to be amplified serve as primers for DNA polymerization

13. DNA Amplification Using PCR Repeated cycles of denaturation, annealing, and DNA synthesis

14. DNA Cloning By PCR Genomic DNA clones: PCR amplification of segment between primers cDNA clones: Reverse transcription of mRNA followed by PCR

15. PCR In Forensic Analysis PCR using primers that flank a VNTR

16. Genetic fingerprint by analyzing several VNTRs

17. Genetic Test Using Allele- Specific Oligonucleotides  A probe  S probe P1P2C1C2C3C4  A allele  S allele -CCTGAGGAG- -CCTGTGGAG-  -globin gene PCR Primer PCR, gel electrophoresis, hybridization

18. Hybridization Using Microarrays Slide with array of DNA probes Genomic DNA or mRNA sample (mRNA→cDNA) DNA sample labeled with fluorescent dye and hybridized Fluorescence measured

19. Gene Expression Patterns In Cancer Cells Characteristic expression patterns in different types of cancer cells

20. Dideoxy DNA Sequencing Each reaction includes one of four ddNTPs ddNTPs block chain growth

21. Fragment sizes indicate positions of each nucleotide

22. Automated Sequencing Of DNA One reaction with four fluorescent labeled ddNTPs

23. Sequencing Genomes Shotgun method: Generate several genomic libraries with different size inserts Perform sequencing reactions on millions of genomic clones Establish order on chromosome based on sequence overlaps

24. Highly Parallel Sequencing Clonal amplification of DNA fragments on solid surface High density array of clonal DNA clusters Sample preparation

25. nucleotide addition imaging by fluorescence or chemiluminescence to detect nucleotide incorporation at each DNA cluster Sequencing by synthesis: repeated cycles

26. Finding DNA Sequences That Encode Proteins –Search open reading frames, splice sites, regulatory elements –Compare to cDNA sequence database –Compare to other species From genome: From cDNA: usually one open reading frame

27. Antibodies to Detect Proteins Antibodies are produced by immune system Billions of forms bind to different antigens Primary antibody recognizes specific antigen; secondary antibody used for detection

28. Western Blotting Complex mixture of proteins separated by polyacrylamide- gel electrophoresis and transferred to membrane Antibody used to detect specific protein

29. Producing Proteins Insert gene into expression vector adjacent to strong promoter Introduce into cells Purify overexpressed protein

30. Locate disease genes using physical markers Physical markers have known locations and are polymorphic Examine relationship between physical markers and disease Co-inheritance indicates nearby location Linkage Analysis

31. Inheritance Patterns Simple mendelian Autosomal dominant Autosomal recessive X-linked recessive Complex genetic diseases: many common diseases, risk dependent upon multiple genes and environment

32. Genome-Wide Association Studies Compare frequency of SNP alleles in healthy and disease populations SNP allele with higher frequency in disease population indicates genetic risk factor

33. Identification of Genetic Risk Factors age-related macular degeneration asthma bipolar disorder coronary artery disease Crohn’s disease diabetes-type 1 diabetes-type 2 obesity prostate cancer rheumatoid arthritis

34. Gene Targeting In Mice

35. RNA Interference Turn off gene expression Introduce dsRNA to degrade specific mRNA

36. Genome Engineering Using CRISPR-Cas9 Targeted genome editing Introduce Cas9 (nuclease) and gRNA for genomic target DS break, repaired by NHEJ, usually inactivates gene Introduction of repair template allows precise editing

37. Generation of Mutant Organisms using CRISPR/Cas9