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Bringing DNA science to more places

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Presentation on theme: "Bringing DNA science to more places"— Presentation transcript:

0 From Genotype to Phenotype
PTC Taster Lab October 2015

1 Bringing DNA science to more places

2 PCR is at the heart of DNA analysis
Molecular diagnostics Text Consumer genomics Text Text Personalized medicine PCR Food and agriculture Text Text Human evolution Text Forensics

3 PTC Taster Lab Links genotype and phenotype
Molecular physiology and genetics of taste Teach essential molecular biology techniques Aligns with standards

4 The PTC lab packs a punch
Students use essential molecular biology techniques to determine genotype DNA extraction PCR Restriction digest Gel electrophoresis First class Second class Complete the miniPCR PTC Taster lab in two 45-min class periods, or in a single 3-h instruction block

5 Experimental Outline What you’ll need: miniPCR
Bluegel electrophoresis system Pipettes, tips and tubes miniPCR PTC lab reagents kit Electrophoresis reagents Please refer to the Teacher’s Guide for details

6 Sense of Taste Cheek cells divide very rapidly.
66 Cheek cells divide very rapidly. Transition: The various membranes in the cell provide a barrier between the cell’s environment and the cytoplasm. In order to retrieve the DNA the membranes have to be broken apart. Sense of Taste

7 ORGAN Tongue CELL Gustatory TISSUE Papillae papillae taste buds
gustatory cells nerves

8 PROTEIN: G-protein coupled receptor bitter taste receptors
----- Meeting Notes (10/20/15 14:20) ----- G Protein receptors make up 50% of drug targets for medications

9 Each human carries a distinctive set of taste receptors which gives them a unique perception of how foods taste Taste is a phenotype Small differences in genotype can change taste perception

10 Ability to taste PTC is Mendelian The TAS2R38 gene
Position (bp) Taster DNA aa non-Taster DNA aa 145 C Pro (P) G Ala (A) 785 T Val (V) 886 A Ile (I) Single nucleotide polymorphisms (SNPs) Genotype Phenotype Homozygous Taster PAV/PAV Intensely bitter Heterozygous Taster PAV/AVI Somewhat bitter Non-taster AVI/AVI Can’t taste

11 Ability to taste PTC is Mendelian The TAS2R38 gene
Single nucleotide polymorphisms (SNPs) SNP1 (145) SNP2 (785) SNP3 (886) taster DNA C G aa P (Pro) A (Ala) V (Val) non-taster T A I (Ile) Genotype Phenotype Homozygous Taster PAV/PAV Intensely bitter Heterozygous Taster PAV/AVI Somewhat bitter Non-taster AVI/AVI Can’t taste

12 Now, let’s try the TASTE test (PTC paper)

13 Central Dogma…Genotype to Phenotype
Differences in DNA = genotype ‘taster’ allele ‘non-taster’ allele DNA TRANSCRIPTION ‘taster’ RNA ‘non-taster’ RNA AAAAAA RNA TRANSLATION Try slide with three columns, one for each genotype ----- Meeting Notes (10/21/15 17:18) ----- i need your help here zeke ‘taster’ protein ‘non-taster’ protein Protein SIGNAL TRANSDUCTION Differences in taste = phenotype

14 Extract DNA From Cheek Cells
Cheek cells divide very rapidly. Transition: The various membranes in the cell provide a barrier between the cell’s environment and the cytoplasm. In order to retrieve the DNA the membranes have to be broken apart. Extract DNA From Cheek Cells Rub gently 5-6 times with a flat-head toothpick

15 Use miniPCR as a Heat Block
DNA extraction PCR Restriction digest Gel electrophoresis Incubate 10 minutes at 95°C in miniPCR

16 Using Windows app: 95C, 10 minutes

17 Next step: PCR Amplify TAS2R38 gene around SNP785
DNA extraction PCR Restriction digest Gel electrophoresis Exponential amplification of the TAS2R38 gene

18 Polymerase Chain Reaction (PCR)
Complex DNA sample Region of interest Amplified DNA (Billions of copies) PCR is used to replicate DNA outside the body

19 PCR: exponential amplification

20 Setting up a PCR experiment…
Template DNA to be amplified Pair of DNA primers DNA polymerase dNTPs Buffer to maintain pH and provide Mg2+ Thermal cycler dCTP dCTP dGTP Taq dATP dTTP primer A T G C dTTP dGTP dTTP dATP dCTP dGTP dATP

21 How does PCR work? Repeat x 30 cycles Denaturation Annealing Extension
denatured DNA DNA + primers DNA + copy Single molecule 94° C ~1B copies 50-60° C 72° C Denaturation Annealing Extension Repeat x 30 cycles

22 Programming the miniPCR…
1 2 3 4 5 6 ----- Meeting Notes (10/21/15 16:56) ----- have easel paper in TWO places around the room with BIG BOLD lettering to match the program requirements...

23 Possible stopping point after PCR complete
DNA extraction PCR Store PCR product up to 48h at room temperature, or long term in fridge or freezer

24 Next step: restriction digest
Interrogate SNP785 taster vs. non-taster variants DNA extraction PCR Restriction digest Gel electrophoresis Second class Beginning of second class period

25 The restriction enzyme Fnu4H1 cuts @ SNP785 Only in the taster allele TAS2R38 variants
TAS2R38 Gene taster variant non-taster variant 5’…GCNGC…3’ 3’…CGNCG…5’ …TGTGCTGCCTT… …ACACGACGGAA… …TGTGTTGCCTT… …ACACAACGGAA… ----- Meeting Notes (10/21/15 16:55) ----- Zeke...can you work your magic with the taster SNP? I can't seem to get the cut right!!! RE …TGTGC TGCCTT… …ACACGA CGGAA… …TGTGTTGCCTT… …ACACAACGGAA…

26 blueGel reduces equipment needs
DNA extraction PCR Restriction digest Gel electrophoresis No need for… big bulky gel chambers, power supplies, illuminators, or UV

27 Homozygous dominant (taster)
Expected results… Homozygous dominant (taster) Homozygous recessive (non-taster) Heterozygous (taster) 300bp 200bp 100bp

28 We hope you’ve enjoyed the lab
We hope you’ve enjoyed the lab! Now you can connect phenotype to genotype in two 45- minutes classes DNA extraction PCR Restriction digest Electrophoresis

29

30 Contact miniPCR with feedback or questions
@miniPCR Facebook.com/miniPCR

31 miniPCR™ Powerful Portable Engaging Affordable

32 21st century DNA gel electrophoresis


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