Presentation is loading. Please wait.

Presentation is loading. Please wait.

Pdi11 (3) pdi1 (2) pdi2 (2) pdi4 (2) pdi6 (2) pdi7 (2) pdi9 (1) pdi3 (2) pdi5 (3) pdi8 (0) pdi10 (1) GeneAccession #'s Chr #T-DNA knockoutComments Pdi1At3g54960.

Similar presentations


Presentation on theme: "Pdi11 (3) pdi1 (2) pdi2 (2) pdi4 (2) pdi6 (2) pdi7 (2) pdi9 (1) pdi3 (2) pdi5 (3) pdi8 (0) pdi10 (1) GeneAccession #'s Chr #T-DNA knockoutComments Pdi1At3g54960."— Presentation transcript:

1 Pdi11 (3) pdi1 (2) pdi2 (2) pdi4 (2) pdi6 (2) pdi7 (2) pdi9 (1) pdi3 (2) pdi5 (3) pdi8 (0) pdi10 (1) GeneAccession #'s Chr #T-DNA knockoutComments Pdi1At3g54960 CAB41088 AL049655 Chr3Salk_148208 A Salk_150463 B Pdi2At5g60640 BAB09837 AB005246 Chr5Salk_017090 A Salk_115574 B Subjects Pdi3At1g52260 AAG51554 AC037424 Chr1Salk_019909 A Sail_302_G10 B Pdi4At3g16110 BAB02677 AB012247 Chr3Salk_048210 A Salk_114777 B Pdi5At1g21750 AAD41430 AC007727 Chr1Salk_010645 Salk_136642 Salk_015253 Pdi6At1g77510 Q9SRG3 AC010704 Chr1Salk_111424 A Salk_026561 B Pdi7At4g27080 T06038 T24A18.30 Chr4Salk_049017 A Salk_052314 B Pdi8At1g35620 AAK62431 AF386986 Chr1 Pdi9At2g32920 AAB91984 AC003033 Chr2Salk_063278 A Sail_595_D09 not availabl Pdi10At1g04980 AAF40463 AC004809 Chr1Sail_548_F05 Pdi11At2g47470 O22263 AY091388 Chr2Salk_046705 A Salk_135268 B Salk_148421 C

2 Genotype - Segregation T-DNA in the Arabidopsis Genome T-DNA – (transfer DNA) the transforming region of DNA in the Ti plasmid of Agrobacterium tumefaciens. It is the vehicle to deliver foreign genes to plant cells. T-DNA T-DNA Flanking Region LBRB KAN Pdi2 1:3

3 PCR Amplified Fragments Cloning and Sequencing How to Map Your T-DNA ? GSP T-DNA Flanking Region GSP LB RB T-DNA

4 Results and Discussion What is a wild type PCR band? What PCR band patterns indicate that a plant is a heterozygote or homozygote? M - + N pr2pr1 pr1 pr3 Normal Mutant Hm Ht Hm

5 PCR Mapping of T-DNAs in Pdi2 Gene R1 primer Wild Type Primer F1 Pdi2 A LB T-DNA 800bp WT ~ 620 bp T-DNA Predicted PCR products F1/LB F1/R1

6 Materials and Solutions: DNA samples and PCR solutions (?) Procedures: 1. Set up PCR (see Protocol I). 2. Check PCR products using agarose gels (see Protocol II). T-DNA Mapping Experiment

7 PCR Reaction Mix Reaction mix: 1 X6 X DNA template (50-100ng) 1.0 ul --- ddH2O18.1 ul108.6 10x Immolase buffer, 2.5 ul15.0 dNTP (25 mM), 0.2 ul 1.2 MgCl2(25mM) 2.0 ul12.0 Primer 1 (100ng/ul) 0.5 ul 3.0 Primer 2 (100ng/ul) 0.5 ul 3.0 Immolase DNA Polymerase 0.2 ul 1.2 (5 U/ul) Total volume 25 ul24 X 6 DNA samples: 1 2 3 4 5 WT, PDI2A-1, PDI2A-2, Positive (+) and Negative control (H2O)

8 PCR Conditions PCR conditions: 95  C for 7 min 35 cycles 95  C for 30 seconds Tm – 5  C, 30 seconds 72  C, extension 1 min/kb 72  C, 7 min 4  C, ~~ Immolase is inactive at room temperature; it needs heat activation at 95  C. Annealing temp : Tm- 5  C

9 T-DNA Mapping Pdi2 A: SALK_115574 F1/R2 (WT Band) WTA1 A2 WT 800bp F1/LB (T-DNA Band) WTA1 A 2WT 620 500 Annealing Temp 55  C MW


Download ppt "Pdi11 (3) pdi1 (2) pdi2 (2) pdi4 (2) pdi6 (2) pdi7 (2) pdi9 (1) pdi3 (2) pdi5 (3) pdi8 (0) pdi10 (1) GeneAccession #'s Chr #T-DNA knockoutComments Pdi1At3g54960."

Similar presentations


Ads by Google