The Flavr Savr Tomato November 25, 2014 Lu Tian. Flavr Savr Tomato The first FDA approved genetically modified food Licensed in 1994 Ripening causes production.

Slides:



Advertisements
Similar presentations
Dr VISHAL SHARMA Assoc. Proff Government Post Graduate College For Girls-11,Chandigarh GENETICALLY MODIFIED CROPS.
Advertisements

Post-Transcriptional Gene Silencing (PTGS) Also called RNA interference or RNAi Process results in down-regulation of a gene at the RNA level (i.e., after.
What are the Methods and Approaches Used to Identify and Study Arabidopsis Seed Knock- Out Mutations? Eric Newton Garen Polatoglu Rena Schweizer.
6.4 Applications of Biotechnology
RECOMBINANT DNA TECHNOLOGY PART 2 Topics Genomic libraries Id a specific clone or sequence within a library Transgenic plants Transgenic animals Timely.
Lecture 18, Chapter 11 Analysis of transgenic plants part I Mat Halter 3/27/12 Plant Genetics, Breeding and Biotechnology (PLSC 452/552), University of.
Microbiology: A Systems Approach, 2 nd ed. Chapter 10: Genetic Engineering- A Revolution in Molecular Biology.
CHAPTER 17 Recombinant DNA and Biotechnology
Post-Transcriptional Gene Silencing (PTGS) Also called RNA interference or RNAi Process results in down-regulation of a gene at the RNA level (i.e., after.
AP Biology: Chapter 14 DNA Technologies
Molecular Techniques.
Transfection. What is transfection? Broadly defined, transfection is the process of artificially introducing nucleic acids (DNA or RNA) into cells, utilizing.
1 Genetics Faculty of Agriculture Instructor: Dr. Jihad Abdallah Topic 13:Recombinant DNA Technology.
How do you identify and clone a gene of interest? Shotgun approach? Is there a better way?
Biotechnology Packet #12 Chapter #9. Introduction Since the 1970’s, humans have been attempted to manipulate and modify genes in a way that was somewhat.
© 2012 Pearson Education, Inc. Lecture by Edward J. Zalisko PowerPoint Lectures for Campbell Biology: Concepts & Connections, Seventh Edition Reece, Taylor,
Biotechnology Methods Producing Recombinant DNAProducing Recombinant DNA Locating Specific GenesLocating Specific Genes Studying DNA SequencesStudying.
Recombinant DNA and Other Topics in Biotechnology
DNA Technologies.
What must DNA do? 1.Replicate to be passed on to the next generation 2.Store information 3.Undergo mutations to provide genetic diversity.
Regulation of Gene Expression
Expression of the Genome The transcriptome. Decoding the Genetic Information  Information encoded in nucleotide sequences contained in discrete units.
RNA interference Definition: RNA interference (RNAi) is a mechanism where the presence of certain fragments.
19.1 Techniques of Molecular Genetics Have Revolutionized Biology
Agricultural uses of DNA technology
Chapter 11: Functional genomics
DNA TO PROTEIN genotype to phenotype Look deep into nature, and then you will understand everything better. Albert Einstein.
Section J Analysis and application of cloning DNA.
Chapter 10: Genetic Engineering- A Revolution in Molecular Biology.
DNA in the Cell Stored in Number of Chromosomes (24 in Human Genome) Tightly coiled threads of DNA and Associated Proteins: Chromatin 3 billion bp in Human.
DNA Technology Ch. 20. The Human Genome The human genome has over 3 billion base pairs 97% does not code for proteins Called “Junk DNA” or “Noncoding.
Trends in Biotechnology Constructing and Screening a DNA Library.
Ch 16. Posttranscriptional Regulation RNA interference (RNAi)
THE CONCEPT OF THE GENOME AS THE COMPLETE SET OF GENES IN A CELL AND OF THE PROTEOME AS THE FULL RANGE OF PROTEINS THAT A CELL IS ABLE TO PRODUCE. THE.
DNA Fingerprinting Maryam Ahmed Khan February 14, 2001.
What is the link?. E – Describe the process of genetic engineering C – Explain the advantages and disadvantages and interpret data A – Evaluate the technology.
DNA Technology. I. Vectors: Things used to transport genes into cells.
Gene Cloning & Creating DNA Libraries. Клонирование генов Что означает термин «клонирование»? Как происходит клонирование генов? Чем это отличается от.
Interfering RNA (干擾RNA)
Lecture 8 A toolbox for mechanistic biologists (continued)
The Flavr Savr Tomato.
Expression of the Genome
DNA Technology Packet #27.
Protein Synthesis.
Technical Aspects of Recombinant DNA and Gene Cloning
RECOMBINANT DNA TECHNOLOGY
RECOMBINANT DNA TECHNOLOGY
Regulation of Gene Expression
Recombinant DNA Technology
PBIO 427/527: Molecular Genetics Lecture 3 - Review
Rhiana Lau MMG C174 Professor Simpson
Consequences of T‐DNA insertion on SWP expression in swp mutant.
Evidence that processed small dsRNAs may mediate sequence-specific mRNA degradation during RNAi in Drosophila embryos  Dun Yang, Hong Lu, James W. Erickson 
In the name of god, the compassionate, the merciful Antisense RNA Dr.sharif Moghaddam By: Niloofar Beiranvand.
RNAi Related Mechanisms Affect Both Transcriptional and Posttranscriptional Transgene Silencing in Drosophila  Manika Pal-Bhadra, Utpal Bhadra, James.
Sherif Abou Elela, Haller Igel, Manuel Ares  Cell 
Protein Synthesis Lecture 5
DNA Technology Packet #50 Chapter #20.
Volume 101, Issue 5, Pages (May 2000)
mRNA Degradation and Translation Control
Noncoding RNA roles in Gene Expression
Volume 21, Issue 3, Pages (February 2006)
RNAi as Random Degradative PCR
Chapter 6.2 McGraw-Hill Ryerson Biology 12 (2011)
Producing DNA fragments eg for manufacturing insulin
Transcription Protein Synthesis.
The Human DiGeorge Syndrome Critical Region Gene 8 and Its D
A Counterdefensive Strategy of Plant Viruses
Presentation transcript:

The Flavr Savr Tomato November 25, 2014 Lu Tian

Flavr Savr Tomato The first FDA approved genetically modified food Licensed in 1994 Ripening causes production of an enzyme Polygalacturonase in a gradual increasing level, which is responsible for softening of the tomato and which becomes the cause of rottening Calgene introduced a gene in plant which synthesize a complementary mRNA to PG gene and inhibiting the synthesis of PG enzyme.

Antisense RNA Antisense RNA (asRNA) is a single-stranded RNA that is complementary to a messenger RNA (mRNA) strand transcribed within a cell.

Put PG gene sequences in the reverse orientation into the vector Transformation Isolate the nuclei used for in vitro transcription Isolate the RNA Hybridize RNA Measure PG activity Lycopene determination

Result

PG gene suppression is the result of RNAi

Promoterantisense cDNApoly A addition signal antisense oligonucleotide mRN A -antisense RNA complex dsRNA Binding of dsRNA-specific nuclease cleavage mRNA is cleaved! Nuclease-ssRNA complex Hybridizes to mRNA sense antisense

Southern blot Two linked T-DNAs Left T-DNA, lanes 1 and 2 (primers 1 and 4); Right T-DNA, lanes 3 and 4 (primers 2 and 3); full insert, lanes 5 and 6 (primers 1 and 2); unique junction region, lanes 7 and 8 (primers 5 and 6). Diagram of the sequenced 13,621-bp T-DNA insertion and flanking genomic regions. DNA probes (bars C and D) and primers (arrows 1–6) used for confirmation PCRs are indicated.

Northern blot

Result Flavr Savr locus contains two linked T-DNAs siRNAs from transgenes accumulate in Flavr Savr tomatoes.