TILLING (Targeting Induced Local Lesions in Genomes) is a method in molecular biology that allows directed identification of mutations in a specific gene.
Classification of Kerogen, Perspective on palynofacies in depositional envi...
Tilling [targeting induce local lesions in genome
1. TILLING
[TARGETING INDUCE LOCAL LESIONS IN GENOME]
Presented By: Prashansa Tayal ,
M.Sc Biotechnology [3rd Sem]
Chaudhary Charan Singh University,
Meerut, U.P. India.
Supervisor : Dr. Pradip Kumar
Department of Biotechnology
C.C.S. University, Meerut
2. TILLING
[Targeting Induce Local Lesions in
Genome]
For Gene Function
GENE MUTATION PHENOTYPIC CHANGE IN MUTATED ORGANISM GENE SEQUENCE
FORWARD GENETIC APPROACH [ PHENOTYPE GENE]
LARGE MUTATED POPULATION HAVE BEEN CREATED
SERVED FOR THE IDENTIFICATION OF GENE UNDERLYING THE CHANGE IN PHENOTYPE
SEQUENCE OF THE GENE CHANGE IN ALTERED PENOTYPE CAN BE ISOLATED BY MAP BASED CLONNING
TIME CONSUMING & LABOUR INTENSIVE
3. REVERSE GENETIC APPROACH [ GENE SEQUENCE PHENOTYPE]
ALTERATION OF GENE
STRUCTURAL ACTIVITY
ANALYSIS OF ASSOCIATED
CHANGE IN PLANT PHENOTYPE
Examples :-
• INSERTIONAL MUTAGENESIS WITH T-DNA
• TRANSPOSONS TAGGING
• GENE SILENCING USING RNA INTERFERENCE
• TILLING
Continued....
5. TILLING
• Alternative to insertional mutagenesis.
• Take advantage of classical mutagenesis, sequence availability & high
throughput for screening nucleotide polymorphism in a target sequence.
• Applied to any plant species, regardless of its genome size, ploidy level/
method of propagation.
• Much smaller populations are required to reach saturation mutagenesis
using TILLING as compared to T- DNA mutagenesis.
• Chemical mutagens provide a high frequency of point mutation,
distributed randomly in the genome.Create a spectrum of
mutationGain of function
alleles -Loss of functions alleles -
Hypomorphic alleles
-
-Missense changes
-Truncation
-Mutation in splice junction
sequences
6. • In contrast to insertional mutagenesis that generates mostly gene knockouts, using
TILLING, it is possible to induce a series of alleles in a targeted locus.
• Does not required transformation processes like RNAi technology & insertional
mutagenesis.
• Non-GMO technology.
• Initially developed as a discovery platform for functional genomics, but it soon
become a valuable tool in crop breeding as an alternative to the transgenic
approach.
TILLING
Continued….
7. GENERAL PROTOCOL
1. Creation of mutated population –
• Chemical mutagenesis [EMS mainly]
• Development of M1 and M2 generations
• DNA extraction from individual M2 plants
• Creation of DNA pools of 5-8 M2 plants
• Setting up an M3 seed bank.
2. Detection of mutation in a targeted sequence-
• PCR amplification of the targeted DNA segment using pooled DNA as a template.
• Detection of mutations [ cleavage by specific endonuclease]
• Identification of the individual M2 plant carrying the mutation.
• Sequencing the target gene segment to confirm the mutation & to determine the type of nucleotide
change.
3. Analysis of the mutant phenotype
9. Major components of TILLING
Procedures
1. Identifying Experimental material – Seeds mainly but other parts of plants can be used.
2. Determining the type & conc. of the mutagen - Mainly EMS creates G : C to A : T
transitions.
3. Creating mutagenized population – M2 population
4. DNA isolation and pooling – from each M2 plant.
5. Primer design and PCR amplification – design a set of primers which are specific to amplify
only the gene of interest.
- PCR amplification is followed by the heteroduplex formation step where the products of the
PCR are first denatured followed by slow annealing to facilitate the formation of heteroduplex
molecules.
6. Mutation detection – by S2 nuclease family [CEL 1, Mung bean nuclease]
7. Validation of mutation by sequencing & crossing
10. REFERENCES
• Kurowska, M., Daszkowska- Golec, A., Gruszka, D., Marzec, M., Szurman, M., Szarejko, I., & Maluszynski, M.
[2011] . TILLING a shortcut in functional genomics. Journal of applied genetics, 52(4),37.
• Tadele, Z., [2016]. Mutagenesis and TILLING to dissect gene function in plants. Current genomics,17(6), 499-
508.