1. D E P A R T M E N T O F P L A N T B R E E D I N G A N D G E N E T I C S
J A W A H A R L A L N E H R U K R I S H I V I S H W A V I D Y A L A Y A
2 2 / 0 7 / 2 0 2 0
J A B A L P U R
2. A SPECIFIC SEQUENCE OF NUCLEOTIDE IN DNA OR
RNA THAT IS LOCATED ON CHROMOSOME AND IS A
FUNCTIONAL UNIT OF INHERITANCE CONTROLLING
THE EXPRESSION OF TRAIT
HAPLOID SET OF CHROMOSOME INCLUDE BOTH
CODING AND NON CODING DNA AS WELL AS
MITOCHONDRIAL DNA AND CHLOROPLAST
STUDY OF THE WHOLE GENOME OF ORGANISM AND
INCORPORATED ELEMENTS FROM GENETICS
3. 1871
FRIEDRICH MIESCHER PUBLISHES HIS
PAPER IDENTIFYING THE PRESENCE
OF ‘NUCLEIN’AND ASSOCIATED
PROTEINS, IN THE CELL NUCLEUS.
1904
WALTER SUTTON AND THEODOR
BOVERI PROPOSE THE
CHROMOSOME THEORY OF
HEREDITY AFTER
1910
ALBRECHT KOSSEL IS AWARDED
THE FIRST NOBEL PRIZE IN
PHYSIOLOGY OR MEDICINE FOR
DISCOVERY OF THE FIVE
NUCLEOTIDE BASES.
1950
ERWIN CHARGAFF FINDS THAT
CONCENTRATIONS OF THYMINE AND
ADENINE, AND CYTOSINE AND GUANINE,
ARE ALWAYS FOUND IN EQUAL
AMOUNTS IN SAMPLES OF DNA.
1952
THE HERSHEY-CHASE
EXPERIMENTS ARE CARRIED OUT
TO DEMONSTRATE THAT DNA,
RATHER THAN PROTEIN, CARRIES
OUR GENETIC INFORMATION.
TIMELINE: HISTORY OF GENOMICS
4. 1953
JAMES WATSON AND FRANCIS
CRICK, WITH CONTRIBUTIONS FROM
ROSALIND FRANKLIN
AND MAURICE WILKINS, DISCOVER
THE DOUBLE HELIX STRUCTURE OF
DNA.
1961
MARSHALL NIRENBERG, HAR GOBIND KHORANA
AND COLLEAGUES, CRACK THE ‘CODE FOR
LIFE’. THEY IDENTIFY HOW THE LETTERS IN DNA
ARE READ IN BLOCKS OF THREE CALLED A
“CODON”. EACH CODON SPECIFIES AN AMINO
ACID WHICH IS ADDED TO THE PROTEIN DURING
SYNTHESIS.
1968
MARSHALL NIRENBERG, HAR GOBIND
KHORANA AND ROBERT HOLLEY SHARE THE
1968 NOBEL PRIZE FOR PHYSIOLOGY AND
MEDICINE FORMER FOR CRACKING THE
GENETIC CODE, AND HOLLEY’S WORK
SEQUENCING THE FIRST tRNA MOLECULE.
1977
FREDERICK SANGER DEVELOPS A DNA
SEQUENCING TECHNIQUE WHICH HE
AND HIS TEAM USE TO SEQUENCE THE
FIRST FULL GENOME – THAT OF A VIRUS
CALLED PHIX174.
1980
FRED SANGER SHARES THE NOBEL
PRIZE FOR CHEMISTRY WITH WALLY
GILBERT AND PAUL BERG, FOR
PIONEERING DNA
SEQUENCING METHODS.
TIMELINE: HISTORY OF GENOMICS
5. 1983
THE POLYMERASE CHAIN
REACTION (PCR) IS DEVELOPED – A
TECHNIQUE USED FOR AMPLIFYING
DNA – BY DR KARY MULLIS AT THE
CETUS CORPORATION IN
CALIFORNIA, USA.
1985
ALEC JEFFREYS DEVELOPS A METHOD FOR
DNA PROFILING. A DNA PROFILE IS
PRODUCED BY COUNTING THE NUMBER OF
SHORT REPEATING SEQUENCES OF DNA
SEQUENCE FOUND AT TEN SPECIFIC
REGIONS OF THE GENOME.
1990
HUMAN GENOME PROJECT IS
LAUNCHED. THE PROJECT AIMS TO
SEQUENCE ALL 3
BILLION LETTERS OF A HUMAN GENOME
IN 15 YEARS.
1995
THE FIRST BACTERIUM GENOME
SEQUENCE IS COMPLETED
(HAEMOPHILUS INFLUENZA).
1996
AN INTERNATIONAL TEAM
COMPLETE SEQUENCING THE
GENOME OF YEAST,
SACCHAROMYCES CEREVISIAE.
TIMELINE: HISTORY OF GENOMICS
6. 1998
JOHN SULSTON AND BOB
WATERSTON PUBLISH THE GENOME
OF THE NEMATODE WORM, C.
ELEGANS.
1999
CHROMOSOME 22 IS THE FIRST HUMAN
CHROMOSOME TO BE SEQUENCED AS
PART OF THE HUMAN GENOME PROJECT.
ENSEMBL GENOME BROWSER
LAUNCHED.
2001
FIRST DRAFT OF THE HUMAN GENOME
SEQUENCE RELEASED.
2002
THE MOUSE IS THE FIRST MAMMAL TO HAVE ITS
FULL GENOME SEQUENCE COMPLETED.
THE MOUSE GENOME IS 14 PER CENT SMALLER
THAN THE HUMAN GENOME, BUT OVER 95 PER
CENT OF THE MOUSE GENOME IS SIMILAR TO
OURS.
2002
THE INTERNATIONAL HAPMAP PROJECT IS
LAUNCHED, WHICH AIMS TO PRODUCE A
‘CATALOGUE’ OF COMMON HUMAN
GENETIC VARIATIONS AND WHERE THEY
ARE FOUND IN THE GENOME.
TIMELINE: HISTORY OF GENOMICS
7. 2003
HUMAN GENOME PROJECT IS
COMPLETED AND CONFIRMS HUMANS
HAVE APPROXIMATELY 20,000–25,000
GENES. THE HUMAN GENOME IS
SEQUENCED TO 99.99 PER CENT
ACCURACY.
2003
THE ENCODE PROJECT IS LAUNCHED BY
THE NATIONAL HUMAN GENOME
RESEARCH INSTITUTE AND AIMS TO
IDENTIFY AND
CHARACTERISE ALL THE GENES IN THE
HUMAN GENOME.
2008
NEXT-GENERATION SEQUENCING
PLATFORMS RESULT IN DRAMATIC DROP
IN SEQUENCING COSTS.
2013
THE U.S. SUPREME COURT RULES
THAT NATURALLY OCCURRING DNA
CANNOT BE PATENTED.
2014
CRISPR/CAS9 GENOME
EDITING IN PLANT
TIMELINE: HISTORY OF GENOMICS
9. about
Types
Branches
Application
Tools
Crop
Improvement
GENOMICS
T. Roderick, 1986
•The study of structure and function of whole of the hereditary
material contains in a genome of a living organism.
•Genomics involves the study of all genes at the DNA mRNA
and proteome level as well as cellular or tissue level.
•The ultimate objective is to obtain DNA sequences of complete
genome and to understand the function of each of
those genes.
11. about
Types
Branches
Application
Tools
Crop
Improvement
RNA SEQUENCING
TRANSCRIPTION REGULATION
G E N O M I C S
•DNA SEQUENCING
•GENETIC MAPPING
•GENETIC PROFILING
•DNA RECOMBINANT
TECHNOLOGY
TRANSCRIPTOMICS
.
PROTEOMICS
.
PHENOMICS
.
INOMICS
METABOLOMICS
.
PROTEIN IDENTIFICATION ,QUANTIFICATION
POST TRANSLATION MODIFICATION
METABOLITE PROFILES, INTERMEDIATE,
HORMONES AND SIGNALING MOLECULE
ELEMENT PROFILING, BIOCHEMICAL
REGULATION, ELEMENT INTERACTION
HORMONES AND SIGNALING MOLECULE
EVALUATION OF TRAITS
LINK BETWEEN GENETIC, EPIGENETIC AND
ENVIRONMENTAL FACTORS
13. about
Types
Branches
Application
Tools
Crop
Improvement
MICROARRAY
A microscopic DNA chip attached
to solid surface used to measure
the expression of 1000 sub-gene
simultaneously.
MASS SPECTROMETRY
Analysis of oligonucleotides
PCR
In-vitro Amplification of specific
DNA or RNA sequence
SEQUENCER
Sequence and analyze whole
genomes.
ELECTROPHORESIS SYSTEM
Isolate DNA templates
ONLINE SOFTWARE'S
Data storage and analysis
Ex-
BLAST
FASTA
MUMmer
DIALIGN
14. about
history
timeline
teamsTools
Crop
Improvement
HERBICIDE TOLERANCE
Glyphosate tolerance in
tomato, tobacco, soybean,
cotton etc.
PATHOGEN RESISTANCE PEST RESISTANCE
CHILLING RESISTANCEFERTILITY RESTORATIONQUALITY IMPROVEMENT
Coat protein gene from TMV
has been transferred to
tobacco.
Insecticidal BT gene has been
isolated from Bacillus
thuringiensis bacteria and
transferred to plant like cotton,
tomato, tobacco
Delayed ripening through
decreasing ethylene
production
Hybrid seed production of
Brassica napus
Gene Glycerol-1-phosphateacyl-
tranceferace enzyme from
arabidopsis into tobacco
23. 0 1
0 2
0 3
•HIGH TECHNICAL SKILL
•EXPANSIVE AND LABORIOUS TECHNIQUE
•LIMITED GENE AVAILABILITY
•LACK OF PROPER MARKERS
•SOME ANNOTATED OPEN READING FRAMES ARE
SUBSEQUENTLY FOUND NOT TO ENCODED PROTEIN
LIMITATIONS
•POST TRANSLATIONAL MODIFICATIONS THAT INFLUENCE
THE PROTEIN FUNCTION AND CELLULAR LOCALIZATION
OFTEN CANNOT BE PREDICTED FROM THE SEQUENCE
24. 01
02
TISSUE CULTURE FREE
TRANSFORMATION
IMPROVED VARIETIES FOR WORLD
AGRICULTURE
TISSUE CULTURE FREE
TRANSFORMATION03
04
F U T U R E
A S P E C T
NON GMO GENOMICS BREEDING
3-D MODELLING OF PLANT USING
GENOTYPES