CG920 Genomics
Finishing Lesson 2
Genes Identification
Jan Hejátko
Functional Genomics and Proteomics of Plants,
CEITEC - Central European Institute of Technology
And
National Centre for Bimolecular Research,
Faculty of Science,
Masaryk University, Brno
hejatko@sci.muni.cz, www.ceitec.eu
2
2
 Identification of Genes Ab Initio
 Constructing gene-enriched libraries using
methylation filtration technology
 EST libraries
 Forward and reverse genetics
 Experimental Genes Identification
 Genomic colinearity and genomic homology
 Structure of genes and searching for them
 Forward and Reverse Genetics Approaches
 Differences between the approaches used
for identification of genes and their function
Outline
(finishing Lesson 02)
3
3
 Alteration of phenotype after mutagenesis
 Forward genetics
 Identification of sequence-specific mutant
and analysis of its phenotype
 Reverse genetics
 Analysis of expression of a particular gene
and its spatiotemporal specifity
 Principles of experimental identification of
genes using forward and revers genetics
Forward and Reverse
Genetics
4
4
 Alteration of phenotype after mutagenesis
 Forward genetics
 Principles of experimental identification of
genes using forward and reverse genetics
Forward Genetics
5
Identification of CKI1 via Activation
Mutagenesis
 CKI1 overexpression mimics cytokinin response
Kakimoto, Science, 1996
NO
hormones
tZ
ctrl1 ctrl2Plasmid Rescue Pro35S::CK1
5
6
Signal Transduction via MSP
NUCLEUS
CYTOKININ
PM
AHK sensor histidine kinases
• AHK2
• AHK3
• CRE1/AHK4/WOL
REGULATION OF TRANSCRIPTION
INTERACTION WITH EFFECTOR PROTEINS
HPt Proteins
• AHP1-6
Response Regulators
• ARR1-24
6
7
7
 Alteration of phenotype after mutagenesis
 Forward genetics
 Identification of insertional mutant and
analysis of its phenotype
 Reverse genetics
 Principles of experimental identification of
genes using forward and revers genetics
Reverse Genetics
8
Identification of insertional
cki1 mutant allele
8
9
CKI1 Regulates Female Gametophyte
Development
 CKI1 is necessary for proper megagametogenesis in Arabidopsis
CKI1/CKI1CKI1/cki1-i
Hejátko et al., Mol Genet Genomics (2003)
9
10
A. ♂ wt x ♀ CKI1/cki1-i
B. ♂ CKI1/cki1-i x ♀ wt
C. ♂ wt x ♀ CKI1/cki1-i
D. ♂ CKI1/cki1-i x ♀ wt
CKI1 specific primers (PCR positive control)
cki1-i specific primers
CKI1 and
Megagametogenesis
 cki1-i is not transmitted through the female gametophyte
10
11
FG 0FG 1FG 2FG 3FG 4
CKI1 and
Megagametogenesis
11
12
cki1-iCKI1
late FG5FG6FG7
24 HAE48 HAE
CKI1 and
Megagametogenesis
Hejátko et al., Mol Genet Genomics (2003)
12
13
13
 Alteration of phenotype after mutagenesis
 Forward genetics
 Identification of insertional mutant and
analysis of its phenotype
 Reverse genetics
 Analysis of expression of a particular gene
and its spatiotemporal specifity
 Principles of experimental identification of
genes using forward and reverse genetics
Forward and Reverse
Genetics
14
CKI1 is Expressed During
Megagametogenesis
FG0-FG1
FG3-FG4
FG4-FG5
FG7
14
15
12 HAP
(hours
after
pollination)
24 HAP48 HAP72 HAP
♀ wt x ♂ ProCKI1:GUS
Paternal CKI1 is Expressed in the
Arabidopsis Sporophyte Early after
Fertilization
24 HAP
Hejátko et al., Mol Genet Genomics (2003)
15
CG920 Genomics
Finishing Lesson 2
Genes Identification
Jan Hejátko
Functional Genomics and Proteomics of Plants,
CEITEC - Central European Institute of Technology
And
National Centre for Bimolecular Research,
Faculty of Science,
Masaryk University, Brno
hejatko@sci.muni.cz, www.ceitec.eu
17
17
 Literature sources for Chapter 03:
 Bioinformatics and Functional Genomics, 2009, Jonathan Pevsner, WilleyBlackwell,
Hobocken, New Jersey
http://www.bioinfbook.org/index.php
 Plant Functional Genomics, ed. Erich Grotewold, 2003, Humana Press,
Totowa, New Jersey
 Mello, C.C. and Conte Jr., D. (2004) Revealing the world of RNA interference.
Nature, 431, 338-342.
 Klinakis et al.. (2000) Genome-wide insertional mutagenesis in human cells by
the Drosophila mobile element Minos. EMBO Rep, 1, 416.
 Hansen et al.. (2003) A large-scale, gene-driven mutagenesis approach for the
functional analysis of the mouse genome. PNAS, 100, 9918.
Literature
18
„Classical genetics“ approach
1. IDENTIFICATION OF PHENOTYPE
2. GENE MAPPING
3. GENE IDENTIFICATION
- position cloning
„Reverse genetics“ approach
1. ISOLATION OF SEQUENCE-SPECIFIC
MUTANT
2. IDENTIFICATION OF
PHENOTYPE
3. PROOF OF CAUSAL RELATIONSHIP
BETWEEN INSERTION AND
PHENOTYPE
RANDOM MUTAGENESIS
„Classical“ genetics versus „reverse genetics“
approaches in functional genomics
EMS
T-DNA
(retro)transposons
18
19
19
 Analysis of Phenotype and Confirmation of Causality Between
Phenotype and Insertional Mutation
 Using unstable insertional mutagens and
isolation of revertant lines
 Co-segregation analysis
 Methods for Identification of Sequence-Specific Mutants
 Preparation of mutants collection
 Searching for sequence-specific mutants using
PCR
 Searching for sequence-specific mutants in
electronic databases
 Identification of independent insertional allele
Outline
 Knocking-out the gene using homologous
recombinantion
 Mutant complementation by the transgene
20
20
 Methods of identification of sequence-specific mutants
 Preparation of mutants collection
Outline
21
• Mobile elements
• Stable elements
 Autonomous transposons (En-1)
 Non-autonomous transposons (dSpm)
 T-DNA
 They contain a gene for transponase, enabling
excision and reintegration into the genome
 At both ends they contain short inverted repeat,
which are recognized by transponase
 mutant of En/Spm transposon, which has lost
autonomy because of mutation in a gene for
transponase
 It can be activated by crossing with a line carrying
the En/Spm transposon
 completely stable, however, its insertion can lead
to chromosome rearrangements (inversions,
deletions, transpositions)
Types of Insertional Mutagens
21
22
22
Searching for sequence-specific mutants
by PCR
Libraries of Insertional
Mutants (plants)
Preparation of transgenic plants
Creating the population of mutants
23
23
Libraries of Insertional
Mutants (animals)
Transfection into human cell cultures (HeLa) or
mouse embryonic stem (ES) cells
Generating a population of mutant cell lines and
frequence-analysis of insertions
in vitro analysis or preparation of library of
insertional mutants by reintroingression ES into
mouse embryos
Technologii inzerční mutageneze lze využít i u živočichů. Zda se využívají
např. transpozony odvozené z Drosophily (transpozon Minos, viz schéma
vlevo nahoře (Klinakis et al., 2000). V tomto případě bylo nutne provést
kotransfekci s tzv. helper plasmiem, kódujícím transponázu (neautonomní
transpozon). Neo kóduje rezistenci k neomycinu, šipky ukazují směr
transkripce řízený přislušnými promotory, pA je polyadenylační signál, ori
je počátek replikace viru SV40, S-P je promotor téhož viru. Pro identifikaci
inzercí „in frame“ se zasaženými geny lze využít transpozony, obsahující
fůzi akceptorových míst sestřihu s ORF reportérového genu, např. lacZneo
(bez AUG kodonu). Tento přístup umožňuje identifikovat inzerce do
aktivních genů prostřednictvím selekce inzerčních mutantů na rezistenci k
neomycinu, resp. vykazující β-galaktozidázovou aktivitu (Klinakis et al.,
2000).
24
24
 Methods of identification of sequence-specific mutants
 Preparation of mutants collection
 Searching for sequence-specific mutants using
PCR
 PCR-based three-dimensional screening
Outline
25
Isolation of sequence-specific
mutants
1. Library of En-1 insertional mutants
• 3000 independent lines
• 5 copies per line on average
• PCR-based three-dimensional screening
• autonomous En/Spm, without selection
25
26
Základy genomiky III, Přístupy reverzní a přímé genetiky
 PCR-based three-dimensional screening
 Isolation of genomic DNA from the individual plants of mutant population and
creating sets of DNA („triads“, rows and columns of triads and individual trays)
p o o l 1 ......p o o l 2 8
28x3-tray pools
90
R
28 x 7 row pools
28 x 5 column pools
35
B
35
B
28 x 3 1-tray pools
3.000 mutant lines of A. thaliana (5 copies of En-1/line)
Isolation of sequence-specific
mutants
27
Základy genomiky III, Přístupy reverzní a přímé genetiky
 PCR-based three-dimensional screening
 Isolation of genomic DNA from the individual plants of mutant
population and creating sets of DNA („triads“, rows and columns of
triads and individual trays)
 Identification of positive „triad“ with PCR, blotting of PCR products
and hybridization of the PCR products with gene-specific probe
Isolation of sequence-specific
mutants
Základy genomiky III, Přístupy reverzní a přímé genetiky
p o o l 1 ......p o o l 2 8
28x3-tray pools
Identification of the PCR product by
hybridization with a gene-specific probe
1. 3-tray pools screen
En-1
En-8130
En-205
Xho67
1262
CKI1 CKI1
En-1
En-8130
En-205Xho67
1262
CKI1 CKI1
(2x2x28=112 PCR reactions)
3.000 mutant lines of A. thaliana (5 copies of En-1/line)
Isolation of sequence-specific
mutants
28
29
Základy genomiky III, Přístupy reverzní a přímé genetiky
 PCR-based three-dimensional screening
 Isolation of genomic DNA from the individual plants of mutant
population and creating sets of DNA („triads“, rows and columns of
triads and individual trays)
 Identification of positive „triad“ with PCR, blotting of PCR products and
hybridization of the PCR products with gene-specific probe
 Identification of the positive line through identification of positive tray,
row and column
Isolation of sequence-specific
mutants
Základy genomiky III, Přístupy reverzní a přímé genetiky
p o o l 1 ......p o o l 2 8
28x3-tray pools
Identification of the PCR product by
hybridization with a gene-specific probe
1. 3-tray pools screen
2. Identification of line carrying
the insertion
En-1
En-8130
En-205
Xho67
1262
CKI1 CKI1
En-1
En-8130
En-205Xho67
1262
CKI1 CKI1
(2x2x28=112 PCR reactions)
(another 5+7+3=15 PCR reactions)
In total: 112+15=127 PCR reactions
9 0
R
7 row pools
5 column pools
3 5
B
3 5
B
3 x 1-tray pools
3.000 mutant lines of A. thaliana (5 copies of En-1/line)
Isolation of sequence-specific
mutants
30
31
31
 Methods of identification of sequence-specific mutants
 Preparation of mutants collection
 Searching for sequence-specific mutants using
PCR
 PCR-based three-dimensional screening
 Hybridization with iPCR products on filters
Outline
32
Insertion library of dSpm mutants
 48.000 lines
 non-autonomous transposon
 SINS (sequenced insertion sites) database
 PCR searching or hybridization with iPCR filters
 The Sainsbury Laboratory (SLAT-lines),
John Innes Centre, Norwich Research Park
 DNA and seeds in Nottingham Seed Stock Centre
http://nasc.nott.ac.uk
 1.2 insertion per line on average
Isolation of sequence-specific
mutants
32
33
T-DNA
 Hybridization with products of iPCR on filters
 Isolation of genomic DNA from the
individoul plants of mutant
population
 Restriction endonuclease cleavage
 Ligation, formation of circular DNA
 Inverse PCR (iPCR) using the TDNA
specific primers
 Preparation of nylon filters with PCR
products in the exact position using
a robot
 Hybridization with a gene-specific
probe
Isolation of sequence-specific
mutants
33
34
34
 Methods of identification of sequence-specific mutants
 Preparation of mutants collection
 Searching for sequence-specific mutants using
PCR
 Searching for sequence-specific mutants in
electronic databases
Outline
35
Preparation of librares from population of A. thaliana
mutated by T-DNA
GABI-Kat (MPIZ, Köln)
Isolation of sequence-specific
mutants
35
36
Searching in electronic libraries of insertional
mutants
36
37
Searching in electronic libraries of insertional mutants
| | | | | | | | | | | | | | | | | | | | | | | |
gtgactaaagtgtaattaataagtga………
1923
13
37
38
38
 Methods for Identification of Sequence-Specific Mutants
 Preparation of mutants collection
 Searching for sequence-specific mutants using
PCR
 Searching for sequence-specific mutants in
electronic databases
Outline
 Knocking-out the gene using homologous
recombinantion
39
Knocking-Out the Gene
39
40
40
 Analysis of Phenotype and Confirmation of Causality Between
Phenotype and Insertional Mutation
 Using unstable insertional mutagens and
isolation of revertant lines
 Co-segregation analysis
 Methods for Identification of Sequence-Specific Mutants
 Preparation of mutants collection
 Searching for sequence-specific mutants using
PCR
 Searching for sequence-specific mutants in
electronic databases
 Identification of independent insertional allele
Outline
 Knocking-out the gene using homologous
recombinantion
 Mutant complementation by the transgene
41
 Presence of multiple insertions in one line
Why is it necessary to analyze the causality
between the insertion and the observed
phenotype?
 Posibility of independent point mutation occurrence
 Insertions of T-DNA are often associated with chromosomal
aberrations (duplications, inversions, deletions)
41
42
 Co-segregation analysis
 Co-segregation of specific fragment, e.g. after insertion of T-DNA (or
exposure to EMS etc.) into the genome of the observed phenotype
cki1::En-1
+ ++ + + + + + ++
Causality between insertion
and phenotype
42
43
 However, excision of transposons is not always entirely accurate
– point mutations occurr – isolation of revertant lines with silent
mutation, or even isolation of the stable mutants
Use of autonomous transposons for the isolation
of new stable mutations and of revertant lines
 Transposons are often characterized by excision and reinsertion
into a nearby region – use for the isolation of new mutant alleles
43
44
Phenotype of silicles cki1::En-1/CKI1
cki1::En-1/CKI1 CKI1/CKI1
44
45
1. Isolation of revertant lines
• PCR-searching in 246 plants of segregating population
• from 90 cki1::En-1 positive plants, 9 plants had both mutant and
standard silicles
Offspring analysis
• confirmation of absention of insertion using PCR
• PCR amplification and cloning the part of the
genomic DNA at the insertion site
• sequencing
Confirmation of phenotype cki1::En-1/CKI1
45
46
Use of autonomous transposons for the
isolation of new stable mutations and
revertant lines
46
47
2. Isolation of a stable mutant line
• analysis of the phenotype of the segregating population
(CKI1/CKI1 CKI1/cki1::En-1)
• PCR analysis of plants with the mutant phenotype – identification of plants
without insertion
• PCR amplification and cloning the part of the genomic DNA at the
insertion site
• sequencing
Confirmation of phenotype cki1::En-1/CKI1
47
48
Use of autonomous transposons for the
isolation of new stable mutations and
revertant lines
48
49
Mutant Line
Complementation
Transposone/T‐DNA
GOI
GO I
49
50
Mutant Line
Complementation
Ranjan et al., 2014
50
51
51
 Phenotype analysis
 Confirmiong the causality between the observed phenotype
and the insertion mutation
 Use of unstable insertion mutagenes and
identification of revertant lines
 Co-segregation analysis
 How reverse genetics explores the gene and
its role?
 Targeted gene silencing
 Searching in the insertion mutant libraries
 Homologous recombination
 Identification of independent allele
Key Concepts
 Mutant line complementation by transgene
52
52
Discussion