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Cry3Aa inheritance in filial generations of Solanum tuberosum

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Title: Cry3Aa inheritance in filial generations of Solanum tuberosum


1
Cry3Aa inheritance in filial generations of
Solanum tuberosum
  • Jeff Skoneczka and Richard Veilleux
  • Department of Horticulture
  • Virginia Polytechnic Institute State University
  • Blacksburg, Virginia

2
Purpose
  • Incorporation of sexual hybrids into production
    systems
  • Easy start-up
  • Economical
  • Difficulties
  • Heterozygosity and polyploidy
  • Transgenics

3
Objectives
  • In a prior study (Johnson 2001), Cry3Aa
    expression in sexual hybrids of potato differed
    depending upon whether the transgene was
    maternally or paternally inherited (using
    independently transformed parents)
  • We wanted to verify a difference in transmission
    through the male and female gametophyte based on
    reciprocal hybrids using the same transgenic
    parent

4
Construct
5
Establishment
  • After confirmation of transformation in vitro,
    transfer plants to greenhouse for breeding.
  • Established plants were used to create reciprocal
    hybrids

6
  • Parental Lines
  • Atlantic - tetraploid commercial cultivar
  • APM-2 heterozygous diploid line with high
    frequency of 2n pollen
  • Single insert transgenic lines of the above,
    denoted by TC1

Hybrid Families
Atlantic TC1 X Katahdin
Katahdin X Atlantic TC1
Atlantic TC1 X Atlantic
Atlantic X Atlantic TC1
Atlantic TC1 self
Atlantic TC1 X wt APM-2
Atlantic TC1 X APM-2 TC1
  • Katahdin tetraploid commercial cultivar

7
Material and methods
  • The seedlings were planted in sets of 16 plants
    per family in three different plantings, two in
    the greenhouse and one in the field
  • Each hybrid plant was screened for transgene
    expression via DAS-ELISA

8
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9
Methods DAS-ELISA
  • Bt endotoxin ELISA kit from Agdia, Inc.
  • Leaf samples ( 200 mg) taken at seedling stage
  • Presence of protein in sample expressed
    colorimetrically
  • OD is read with plate reader at 405 nm and
    converted to Absorption Ratio (AR)
  • AR (OD of test plant)/(OD of negative control)
  • Examine segregation ratios to verify gene copy
    number as well as transgene expression levels

10
96-well ELISA plate
11
Mean absorption ratios (AR) of Cry3Aa expressing
plants in four hybrid families of tetraploid
potato first greenhouse trials of 16 plants per
family
12
Segregation ratios of Cry3Aa expressing and
non-expressing plants in four hybrid families of
tetraploid potato first greenhouse trials of 16
plants per family
  • A segregation ratio significantly different from
    11 was observed in one family

13
Mean absorption ratios (AR) of Cry3Aa expressing
plants in five hybrid families of tetraploid
potato second greenhouse trials of 16 plants
per family
Again, expression levels not significant, however
14
Segregation ratios of Cry3Aa expressing and
non-expressing plants in five hybrid families of
tetraploid potato second greenhouse trials of
16 plants per family
High expected ratio due to APM-2 having high
frequency of 2n pollen
15
Segregation ratios of Cry3Aa expressing and
non-expressing plants in two hybrid families of
tetraploid potato field trial
Results slightly significant at 95 confidence
level
16
Pooled Data
17
Conclusions
  • Levels of Cry3Aa expression do not differ between
    reciprocal hybrids
  • The transmission rate of the Cry3Aa gene appears
    to differ in reciprocal hybrids between Atlantic
    and Katahdin
  • An unexpectedly greater number of expressers to
    non expressers was observed in three separate
    sets of hybrids

18
Possible causes of different frequencies of
Cry3Aa expressing hybrids in reciprocal hybrids
  • More than a single copy of the transgene exists
    in Atlantic TC1 accompanied by transgene
    silencing in Katahdin X Atlantic TC1
  • Preferential gametic selection

19
With more than one copy of the transgene in
Atlantic TC1
  • Expect higher expressers to non-expressers in
    both Atlantic TC1 X Katahdin and Katahdin X
    Atlantic TC1
  • Expect gene silencing in Katahdin X Atlantic TC1
    non-expressers
  • PCR of non-expressers

20
Methods
  • DNA extraction (Sigma Extract-N-Amp)
  • Primers to amplify Cry3Aa
  • Forward 5GAGCTGCAAGGCCTTCAAAACAAT
  • Reverse 5TCTAGCACGCTAAGGGTCATCTCT
  • 1 cycle 4 min 94ºC 40 cycles 1 min 94ºC, 1
    min 58ºC, 1.5 min 72ºC 1 cycle 5 min 72ºC
  • 1.0 agarose gel
  • Stain with ethidium bromide

21
PCR results of amplification of genomic DNA of
expressing and non-expressing progeny of Katahdin
x Atlantic TC1
500bp
Results confirm observed segregation ratio from
ELISA
22
Conclusion
  • PCR results agree with ELISA results
  • If not transgene silencingthen gametic
    selection?
  • How does segregation compare in a different
    hybrid using Atlantic TC1 as female parent?

23
In order to determine if the phenomenon of
unexpectedly high numbers of transgenic progeny
were obtained from Atlantic TC1 as a female
parent and to verify the single transgene copy,
we examined a cross between Atlantic and the 2n
pollen-producing diploid hybrid, APM-2
24
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25
Conclusions
  • Single transgene copy in Atlantic TC1 was
    supported by segregation data in four of five
    families
  • Absence of the transgene in non-expressers was
    verified by PCR in two families so transgene
    silencing does not appear to be the cause
  • The unexpectedly high frequency of Cry3Aa
    expressers in Atlantic TC1 X Katahdin is likely
    due to preferential selection of transgenic
    female gametes in this cross

26
Acknowledgements
  • Dave Douches
  • Richard Veilleux
  • Sue Tolin
  • Vladamir Shulaev
  • Suzanne Piovano
  • My fellow graduate students
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