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Welcome
Cisgenesis strongly improves
    Introgression and Induced Translocation
              breeding of plants.




2
Introduction


    Why cisgenic approach?


    Prerequisites for cisgenic approach


    Method to develop cisgenic plant


    Conclusion

3
Concept of cisgenesis introduced by Dutch
    researchers Schouten, Krens and Jacobsen (2006)




4
How can we go for genetic improvement?

            g           PLANT VARIETIES
          d in
       ree




                     Modern
     lb




                     insights        GMO
       ca




                  &techniques    REGULATIONS
                    including
   ssi




                 biotechnology
Cla




 5
Overview of existing Technologies




6
Key terms

    • Cisgenesis is the genetic modification of a recipient plant with a
      natural gene (includes its introns and is flanked by its native
      promoter and terminator in the normal sense orientation) from a
      crossable sexually compatible plant

    • A cisgene is a natural gene, coding for an (agricultural) trait,
      from the crop plant itself or from a sexually compatible donor
      plant that can be used in conventional breeding.




7
Contd...

     The gene pool for cisgenesis is identical to the gene pool available

      for classical breeding.
     Cisgenic plants can harbor one or more cisgenes, do not contain any

      transgenes.
     No foreign DNA, such as selection marker genes and vector-

      backbone sequences, should remain in the final cisgenic plant.



          The author of ‘Invasion of Genes - Genetic Heritage of India’
                           Dr B. S. Ahloowalia said:
          “Cisgenics removes all fears associated with transgenic crops.”




8
Contd…
• Transgenesis is   the     genetic
  modification of a recipient plant
  with one or more genes from any
  non-plant organism, or from a
  donor plant that is sexually
  incompatible with the recipient
  plant.

• This includes gene sequences of
  any origin in the anti-sense
  orientation,      any    artificial
  combination of a coding sequence
  and a regulatory sequence, such as
  a promoter from another gene, or
  a synthetic gene.

  9
Contd…

     • Traditional or conventional breeding: uses all classical and
       modern insights and techniques, including those related to
       biotechnology, however, without genetic modification.

     • It includes a number of techniques that are not regarded as
       genetic modification or that are exempted from the GMO-
       legislation.

     • Particularly the European Directive 2001/18/EC on the deliberate
       release of GMOs into the environment
                                         (European Parliament, 2001)




10
Contd…
     • Translocations   or interchanges:
       structural changes in chromosomes,
       where segments of non homologous
       chromosomes      have    exchanged
       positions.

      Why    interchanges important for
       plant breeders, geneticists &
       evolutionists?

      Interchanges bring about changes in
       linkage relationship, changes in
       chromosome structure & behavior
       by which variability is created.



11
Traditional breeding 

12
Why cisgenic approach?

      Some plant spp. difficult to breed by classical method

        e.g. woody plants- don’t flower for many years, intolerant to
       inbreeding, highly heterozygous.



      Some plant spp. are naturally sterile / are part of a highly

       desired and commercially widespread clone whose genotype
       needs to remain intact.

       e.g. potato, apple, grape, and banana.



13
To appreciate cisgenesis……

       1st we need to understand the problems related to…

     1. Transgenic approach

     2. Traditional breeding and

     3. Translocation breeding.




14
What is the problem with transgenesis?

                                                  B.t
 Transferred gene usually derives from an
     alien species.

• Extends the gene pool of the recipient
     species.

• Such a novel gene might provide the
     target plant with a new trait that neither
     occurs in the recipient species in nature
     nor can be introduced through traditional
     breeding.




15
Contd…

      In recipient species fitness may change in various ways:

          Through gene flow between a GM crop and its wild relatives
         potentially creating shifts in natural vegetation.



      The generation of these new ‘unnatural’ gene combinations is

         regarded as both unethical and having potential long-term risks
         for   health   and    environment.(non-targeted      organisms/soil
         ecosystems)




                                         den Nijs et.al., 2004
16
T
     a
     r
     g
     e
     t

     p
     l
     a
     n
     t




         GENE FLOW
17                   FITNESS OF THE POPULATION
How cisgenic plants can overcome problems of
                   transgenic plants?


                Transgenesis




18
What is the problem with introgression breeding?

     High-quality genotype (cultivar) X wild plant (gene of
                                                      interest).
     The wild plant, passes genes of interest to the progeny, but also
     deleterious genes.

     This ‘linkage drag’ tremendously slow down the breeding process,
     esp. if the gene of interest is genetically tightly linked to one or
     more deleterious genes.

     Quality of crop is ruined.

     To reduce linkage drag, need successive generations of
     recurrent backcrossing with the cultivated plant and
     simultaneous selection for the trait.
19
Contd..



       As     apple    cultivars    are   self-incompatible    and    highly
        heterozygous, the phenotype of a cultivar is unique and
        breeding       produces     genotypes   with   new     and    distinct
        characteristics.



       Limited    Popularity of the new cultivars carrying disease
        resistance genes since originality of cultivar lost.




                                                (Gardiner et al., 2007)
20
How cisgenesis can overcome problems of
             introgression breeding?


               Introgression
                 breeding




21
Induced Translocation breeding

      Chromosome pairing and recombination in common wheat is largely

       governed by the gene Phi, located on the long arm of chromosome 5B,
       which ensures that only homologous chromosomes can pair and
       recombine.



      Sears (1956) used ionizing radiation treatment to induce chromosome

       breaks and transferred a gene conditioning resistance to:
      leaf rust caused by   Puccinia recondita f. sp. tritici from

       Ae. umbellulata Zhuk. to wheat.

                                                        Riley & Chapman,1958;
                                                        Sears & Okamoto, 1958;
                                                        Sears, 1976;
22
Major problem in induced translocation breeding.

      Radiation treatment causes random chromosome breaks.

      The majority of translocations resulting from radiation

       treatments were formed between non-homoeologous chromosome
       arms.
      These non-compensating translocations are genetically

       unbalanced, and lead to reduced agronomic performance.



       The radiation-induced Sr26 transfer, derived from A. elongatum,
       the translocation causes a reduction of about 10% in yield



23                                                 The et al., 1988
24
Is Cisgenesis efficient method in crops? Yes…

      Particularly efficient method for cross-fertilizing heterozygous

       plants that propagate vegetatively, such as potato, apple and
       banana.
      Cisgenesis   might   also   supplement    classical   breeding   for
       improving traits with. limited natural allelic variation in cultivars
       and wild species
      E.g. expression of an endogenous phytase gene in barley through

       the insertion of extra gene copies of the endogenous phytase
       gene isolated from barley itself



25
The prerequisites for cisgenesis….


      Sequence information of the plant.

      The isolation and characterization of genes of interest from

      crossable relatives.




26
Web site address for data base info..




27
28
Solutions via cisgenesis




29
Development of a cisgenic apple plant.




                             Thalia Vanblaere et.al.,2011
30
Present day Apple
                           (Malus x domestica) cultivars
                      are susceptible to Apple scab which is
                                  caused by the
                             fungus Venturia inaequalis
     early symptoms




31
Apple growers spray on an average 15 times in one season to control
                                the disease.




                                       Spraying fungicides in Apple orchard



                                                     Patocchi et al., 2004
32
Any natural resistance? Yes……..
  Source natural resistance to diseases is known .


  Classical breeding has developed scab resistant cultivars, mostly
      by introgression of Vf resistance from Malus floribunda 821




                                       (Lespinasse,1989; MacHardy, 1996)




33
Several apple scab resistance genes




       Identified and were mapped on different linkage
                 groups of the Apple genome.

34
Impact of Vf genes in conventionally bred Apple




35
 Only   Vf locus has been positionally cloned

                                        ( Vinatzer et al., 2001)



      Proved to consists of a gene cluster with four
        paralogs :
     1. HcrVf1
     2. HcrVf2
     3. HcrVf3 and
     4. HcrVf4
                                         ( Xu and Korban 2002)


36
 Initially, only the   HcrVf2 gene was tested by overexpression using
       the CaMV35S promoter & also own promoter and nos terminator,in

       scab susceptible Apple plants.




      Only one resistance encoding gene, HcrVf2, has been isolated and

       proven functional to date in cvs. Gala and Elstar.


                                                Belfanti et al., 2004;



                                                Szankowski et al., 2009;

                                                                           Joshi,
37                                              2010.
 In Transgenic Apple, for successful transformation marker gene
       nptII & other regulators added.

                                                      Joshi, (2010)
38
But people don’t need Transgenic Apple……..


      A large proportion of the consumers in Europe view genetically
       modified foods as a risk to both health and the environment

                                                (Gaskell et al., 2000)




                                                  CISGENIC




39
Cisgenic plants are produced by the same transformation
                  techniques as transgenic plants.




40
Construction of vector




                              17434 bp




41
 In order to develop marker-free plants the
      chemically inducible recombinase system reported in
      strawberry was applied to apple.
                                    Schaart et al., (2004)




42
Method to develop cisgenic plants
  Technique used: 2 independent regeneration                  step
      with 1 binary vector

 Transformation with stable integration using positive selection
   e.g. on kanamycin (nptII)



     Removal of marker by chemical induction of Recombinase R activity
                       ( Decamethosone treatment)



     Selection for marker free plants using negative selection (codA) on
                    5-Fluro cytosine (toxic 5-Fluro uracil)

43                                                      Schaart et.al.,2004
Clean vector system


T-DNA insert in transgenic line

 RB                            RS R-LBD Recombinase CodA-NptII fusion RS LB
       prom HcrVf2      term



     Recombination

     RB                         RS
                                     R-LBD Recombinase CodA-NptII fusion RS LB
       prom   HcrVf2     term


 T-DNA insert after cisgenic line
                                                           RS LB
                           RB
                                prom                term
                                         HcrVf2
44
10 transgenic lines were
             regenerated     through
             selection on Kanamycin medium




     8 out of 10 lines have backbone integration (nptII)
45
‘Gala’ scab susceptible cultivar
HcrVf2         Florina,classical bred cv. Vf resistance




 3 cisgenic lines are derived
CodA marker gene

                        pMF vector




nptII (backbone)

                                                  46
Gene expression analysis by PCR of cDNA
     Transgenic            Transgenic


                  Cisgenic lines   Cisgenic lines




47
Copy number by southern Blot




1 copy of nptII in all transgenic lines


                                          1 copy of HcrVf2 in C7.1.49 & C 11.1.53

                                          2 copies of HcrVf2 in T12.1 (C12.1.49)


48
49
A cisgenic GM strategy for durable
                  resistance based on
                    R and Avr genes


     The new concept : HEALTHY POTATO




                              Haverkort, A. J. et al.,2007

50
Late blight of potato deadly disease in potato.

      Phytophthora resistance in potato is easily broken.

      A better strategy is needded for Sustainable resistance

      Many R-genes are available in crossable wild species,   enabling

     the development of a resistance strategy

      With useful molecular knowledge Avr-genes from the pathogen.




51
52
List of R genes and Avr genes




53
Approach:

      Cloning of R genes
      Marker free transformation
      Cisgene field tests




54
55
Endogenous Fungal Resistance Genes

     Plants have been genetically engineered with

      either:
      Endogenous gene 1:   V. vinifera thaumatin-like protein
        gene (vvtl-1) for fungal disease resistance or


      Endogenous gene 2: 2S albumin gene (alb) from

      grapevine


56
Genes are expressed via bidirectional promoter system




57
58
Cisgenic Approach for Improving the Bioavailability
               of Phosphate in the Barley Grain.




                                     Holme I B et al.,2012

59
leading to water pollution…….




60
PAPhy (purple acid phosphatase)


      Two types: HvPAPhy_a and HvPAPhy_b.


      HvPAPhy_a    is preferentially synthesized during seed
       development and stored as preformed phytase in the
       mature grain,
      HvPAPhy_b      is  preferentially   synthesized  during
       germination.

     Therefore ,the HvPAPhy_a gene as a candidate for our
       cisgenic approach.




61
62
Phytase Activities in Cisgenic Barley Seeds



                                                  Revealed a
                                                   positive
                                                 correlation
                                                between gene
                                               dosage and gene
                                               expression of the
                                                phytase gene.




63
Modifying Plant Growth using GA-associated cisgenes.




                    POPLAR TRE
                               ES




                                           Han K et.al.,2010
64
 The transfer of entire native genes that play roles in

      biosynthesis or signaling of gibberellic acids (GAs),
      including their 5’ and 3’ proximal regulatory regions,
      impart changes in growth rate and stature in poplar
      trees.




65
 Five different cisgenes :
         GA20ox7,GA2ox2, GAI1, RGL 1_1, and RGL 1_2 .
      GA20oxidase catalyzes the penultimate step in the biosynthetic
        GA pathway, in turn promote cell division and elongation.
      The other genes tend to repress or attenuate active GA
        actions.
     a) GA degradation by GA2ox2.
     b) DELLA domain proteins that attenuate GA signals.




66
 Plants transformed with GA20ox7 cisgene had a higher rate and
       frequency of regeneration of transgenic shoots during antibiotic
       selection.


      The average stem volume of the GA20ox7 transformed plants
       increased by 40% compared with the transgenic (empty vector)
       controls.


      GA20ox7 gene expression was also statistically associated with
       the growth enhancement.




67
68
69
Thank you

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Cisgenics- Clean marker assisted Technology

  • 2. Cisgenesis strongly improves Introgression and Induced Translocation breeding of plants. 2
  • 3. Introduction Why cisgenic approach? Prerequisites for cisgenic approach Method to develop cisgenic plant Conclusion 3
  • 4. Concept of cisgenesis introduced by Dutch researchers Schouten, Krens and Jacobsen (2006) 4
  • 5. How can we go for genetic improvement? g PLANT VARIETIES d in ree Modern lb insights GMO ca &techniques REGULATIONS including ssi biotechnology Cla 5
  • 6. Overview of existing Technologies 6
  • 7. Key terms • Cisgenesis is the genetic modification of a recipient plant with a natural gene (includes its introns and is flanked by its native promoter and terminator in the normal sense orientation) from a crossable sexually compatible plant • A cisgene is a natural gene, coding for an (agricultural) trait, from the crop plant itself or from a sexually compatible donor plant that can be used in conventional breeding. 7
  • 8. Contd...  The gene pool for cisgenesis is identical to the gene pool available for classical breeding.  Cisgenic plants can harbor one or more cisgenes, do not contain any transgenes.  No foreign DNA, such as selection marker genes and vector- backbone sequences, should remain in the final cisgenic plant. The author of ‘Invasion of Genes - Genetic Heritage of India’ Dr B. S. Ahloowalia said: “Cisgenics removes all fears associated with transgenic crops.” 8
  • 9. Contd… • Transgenesis is the genetic modification of a recipient plant with one or more genes from any non-plant organism, or from a donor plant that is sexually incompatible with the recipient plant. • This includes gene sequences of any origin in the anti-sense orientation, any artificial combination of a coding sequence and a regulatory sequence, such as a promoter from another gene, or a synthetic gene. 9
  • 10. Contd… • Traditional or conventional breeding: uses all classical and modern insights and techniques, including those related to biotechnology, however, without genetic modification. • It includes a number of techniques that are not regarded as genetic modification or that are exempted from the GMO- legislation. • Particularly the European Directive 2001/18/EC on the deliberate release of GMOs into the environment (European Parliament, 2001) 10
  • 11. Contd… • Translocations or interchanges: structural changes in chromosomes, where segments of non homologous chromosomes have exchanged positions.  Why interchanges important for plant breeders, geneticists & evolutionists?  Interchanges bring about changes in linkage relationship, changes in chromosome structure & behavior by which variability is created. 11
  • 13. Why cisgenic approach?  Some plant spp. difficult to breed by classical method e.g. woody plants- don’t flower for many years, intolerant to inbreeding, highly heterozygous.  Some plant spp. are naturally sterile / are part of a highly desired and commercially widespread clone whose genotype needs to remain intact. e.g. potato, apple, grape, and banana. 13
  • 14. To appreciate cisgenesis…… 1st we need to understand the problems related to… 1. Transgenic approach 2. Traditional breeding and 3. Translocation breeding. 14
  • 15. What is the problem with transgenesis? B.t  Transferred gene usually derives from an alien species. • Extends the gene pool of the recipient species. • Such a novel gene might provide the target plant with a new trait that neither occurs in the recipient species in nature nor can be introduced through traditional breeding. 15
  • 16. Contd…  In recipient species fitness may change in various ways:  Through gene flow between a GM crop and its wild relatives potentially creating shifts in natural vegetation.  The generation of these new ‘unnatural’ gene combinations is regarded as both unethical and having potential long-term risks for health and environment.(non-targeted organisms/soil ecosystems) den Nijs et.al., 2004 16
  • 17. T a r g e t p l a n t GENE FLOW 17 FITNESS OF THE POPULATION
  • 18. How cisgenic plants can overcome problems of transgenic plants? Transgenesis 18
  • 19. What is the problem with introgression breeding? High-quality genotype (cultivar) X wild plant (gene of interest). The wild plant, passes genes of interest to the progeny, but also deleterious genes. This ‘linkage drag’ tremendously slow down the breeding process, esp. if the gene of interest is genetically tightly linked to one or more deleterious genes. Quality of crop is ruined. To reduce linkage drag, need successive generations of recurrent backcrossing with the cultivated plant and simultaneous selection for the trait. 19
  • 20. Contd..  As apple cultivars are self-incompatible and highly heterozygous, the phenotype of a cultivar is unique and breeding produces genotypes with new and distinct characteristics.  Limited Popularity of the new cultivars carrying disease resistance genes since originality of cultivar lost. (Gardiner et al., 2007) 20
  • 21. How cisgenesis can overcome problems of introgression breeding? Introgression breeding 21
  • 22. Induced Translocation breeding  Chromosome pairing and recombination in common wheat is largely governed by the gene Phi, located on the long arm of chromosome 5B, which ensures that only homologous chromosomes can pair and recombine.  Sears (1956) used ionizing radiation treatment to induce chromosome breaks and transferred a gene conditioning resistance to:  leaf rust caused by Puccinia recondita f. sp. tritici from Ae. umbellulata Zhuk. to wheat. Riley & Chapman,1958; Sears & Okamoto, 1958; Sears, 1976; 22
  • 23. Major problem in induced translocation breeding.  Radiation treatment causes random chromosome breaks.  The majority of translocations resulting from radiation treatments were formed between non-homoeologous chromosome arms.  These non-compensating translocations are genetically unbalanced, and lead to reduced agronomic performance. The radiation-induced Sr26 transfer, derived from A. elongatum, the translocation causes a reduction of about 10% in yield 23 The et al., 1988
  • 24. 24
  • 25. Is Cisgenesis efficient method in crops? Yes…  Particularly efficient method for cross-fertilizing heterozygous plants that propagate vegetatively, such as potato, apple and banana.  Cisgenesis might also supplement classical breeding for improving traits with. limited natural allelic variation in cultivars and wild species  E.g. expression of an endogenous phytase gene in barley through the insertion of extra gene copies of the endogenous phytase gene isolated from barley itself 25
  • 26. The prerequisites for cisgenesis…. Sequence information of the plant. The isolation and characterization of genes of interest from crossable relatives. 26
  • 27. Web site address for data base info.. 27
  • 28. 28
  • 30. Development of a cisgenic apple plant. Thalia Vanblaere et.al.,2011 30
  • 31. Present day Apple (Malus x domestica) cultivars are susceptible to Apple scab which is caused by the fungus Venturia inaequalis early symptoms 31
  • 32. Apple growers spray on an average 15 times in one season to control the disease. Spraying fungicides in Apple orchard Patocchi et al., 2004 32
  • 33. Any natural resistance? Yes……..  Source natural resistance to diseases is known .  Classical breeding has developed scab resistant cultivars, mostly by introgression of Vf resistance from Malus floribunda 821 (Lespinasse,1989; MacHardy, 1996) 33
  • 34. Several apple scab resistance genes Identified and were mapped on different linkage groups of the Apple genome. 34
  • 35. Impact of Vf genes in conventionally bred Apple 35
  • 36.  Only Vf locus has been positionally cloned ( Vinatzer et al., 2001)  Proved to consists of a gene cluster with four paralogs : 1. HcrVf1 2. HcrVf2 3. HcrVf3 and 4. HcrVf4 ( Xu and Korban 2002) 36
  • 37.  Initially, only the HcrVf2 gene was tested by overexpression using the CaMV35S promoter & also own promoter and nos terminator,in scab susceptible Apple plants.  Only one resistance encoding gene, HcrVf2, has been isolated and proven functional to date in cvs. Gala and Elstar. Belfanti et al., 2004; Szankowski et al., 2009; Joshi, 37 2010.
  • 38.  In Transgenic Apple, for successful transformation marker gene nptII & other regulators added. Joshi, (2010) 38
  • 39. But people don’t need Transgenic Apple……..  A large proportion of the consumers in Europe view genetically modified foods as a risk to both health and the environment (Gaskell et al., 2000) CISGENIC 39
  • 40. Cisgenic plants are produced by the same transformation techniques as transgenic plants. 40
  • 41. Construction of vector 17434 bp 41
  • 42.  In order to develop marker-free plants the chemically inducible recombinase system reported in strawberry was applied to apple. Schaart et al., (2004) 42
  • 43. Method to develop cisgenic plants  Technique used: 2 independent regeneration step with 1 binary vector Transformation with stable integration using positive selection e.g. on kanamycin (nptII) Removal of marker by chemical induction of Recombinase R activity ( Decamethosone treatment) Selection for marker free plants using negative selection (codA) on 5-Fluro cytosine (toxic 5-Fluro uracil) 43 Schaart et.al.,2004
  • 44. Clean vector system T-DNA insert in transgenic line RB RS R-LBD Recombinase CodA-NptII fusion RS LB prom HcrVf2 term Recombination RB RS R-LBD Recombinase CodA-NptII fusion RS LB prom HcrVf2 term T-DNA insert after cisgenic line RS LB RB prom term HcrVf2 44
  • 45. 10 transgenic lines were regenerated through selection on Kanamycin medium 8 out of 10 lines have backbone integration (nptII) 45
  • 46. ‘Gala’ scab susceptible cultivar HcrVf2 Florina,classical bred cv. Vf resistance 3 cisgenic lines are derived CodA marker gene pMF vector nptII (backbone) 46
  • 47. Gene expression analysis by PCR of cDNA Transgenic Transgenic Cisgenic lines Cisgenic lines 47
  • 48. Copy number by southern Blot 1 copy of nptII in all transgenic lines 1 copy of HcrVf2 in C7.1.49 & C 11.1.53 2 copies of HcrVf2 in T12.1 (C12.1.49) 48
  • 49. 49
  • 50. A cisgenic GM strategy for durable resistance based on R and Avr genes The new concept : HEALTHY POTATO Haverkort, A. J. et al.,2007 50
  • 51. Late blight of potato deadly disease in potato. Phytophthora resistance in potato is easily broken. A better strategy is needded for Sustainable resistance Many R-genes are available in crossable wild species, enabling the development of a resistance strategy With useful molecular knowledge Avr-genes from the pathogen. 51
  • 52. 52
  • 53. List of R genes and Avr genes 53
  • 54. Approach: Cloning of R genes Marker free transformation Cisgene field tests 54
  • 55. 55
  • 56. Endogenous Fungal Resistance Genes Plants have been genetically engineered with either:  Endogenous gene 1: V. vinifera thaumatin-like protein gene (vvtl-1) for fungal disease resistance or  Endogenous gene 2: 2S albumin gene (alb) from grapevine 56
  • 57. Genes are expressed via bidirectional promoter system 57
  • 58. 58
  • 59. Cisgenic Approach for Improving the Bioavailability of Phosphate in the Barley Grain. Holme I B et al.,2012 59
  • 60. leading to water pollution……. 60
  • 61. PAPhy (purple acid phosphatase)  Two types: HvPAPhy_a and HvPAPhy_b.  HvPAPhy_a is preferentially synthesized during seed development and stored as preformed phytase in the mature grain,  HvPAPhy_b is preferentially synthesized during germination. Therefore ,the HvPAPhy_a gene as a candidate for our cisgenic approach. 61
  • 62. 62
  • 63. Phytase Activities in Cisgenic Barley Seeds Revealed a positive correlation between gene dosage and gene expression of the phytase gene. 63
  • 64. Modifying Plant Growth using GA-associated cisgenes. POPLAR TRE ES Han K et.al.,2010 64
  • 65.  The transfer of entire native genes that play roles in biosynthesis or signaling of gibberellic acids (GAs), including their 5’ and 3’ proximal regulatory regions, impart changes in growth rate and stature in poplar trees. 65
  • 66.  Five different cisgenes : GA20ox7,GA2ox2, GAI1, RGL 1_1, and RGL 1_2 .  GA20oxidase catalyzes the penultimate step in the biosynthetic GA pathway, in turn promote cell division and elongation.  The other genes tend to repress or attenuate active GA actions. a) GA degradation by GA2ox2. b) DELLA domain proteins that attenuate GA signals. 66
  • 67.  Plants transformed with GA20ox7 cisgene had a higher rate and frequency of regeneration of transgenic shoots during antibiotic selection.  The average stem volume of the GA20ox7 transformed plants increased by 40% compared with the transgenic (empty vector) controls.  GA20ox7 gene expression was also statistically associated with the growth enhancement. 67
  • 68. 68
  • 69. 69