Methods for plant transformation using spectinomycin selection

• US 8,357,834 B2
• Filed: 08/18/2011
• Issued: 01/22/2013
• Est. Priority Date: 03/09/2007
• Status: Active Grant

• Current Assignee: Monsanto Technology LLC (Bayer AG)
• Original Assignee: Monsanto Technology LLC (Bayer AG)
• Inventors: Martinell, Brian, Petersen, Michael, Somers, David, Wan, Yuechun, Williams, Edward, Ye, Xudong
• Primary Examiner(s): Fox, David T
• Application Number:
  US13/213,015
• Publication Number:
  US 20120073015A1
• Time in Patent Office: 523 Days
• Field of Search: None
• US Class Current: 800/278
• CPC Class Codes: A01H 4/003 Cutting apparatus specially adapted for tissue culture
• CPC Class Codes: A01H 4/008 Methods for regeneration to complete plants
• CPC Class Codes: A01H 6/202 Brassica napus [canola]
• CPC Class Codes: A01H 6/4684 Zea mays [maize]
• CPC Class Codes: A01H 6/542 Glycine max [soybean]
• CPC Class Codes: A01H 6/604 Gossypium [cotton]
• CPC Class Codes: C12N 1/205 Bacterial isolates
• CPC Class Codes: C12N 15/8201 Methods for introducing genetic material into plant cells, e.g. DNA, RNA, stable or transient incorporation, tissue culture methods adapted for transformation
• CPC Class Codes: C12N 15/8202 by biological means, e.g. cell mediated or natural vector
• CPC Class Codes: C12N 15/8205 Agrobacterium mediated transformation
• CPC Class Codes: C12N 15/8209 Selection, visualisation of transformants, reporter constructs, e.g. antibiotic resistance markers
• CPC Class Codes: C12N 15/8221 Transit peptides
• CPC Class Codes: C12N 15/8261 with agronomic (input) traits, e.g. crop yield
• CPC Class Codes: C12N 15/8265 Transgene containment, e.g. gene dispersal
• CPC Class Codes: C12N 15/8271 for stress resistance, e.g. heavy metal resistance
• CPC Class Codes: C12N 15/8274 for herbicide resistance
• CPC Class Codes: C12N 15/8275 Glyphosate
• CPC Class Codes: C12N 15/8277 Phosphinotricin
• CPC Class Codes: C12N 15/8281 for bacterial resistance
• CPC Class Codes: C12N 5/0025 Culture media for plant cell or plant tissue culture
• CPC Class Codes: C12N 5/04 : Plant cells or tissues culture media C12N5/0025
• CPC Class Codes: C12N 9/1029 : transferring groups other than amino-acyl groups (2.3.1)
• CPC Class Codes: C12R 2001/41 : Rhizobium
• CPC Class Codes: C12Y 203/01081 : Aminoglycoside N3'-acetyltransferase (2.3.1.81)
• CPC Class Codes: G01N 33/0098 : Plants or trees wood G01N33/46

Abstract

The present invention relates to methods and compositions for transforming soybean, corn, cotton, or canola explants using spectinomycin as a selective agent for transformation of the explants. The method may further comprise treatment of the explants with cytokinin during the transformation and regeneration process.

Claims

1. A method of producing a transgenic plant comprising:

(a) transforming at least a first soybean or cotton seed explant with a first heterologous nucleic acid sequence comprising a selectable marker conferring tolerance to spectinomycin to produce transformed cells, wherein the selectable marker gene comprises an aadA gene fused to a sequence encoding a chloroplast transit peptide; and

(b) regenerating a transgenic plant from the transformed cells, wherein the explant is contacted, prior to, concurrently with, and/or following step (a) or step (b), with at least a first media comprising spectinomycin to select transformed cells comprising said selectable marker.

2. The method of claim 1, wherein the first seed explant is retransformed.

3. The method of claim 1, wherein the explant is stored at a temperature of between 0-15°

C. for between 1 hour and 7 days prior to step (a).

4. The method of claim 1, wherein the explant comprises an embryonic meristem.

5. The method of claim 1, wherein the media comprises from about 15 mg/L to about 1500 mg/L spectinomycin.

6. The method of claim 1, wherein the cells of the explant comprise a coding sequence conferring tolerance to glyphosate, bialaphos, phosphinothricin, Basta, glufosinate, 2,4-D, kanamycin and related aminoglycosides, hygromycin, streptomycin, ampicillin, or dicamba.

7. The method of claim 1, wherein during or following step (a), explants are grown in the presence of a selective agent at 35°

C.-40°

C. and/or are grown under lighting conditions that allow for normal plastid development.

8. The method of claim 7, wherein growth at 35°

-40°

C. is performed for 1-7 days or the lighting conditions comprise at least 5μ

Einsteins with about a 16 hour light/8 dark photoperiod.

9. The method of claim 1 wherein step (a) comprises growing an explant on a co-culture medium comprising spectinomycin.

10. The method of claim 9, wherein the explant is not contacted with a medium comprising spectinomycin after being transferred from a co-culture medium.

11. The method of claim 9, wherein the explant is contacted with a medium comprising spectinomycin after being transferred from a co-culture medium.

12. The method of claim 1, wherein the explant that is regenerating into a plant is transferred to soil or soil substitute for rooting without pre-rooting in aseptic media.

13. The method of claim 1, wherein the heterologous nucleic acid further comprises a coding sequence that confers a trait of agronomic interest or improved end use.

14. The method of claim 1, wherein step (a) comprises transforming the cell of the explant with at least a second heterologous nucleic acid.

15. The method of claim 14, wherein the first and second heterologous nucleic acids are integrated at different loci within the genome of the cell.

16. The method of claim 1, further comprising, prior to step (a), the step of priming the seed, wherein the priming comprises contacting the seed with a cytokinin.

17. The method of claim 1, further comprising contacting the explant with a cytokinin prior to, concurrently with and/or following step (b).

18. The method of claim 17 wherein the cytokinin is selected from the group consisting of thidiazuron, BAP (6-Benzylaminopurine), kinetin, CPPU (N-(2-Chloro-4-pyridyl)-N′

-phenylurea), 2iP (6-(y,y-Dimethylallylamino) purine), Zeatin, Zeatin-riboside, Adenine, and TIBA (2,3,5-Triiodobenzoic acid).

19. The method of claim 1, wherein step (a) comprises contacting the explant with recombinant Rhizobiaceae comprising said heterologous nucleic acid, wherein the Rhizobiaceae have been exposed to thidiazuron prior to or concurrently with contacting the explant with the recombinant Rhizobiaceae.

20. The method of claim 19, wherein the Rhizobiaceae is exposed to thidiazuron for from about 1 to 5 days prior to contacting the explant with the recombinant Rhizobiaceae.

21. The method of claim 19, wherein the Rhizobiaceae are suspended in the presence of a selective agent active against an untransformed explant prior to contacting the explants with the Rhizobiaceae.

22. The method of claim 19, wherein the Rhizobiaceae are selected from the group consisting of:

Agrobacteria, Sinorhizobia, Mesorhizobia, and Rhizobia.

23. The method of claim 19, wherein the explants are grown in the presence of a fungicide prior to, during, or subsequent to step (a).

24. The method of claim 23, wherein the explants are grown in the presence of a fungicide and DMSO.

25. The method of claim 24, wherein the explants are grown in the presence of nystatin, thiabendazole, and DMSO.

26. The method of claim 6, wherein the explant is a soybean explant.

27. The method of claim 13, further comprising the step of

(c) obtaining a progeny plant of any generation of the transgenic plant that comprises the gene conferring the trait of interest and lacks the selectable marker.

28. The method of claim 1, wherein the heterologous nucleic acid comprises a first DNA segment comprising left and right T-DNA borders flanking a gene conferring a trait of interest;

and a second DNA segment comprising a second set of left and right T-DNA borders flanking said selectable marker conferring tolerance to spectinomycin.

29. The method of claim 28, further comprising the step of

(c) obtaining a progeny plant of any generation of the transgenic plant that comprises the gene conferring the trait of interest and lacks the selectable marker.

30. The method of claim 1, wherein the heterologous nucleic acid comprises right and left T-DNA borders and first and second DNA segments, wherein the first DNA segment comprises a gene of interest located after the right border, and wherein the second DNA segment comprises the selectable marker located after the left border.

31. The method of claim 1, wherein the heterologous nucleic acid comprises first and second right T-DNA borders, wherein a first DNA segment comprising a gene of interest is located after the first right border and a second DNA segment comprising the selectable marker is located after the second right border.

32. The method of claim 1, comprising culturing said explant on media lacking spectinomycin for from about 1 to about 7 days during step (b).

33. The method of claim 1, wherein contacting the explant with at least a first media comprising spectinomycin is for from about 15 minutes to about 7 days.

34. The method of claim 1, wherein the selectable marker is encoded by aadA.

35. The method of claim 34, wherein aadA comprises SEQ ID NO:

1.

36. The method of claim 34, wherein aadA comprises SEQ ID NO:

2.

37. The method of claim 1, wherein the explant is further defined as having been maintained prior to step (b) under conditions wherein the explant does not germinate and remains viable and competent for genetic transformation.

38. The method of claim 37, wherein said conditions comprise dehydrating the explant or a seed comprising the explant.

39. The method of claim 38, further defined as comprising increasing the moisture content of the explant prior to or concurrently with step (b).

40. The method of claim 37, wherein said conditions comprise an internal moisture content of the explant of from about 3% to about 25%.

41. The method of claim 40, wherein said conditions comprise an internal moisture content of the explant of from about 3% to about 16%.

42. The method of claim 37, wherein said conditions comprise a temperature of between about −

80°

C. and about 60°

C.

43. The method of claim 37, further defined as comprising priming the explant or a seed comprising the explant prior to step (b).

44. The method of claim 43, wherein priming the seed comprises contacting the explant or a seed comprising the explant with an aqueous solution comprising water, a plant growth regulator, a selection agent, or a cell membrane conditioner.

45. The method of claim 1, wherein transforming at least a first cell of the explant with a heterologous nucleic acid is carried out by bacterially-mediated transformation or microprojectile bombardment.

46. The method of claim 1, wherein the explant is further defined as having been excised from a seed comprising 3% to 25% internal moisture content, or a hydrated or germinating seed comprising 26% to 80% internal moisture content, or comprises a tissue of the group consisting of:

meristem, immature embryo, embryo, embryonic axis, cotyledon, hypocotyl, mesocotyl, leaf, primary leaf base, leaf disc, shoot tip, and plumule.

47. The method of claim 46, wherein the explant is further defined as having been excised from a germinated or imbibed seed.

48. The method of claim 1, wherein the explant is not contacted with a media comprising spectinomycin subsequent to step (a).

49. The method of claim 1, wherein the first media is a liquid.

50. The method of claim 1, wherein one or more of steps (a)-(b) are automated.