Markers for Salinity Tolerance in Wheat Plants and the Use Thereof in Breeding Programs

• US 20080028480A1
• Filed: 06/14/2005
• Published: 01/31/2008
• Est. Priority Date: 06/14/2004
• Status: Abandoned Application

• Current Assignee: Evans Lagudah, Megan Lindsay, Rana Munns, Richard James, Shaobai Huang, Wolfgang Spielmeyer
• Original Assignee: Evans Lagudah, Megan Lindsay, Rana Munns, Richard James, Shaobai Huang, Wolfgang Spielmeyer
• Inventors: Spielmeyer, Wolfgang, James, Richard, Munns, Rana, Huang, ShaoBai, Lindsay, Megan, Lagudah, Evans
• Application Number:
  US11/629,835
• Publication Number:
  US 20080028480A1
• Time in Patent Office: Days
• US Class Current: 800/260
• CPC Class Codes: C07K 14/415 from plants
• CPC Class Codes: C12Q 1/6895 for plants, fungi or algae
• CPC Class Codes: C12Q 2600/13 Plant traits
• CPC Class Codes: C12Q 2600/156 Polymorphic or mutational markers
• CPC Class Codes: Y02A 40/135 Plants tolerant to salinity

Abstract

The present invention relates to markers of a Nax locus of wheat plants, particularly durum wheat, linked to reduced sodium accumulation, as well as enhanced tolerance to saline and/or sodic soils. The present invention also relates to the use of these markers in breeding programs to produce plants with reduced sodium accumulation, as well as enhanced tolerance to saline and/or sodic soils. Furthermore, the invention relates to plants produced by these breeding programs.

Claims

1. A method of identifying a wheat plant having a phenotype of enhanced tolerance to saline and/or sodic soils, and/or reduced sodium accumulation in an aerial part of the plant, the method comprising detecting a nucleic acid molecule of the plant, wherein the nucleic acid molecule is linked to a Nax1 locus of wheat that comprises an allele that confers on the plant the phenotype of enhanced tolerance to saline and/or sodic soils and/or reduced sodium accumulation in an aerial part of the plant.

3. The method of claim 1 which comprises:

i) hybridising a second nucleic acid molecule to said nucleic acid molecule which is obtained from said plant,

ii) optionally hybridising at least one other nucleic acid molecule to said nucleic acid molecule which is obtained from said plant; and

iii) detecting a product of said hybridising step(s) or the absence of a product from said hybridising step(s).

4. The method of claim 3, wherein the second nucleic acid molecule is used as a primer to reverse transcribe or replicate at least a portion of the nucleic acid molecule.

5. The method of claim 1, wherein the nucleic acid is detected using a technique selected from the group consisting of:

restriction fragment length polymorphism analysis, amplification fragment length polymorphism analysis, microsatellite amplification and/or nucleic acid sequencing.

6. The method of claim 1 which comprises nucleic acid amplification.

8. The method of claim 6, wherein the amplification is performed using primers which amplify a polymorphic GA-repeat, wherein the polymorphic GA-repeat can be amplified using the primers ATCGCATGATGCACGTAGAG (SEQ ID NO:

11) and ACATGCATGCCTACCTAATGG (SEQ ID NO;

     12).

9. The method of claim 6, wherein the amplification is 5 performed using primers which amplify a polymorphic GA-repeat, wherein the polymorphic GA-repeat can be amplified using the primers ATCGCATGATGCACGTAGAG (SEQ ID NO:

11) and GTGGGGGAGGCCGGCCAC (SEQ ID NO;

     15).

10. The method of claim 6, wherein the amplification is performed using a primer comprising the sequence ATCGCATGATGCACGTAGAG (SEQ ID NO:

11), in conjunction with a primer comprising the sequence ACATGCATGCCTACCTAATGG (SEQ ID NO;

     12) or GTGGGGGAGGCCGGCCAC (SEQ ID NO;

     15), or at least one primer which is a variant of any one of said primers.

11. The method of claim 6, wherein the amplification is performed using primers which amplify a polymorphic repeat, wherein the polymorphic repeat can be amplified using the primer pairs selected from:

i) ACATCCACGTTTATGTTGTTG (SEQ ID NO;

     13) and TTGGTTGCTCAACGTTTACTT (SEQ ID NO;

     14),

ii) TGTGGTGCATCACAGGGCTGTTC (SEQ ID NO;

21) and AGCGCTTGCATACTCGTCCGG (SEQ ID NO;

22), and

iii) AGCAATGAGGATGGTGCTTTCTC (SEQ ID NO;

23) and TGTGAGCGACTCCTCGATTTCAG (SEQ ID NO;

24).

12. The method of claim 6, wherein the amplification is performed using primers pairs comprising the sequences selected from:

i) ACATCCACGTTTATGTTGTTG (SEQ ID NO;

     13) and TTGGTTGCTCAACGTTTACTT (SEQ ID NO;

     14), or at least one primer which is a variant of any one of said primers,

ii) TGTGGTGCATCACAGGGCTGTTC (SEQ ID NO;

21) and AGCGCTTGCATACTCGTCCGG (SEQ ID NO;

22), or at least one primer which is a variant of any one of said primers, and

iii) AGCAATGAGGATGGTGCTTTCTC (SEQ ID NO;

23) and TGTGAGCGACTCCTCGATTTCAG (SEQ ID NO;

24) or at least one primer which is a variant of any one of said primers.

13. A method of selecting a wheat plant from a population of wheat plants, the method comprising;

i) crossing two wheat plants of which at least one plant comprises a Nax1 locus comprising an allele which confers on the plant a phenotype of enhanced tolerance to saline and/or sodic soils, and/or reduced sodium accumulation in an aerial part of the plant, and

ii) screening progeny plants from the cross for the presence or absence of said Nax1 locus by a method of claim 1,

wherein progeny with said allele have a phenotype of enhanced tolerance to saline and/or sodic soils, and/or reduced sodium accumulation in an aerial part of the plant, when compared to progeny lacking said allele.

16. The method of claim 13, wherein the wheat is tetraploid wheat, preferably durum wheat, or at least one of the wheat plants of step i) is a hexaploid wheat plant.

19. The method of claim 13, wherein the cross is between a durum wheat plant comprising said allele and a hexaploid wheat plant lacking said allele.

20. The method of claim 13, wherein one of the wheat plants is Line 149, Line 150, Line 151 or a progenitor or progeny plant thereof comprising said allele.

21. A method of introducing a Nax1 locus into the genome of a wheat plant lacking said locus, the method comprising;

i) crossing a first parent wheat plant with a second parent wheat plant, wherein the second plant comprises a Nax1 locus which comprises an allele which confers on the second plant a phenotype of enhanced tolerance to saline and/or sodic soils and/or reduced sodium accumulation in an aerial part of the plant, and

ii) backcrossing the progeny of the cross of step i) with plants of the same genotype as the first parent plant for a sufficient number of times to produce a plant with a majority of the genotype of the first parent but comprising said allele,

wherein progeny plants are screened for the presence or absence of said allele by a method of claim 1.

23. The method of claim 21, wherein the first and/or second parent wheat plant is a durum wheat plant, or the first parent wheat plant is a hexaploid wheat plant.

25. The method of claim 21, wherein one of the wheat plants is Line 149, Line 150, Line 151 or a progenitor or progeny plant thereof comprising said allele.

2. (canceled)

7. (canceled)

14-15. -15. (canceled)

17-18. -18. (canceled)

22. (canceled)

24. (canceled)

26-27. -27. (canceled)

28. A wheat plant comprising an allele of the Nax1 gene on chromosome 2AL which confers on the wheat plant a phenotype of enhanced tolerance to saline and/or sodic soils, and/or reduced sodium accumulation in an aerial part of the plant.

29. A seed of a wheat plant of claim 28.

30. A product produced from a wheat plant of claim 28 or a seed of claim 29, wherein the product comprises genetic material comprising an allele of the Nax1 gene on chromosome 2AL which confers on the wheat plant a phenotype of enhanced tolerance to saline and/or sodic soils, and/or reduced sodium accumulation in an aerial part of the plant.

32. The product of claim 30, wherein the product is a food product.

31. (canceled)

33-39. -39. (canceled)