Diagnostic molecular markers for seed lot purity traits in soybeans

• US 10,172,305 B2
• Filed: 04/26/2012
• Issued: 01/08/2019
• Est. Priority Date: 04/29/2011
• Status: Active Grant

• Current Assignee: Monsanto Technology LLC (Bayer AG)
• Original Assignee: Monsanto Technology LLC (Bayer AG)
• Inventors: Yates, Jennifer, Kleiss, Holly, Tamulonis, John P., Wooten, Jr., David R., Wu, Kunsheng
• Primary Examiner(s): Page, Brent T
• Application Number:
  US14/114,642
• Publication Number:
  US 20140115732A1
• Time in Patent Office: 2,448 Days
• Field of Search: None
• CPC Class Codes: A01H 1/045 using molecular markers
• CPC Class Codes: A01H 5/10 Seeds
• CPC Class Codes: A01H 6/542 Glycine max [soybean]
• CPC Class Codes: C07K 14/415 from plants
• CPC Class Codes: C12N 9/0073 with NADH or NADPH as one donor, and incorporation of one atom of oxygen 1.14.13
• CPC Class Codes: C12Y 114/13088 Flavonoid 3',5'-hydroxylase (1.14.13.88)

Abstract

The present invention is in the field of plant breeding. More specifically, the invention includes a method for breeding and selecting plants that uniform for one or more seed lot purity traits such as, such as distinct flower color, pubescence color, hilum color, and pod wall color. The invention further includes molecular markers associated with distinct flower color, pubescence color, hilum color, and pod wall color for uses in a breeding program.

Claims

1. A method of molecular marker assisted soybean breeding, the method comprising the steps of:

a) genotyping two parental soybean plants to determine the allelic state of each parental soybean plant with regard to each of;

(i) whether the parental soybean plant comprises the W1 Locus “

DD”

allelic form (W1 allele) represented by SEQ ID NO;

1 or the W1 Locus “

II”

allelic form (w1 allele) represented by SEQ ID NO;

2;

(ii) whether the parental soybean plant comprises the T Locus “

CC”

or “

TT”

allelic form of the molecular marker represented by SEQ ID NO;

8 (M0243191);

(iii) whether the parental soybean plant comprises the Td Locus “

II”

allelic form represented by SEQ ID NO;

13 or the Td Locus “

DD”

allelic form represented by SEQ ID NO;

14;

(iv) whether the parental soybean plant comprises the R locus “

AA”

or “

TT”

allelic form of the molecular marker represented by SEQ ID NO;

19 (M0100925); and

(v) for the haplotype defined by the molecular markers represented by SEQ ID NO;

26 (M0202726), SEQ ID NO;

33 (M0119618), and SEQ ID NO;

40 (M0094170), whether the parental soybean plant comprises the L2 Locus “

AA”

or “

TT”

allelic form of the molecular marker represented by SEQ ID NO;

26 (M0202726), whether the parental soybean plant comprises the L2 Locus “

AA”

or “

TT”

allelic form of the molecular marker represented by SEQ ID NO;

33 (M0119618), and whether the parental soybean plant comprises the L2 Locus “

AA”

or “

GG”

allelic form of the molecular marker represented by SEQ ID NO;

40 (M0094170);

(b) crossing the two parental soybean plants genotyped in step (a) to generate an F₁ population of soybean plants;

(c) obtaining a DNA or RNA sample from a tissue of at least one F₁ soybean plant of the F₁ population generated by the cross in step (b);

(d) determining by a nucleic acid based analyses, for at least the allelic forms in step (a) that differ between the two crossed parental plants, the allelic state of the F₁ soybean plant; and

(e) selecting based on the determination of allelic state in step d an F₁ soybean plant for use in a soybean breeding program that is a true F₁ soybean plant and not the result of self-pollination of one of the parental soybean plants.

2. The method of claim 1, further comprising:

(f) self-crossing the true F₁ soybean plant selected in step (e) to generate an F₂ population of soybean plants;

(g) obtaining a DNA or RNA sample from a tissue of at least one soybean plant of the F₂ population generated by the cross in step (f) and;

(i) determining whether the allelic state of the F₂ soybean plant comprises the W1 Locus “

DD”

allelic form (W1 allele) represented by SEQ ID NO;

1 or the W1 Locus “

II”

allelic form (w1 allele) represented by SEQ ID NO;

2;

(ii) determining whether the allelic state of the F₂ soybean plant comprises the T Locus “

CC”

or “

TT”

allelic form of the molecular marker represented by SEQ ID NO;

8 (M0243191);

(iii) determining whether the allelic state of the F₂ soybean plant comprises the Td Locus “

II”

allelic form represented by SEQ ID NO;

13 or the Td Locus “

DD”

allelic form represented by SEQ ID NO;

14;

(iv) determining whether the allelic state of the F₂ soybean plant comprises the R locus “

AA”

or “

TT”

allelic form of the molecular marker represented by SEQ ID NO;

19 (M0100925); and

(v) determining the allelic state for the haplotype defined by the molecular markers represented by SEQ ID NO;

26 (M0202726), SEQ ID NO;

33 (M0119618), and SEQ ID NO;

40 (M0094170), whether the F₂ soybean plant comprises the L2 Locus “

AA”

or “

TT”

allelic form of the molecular marker represented by SEQ ID NO;

26 (M0202726), whether the F₂ soybean plant comprises the L2 Locus “

AA”

or “

TT”

allelic form of the molecular marker represented by SEQ ID NO;

33 (M0119618), and whether the F₂ soybean plant comprises the L2 Locus “

AA”

or “

GG”

allelic form of the molecular marker represented by SEQ ID NO;

40 (M0094170); and

(g) selecting based on at least the determination of allelic state in (i), (ii), (iii), (iv), and (v) an F₂ soybean plant that is homozygous and not segregating for the determined alleles.

3. The method of claim 2 further comprising self-crossing the selected F₂ soybean plant to generate an F₃ population of soybean plants.

4. The method of claim 3 further comprising determining the allelic state as determined in claim 2 of at least one generated F₃ plant or any progeny or descendent thereof in a successive generation to determine whether the seed lot purity traits of flower, pubescence, hilum, and pod wall color have been fixed and/or to validate visual observations of flower color, pubescence color, pod wall color, and hilum color.