QTLs associated with and methods for identifying shatter resistance in canola
Markers associated with shatter resistance in Brassica are provided. Methods of identifying shatter resistant and susceptible plants, using the markers are provided. Methods for identifying and isolating QTLs are a feature of the invention, as are QTLs associated with shatter resistance in Brassica.
1. A method of producing a Brassica plant or germplasm that exhibits pod shatter resistance, the method comprising crossing a first plant comprising a pod shatter resistance locus with a second plant lacking the pod shatter resistance locus to produce progeny seed for a nucleic acid, screening a population of progeny seed or a progeny plant grown therefrom, wherein the first plant comprises a quantitative trait locus (QTL) on linkage group N4 and detecting in the progeny plant or germplasm at least one allele of the at least one QTL that is associated with the shatter resistance, wherein the QTL is localized to linkage group N4, wherein said linkage group comprises at least one marker that is associated with the resistance to shatter with a statistical significance of p≤0.01, wherein the QTL is localized to a chromosomal interval flanked by and including markers N88514-001-K001 and N88537-001-K001 on linkage group N4; and wherein the marker comprises an allele selected from the group consisting of a C at a position corresponding to 201 of SEQ ID NO: 17, a G at a position corresponding to 151 of SEQ ID NO: 15, an A at a position corresponding to 201 of SEQ ID NO: 25, an A at a position corresponding to 201 of SEQ ID NO: 23, and A at a position corresponding to 101 of SEQ ID NO: 26, an A at a position corresponding to 201 of SEQ ID NO: 22, an A at a position corresponding to 201 of SEQ ID NO: 30, a C at a position corresponding to 201 of SEQ ID NO: 32, a G at a position corresponding to 201 of SEQ ID NO: 37, and a T at a position corresponding to 501 of SEQ ID NO: 14, thereby producing the Brassica plant or germplasm that will exhibit shatter resistance.
2. The method of claim 1 , wherein the marker comprises at least five alleles selected from the group consisting of a C at a position corresponding to 201 of SEQ ID NO: 17, a G at a position corresponding to 151 of SEQ ID NO: 15, an A at a position corresponding to 201 of SEQ ID NO: 25, an A at a position corresponding to 201 of SEQ ID NO: 23, an A at a position corresponding to 101 of SEQ ID NO: 26, an A at a position corresponding to 201 of SEQ ID NO: 22, an A at a position corresponding to 201 of SEQ ID NO: 30, a C at a position corresponding to 201 of SEQ ID NO: 32, a G at a position corresponding to 201 of SEQ ID NO: 37, and a T at a position corresponding to 501 of SEQ ID NO: 14.
3. The method of claim 1 , further comprising detecting at least one marker selected from the group consisting of:
N05943-1-Q1 (SEQ ID NO:10); N06007-1-Q1 (SEQ ID NO:11); N10105-001-Q-001 (SEQ ID NO:12); N08181-1-Q1 (SEQ ID NO:13); N06675-1-Q1 (SEQ ID NO:14); N001KH2-001-Q001 (SEQ ID NO:15); N29313-001-Q001 (SEQ ID NO:16); N88512-001-K001 (SEQ ID NO:17); N88514-001-KO01 (SEQ ID NO:18); N88515-001-K01 (SEQ ID NO:19); N88516-001-KO01 (SEQ ID NO:20); N88517-001-K01 (SEQ ID NO:21); N88518-001-K001 (SEQ ID NO:22); N88519-001-K001 (SEQ ID NO:23); N88520-001-K001 (SEQ ID NO:24); N88521-001-K001 (SEQ ID NO:25); N001KFE-001-Q001 (SEQ ID NO:26); N88522-001-K001 (SEQ ID NO:27); N88523-001-K001 (SEQ ID NO:28); N88524-001-K001 (SEQ ID NO:29); N88525-001-K001 (SEQ ID NO:30); N88529-001-K001 (SEQ ID NO:31); N88530-001-K001 (SEQ ID NO:32); N88531-001-K001 (SEQ ID NO:33); N88533-001-K001 (SEQ ID NO:34); N88535-001-K001 (SEQ ID NO:35); N88536-001-K001 (SEQ ID NO:36); N88537-001-K001 (SEQ ID NO:37).
4. The method of claim 3 , wherein the detecting comprises detecting at least one marker selected from the group consisting of: N88514-001-K001 (SEQ ID NO:18); N88515-001-K001 (SEQ ID NO:19); N88516-001-K001 (SEQ ID NO:20); N88517-001-K001 (SEQ ID NO:21); N88518-001-K001 (SEQ ID NO:22); N88519-001-K001 (SEQ ID NO:23); N88520-001-K001 (SEQ ID NO:24); N88521-001-K001 (SEQ ID NO:25); N001KFE-001-Q001 (SEQ ID NO:26); N88522-001-K001 (SEQ ID NO:27); N88523-001-K001 (SEQ ID NO:28); N88524-001-K001 (SEQ ID NO:29); N88525-001-K001 (SEQ ID NO:30); N88529-001-K001 (SEQ ID NO:31); N88530-001-K001 (SEQ ID NO:32); N88531-001-K001 (SEQ ID NO:33); N88533-001-K001 (SEQ ID NO:34); N88535-001-K001 (SEQ ID NO:35); N88536-001-K001 (SEQ ID NO:36); and N88537-001-K001 (SEQ ID NO:37).
5. The method of claim 3 , further comprising detecting a second marker located in a different linkage group.
6. The method of claim 1 , wherein the plant is Brassica napus; Brassica juncea; Brassica rapa; Brassica oleracea ; or Brassica carinata.
7. The method of claim 6 , wherein the plant is Brassica napus (canola).
8. The method of claim 7 , wherein the plant is spring canola.
9. The method of claim 7 , wherein the plant is winter canola.
10. The method of claim 7 , wherein the plant is semi-winter canola.
11. A method of producing an F1 hybrid seed, wherein the F1 hybrid plant derived from the F1 hybrid seed is exhibits shatter resistance, the method comprising cross pollinating the identified plant or progeny thereof of claim 1 with a second plant, wherein the second plant lacks the at least one allele of the at least one QTL detected in the identified plant.
12. A method of marker assisted selection (MAS) of a quantitative trait locus (QTL) associated with shatter resistance in Brassica , the method comprising the steps of:
(a) producing the Brassica plant according to claim 1 ;
(b) crossing the Brassica plant with a different Brassica plant to produce progeny;
(c) evaluating the progeny for the allele associated with the shatter resistance; and
(d) selecting progeny plants that possess the allele.
13. The method of claim 12 , wherein the Brassica plant of step (a) is a member of a segregating population.
14. The method of claim 12 , wherein the marker assisted selection is performed using high throughput screening.
15. A method of producing a Brassica plant or germplasm that exhibits pod shatter resistance, the method comprising:
a) isolating at least one nucleic acid from a Brassica plant selected from a population of Brassica plants;
b) detecting by way of amplifying marker loci or portions thereof from the nucleic acid of a), thereby producing a plurality of amplicons for pod shatter resistance alleles located on maize chromosome 4 and further located within and including markers N05943-1-Q1 and N06675-1-Q1, wherein the amplicons comprise at least five alleles favorable for shatter resistance selected from the group consisting of a C at a position corresponding to 201 of SEQ ID NO: 17, a G at a position corresponding to 151 of SEQ ID NO: 15, an A at a position corresponding to 201 of SEQ ID NO: 25, an A at a position corresponding to 201 of SEQ ID NO: 23, an A at a position corresponding to 101 of SEQ ID NO: 26, an A at a position corresponding to 201 of SEQ ID NO: 22, an A at a position corresponding to 201 of SEQ ID NO: 30, a C at a position corresponding to 201 of SEQ ID NO: 32, a G at a position corresponding to 201 of SEQ ID NO: 37, and a T at a position corresponding to 501 of SEQ ID NO: 14;
c) selecting a first plant from the population of a) based on the presence of the at least five alleles detected in b);
d) crossing the first plant with a second plant, wherein the second maize plant does not have in its genome at least one of the at least five alleles favorable for shatter resistance; and
e) producing a progeny plant having improved pod-shatter resistance from the cross of d) wherein said progeny plant comprises the at least five alleles favorable for shatter resistance detected in b).