Maize cytoplasmic male sterility (CMS) S-type restorer Rf3 gene, molecular markers and their use
View Patent ↗The present disclosure provides a method for selecting a plant comprising a functional restorer gene for maize S-type cytoplasmic male sterility comprising the steps of (a) screening a population of plants for at least one marker nucleic acid, wherein the marker nucleic acid comprises an allele linked to the functional restorer gene for maize S-type cytoplasmic male sterility; (b) detecting the marker nucleic acid; (c) identifying a plant comprising the marker nucleic acid; and (d) selecting the plant comprising the marker nucleic acid, wherein the plant comprising the marker nucleic acid further comprises the functional restorer gene for maize S-type cytoplasmic male sterility. The present disclosure also provides methods for restoring fertility in a progeny of an S-type cytoplasmic male sterile plant and methods for transferring an Rf3 gene into a progeny plant.
1. A method for restoring fertility in a maize plant, the method comprising the steps of:
(a) crossing a female maize plant with a male maize plant to generate a population of progeny maize plants,
wherein the female maize plant is an S-type cytoplasmic male sterile maize plant, and
wherein the male maize plant possesses a functional Rf3 restorer gene for S-type cytoplasmic male sterility;
(b) screening the population of progeny maize plants to identify a fertile progeny maize plant comprising marker nucleic acid Mo17-14388 comprising an allele linked to the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility by extracting nucleic acids from the progeny plants and detecting the marker nucleic acid Mo17-14388;
(c) selecting the fertile progeny maize plant comprising the marker nucleic acid Mo17-14388 comprising the allele linked to the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility; and
(d) propagating the fertile progeny maize plant, wherein the fertile progeny maize plant comprises the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility.
2. A method for restoring fertility in a maize plant, the method comprising the steps of:
(a) crossing a female maize plant with a male maize plant to generate a population of progeny maize plants,
wherein the female maize plant is an S-type cytoplasmic male sterile maize plant, and
wherein the male maize plant possesses a functional Rf3 restorer gene for S-type cytoplasmic male sterility;
(b) screening the population of progeny maize plants to identify a fertile progeny maize plant comprising marker nucleic acid DASCMS-SRf39 comprising an allele linked to the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility by extracting nucleic acids from the progeny plants and detecting the marker nucleic acid DASCMS-SRf39;
(c) selecting the fertile progeny maize plant comprising the marker nucleic acid DASCMS-SRf39 comprising the allele linked to the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility; and
(d) propagating the fertile progeny maize plant, wherein the fertile progeny maize plant comprises the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility.
3. The method of claim 1 , wherein the marker nucleic acid Mo17-14388 is selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 12, and SEQ ID NO: 23, and any combination thereof.
4. The method of claim 2 , wherein the marker nucleic acid DASCMS-SRf39 is selected from the group consisting of SEQ ID NO: 86, SEQ ID NO: 87, and SEQ ID NO: 88, and any combination thereof.
5. The method of claim 1 , wherein the marker nucleic acid Mo17-14388 is located on chromosome 2 within 8.3 Mb of the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility.
6. The method of claim 1 , the method further comprising introducing the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility into the male plant.
7. The method of claim 6 , wherein the introducing is selected from the group consisting of transformation, crossing, backcrossing, homologous recombination, and mutagenesis.
8. The method of claim 1 , wherein the progeny maize plant is a hybrid maize plant.
9. The method of claim 8 , wherein the hybrid maize plant belongs to the Stiff Stalk heterotic group.
10. The method of claim 1 , said screening comprising the steps of:
isolating nucleic acid molecules from the population of progeny maize plants;
contacting the isolated nucleic acid molecules with a set of oligonucleotides; and
amplifying the isolated nucleic acid molecules and the oligonucleotides to produce an amplicon, wherein the amplicon comprises a detectable signal that is indicative of the presence of the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility.
11. The method of claim 6 , wherein the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility consists essentially of SEQ ID NO: 92.
12. The method of claim 11 , wherein the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility is comprised in an organism selected from the group consisting of a plant, a yeast, a bacterium, and a virus.
13. The method of claim 12 , wherein the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility is comprised in a plant cell.
14. The method of claim 9 , wherein the female maize plant or the male maize plant of the hybrid maize plant belongs to the Stiff Stalk heterotic group.
15. The method of claim 2 , wherein the marker nucleic acid DASCMS-SRf39 is located on chromosome 2 within 8.3 Mb of the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility.
16. The method of claim 2 , wherein the marker nucleic acid DASCMS-SRf39 is located on chromosome 2 within 1.3 Mb of the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility.
17. The method of claim 2 , wherein the marker nucleic acid DASCMS-SRf39 is located on chromosome 2 within 0.5 Mb of the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility.
18. The method of claim 2 , wherein the marker nucleic acid DASCMS-SRf39 is located on chromosome 2 within 100 kb of the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility.
19. The method of claim 2 , the method further comprising introducing the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility into the male plant.
20. The method of claim 19 , wherein the introducing is selected from the group consisting of transformation, crossing, backcrossing, homologous recombination, and mutagenesis.
21. The method of claim 2 , wherein the progeny maize plant is a hybrid maize plant.
22. The method of claim 21 , wherein the hybrid maize plant belongs to the Stiff Stalk heterotic group.
23. The method of claim 2 , said screening comprising the steps of:
isolating nucleic acid molecules from the population of progeny maize plants;
contacting the isolated nucleic acid molecules with a set of oligonucleotides; and
amplifying the isolated nucleic acid molecules and the oligonucleotides to produce an amplicon, wherein the amplicon comprises a detectable signal that is indicative of the presence of the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility.
24. The method of claim 19 , wherein the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility consists essentially of SEQ ID NO: 92.
25. The method of claim 24 , wherein the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility is comprised in an organism selected from the group consisting of a plant, a yeast, a bacterium, and a virus.
26. The method of claim 25 , wherein the functional Rf3 restorer gene for maize S-type cytoplasmic male sterility is comprised in a plant cell.
27. The method of claim 22 , wherein the female maize plant or the male maize plant of the hybrid maize plant belongs to the Stiff Stalk heterotic group.