The present invention relates to methods for providing cytoplasmic male sterile Petroselinum plants, cytoplasmic male sterile Petroselinum crispum plants and to seeds, cells, tissues and plant parts thereof. Specifically the present invention relates to a method for providing a cytoplasmic male sterile Petroselinum crispum plant comprising: (a) providing first protoplasts obtained from a plant selected from the group consisting of Daucus carota L., Foeniculum vulgare Mill., Apium graveolens L., and Pastinaca sativa L., wherein the first protoplasts have a substantially inactivated nuclear genome and a substantially non-modified cytoplasm; (b) providing second protoplasts obtained from Petroselinum crispum wherein the second protoplasts have a substantially inactivated cytoplasm and a substantially non-modified nuclear genome; (c) fusing said first and second protoplasts; and (d) obtaining from the fusion product of said first and second protoplasts a cytoplasmic male sterile Petroselinum crispum plant.

The present invention relates to cytoplasmic male sterile (CMS) Cichorium plants and especially to cytoplasmic male sterile (CMS) green chicory plants; cytoplasmic male sterile (CMS) radicchio rosso plants; cytoplasmic male sterile (CMS) red leaved chicory plants, cytoplasmic male sterile (CMS) Treviso plants, cytoplasmic male sterile (CMS) white chicory plants, cytoplasmic male sterile (CMS) sugar loaf plants, cytoplasmic male sterile (CMS) Belgian endive plants, cytoplasmic male sterile (CMS) witloof plants, cytoplasmic male sterile (CMS) Catalogna plants, cytoplasmic male sterile (CMS) C. intybus var. foliosum plants, cytoplasmic male sterile (CMS) C. endivia plants and cytoplasmic male sterile (CMS) C. intybus L. var. sativum plants. The present invention further relates to methods for identifying cytoplasmic male sterile (CMS) Cichorium plants and mitochondrial nucleic acid sequences providing cytoplasmic male sterility (CMS) in Cichorium plants.

The present disclosure relates to a fertility gene and the use thereof, and relates to the biotechnology field, particularly to a method of plant hybrid breeding including creation of a sterile line and preparation of hybrid seeds, more particularly to a fertility gene FL2, a mutant thereof and use thereof in hybrid breeding.

The present disclosure relates to a fertility gene and the use thereof, and relates to the biotechnology field, particularly to a method of plant hybrid breeding including creation of a sterile line and preparation of hybrid seeds, more particularly to a fertility gene FL2, a mutant thereof and use thereof in hybrid breeding.

Methods for increasing hybrid seed production are provided. Increased hybrid seed production is achieved through higher outcrossing rates in cytoplasmic male sterile (CMS) lines of rice by introgressing the long stigma trait of Oryza longistaminata. CMS lines having higher outcrossing rates capable of high hybrid seed set are also provided.

The present invention relates to non-transgenic and transgenic plants, preferably crop plants, having biological activity of a haploid inducer and comprising a polynucleotide which comprises a nucleotide sequence encoding a centromer histone H3 (CENH3) protein, wherein the polynucleotide comprises at least one mutation causing an alteration of the amino acid sequence of the CENH3 protein, and to a part of the part. Further, the invention provides methods of generating the inducer plants, methods of generating haploid and double haploid plants using the inducer plants as well as methods of facilitating cytoplasm exchange.

The present invention concerns plants, seeds and cells of the genus Diplotaxis having cytoplasmic male sterility, and more particularly plants, seeds and cells of the species Diplotaxis tenuifolia. The cytoplasmic male sterility is preferably that imported from Raphanus sativus, known as Ogura sterility. The invention also concerns methods for obtaining Diplotaxis tenuifolia plants carrying cytoplasmic male sterility, as well as various uses for the cytoplasmic male sterility of the plants of the invention.

Provided is a method for producing a rice F1 seed, including crossing a rice male sterile line of Koshihikari containing one or more genes selected from the group consisting of the sd1 gene, the Gn1 gene and the hd1 gene derived from Oryza sativa L. cultivar Habataki, or a rice male sterile line exhibiting semi-waxiness as a seed parent, with a rice fertility restorer line as a pollen parent, and collecting the first filial generation seed (F1 seed) from the post-crossing seed parent; and a rice male sterile line containing one or more genes selected from the group consisting of the sd1 gene, the Gn1 gene and the hd1 gene derived from Oryza sativa L. cultivar Habataki.

The present disclosure relates to a fertility gene and the use thereof, and relates to the biotechnology field, particularly to a method of plant hybrid breeding including creation of a sterile line and preparation of hybrid seeds, more particularly to a fertility gene FL2, a mutant thereof and use thereof in hybrid breeding.

A newly identified protein that is encoded by a polynucleotide sequence associated with cytoplasmic male sterility restorer activity (Rf3) is described. The cytoplasmic male sterility restorer gene can be inserted through breeding introgression into plant genomes to restore cytoplasmic male sterility in plants. Further applications of the newly identified polynucleotide sequence associated with cytoplasmic male sterility restorer activity include a mutation (rf3) which results in cytoplasmic male sterility. The cytoplasmic male sterility restorer gene can be inserted through breeding introgression into plant genomes to result in cytoplasmic male sterility in plants. Methods for detecting the cytoplasmic male sterility restorer (Rf3) and the cytoplasmic male sterility (rf3) gene sequences are further described.