EP2114126A2

EP2114126A2 - Production of hybrid lactuca sativa seeds

Info

Publication number: EP2114126A2
Application number: EP08775629A
Authority: EP
Inventors: Hervé MICHEL; Thierry Soussin
Original assignee: Vilmorin SA
Current assignee: Vilmorin SA
Priority date: 2007-03-05
Filing date: 2008-03-05
Publication date: 2009-11-11
Also published as: NZ579489A; BRPI0808266A2; US20100306882A1; WO2008132310A3; FR2913304A1; JP2014168478A; MX2009009498A; IL200649A0; CA2679333A1; CN104472338A; AU2008244195B2; AU2008244195A1; US8716551B2; JP2010519923A; IL200649A; ZA200906117B; RU2009131326A; RU2593940C2; CA2679333C; JP5627894B2

Abstract

The present invention relates to hybrid Lactuca sativa seeds which have a male sterile genotype and which are heterozygous for at least one distinct gene which confers a detectable phenotype on the plants derived from these seeds. The invention also relates to a method for producing hybrid Lactuca sativa seeds, comprising a step of cultivating phenotypically male-sterile plants and phenotypically male-fertile plants in a closed medium, a step of pollinating by means of dipterans introduced into the closed medium at the time the plants are flowering, and a step of harvesting the seeds produced by the male-sterile plants.

Description

PRODUCTION OF LACTUCA SATIVA HYBRID SEEDS

The present invention relates to hybrid lettuce (Lactuca sativa) seeds, as well as to a process for producing said seeds. The invention also relates to hybrid Lactuca sativa plants, as well as hybrid Lactuca sativa plant cells.

Reasons for producing large-scale hybrid plant seeds include heterosis (or hybrid vigor), homeostasis (stability of the plant in different environments), the possibility of accumulating resistance genes to insects, fungi, bacteria or viruses, or adaptation to abiotic stresses, such as, for example, resistance to extreme temperatures, that is to say temperatures below 5 ° C or above 30 ° C. ⁰ C, or resistance to low light. It has been found that in Lactuca sativa (cultured lettuce), it is impossible or very difficult to combine certain resistance genes in a homozygous line, the genes in question being located on the same locus (one on each allele), or on very close loci. The production of hybrid F1 hybrid lettuces would be of great interest, in particular by allowing the production on a commercial scale, of hybrids combining several genes of agricultural interest co-dominant or dominant borne by the different alleles of the same locus or locus. very close. The genus Lactuca comprises more than 100 species, including Lactuca sativa (cultivated species), Lactuca saligna (wild species), Lactuca serriola (wild species) and Lactuca virosa (wild species). Lactuca sativa is a diploid species (2n = 18), largely self-pollinated, with 98% self-pollination. The stamens (male organs) are grouped and form a staminal tube in which open the pollen sacs of the anthers. The pistil (female organ) consists of an ovary, a style, and a bifid stigma. At the opening of the flower, the style extends inside the staminal tube, so the stigma is covered with pollen and the plant is self-fertilized. A Lactuca sativa plant usually gives 0.5 to 6 grams, or even up to 10 grams of seeds depending on the growing conditions, with each gram generally having 600 to 1000 seeds.

A typical technique for large-scale hybrid plant production is to cultivate the two varieties used as "relatives" in close proximity to each other and to use insects for pollination. Male sterility to avoid contamination due to self-pollination. The seeds are then harvested on the male-sterile parent.

This technique makes it possible to accumulate genes of interest present in homozygous form in each of the parents while maintaining plot homogeneity, the F1 generation presenting a 100% homogeneous phenotype at the harvest stage (before the opening of the flowers).

It turns out that it is very difficult to produce hybrid lettuce (Lactuca sativa) on a large scale by this technique. Indeed, the Lactuca sativa flower opens only once, for a period of only a few hours, for example from one to four hours, at a time of the day (early morning) during which the insects classical pollinators such as some species I \> W v »fc w" *

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bees (Apis mellifera) or bumble bees (Bombus spp.) are not active.

The pollination of Lactuca sativa is not done through the wind.

The identification of a pollinator insect that can be used for the production of hybrid lettuces thus faces many difficulties, in particular: the duration of opening of the flowers is both short and morning, which makes it difficult to identify an insect visiting these flowers; the flowers open only once, therefore the pollinating insect chosen must be an insect visiting the flowers every day to ensure that a maximum number of sterile male flowers are pollinated.

Moreover, the production of F1 hybrids requires the availability of a "male" line and a "female" line. The "female" line can be obtained by manual castration of the plant. However, in the case of lettuce, each flower opens only once and for a very short time (a few hours), this method can hardly be implemented on a commercial scale because of the hand of very important work that it would require.

The "female" line can also be obtained through the introduction of gene-type (or nuclear) or cytoplasmic sterility, manifested by the absence of anthers, empty anthers or non-viable pollen. This sterility is transmitted to the offspring partially in the case of nuclear (or gene) sterility, or totally in the case of cytoplasmic sterility. In their works, Goubara & Takasaki {Appl. Entomo. Zool. 38 (4): 571-581, 2003 [I]) conducted open and closed field experiments to identify potential pollinating insects that could be used for the production of hybrid Lactuca sativa lettuce. Among 22 insects observed (21 species of bees and one species of nectar-eating maggot, Syrphidae Eristalis tenax), the bee Lagioglossum villosulum trichopsis was selected as the best pollinator.

Goubara & Takasaki (Applying Entomology, Zool 39 (1): 163-169, 2004

[2]) also conducted small-scale hybridization assays between lettuce carrying a male sterility gene and a closed male-fertile lettuce in the presence of the bee Lagioglossum villosulum trichopse. The authors state that they have obtained F1 hybrid lettuce, but with a very low yield.

No other hybrid Lactuca sativa production experiment using a pollinating insect is known at this time.

To date, no variety of hybrid lettuce F1 is produced on a commercial scale.

According to the invention, the following terms are understood as follows:

By culture lettuce is meant the species Lactuca sativa. There are five main cultigroups of cultivated lettuce (see Figure 1): Lactuca sativa var. angustana (asparagus lettuce); Lactuca sativa var. capitata (head lettuce, lettuce butter); Lactuca sativa var. crispa (Batavia or Iceberg lettuce); Lactuca sativa var. longifolia (romaine lettuce) and Lactuca sativa var. acephala (curly lettuce, lettuce to be cut). The invention encompasses the use of each of these different types of lettuce.

- Pollination refers to transporting pollen from the anther to the stigma of the same or another flower. This sexed system is the preferred method of reproduction of flowering plants (angiosperms and gymnosperms). It allows the pollen grain to reach the stigma, then form through the style a pollen tube leading to the egg to fertilize it. By self-pollination, we mean the pollination of an individual or a biotype by its own pollen, the resulting individuals are said to be self-pollinated. - The term autogamy refers to the ability of a plant to self-pollinate, both gametes coming from the same individual.

The term allogamy refers to the phenomenon in which the flowers of an individual are pollinated by pollen from one or more other individuals.

- By insect pollinator, we mean an insect (among others bees, butterflies, Diptera or some beetles) which, exploring the flowers (for example in search of nectar) rubs with the stamens, collecting some grains of pollen that he will eventually leave on another flower.

The term locus refers to the location of a gene or allele on a chromosome. - By alleles means variants within a species, a gene located at a given chromosomal location (locus). Different alleles of a gene give rise to different expressions of a character.

Cluster means two or more genes positioned close to each other on the same chromosome. The clusters of resistance genes identified in lettuce have been described by Kesseli et al. [12].

By dominant gene is meant a gene that confers a phenotype, whether it is present on both chromosomes of the pair or on only one. By recessive gene is meant a gene which confers a phenotype only when it is present on each of the two homogeneous chromosomes.

By codominance is meant the property of two genes alleles to express one and the other, in the phenotype, the characters they determine. In a heterozygous subject carrying two codominant allele genes, the genotype will be completely expressed in the phenotype with regard to the information carried by these genes.

By heterozygote is meant a cell or an individual that has two distinct allelic genes on a specific locus of the same pair of chromosomes.

By homozygote is meant a cell or an individual that has two identical allelic genes on a specific locus of the same pair of chromosomes.

Hybrid means the product of the cross between individuals of different genetic makeup, preferably of the same species.

By F1 hybrid is meant the first generation resulting from a cross between individuals of different genetic makeup. As a result, F1 hybrids are heterozygous for at least one gene. yo / uuu 1

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By backcross (or return cross, or "backcross"), we mean the crossing between a hybrid and one of his parents.

By cultivar, we mean a variety.

By genotype, we mean all the genetic material carried by an individual, which constitutes his hereditary heritage.

The term phenotype refers to the set of apparent morphological or functional characteristics of an individual, which correspond to both the expressed part of the genotype and phenomena determined by the external environment. By phenotype of agricultural interest, is meant a phenotype, resulting for example from a cross between two homozygous genotypes, having characteristics of interest from the agricultural point of view, such as, inter alia, the accumulation of resistance characters to different pathogens or insects, hybrid vigor (that is, the average level of one trait of the hybrid being greater than the mean level of both parents), homeostasis, adaptability to abiotic stresses, characteristics morphological characteristics such as color, shape, flexible or rigid nature of the leaves, nutrient composition or taste qualities of the plant.

By heterosis or hybrid vigor, we mean the phenomenon according to which a hybrid F1 is significantly superior to the best of its parents as to one or more characters, especially as regards vigor. rei / EN 2008/000 289

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Homeostasis refers to the ability of a plant to adapt to its environment or even to several environmental characteristics.

- The term male sterile means a plant unable to reproduce by self-pollination, because of sterility of the male elements of the flowers. For example, the pollen may not be functional, or there may be structural abnormalities of the male reproductive organs, for example at the anther feeder (tapetum).

Cytoplasmic male sterility means sterility that is homogeneously transmitted by the mother according to cytoplasmic inheritance. - By nuclear male sterility (or gene) means Mendelian inheritance sterility carried by the DNA of the nucleus, which may be either dependent on a recessive gene or dependent on a dominant gene. Monogenic male sterility means male sterility carried by a single gene.

By plurigenic male sterility is meant male sterility carried by several genes.

Resistance means the ability of a variety to restrict the growth and development of a particular pathogen or pest and / or the damage they cause, in comparison with susceptible varieties and under similar conditions, environmental and pressure levels of this pathogen or pest. These varieties may, however, express some symptoms of the disease or some damage in case of strong pressure of this pathogen or this pest. UUU £ 0 9

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Standard or high resistance refers to the ability of a variety to severely restrict the growth and development of a particular pathogen or pest under normal pressure conditions, in comparison with susceptible varieties. These varieties may, however, express symptoms or damage under severe pressure from this pathogen or pest. Intermediate or moderate resistance refers to the ability of a variety to restrict the growth and development of a specific pathogen or pest, but may express more symptoms or damage in comparison to high / standard resistance varieties. . Intermediate resistance varieties will show less severe symptoms or damage than those observed on susceptible varieties under similar environmental and / or pathogen or pest pressure conditions.

Molecular marker means a specific DNA fragment that can be identified within the complete genome of an individual and that can be used to locate a gene of interest or to verify whether an individual has inherited a particular characteristic of a gene. parent organism. It may or may not be a coding sequence. In a genetic cross, the gene of interest will generally remain linked to the molecular marker. The detection of the molecular marker then makes it possible to select the individuals presenting the gene of interest without it being necessary to know the sequence of this gene.

In the agronomic field, the use of molecular markers makes it possible to quickly test the plants being selected and to retain those that possess the * WWV & W »

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characteristics sought. In some cases, the presence of markers associated with a character, allows the breeder to overcome certain tests or phenotypic observations. In particular, the use of a molecular marker specific for a male sterility gene, preferably a dominant male sterility gene, allows an early selection, before flowering, of the male sterile plants. This selection makes it possible to eliminate fertile male plants that may be part of the plant population used as supposedly "female" parents (sterile males) for the production of hybrid seeds, for example in the case where a dominant gene of male sterility is used, and therefore to reduce the risk of contamination related to the self - fertilization of these fertile male plants.

The subject of the present invention is seeds, plants and cells of hybrid Lactuca sativa plants characterized in that they have a sterile male genotype, and are heterozygous for at least one gene not involved in male sterility and conferring a detectable phenotype on the subject. plant.

Male sterility carried by seeds, plants or plant cells Lactuca sativa, may be of nuclear or cytoplasmic origin. In the case where it is cytoplasmic, sterility is transmitted by the female parent. It is often due to an interaction between the mitochondria present in the cytoplasm and nuclear genes. Cytoplasmic male sterility is characterized by the appearance of progeny with a sterile male 100% phenotype in the absence of a fertility-restoring gene in the male parent genome. Male fertility can be restored at the offspring level by the presence of a gene fertility restorer (Rf) in the genome of the "male" parent.

More particularly, the invention relates to the case where the sterile male genotype involves at least one nuclear gene and wherein the seed, the cell or the plant is heterozygous for the gene (s) at the origin of the male sterility. Nuclear male sterility is caused by one or more genes of male sterility transmitted by the DNA of the nucleus, this or these genes being able to be dominant or recessive.

Among these genes of male sterility, there is notably the dominant nuclear Ms7 gene described by Ryder

(J.Amer.Soc.Hort.Sci 96 (6) 826-828, 1971 [8]). Sterile male plants are heterozygous, Ms7ms7. Fertile plants are homozygous ms7ms7. Obtaining homozygotes dominant Ms7Ms7 remains very difficult or impossible. Moreover, according to Ryder, the dominance of this male sterility is a hindrance to the usefulness of this gene for the production of hybrid lettuce. A sample of Lactuca sativa seeds obtained by the process of the present invention, deposited at NCIMB (NCIMB Ltd., Ferguson Building, Craibstone Estate, Bucksburn, Aberdeen, A21 9YA, Scotland, UK) on February 13, 2007 under accession number NCIMB 41470, is a source of the Ms7 gene. Moreover, the RAPD BA05-675 molecular marker (SEQ ID 2) developed by the inventors has a particular interest in helping the selection of male sterile lettuce plants Ms7, insofar as it allows the establishment of a molecular test at an early stage before flowering to identify the sterile male plants that will be used for the next crossing. The detection of this marker, the sequence of which is shown in FIG. 8, makes it possible to identify a sterile male plant in 96% of cases on average, all types of lettuce combined (Table 18).

Three recessive male sterility genes, ms1, ms2, and ms3, have also been identified by Lindqvist (Heriditas 46: 387-470, 1960 [3]), and three others, ms4, ms5, and ms6, by Ryder (Proc. Soc Hort Sci 83: 585-595, 1963 [6], Proc.Am.Soc.Hr. Sci 91: 366-368, 1967 [7]). However, in his 1979 book {Leafy Salad Vegetables, p. 30 [9]), Ryder states that since the sterility genes ms1, ms2, ms3, ms4, ms5, ms6 and Ms7 are all nuclear, it is unlikely that they could be used to produce F1 hybrids. the inventors have successfully obtained seeds, plants and hybrid cells using male sterility of nuclear origin.

Nuclear male sterility can be plurigenic or monogenic. In the case where it is plurigenic, it can for example be obtained by means of a complex of recessive genes, for example by combining the genes ms1, ms2 and ms3 mentioned above. The invention preferably relates to the case where the male sterility is monogenic.

Nuclear male sterility may be dominant or recessive. In particular the invention relates to the case where the male sterility gene is monogenic dominant. More particularly, the invention relates to the case where the male sterility is conferred by the dominant Ms7 gene mentioned above. Preferably, the genome of the seeds, plants or cells of the invention comprises a double-stranded DNA sequence of 650 to 700 nucleotides, for example 655 to 695, 660 to 690, 665 to 685, 670 to 680, 673 to 677 nucleotides, or 674, 675 or 676 nucleotides, the 5 'ends of each of the two strands begin with the sequence '5' TGCGTTCCAC 3 '"(SEQ ID NO: 1). According to one preferred embodiment, the genome of seeds, plants or cells of the invention comprises the nucleotide sequence illustrated in FIG. 8 (SEQ ID No. 2) or a sequence derived from this sequence in which 1 to 10, preferably 1 to 5 or 1 to 3 nucleotides have been replaced by others, deleted or added.

The invention preferably relates to the case where the detectable phenotype conferred by the heterozygous gene (s) is a phenotype of agricultural interest, such as, for example, resistance to different pathogens or insects, hybrid vigor (or heterosis), homeostasis.

(stability of the plant in different environments), adaptation to abiotic stress such as for example extreme temperatures or low luminosities, a yield superior to that of the varieties from which a hybrid is derived, the morphological characteristics such as the color, the shape, size, softness or stiffness of the leaves, the nutrient composition or taste qualities of the plant.

In addition, the inventors have observed that, surprisingly, the hybrid plants derived from the seeds according to the invention resulting from various crosses between different lettuces grown in winter and in the temperate region had a faster growth, reaching maturity on average 7 at 10 days earlier than the parent plants cultivated under the same conditions. It has also been observed that the homogeneity of intraparocal development of F1 hybrids (on about 30 plants per plot) is greater than that of plots of lineages (parent plants). In other words, the number of plants with a delay or an advance in their development compared to all the plants of the same plot is significantly lower on the F1 hybrid plots than on the plots of lineage varieties. Therefore, these characteristics of the F1 hybrids not only shorten the lettuce production cycles but also condense the crop over a shorter period of time.

The phenotype of agricultural interest can in particular be conferred by one or more standard or intermediate resistance genes to infection by a virus, a bacterium, an insect or a fungus, and more particularly still to one of the following fungi: Bremia lactucae , Fusarium oxysporum, Sclerotinia minor or sclerotorum, Botrytis cinerea, Rhizitonia solani, Microdochium panattonianum, Verticiulium dahliae, Erysiphe chicocearum or Pithium tracheiphilum, - one of the following insects: Nasonovia ribisnigri, Myzus persicae, Macrosiphum euphorbia, Nematodes pratylenchus or meloidogyne, leafminers Liriomyza huidobrensis or Pemphigus busarius; at one of the following bacteria: pseudomonas, xanthomonas or rhizomonas; or one of the following viruses: LMV (lettuce mosaic virus), TSWV (tanned tomato blotch virus), "Big vein" (or large vein disease composed of LBW viruses). large rib of lettuce) and MILV (Mirafiori lettuce virus), TBSV (tomato stunting virus), LNSV (necrotic lettuce stain virus), TuMV (turnip mosaic virus), CMV (cucumber mosaic virus) or BWYV (beet yellows virus). In the case where the phenotype of agricultural interest is conferred by one or more standard or intermediate resistance genes to an infection by a virus, a bacterium, an insect or a fungus, the said standard or intermediate resistance gene conferring this phenotype can in particular, be chosen from the Bremia resistance genes Dm10, R17, Dm5, Dm8, R36, R37 (genes located on cluster 1 of Lactuca sativa), DmI, Dm2, Dm3, Dm6, Dml4, Dml5, Dml6 and Dml8 (genes located on cluster 2 of Lactuca sativa), Dm4, Dm7, DmI1, R38 (genes located on cluster 4 of Lactuca sativa); or the TuMV resistance gene Tu located on cluster 1; the Nr Nasonovia resistance gene located on cluster 2; or among the LMV resistance mol1 and mol2 genes located on the cluster 4. The clusters 1, 2 and 4 cited above are in particular defined by Michelmore RW (Plant Pathol., 1987, vol 36, no 4 : 499-514 [4], Theor Appl. Genet., 1993, vol 85, no 8: 985-993 [5]). The phenotype of agricultural interest may be more particularly conferred by one or more standard or intermediate resistance genes to one of the main diseases affecting lettuce, Brβmia lactucae, a fungus which causes on the inner side of the blade a whitish down and powdery. Bremia also has a high potential for adaptation which leads to the emergence of new breeds capable of circumventing the resistance already introduced by breeders in the varieties.

The invention still more preferably relates to the case where the seeds, plants or cells of Lactuca sativa plants are heterozygous for at least two genes not involved in male sterility and conferring a detectable phenotype on the plant. Even more preferably, the two or more genes conferring a detectable phenotype on the plant are located on the same cluster, for example on a cluster of resistance genes such as cluster 1, 2 or 4 of Lactuca sativa. The subject of the invention is also a population of Lactuca sativa hybrid seeds having a sterile male genotype, and heterozygous for at least one gene not involved in male sterility and conferring a detectable phenotype on the plants derived from these seeds, possibly having the additional characteristics. seeds described above, such that said population comprises at least 10 ⁵ seeds, preferably at least 10 ⁶ , and even more preferably at least 10 ⁷ seeds. In the case where the seeds are obtained by crossing between two Lactuca sativa plants, one of which ("female" parent) carries a male nuclear sterility conferred by one or more dominant genes, and that the plants used as "female" parents are themselves from a cross, the plants used as "female" parents are necessarily heterozygous for the sterility gene. In order for them to be homozygous for the dominant male sterility gene or genes, the two plants from which the plants used as "female" parents are derived by crossing should themselves be carrying the male sterility gene. if that was the case a cross between these two plants would be impossible. Consequently, the seed population according to the invention resulting from the cross between two types of Lactuca sativa plants, one of which ("female" parent) carries a male nuclear sterility conferred by one or more dominant genes, is composed of , due to the phenomenon of segregation of the chromosomes during meiosis, Lactuca sativa seeds carrying the dominant gene (s) of male sterility, and non-bearing seeds of this or these genes. In the case where the male sterility carried by the "female" parent is monogenic and dominant, the proportion of sterile male seeds is generally at least 40%. 0028 9

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The present invention has notably been carried out following the observation by the inventors that, although diptera are not usual pollinating insects of Lactuca sativa flowers, and are also not known as feeding on their nectar, these insects, especially the species Calliphora vomitaria, Calliphora erythrocephala, and Lucilia caesar, when introduced in excess in a closed environment, act as pollinators of Lactuca sativa.

Also, the subject of the present invention is also the use of insects of the order Diptera for effecting pollination in a closed medium, of sterile male Lactuca sativa plants, by fertile male plants, in particular with a view to obtaining Lactuca sativa hybrid plants. Preferably, the sterile male Lactuca sativa plants used have male sterility carried by a single dominant gene, preferably the male Ms7 sterility mentioned above. The fertile male plants used are preferably Lactuca sativa plants, and even more preferably a cultivar.

The closed medium according to the invention may in particular be a greenhouse, a cage or a tunnel, with an area greater preferably 30 m ² , even more preferably 300 m ² , for example 30 to 1500 m ² or 50 to 300 m ^2. 1000 m ² . The height of the closed medium is normally between 2m and 4m, preferably between 2.5m and 3.5m, for example 3m. It may include ventilation means, watering, temperature control and brightness. Preferably, said closed medium is an enclosure hermetic to insects.

Diptera used should preferably be present at a concentration of at least 100 Diptera per m ² , preferably at least 250 Diptera per m ² , for example 100 to 1000 Diptera per m ² . The concentration may also be determined in number of diptera per m ³ , and is preferably at least 25 diptera per m ³ , preferably at least 50 diptera per m ³ , more preferably at least 75 diptera per m ³ , for example from 25 to 500 Diptera per m ³ or from 75 to 250 Diptera per m ³ .

The subject of the present invention is also a process for obtaining hybrid Lactuca sativa seeds, comprising: a step of culture in a closed medium, of plants

Phytotypically male sterile Lactuca sativa used as "female" parents and phenotypically male fertile Lactuca sativa plants used as "male" parents, close to each other, with one of the two parents having the additional characteristic of be homozygous for a gene conferring on it a detectable phenotype other than male sterility, the other parent not carrying this gene;

a pollination step by dipterans introduced into the closed medium at the time of flowering of the plants at a concentration greater than 100 Diptera per m ² , preferably at least 250 Diptera per m ² ; and a step of harvesting the seeds produced by the sterile male plants.

Preferably, the second parent is also homozygous for at least one gene conferring a detectable phenotype other than male sterility, not worn by the other parent. Preferably, said closed medium is an enclosure hermetic to insects.

It has been found to be better when Diptera are in excess, so their concentration is preferentially, greater than 400 Diptera per m ² , and even more preferably greater than 500 Diptera per m ² .

Diptera can be introduced as eggs, larvae, pupae or adults. They are preferably introduced in the form of pupae.

The diptera used are preferably brachycers, for example cyclopharynic brachycers, more preferably brachycera from the family Muscidae or Calliphorida, for example Calliphora vomitaria, Calliphora erythrocephala or Lucilia caesar. A better yield is normally obtained if the introduction of dipterans is repeated at least once a week, preferably twice a week, for at least 3 to 4 weeks.

Likewise, a better yield is normally obtained if the number of sterile male plants in the closed medium is greater than the number of fertile male plants. The number of sterile male plants in the closed medium, for example is at least 2000, and the number of fertile male plants for example at least 1000.

The implementation of the method according to the invention requires that there is a match of flowering between the two parents. The latter can be obtained by selection on this trait or by appropriate cultural practices.

Preferably, the male sterility of the plants used as female parents is monogenic, dominant and nuclear, and even more preferably conferred by the Ms7 gene.

Preferably, the genome of the plants used as female parents comprises a double-stranded DNA sequence of 650 to 700 nucleotides, for example 655 to 695, 660 to 690, 665 to 8/000289

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685, 670 to 680, 673 to 677 nucleotides, or 674, 675 or 676 nucleotides, whose 5 'ends of each of the two strands begin with the sequence' 5 'TGCGTTCCAC 3'"(SEQ ID NO ^: 1). According to one preferred embodiment, the genome of the plants used as female parents comprises the nucleotide sequence illustrated in FIG. 8 (SEQ ID No. 2) or a sequence derived from this sequence in which 1 to 10, preferably 1 to 5 or another 1 to 3 nucleotides were replaced by others, deleted or added. As explained above, it is not possible, due to the phenomenon of chromosome segregation during meiosis, to obtain by conventional crossing techniques, a homogeneous population of plants used as "female" parents carrying a dominant gene of male sterility. Accordingly, in the case where a dominant male sterility gene is used, the plants used as female parents can be obtained by a method comprising: a crossing step between Lactuca sativa plants heterozygous for a dominant nuclear male sterility gene and fertile male Lactuca sativa plants not carrying sterility genes, a step of culturing seed from said cross, and a step of removing plants having a fertile male phenotype.

The removal step of plants having a fertile male phenotype may for example be carried out manually based on a visible character to distinguish sterile male Lactuca sativa plants from fertile male Lactuca sativa plants. For example, in the case of sterility linked to the Ms7 gene, sorting can be performed using the fact that the capitules of sterile male plants remain open longer than those of the plants.

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fertile males, and sterile male plants do not show pollen.

According to an alternative implementation, the plant elimination step having a fertile male phenotype is performed by means of detecting in a sample of each of the plants the absence of a gene-specific molecular marker. dominant male sterility. For example, it may be a RAPD (Random Amplification of Polymorphic DNA) marker with a length of about 675 base pairs (for example 650 to 700, 655 to 695, 660 to 690, 665 to 685, 670 to 680, 673 to 677, 674, 675 or 676 base pairs) whose 5 'ends of each of the two strands begin with the sequence' 5 'TGCGTTCCAC 3' "(SEQ ID No. 1), such as the BA05 marker. -675 (SEQ ID 2) developed by the inventors or a Sequenced Characterized Amplified Region Marker (SCAR) marker, a Cleaved Amplified Polymorphic Sequence (CAPS) marker, or any other marker generally referred to as STS (Sequence). Tagged Site), developed from this RAPD marker. According to a preferred embodiment, the detection of the presence or absence of a specific molecular marker of a dominant gene of male sterility is carried out before the flowering of the plants used as female parents, preferably at an early stage of growth. plants, for example in the 1 to 5 leaf stage, more preferably in the 1 to 2 leaf stage.

Preferably, the molecular marker used makes it possible to detect sterile male plants with a sensitivity of at least 70%, 75%, 80%, 85%, 95%, 98% or 99%, or 100%, the sensitivity being defined as the ratio of the number of sterile male plants with the molecular marker (true positives) to the sum of the number of true positives and the number of male sterile plants lacking the molecular marker (false negatives) (see Table 17). Preferably also, the molecular marker used makes it possible to detect sterile male plants with a specificity of at least 70%, 75%, 80%, 85%, 95%, 98% or 99%, or else of 100%, the specificity being defined as the ratio of the number of fertile male plants lacking the molecular marker (true negatives) to the sum of the number of true negatives and the number of male fertile plants with the molecular marker (false positives)

(see Table 17).

The MMS (mass of one thousand seeds) of the seeds obtained according to the process of the invention is generally at least 10%, or even at least 20%, or even at least 30% greater than the MMS of the seeds obtained. by self-fertilization of fertile male Lactuca sativa plants used as "male" parents.

The invention also relates to a seed population that can be obtained according to the method described above, and comprising at least 10 ⁵ seeds, preferably 10 ⁶ seeds and even more preferably 10 ⁷ seeds.

Brief description of the drawings Figure 1: Genealogy of Lactuca sativa

Figure 2: arrangement of lettuce used as "male" and "female" parents in trial 1 Figure 3: arrangement of lettuce used as "male" and "female" parents in trial 2 Figure 4: genotyping of the 50 hybrid plants of the test 10: amplification profile of the molecular marker SCW09 after digestion with Taql. The marker SCW09 marks the Dm6 and Dml8 genes of resistance to Bremia lactucae. A = witness Dml8 + / Dml8 +, B = Dml8- / Dml8- control; C = Dm6 + control; D = undigested by Taql.

Figure 5: genotyping of the 50 hybrid plants of the test 10: amplification profile of the molecular marker B1 which marks the Dm3 gene for resistance to Bremia lactucae. A = witness

Dm3 +; B = Dm3- control.

Figure 6: Electrophoretic profile of the primer OPBA05 with the marker BA05-675 (arrow). Agarose gel electrophoresis at 1.0% for 45 h to 190 V. M: 100-bp ladder molecular weight marker (Pharmacia Biotech, ref.

27.4001.01)

Figure 7: Mapping the BA05-675 molecular marker associated with the Ms7 locus in lettuce, Lactuca sativa (distance calculated according to Kosambi function). Figure 8: 5 '-3' nucleotide sequence of BA05-675 marker associated with Ms7 male sterility in lettuce, Lactuca sativa. (SEQ ID 2)

Examples

EXAMPLE 1: PRODUCTION OF HYBRID MILK SEEDS

The sterile male Lactuca sativa plants used in the various assays described below as "female" parents carry the Ms7 sterility gene. These plants come from a 5 ^th generation backcross

(BC5) of a shelter butter lettuce carrying the Ms7 gene (X

Girelle 94-9538-1) obtainable from various research organizations such as INRA, USDA, etc. As the Ms7 gene is dominant, a cross between two plants carrying the Ms7 gene is impossible. Consequently, plants with a male sterility phenotype are necessarily heterozygous for the Ms7 gene and can not be obtained only through the cross between plants Ms7 / ms7 (sterile) and ms7 / ms7 (fertile).

As a result, a purification step is necessary to eliminate fertile male plants. The latter is made possible by the fact that the Ms7 / ms7 plants do not have pollen and the heads of the Ms7 / ms7 plants remain open longer than those of the ms7 / ms7 plants.

Trial 1 As part of this first test:

450 plants Lactuca sativa butters shelter from a 3 ^rd generation backcross (BC3) butters lettuce Ms7 with butter lettuce cultivar Nacre / Cambria Dml8 / R38 (Dml8 resistance genes of cluster 2 and R38 cluster 4) a combination sensitive to Bremia lactucae race 24 (B124), were used as "female" parents (about half of them being sterile males); and 100 Lactuca sativa plants from the BRA butterfly cultivar Dml8 / R37 (Cluster 2 DML8 and Cluster R37 resistance genes), a combination resistant to B124, were used as "male" relatives.

Both parents have a perfect match of flowering which allows fertilization as homogeneous as possible.

The plants were placed in a chamber sealed to insects of 36 m ² (dutch type greenhouse with possibility of control of humidity and temperature, 11m x 3.30 m) as follows (see Figure 2) : plants used as "male" parents, have been arranged in two rows along the edges of the enclosure closed, the plants being spaced 20 cm apart, and the plants used as "female" parents were arranged in seven rows between the two rows of "male" plants, at a distance of 50 cm from them, the plants being spaced 15cm, and the rows of 25 cm.

Sowing was done in week 13 and planting in week 16.

Because of the dominant character of the Ms7 gene, a purification (elimination) stage of the plants used as female parents with a fertile male phenotype was necessary. This step was carried out manually in weeks 26 and 27 using the fact that the Ms7 / ms7 plants do not have pollen and that the heads of the plants Ms7 / ms7 (sterile males) remain open longer than those of the plants ms7 / ms7 (fertile males).

Of the 450 plants used as female parents, 217 were sterile males and were actually used.

Two insect species of the order Diptera and the family Calliphorida were used as pollinating insects: Calliphora vomitaria flies and Calliphora erythrocephala maggots (also called blue flies or meat flies) working at 15 -20 ° C, and - Lucilia caesar flies called 'pinkies' (also called green flies of corpses), working at 20-25 ° C. Insect pollinator contributions were made bi-weekly during weeks 28 to 31 at a rate of 300 flies per m ² per intake.

Harvesting of male sterile plants ("female" parents) and fertile male plants ("male" parents) also used as a selfing control was carried out in week 33.

The plants were dried, beaten, and then the seeds were passed on a pulsed air column to complete the cleaning and remove residual light waste and calibrated in length and width.

A sample of 2,500 seeds obtained in Trial 1 was deposited on February 13, 2007 at NCIMB (NCIMB Ltd., Ferguson Building, Craibstone Estate, Bucksburn, Aberdeen, A21 9YA, Scotland, UK) under accession number NCIMB 41470.

Trial 2 A second similar trial was carried out on a larger scale in a closed, insect-tight enclosure of 336 m ² (length: 56 m, width: 6 m, height: 3 m). As part of this second test:

3000 Lactuca sativa plant butters shelter from a 4 ^th generation backcross (BC4) butter lettuce Ms7 with butter lettuce cultivar

Mother-of-pearl / Cambria Dml8 / R38 in Bremia (B124 sensitive combination), were used as "female" parents (about half of them were sterile males); and

1500 Lactuca sativa plants from a BRA-resistant butterfly cultivar Dml8 / R37 resistant to B124 were used as "male" parents. The plants were placed in the closed chamber in the following manner (see Figure 3): the plants used as "male" parents were arranged in four rows: one row along each edge of the closed chamber ( at 80 cm) and two rows in the center (spaced 20 cm apart), the plants being staggered and spaced 15 cm apart, and the plants used as "female" parents were arranged in eight rows between the rows of plants fertile males, at 65 and 70 cm of these, the plants being spaced 15cm, and the rows of 25 cm.

Sowing was done in week 12 and planting in week 16.

Similar to what was done in Run 1, a purification (elimination) stage of the plants used as female parents with a fertile male phenotype was required. This step was carried out manually in weeks 25 and 26 using the fact that the Ms7 / ms7 plants do not have pollen and that the heads of the plants Ms7 / ms7 (sterile males) remain open longer than those of the plants ms7 / ms7 (fertile males).

Of the 3000 plants used as female parents, 1250 were sterile males and were actually used. 16 plants ms7 / ms7 (fertile males) were however preserved during the purification and self-fertilized under a hermetic enclosure constituted by a net or a canvas not allowing the insects to pass, in order to be used as a witness of self-fertilization . The pollinating insects used are the same as in Trial 1.

Insect pollinator intakes were carried out at weekly intervals during weeks 25 to 29 at a rate of 1100 flies per m ² on average per intake.

At the same time, 10 fertile male (male parents) and 16 fertile ms7 / ms7 plants preserved during the purification stage were self-fertilized under a hermetic enclosure constituted by a net or a canvas that did not allow the insects to pass, in order to serve as self - pollination indicators.

Harvesting of sterile male plants ('female' parents) as well as 10 fertile male (male parents) and 16 fertile 7 ms7 / ms7 plants preserved during the purification stage used as selfing controls was carried out in vitro. week 33. The plants were dried, beaten and then the seeds were passed through a pulsed air column to complete the cleaning and remove residual light waste and calibrated in length and width. A sample of the seeds obtained was sown and the resistance of the plants obtained with B124 was tested according to an official protocol of GEVES (Group of Study and Control of Varieties and Seeds). The plants proved to be resistant to B124. Results of tests 1 and 2

The results of tests 1 and 2 are presented in the tables below.

Table 1: Comparison of seed masses harvested in trials 1 and 2

Table 2: Comparison of the calibrations of hybrid seeds and seeds from inbreeding controls produced in trials 1 and 2

Table 3: Comparison of MMS (masses of thousand seeds) of hybrid seeds and seeds from inbreeding controls produced in trials 1 and 2

Discussion

In the first trial, 730 grams of seeds were obtained from the 217 male sterile Lactuca sativa plants (female parent), giving a yield of 3.36 grams per plant, corresponding to a ratio of 15.30% of the self-contained control. fertilized (male parent).

In the second trial, 7,730 kg of seeds were obtained from 1170 sterile male Lactua sativa plants (female parent), representing a yield of 6.60 grams per plant, corresponding to a ratio of 50% of the average of two self-fertilized controls ("male" parents and "female" female parents, fertile ms / ms preserved during the purification and fertilized under an enclosure hermetic to insects). In the second trial, the rate of useful seeds after calibration of the F1 hybrids is 10% higher than the self-fertilizing control.

In both tests, the MMS (mass of one thousand seeds) of the F1 hybrid is 20-30% greater than the self-fertilizing control.

The plants obtained from the seeds obtained according to the second test are very resistant to B124.

Trials 3 to 8 Six similar trials were launched in parallel with different types of butter and batavia lettuce in 3.3mx 1.1m insect proof cages each containing 8 Lactuca sativa plants used as "female" parents (50% sterile male). , resulting from backcrossing between Lactuca sativa plants carrying the Ms7 gene and fertile Lactuca sativa plants), and 4 fertile male Lactuca sativa plants used as "male" parents, placed in a ventilated greenhouse. Seeding was done in week 22, planting in week 27, sorting between "female" sterile male and fertile male plants at the beginning of flowering in week 31, fly intakes in weeks 32, 33 and 34 due one feed per week for three weeks, about 100 flies / m ² , and harvest in week 37.

Results of tests 3 to 8

- Cage 1: CHARLIN (68/12624) * CHARLIN (butter) 1 female plant: 9.20 gr

1 male plant: 28.30 gr

- Cage 2: CHARLIN (BC / 77) * CHARLIN (butter) 1 female plant: 5.45 gr 1 male plant: 19.40 gr

- Cage 3: BRA 68/12588 (head lettuce) * BRA 68/12588

6 female plants: plant 1 7.00 gr plant 2 2.00 gr plant 3 5.20 gr plant 4 3.40 gr plant 5 9.60 gr plant 6 8.40 average gr: 5.9 gr / plant 1 male plant: 34.40 gr

- Cage 4: BRA 68/12588 * BRA 68/12588 4 female plants: plant 1: 11.95 gr plant 2: 7.15 gr plant 3: 15.90 gr plant 4: 11.90 average gr: 11.25 qr / plant 1 male plant: 29.00 gr

- Cage 5: BVA 68/12553 (batavia shelter lettuce) * BVA 68/12553 5 female plants: plant 1: 3.50 gr plant 2: 1.30 gr plant 3: 2.20 gr plant 4: 1.70 gr plant 5: 4.20 gr average : 3.30 gr / plant 1 male plant: 3.60 gr

- Cage 6: BVA 68/12553 * BVA 68/12553 3 female plants: plant 1: 4.60 gr plant 2: 3.20 gr plant 3: 3.70 gr average: 3.80 gr / plant 1 male plant: 23.40 gr

Discussion The means of production of "female" parents ranged from 3.3g to 11.2g / plant, the Batavia typology (BVA 68/12553) having a much lower yield (about 3.5g / plant) compared to a butter typology ( Charlin, BRA 68/12588) about 8.5 g / plant, which may suggest that there is a strong implication of the typology on the final yield. Trial 9

A new production trial was conducted under small insulated cages 0.40m in diameter, placed in a greenhouse ventilated in the ground.

Seeding was done in week 22, repotting in week 25, sorting between "female" sterile male and fertile male plants at the beginning of flowering in week 30, planting in week 31, fly in weeks 32 , 33 and 34 at a weekly intake for 3 weeks, about 100 flies / m ² , and harvest in week 35. Results

The results obtained are summarized in Tables 4 and 5 below.

Table 4: Seed production by "male" and "female" parents Charlin (shelter butter)

Table 5: Seed production by "male" and "female" parents BVA 68/12553 (batavia) _"

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Discussion

The results are satisfactory insofar as the average production obtained for the batavia lettuce (BVA 68/12553) is about lgr / plant against 1.7 gr / plant for the self-fertilized control, and the average production obtained for the lettuce butter of shelter (Charlin) is about lgr / plant, at the same level as the self-fertilized control.

Test 10: Dm3 / Dml8 cumulation by hybrid combination

Fl hybrid lettuces combining two dominant genes Dm3 and

Dml8 resistance to Bremia lactucae respectively race 24

(B124) and race 23 (B123), belonging to cluster 2 and located on the same locus were obtained according to the method described in the tests described above.

Plants used as "female" parents (06/30443: MS7 / 2INACREXDEVONIAxCAMBRIA) carry the Dml8 and R38 resistance genes. Plants used as "male" parents are sheltering butters of the resistance gene Dm3 (BC: 06/30443 * Rex or BC: 06/30443 *

Melina).

The following five crosses were made:

- 06/30443/01 (MS7 / 21xNACRExDEVONIAxCAMBRIA-01) Dml8 / R38 * Rex Dm3

- 06/30443/10 (MS7 / 21xNACRExDEVONIAxCAMBRIA-10) Dml8 / R38 Rex Dm3

- 06/30443/02 (MS7 / 2IXNACREXDEVONIAXCAMBRIA- 02) Dml8 / R38 Melina Dm3 - 06/30443/03 (MS7 / 21xNACRExDEVONIAxCAMBRIA-03) Dml8 / R38 Melina Dm3

- 06/30443/04 (MS7 / 2IXNACREXDEVONIAXCAMBRIA- 04) Dml8 / R38 Melina Dm3

Seeds from these five crosses were sown and leaf disc inoculation and molecular marking tests were performed on Fl plants, as well as on "male" (Rex / Melina) and "female" parents.

I - Inoculation tests on leaf discs

Material: The plant material consists of leaf discs 1.5 cm in diameter at the rate of 5 disks per plant and per breed, 10 plants per origin and two Bremia lactucae breeds (B124 which attacks Dml8 / R38 Dm3 confers a resistance, and B123 which attacks Dm3 / R38 cumulation and to which Dml8 confers a resistance). Thus 80 plants were tested in total on two races.

Technique: The leaf discs are inoculated by spraying sporocysts with breeds Bremia B123 and B124 separately.

1 / Collection of leaf discs: Five leaf discs per plant are taken and deposited on a double layer of moistened blotting paper. Each box contains 6 lines of test discs and a sensitive control line. 2 / Inoculation: the amount of inoculum required to inoculate 6 boxes of leaf discs is 11 ml. A stock solution of Tween 80 is prepared at the rate of 4 drops of Tween 80 added to 100 ml of demineralized water. The amount of extraction solution for the inoculum volume is 5 ml of Tween 80 stock solution per 100 ml of inoculum. The inoculum is made by detaching the sporocysts in tap water with 5% tween 80 stock solution. The sporocysts are taken at 1 plant / ml of inoculum, to obtain a concentration of sporocysts close to of 10 ⁸ spores / ml. Filtration is carried out by passing the solution on a wipe in a 250 ml beaker. 3 / Spraying: the inoculation takes place on the same day as the collection of leaf discs. The volume of inoculum solution is measured then the spread boxes are inoculated. The inoculum is uniformly sprayed into fine droplets over the entire surface of each disc. The dishes are closed hermetically and incubated in module at 15 ° C, 14 hours of day, 10 hours of night for 7 days.

Results: The results of the inoculations are presented in Tables 6 to 13 below (S = sensitive, R = resistant). Hybrids from different crosses are resistant to both races B123 and B124, indicating the presence of both cluster 2 Dml8 and Dm3 genes.

Table Female plants »30443 (Dml8 / R38l

MS7 / 21xNACRExDEVONIAxCAMBRIA: Resistant B123 and sensitive B124.

. *

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Table 7: "Male" plants Melina (Dm3): sensitive B123 and resistant B124 (test on 10 plants)

Table 8: Crossover 06/30443/02 * Melina (Dml8 / R38 * Dm3) = MS7 / 2IXNACREXDEVONIAXCAMBRIA-02 * MELINA.

Table 9: Crossover 06/30443/03 * Melina (Dml8 / R38 * Dm3) = MS7 / 2IxNACRExDEVONIAxCAMBRIA- 03 * MELINA.

Table 10: Crossover 06/30443/04 * Melina (Dml8 / R38 * Dm3) = MS7 / 2IXNACREXDEVONIAXCAMBRIA- 03 * MELINA.

Table 11: "male" Rex plants (Dm3): sensitive B123 and resistant B124 (test on 10 plants)

Table 12: Crossover 06/30443/01 * Rex (Dml8 / R38 * Dm3; MS7 / 21xNACRExDEVONIAxCAMBRIA-01 * REX.

Table 13 Crossover 06/30443/10 * Rex (Dml8 / R38 * Dm3) MS7 / 21xNACRExDEVONIAxCAMBRIA-10 * REX.

II - Molecular Marking

The use of 2 molecular markers makes it possible to highlight the accumulation of two closely related genes (located on the same locus), dominant, of resistance to two strains of Bremia lactucae in Lactuca sativa. Method:

1 / Plant material: the plant material consists of leaf discs 1.5 cm in diameter at the rate of one disc per plant. DNA from 5 to 10 plants per genotype (ie 50 .

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plants in total) was obtained from a CTAB / chloroform extraction followed by resuspension in a 0.1X TE solution at a concentration of 5 ng / μl. 2 / Genotyping: markers SCW09 and Bl described respectively by Maisonneuve et al. [10] and Kuang H. et al. [11] were used to genotype the 50 plants (Table 14). The PCR conditions are described in Table 15. The PCR cycles of SCW09 and B1 are respectively:

- 94 ° C / 30s - 94 ° C / 1 min, 60 ° C / 1n, 72 ° C / 2min; 40 cycles - 72 ° C / 5min - 4 ° C;

- 94 ° C / 30s - 94 ° C / lmn, 63 ° C / lmn, 72 ° C / 2min; 40 cycles - 72 ° C / 5min - 8 ° C.

The SCW09 marker was enzymatically digested with the Taq I enzyme prior to the migration step (Buffer IX, BSA IX and Taq I IU). The electrophoresis was carried out on a 2% agarose gel (SCW09) or 1.5% (B1) in a buffer of IX TBE for Ih (B1) at 1:30 (SCW09) with a constant voltage of 220 V. The electrophoretic profiles were revealed by ethidium bromide (BET) staining under a UV lamp.

Table 14: Characteristics of SCW09 and Bl Markers

. %

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Table 15: PCR Conditions for SCW09 and Bl Markers

Results

The results are shown in Table 16 and Figures 4 and 5. The REX and MELINA genotypes have Dml8- / Dml8- and Dm3 + profiles. Genotype 06/30443 has a Dml8 + / Dml8 + and Dm3- profile. All crosses with one or the other parents (REX or MELINA) have profiles Dml8 + / Dml8- and Dm3 + that is resistant for Dml8 and Dm3.

Table 16: Genotyping results with markers SCW09 and Bl (S = sensitive, R = resistant)

EXAMPLE 2 IDENTIFICATION OF A MOLECULAR MARKER OF THE Ms7 GENE

The method for obtaining a molecular marker associated with the Ms7 male sterility in Lactuca sativa (lettuce) described below is given for information only.

1 - Construction of populations for the development of a marker linked to the Ms7 nuclear male sterility in lettuce (L. sativa).

Two populations of different types of lettuce with male Ms7 sterility were performed by backcrossing. Two recurrent fourth-generation (BC4) populations of 200 plants thus obtained were then phenotyped on the "absence of viable pollen" character corresponding to the sterile male phenotype. Two phenotypic groups were identified as fertile male (F) or male sterile (S) at a ratio of 1: 1. This ratio confirms the dominant monogenic nature of male sterility brought by the heterozygous parent at the Ms7 locus.

2 - Extraction of DNA from lettuce plants. DNA extraction was performed according to the modified CTAB protocol (Tomas et al., 1989 [20], Doyle et al., 1990 [15], Edwards et al., 1991 [16]) on young fresh leaves. Fresh leaf disks obtained using a 1.5 ml tube are ground in 500 μl of extraction buffer (0.1M tris-HCl, 0.7M NaCl, 10mM EDTA, 1% CTAB, Mercaptoethanol 1%). The crushed material is incubated for 1 h at 65 ° C. and mixed 2-3 times by inversion during the incubation.

200 μl of a solution of chloroform: isoamyl alcohol 24: 1 are then added and mixed by inversion. After centrifugation at 6000 rpm for 10 minutes at 20 ^° C., 400 μl of supernatant are recovered and mixed with 400 μl of isopropanol.

After Ih at -20 ^° C., the mixture is centrifuged at 6000 rpm for 10 minutes at ^{40 °} C. The tubes are emptied. The DNA pellet fixed to the bottom of the tube is allowed to air dry for 12 hours.

The DNA is resuspended in 200 μl of 0.1X TE solution (1 mM Tris-HCl, 0.1 mM EDTA). The final concentration is measured by Lambda DNA-Hind III digest assay on 1% agarose gel.

3 - Search for a RAPD marker associated with male Ms7 sterility in L. sativa by the method of BSA (BuIk Segregant Anaysis).

In order to identify a molecular marker associated with male Ms7 sterility, the RAPD ^® 10mer kits from Operon Technologies Inc. (Huntsville, AL 35805, USA) and the method of BuIk Segregant Analysis (Michelmore et al., 1991 [17 ] and Paran et al., 1991 [18]) were used.

From the phenotyping of the two BC4 populations described above, 2 samples of mixtures of 10 plants were made for the two groups "male sterile" and "male fertile". 1200 primers Operon Biotechnologies Inc. (Huntsville, AL 35805, USA) from OPA-01 to OPBH-20 were tested by the RAPD technique described by William et al., 1990 [22] and, Welsh et al., 1990 [ 21] out of 4 samples per population. The primers demonstrating a "sterile male" specimen specific band and having an easy reading electrophoresis profile were selected.

The PCR reaction is carried out in a total reaction volume of 25 μl consisting of IX PCR buffer, 3 mM MgCl 2, 200 μM of dNTPs, 400 nM of primer, 1 unit of AmpliTaq DNA polymerase (Perkin-Elmer cetus). The PCR reaction consists of several cycles described as follows: 1 step at 94 ° C for 30 sec; 45 cycles at 94 ^° C. for 1 min then 35 ° C. for 1 min and finally 72 ^° C. for 2 min and a final elongation carried out at 72 ^° C. for 5 min, the reaction then being stored at ^{40 °} C.

The amplification products are separated on a 2% agarose gel under the following electrophoresis conditions: TBE IX migration buffer (Tris-Borate-EDTA) at 190V for 2H15.

In order to validate the retained RAPD primers, each of the 200 plants of the two BC4 populations was tested individually for the OPBA05 primer having the sequence '5' TGCGTTCCAC 3 '"(SEQ ID No. 1) and to which a marker of 675 corresponds. pb, BA05-675 (SEQ ID NO: 2), which co-segregates with Ms7. The electophoretic profile obtained for this marker is shown in Figure 6. A validation of this marker on different types of lettuce (batavia, butter, iceberg, Roman, oak leaf and lollo rossa) was carried out on approximately 25 plants of 12 populations. . The conditions for carrying out the test are identical to those described above for the extraction, amplification and electrophoresis steps. The calculation of the sensitivity and specificity of RAPD marker BA05-675 shows different values, according to the typologies, and mean values of 96% and 94% respectively (see Tables 17 and 18).

Table 17: Detail of the calculation of the predictive values, sensitivity and specificity of the molecular markers retained. PHENO'ΓYPE

Male Sterile Male Fertile

Predictive value

MARKER Number of positive number 1 true false positive positives = #VP / (present (#VP) (#FP) (#VP + #FP) rπ

Number of Predictive Value or Number of True Negative Negative 0 Negative Negative Number = #VN / [O]) (#FN) (#VN) (#VN + #FN)

SENSITIVITY SPECIFIC

= #VP / = #VN / (#VP + #FN) (#VN + #FP)

Table 18 Results by lettuce typology and mean value of the calculation of the sensitivity (S *) and the specificity (F **) of the BA05-675 molecular marker associated with Ms7.

4 - Genetic mapping of the marker BA05-675 associated with the male sterility Ms7 in the species Lactuca sativa. WH F

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From the 200 plants of a BC4 disjunction population for Ms7 described above, genetic mapping

(William et al., 1993 [23]) of the marker BA05-675 associated with

6700 AE Wageningen, The Netherlands). The statistical test of the

X ² allowed to test the null hypothesis of a 1: 1 Mendelian type segregation (test not significant at p> 0.05) for the dominant BA05-675 marker (see Table 19). A binding test with a likelihood ratio (or LOD score) greater than or equal to 3.0 allowed this marker to be mapped to 1.8 cM Ms7 (FIG. 6).

Table 19: BA05-675 Molecular Marker Segregation Reports Associated with Ms7 and Results of the X ² Test at 1 ddl according to the null hypothesis of a 1: 1 Mendelian type segregation. (F: number of fertile male plants, S: number of sterile male plants)

5 - Cloning and sequencing of the molecular marker RAPD BA05-

675 associated with male sterility in lettuce, Lactuca sativa.

From the agarose gel electrophoretic profile, the 675 bp DNA fragment was isolated and resuspended in TE buffer (10 mM Tris-Cl, 1 mM EDTA) and then re-amplified according to the PCR conditions described herein. -above. The re-amplified isolated fragment was cloned using the pCR ^® commercial kit 4-T0P0 ^® (Invitrogen, Carlsbad, California 92008, USA). After verification of cloning, DNA extractions (system Midiprep) were performed using the Promega Column Purification Kit (Madison, WI, USA).

The purified clones concentrated at 75 ng / μl were sequenced by Cogenics (38944 Meylan, France). The sequence of the BA05-675 marker described in FIG. 8 was thus obtained (SEQ ID No. 2).

6- Results

The study conducted by the inventors made it possible to define a RAPD marker, BA05-675 (SEQ ID No. 2), the sequence of which is shown in FIG. 8, which is 1.8 cM apart from Ms7 (FIG. with an average sensitivity and specificity of 96% and 94%, respectively, irrespective of the lettuce typology (Table 18). The evaluation of this marker on the individual plants of the 2 BC4 populations made it possible to estimate that the predictive value (Altman 1994a [13]) of identification of male sterile plants is on average close to 97%.

Bibliography

1. Goubara & Takasaki (2003) Flower visitors of lettuce under field and enclosure conditions, Appl. Entomo. Zool. 38 (4): 571-581.

2. Goubara & Takasaki (2004) Pollination effects of the sweat bee Lasioglossum vilosulum trichopsis on genic-male lettuce, Appl. Entomo. Zool. 39 (1): 163-169, 2004.

3. Lindqvist, K. (1960) Inheritance Studies in Lettuce, Heriditas 46: 387-470.

4. Michelmore, RW et al. (1987) Genetic analysis of resistance factors to downey mildew in lettuce, Plant Pathol., Vol. 36, No. 4: 499-514. 5. Michelmore, RW et al. (1993) Development of reliable PCR-based markers linked to downey mildew resistance genes in lettuce, Theor. Appl. Genet., Vol. 85, No. 8: 985-993.

6. Ryder, E. J. (1963) An epistatically controlled sterile pollen in lettuce (Lactuca sativa L.), Proc. Am. Soc.

Hort. Sci. 96: 826-828

7. Ryder, E.J. (1967) A sterile recessive gene in lettuce, Proc. Am. Soc. Hort. Sci 91: 366-368

8. Ryder, E. J. (1971) Genetic Studies in Lettuce (Lactuca sativa L.), J.Amer.Soc.Hort. Sci 96 (6) 826-828.

9. Ryder, E.J. (1979) Leafy Salad Vegetables, Avi. Pub. Co., page 30.

10. Maisonneuve, B. et al. (1994) Rapid mapping of two genes for resistance to downy mildew from Lactuca serriola to existing clusters of resistance genes, Theor. Appl. Broom. 89: 96-104.

11. Kuang H., et al. (2004) Multiple genetic processes in heterogeneous spleens of evolution within the major cluster disease resistance genes in lettuce, The plant cell, Vol. 16, 2870-2894.

12. Kesseli R.V., et al. (1994) Lactuca sativa (lettuce) constructed from RFLP and RAPD markers, Genetics 136: 1435-1446.

13. Altman D.G., Bland J.M., 1994a. Statistics Notes: Diagnostic tests 1: sensitivity and specificity. British

Medical Journal, 308: 1552.

14. Altman DG, Bland JM, 1994b. Statistics Notes: Diagnostic tests 2: predictive values. British Medical Journal, 30: 102. 15. Doyle JJ, and Doyle JL, 1990. Isolation of plant DNA from fresh tissue. Focus 12,13-15. 16. Edwards K., Johnstone C. and Thompson C, 1991. A simple and rapid method for the preparation of plant genomic DNA for PCR analysis. Nucleic Acid Res 19: 1349.

17. Michelmore RW, Paran I., Kesseli RV, 1991. Identification of markers linked to disease-resistance genes by bulked segregant analysis: a rapid method to detect markers in specifies genomic regions by using segregating populations Proc Natl Acad Sci USA 88: 9828 - 9832. 18. Paran I., Kesseli R., Michelmore RW, 1991. Identification of restriction fragment length polymorphism and random amplified polymorphic DNA markers linked to downy mildew genes in lettuce, using near-isogenic a Genome 34: 1021-1027. 19. Stam P., & J. W. van Ooijen, 1996. JoinMap, version 2.0. Software for the calculation of genetic linkage maps. Ed. CPRO-DLO, 60 pp.

20. Tomas H.T., and Tanksley S.D., 1989. A rapid and inexpensive method for the isolation of total DNA from dehydrated plant tissue. Plant Mol Biol Rep 12: 106-109.

21. Welsh J, McClelland M., 1990. Fingerprinting genomes using PCR with arbitrary primers. Nucleic Acids Res, 18: 7213-7218.

22. Williams J.K.G., Kubelik A.R., Livak K. J., Rafalsky J.A., Tynger S.V., 1990. DNA polymorphism amplified by arbitrary primers are useful as genetic markers. Nucleic Acids Res, 18: 6531-6535.

23. Williams J.K. G., Reiter R.S., Young R.M., Scolnik P.A., 1993. Genetic mapping of mutations using phenotypic pools and mapped RAPD markers. Nucleic Acids Res., 21 (11): 2697-2702.

Claims

claims

1. Hybrid Lactuca sativa seed, characterized in that it has a sterile male genotype, and is heterozygous for at least one distinct gene conferring a detectable phenotype on the plant derived from this seed.

2. Seed according to claim 1, such that said sterile male genotype involves at least one nuclear gene and said seed is heterozygous for the gene (s) at the origin of the male sterility.

3. Seed according to claim 2, wherein the male sterility is monogenic.

4. Seed according to claim 3, such that the male sterility gene is dominant.

The seed of claim 1, wherein said sterile male genotype is conferred by the Ms7 sterility gene.

6. Seed according to any one of claims 1 to 5 characterized in that its genome comprises a sequence

Double-stranded DNA of 650 to 700 nucleotides, the 5 'ends of both strands begin with the TGCGTTCCAC sequence (SEQ ID N ⁰ I).

Seed according to any one of claims 1 to 6, such that said phenotype is a phenotype of agricultural interest.

8. A seed according to any of claims 1 to 7, such that said phenotype is conferred by a standard resistance or intermediate resistance gene to infection by a virus, bacteria, insect or fungus.

9. Seed according to any one of claims 1 to 8, such that said phenotype is a standard or intermediate resistance to one of the following fungi: Bremia lactucae, Fusarium oxysporum, Sclerotinia minor or sclerotorum, Botrytis cinerea, Rhizictonia solani, Microdochium Panattonianum, Verticiulium dahliae, Erysiphe chicocearum or Pithium tracheiphilum, to any of the following insects: Nasonovia ribisnigri, Myzus persicae, Macrosiphum euphorbia, Nematodes pratylenchus or meloidogyne, leafminers liriomyza huidobrensis or Pemphigus busarius, to any of the following: pseudomonas, xanthomonas or rhizomonas, or one of the following viruses: LMV, TSWV, "Big vein", TBSV, LNSV, TuMV, CMV or BWYV.

The seed of claim 8 or 9, wherein said seed has a second separate standard or intermediate resistance gene in heterozygous form.

Seed according to claim 8 or 10, wherein said standard or intermediate resistance gene or genes are selected from the following bremia resistance genes: DmIO, R17, Dm5 / Dm8, R36 / R37 (cluster 1), DmI, Dm2 , Dm3, Dm6, DmI4, Dm15, Dml6, Dml8 (cluster 2), or Dm4, Dm7, DmI1, R38 (cluster 4); or TuMV resistance gene Tu (cluster 1); the Nr gene of Nasonovia resistance (cluster 2); or the mol.l, mol.2 genes of resistance to LMV (cluster 4).

12. Plant of lactuca sativa hybrid, characterized in that it:

has a heterozygous sterile male genotype, and is heterozygous for at least one distinct gene conferring on it a detectable phenotype.

13. Plant according to claim 12, such that said sterile male genotype is of nuclear origin and said plant is heterozygous for the gene (s) at the origin of the male sterility.

The plant of claim 13, wherein the male sterility is monogenic.

The plant of claim 14, wherein the male sterility gene is dominant

The plant of claim 12, wherein said sterile male genotype is conferred by the Ms7 sterility gene.

Cell of a hybrid lactuca sativa plant, characterized in that it:

has a heterozygous sterile male genotype, and is heterozygous for at least one distinct gene conferring a detectable phenotype on the plant.

18. A cell according to claim 17, such that said sterile male genotype is of nuclear origin and that said cell is heterozygous for the gene (s) responsible for the male sterility.

The cell of claim 18, wherein the male sterility is monogenic.

The cell of claim 19, wherein the male sterility gene is dominant

The cell of claim 17, such that said sterile male genotype is conferred by the Ms7 sterility gene.

22. seed population according to any one of claims 1 to 11, such that said population comprises at least 10 ⁵ seeds, preferably at least 10 ^6.

23. Seed population according to claim 22, comprising at least 10 ⁷ seeds.

24. A population of lactuca sativa seeds comprising at least 40% seeds according to any one of claims 1 to 11.

25. The population of claim 24 wherein the other seeds do not include the male sterility gene.

26. Use of insects of the order Diptera at a concentration greater than 100 Diptera per m ² or 25 Diptera per m ³ to effect pollination in closed medium of sterile male Lactuca sativa plants by male plants fertile.

27. Use according to claim 26, wherein the diptera are present at a concentration of at least 250 Diptera per m ² or at least 75 Diptera per m ³ .

28. Use according to claim 26, to obtain hybrid Lactuca sativa plants.

29. Use according to any of claims 26 to 28, wherein the sterile male Lactuca sativa plants have male sterility carried by a single dominant gene, preferably male Ms7 sterility.

30. Use according to any one of claims 26 to 29, wherein the fertile male plants are also Lactuca sativa plants, preferably a cultivar.

31. Process for obtaining hybrid Lactuca sativa seeds, comprising: - a step of culture in a closed medium, of sterile phenotypically male Lactuca sativa plants used as "female" parents and of phenotypically fertile male Lactuca sativa plants used as than "male" relatives, close to each other, one of the two parents having as an additional feature the fact of being homozygous for a gene conferring on it a detectable phenotype other than male sterility, the other parent not carrying this gene; a pollination step by dipterans introduced into the closed environment at the time of flowering of the plants at a concentration greater than 100 Diptera per m ² or 25 diptera per m ³ , preferably at least 250 diptera per m ² or at least 75 dipteres per m ³ ; and a step of harvesting the seeds produced by the sterile male plants.

32. The method of claim 31, wherein the second parent is also homozygous for at least one gene conferring a detectable phenotype other than male sterility, not worn by the other parent.

33. The method of claim 31 or 32, wherein said introduced Diptera concentration is greater than 400 Diptera per m ² , preferably greater than 500 Diptera per m ² .

34. Process according to any one of claims 31 to 33, in which said dipteres are introduced in the form of pupae.

35. Process according to any one of claims 31 to

34, wherein said closed medium is an enclosure sealed to insects.

36. Process according to any one of claims 31 to

35, wherein said dipterans are brachycers, preferably cyclopharyness brachycers.

37. The method of claim 36, wherein said dipteres belong to the family Calliphoridae or Muscidae.

38. The method of claim 37 wherein said diptera are Calliphora vomitaria, desCalliphora erythrocephala or Lucilia caesar.

39. Process according to any one of claims 31 to

38, where in the closed medium, the number of male sterile plants is greater than the number of fertile male plants.

40. Process according to any one of claims 31 to

39, where in the closed medium, the number of male sterile plants is at least 2000, and the number of male fertile plants is at least 1000.

41. Process according to any one of claims 31 to

40, where the introduction of Diptera is renewed at least once a week for 3 to 4 weeks.

42. Process according to any one of claims 31 to

41, wherein the male sterility of the plants used as female parents is of monogenic, dominant and nuclear origin, and wherein the plants used as female parents are obtained by a process comprising:

a step of crossing between Lactuca sativa plants heterozygous for a dominant male nuclear sterility gene and fertile male Lactuca sativa plants not carrying sterility genes; a step of cultivating the seeds resulting from said crossing, and a step of elimination of plants with a fertile male phenotype.

The method of claim 42, wherein the step of removing plants having a fertile male phenotype is achieved by detecting in a sample of each of the plants the absence of a specific molecular marker of the dominant gene of male sterility.

44. The method of claim 42 or 43, wherein the male sterility of the plants used as female parents is conferred by the Ms7 gene.

45. The method according to claim 31, wherein the genome of the plants used as female parents comprises a double-stranded DNA sequence of 650 to 700 nucleotides in which the 5 'ends of each of the two strands start with the TGCGTTCCAC sequence. (SEQ ID NO: 1)

46. Population of seeds obtainable according to any one of claims 31 to 45, comprising at least 10 ⁵ seeds, preferably 10 ⁶ seeds and even more preferably 10 ⁷ seeds.

47. Seed population according to claim 46, such that the MMS (mass of thousand seeds) is greater by at least 10%, preferably by at least 20% and even more preferentially by at least 30% in the MMS of the seeds. seeds obtained by self-fertilization of fertile male Lactuca sativa plants used as "male" parents.