Hervé Serieys

Potential gene flow from cultivated sunflower to volunteer, wild Helianthus species in Europe

Abstract The possibility of gene flow between cultivated and wild species of different crops was assessed, focussing on sunflower and its wild relatives or cultivated forms (annual Helianthus annuus, H. argophyllus, H. bolanderi, H. petiolaris, and perennial rigidus, H. tuberosus). Data were compiled from the literature and an attempt was made at determining the efficiency of possible crosses between annual and perennial species. The risk of a cultivated allele escaping from sunflower to uncontrolled forms (volunteers, H. annuus and H. tuberosus feral forms) was addressed, the fate of such alleles in the wild also being examined. An attempt was made to define some of the pressures likely to limit the spread of wild forms in nature, or that could prevent or impede the spread and increase the frequency of alleles from cultivated plants. Risks of spread of transgenes from sunflower varieties in Europe where feral forms are present but no natural Helianthus species were assessed. The emergence of transgenic or biologically engineered varieties of sunflower demands that attention be focussed on this field.

Structure of wild annual sunflower (Helianthus annuus L.) accessions based on agro-morphological traits

Seventy-seven wild sunflower accessions from USA were compared in France (Mauguio) for 13 quantitative characters using multivariate methods, including clustering, principal component and canonical discriminate analyzes to assess the patterns of morphological and climatic variation. Geographic and climatic data from their sampled sites such as latitude, longitude, elevation, rain fall, temperature, number of rain fall days, temperature range, and sunniness were also analyzed and we sought for correlations of climatic variables and morphological traits. Climatic data clustered the accessions into four groups. Principal component analysis was used to summarize the characteristic habits of annual wild sunflower sampled sites in terms of geography and climates, thus we characterized the ecogeographical profiles of wild sunflowers. As we studied the traits in a common environment we speculated whether local adaptation patterns are sustained by our data. Indeed traits shared by accessions that belong to climatic clusters are suggested to be due to local adaptation.

Diversity of Jerusalem artichoke clones (Helianthus tuberosus L.) from the INRA-Montpellier collection.

INRA hosted the national Jerusalem artichoke collection in Rennes and Clermont-Ferrand until 2005. It now takes place in Montpellier. The list of cultivar-clones and of wild accessions is provided as well as main data on expected yield, earliness, female fertility, and disease susceptibility to viruses and Oidium. Descriptions of some traits (anthocyanin, ramification, chlorophyll) were reported. Data was collected from a hydroponic experimental design which was set up with two repeats at Mauguio and Montpellier. The experimental yields are shown for nine clones chosen for agronomic production of tubers and the pictures of tubers are given.

Specifying the introgressed regions from H. argophyllus in cultivated sunflower (Helianthus annuus L.) to mark Phomopsis resistance genes

A method based upon targetting of introgressed markers in a Phomopsis-resistant line (R) of cultivated sunflower, issuing from a H. argophyllus cross was used to mark the Phomopsis resistance regions. Our study was based upon 203 F3 families derived from a cross between an inbred line susceptible to Phomopsis (S1) and the introgressed resistant line (R). Families were checked for Phomopsis resistance level in a design with replicated plots and natural infection was re-inforced by pieces of contaminated stems. Thirty four primers were employed for RAPD analysis. Out of 102 polymorphic fragments between (S1) and H. argophyllus, seven were still present in (R) suggesting that they marked introgressions of H. argophyllus into (R). The F2 plants were scored for the presence or absence of 19 fragments obtained from five primers, and the relationships between the presence/absence of fragments in F2 plants and Phomopsis resistance/susceptiblity in the F3 progenies was determined by using an analysis of variance. We found that at least two introgressed regions, as well as favourable factors from sunflower, contributed to the level of Phomopsis resistance in cultivated sunflower.

Construction of a crop—wild hybrid population for broadening genetic diversity in cultivated sunflower and first evaluation of its combining ability: the concept of neodomestication

The genetic base of sunflower elite lines is very narrow, due to many years of selection and breeding. To broaden the genetic diversity of the cultivated sunflower, in 1995 73 wild sunflower populations were crossed with 3 cultivated lines (Testers), and 219 hybrid offspring’s were evaluated in the field. GCA and SCA effects were computed suggesting for all traits a genetic potential for improvement through selection. Study of the hybrids revealed that the wild accessions bear different genetic abilities to combine with the testers for traits of morphological architecture, phenology and yield (seed weight and seed oil). The variance due to GCA and SCA showed that gene action was additive for days to flowering, branching and plant height. Genotypes derived from the same geographic origin may have either good or poor general combing ability. The correlation between GCA and per se genotype performance was positive for all traits except for seed oil content. This was the first attempt to evaluate wild-cultivated hybrids in sunflower on a large scale and will be the starting point for the management of hybrid Helianthus annuus populations for breeding. GCA and SCA estimations will facilitate the definition of strategies to manage and exploit the natural diversity for this crop.

Transfer of architectural traits from perennial Helianthus mollis Lam. to sunflower (H. annuus L.) and localisation of introgression

Common sunflower (i.e., Helianthus annuus) is occasionally crossed with other Helianthus species to gain favourable agronomic traits. An interspecific cross between H. annuus and Helianthus mollis was used to examine events that occurred during the five first generations. First generation hybrid plants were verified using GISH, and F1 hybrid (#17) was back-crossed to common sunflower to obtain BC1 (#4) and BC2 (#21). Some BC2 progeny possessed new traits, i.e., compact (Compact plant architecture is due to short inter-node length, short petiole length and short leaf lamina length) architecture without and with corrugated leaves, which were not observed in the parents. These traits were selected for and fixed after the BC2-S3 (#18) to produce a H. mollis introgression line (namely HM374). Although the size of the population was small, we tentatively construct a genetic map using data from the BC2 generation. Two linkage groups were identified carrying H. mollis specific AFLP markers that were associated with compact plant architecture, and one unlinked marker was shown to explain variation for the corrugated leaves. Introgression line HM374 was used to test the inheritance of compact plant architecture in a cross with an elite high oleic line, OL75HO. Microsatellite (SSR) markers were used to genotype F1 and F2 offspring’s. Our data suggested that the line HM374 was still heterozygous for introgression after eight generations. HM374 displays new architecture traits (i.e. compact architecture with or without corrugated leaves) and carries H. mollis fragments anchored on LG1 and LG11 of sunflower public map.

Evaluation of Parameters Accounting for Phomopsis Resistance Using Natural Infection and Artificial Inoculation on Recombinant Inbred Lines From a Cross Between Susceptible and Resistant Sunflower

HA89, a sunflower line susceptible to Phomopsis, was crossed with a resistant line, LR4-17. Two hundred and forty-one F2/F3 progenies and 232 recombinant inbred (RI) lines were derived from this cross. F2/F3 progenies were tested in semi-natural infections in 1994. F7, F8 and F9 were tested with semi-natural infections in 1997, 1998 and 1999, respectively. F7 RI lines were artificially infected with Phomopsis mycelium on leaves in 1997. Family effects were significant in F2/F3 progenies for attack rates on stems and encircling spots rates on stems after semi-natural infections. Line effects were significant for attack rates on stems and encircling spot rates in F7 and F8. F7 RI lines showed a high heritability for speed of necrosis on leaf blades after artificial infection. Continuous and unimodal distributions were observed for attack rates on stems in all experiments done in semi-natural conditions. In contrast, speed of necrosis on leaf blades showed a bimodal distribution. Significant rank correlations were observed between the speed of necrosis on leaf blades and the attack rates on stems. It is suggested that resistance to Phomopsis is the consequence of several mechanisms, independently inherited. It was concluded that speed of necrosis on leaf blades in artificial infections and attack rates on stems in natural infections should be retained as parameters for quantitative trait locus mapping of Phomopsis resistance.

Partial hybridization in crosses between cultivated sunflower and the perennial Helianthus mollis: effect of in vitro culture compared to natural crosses

Abstract. Eighty-four plants obtained from the pollination of the annual diploid cultivated sunflower, Helianthus annuus, by the perennial diploid species H. mollis were obtained naturally from mature seeds (62 plants) or following embryo rescue procedures (22 plants) and subsequently studied for phenotype traits and DNA markers. Twenty-two plants were obtained from the reverse cross as a result of natural seed development. The level of hybridization was determined using random amplified polymorphic DNA and restriction fragment length polymorphism markers. All of the resulting plants were found to be diploid 2n=34. Reciprocal crosses led to different progenies, with phenotypes that were predominantly similar to that of the female sunflower or the H. mollis type. The embryo rescue procedure enhanced the level of hybridization, whereas natural seed development led to fewer hybrids. Molecular markers unique to the female or the male parent indicated mechanisms leading to partial hybridization.