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1.
Planta ; 241(5): 1241-54, 2015 May.
Article in English | MEDLINE | ID: mdl-25656052

ABSTRACT

MAIN CONCLUSION: Switches between pollination syndromes have happened frequently during angiosperm evolution. Using QTL mapping and reciprocal introgressions, we show that changes in reproductive organ morphology have a simple genetic basis. In animal-pollinated plants, flowers have evolved to optimize pollination efficiency by different pollinator guilds and hence reproductive success. The two Petunia species, P. axillaris and P. exserta, display pollination syndromes adapted to moth or hummingbird pollination. For the floral traits color and scent, genetic loci of large phenotypic effect have been well documented. However, such large-effect loci may be typical for shifts in simple biochemical traits, whereas the evolution of morphological traits may involve multiple mutations of small phenotypic effect. Here, we performed a quantitative trait locus (QTL) analysis of floral morphology, followed by an in-depth study of pistil and stamen morphology and the introgression of individual QTL into reciprocal parental backgrounds. Two QTLs, on chromosomes II and V, are sufficient to explain the interspecific difference in pistil and stamen length. Since most of the difference in organ length is caused by differences in cell number, genes underlying these QTLs are likely to be involved in cell cycle regulation. Interestingly, conservation of the locus on chromosome II in a different P. axillaris subspecies suggests that the evolution of organ elongation was initiated on chromosome II in adaptation to different pollinators. We recently showed that QTLs for pistil and stamen length on chromosome II are tightly linked to QTLs for petal color and volatile emission. Linkage of multiple traits will enable major phenotypic change within a few generations in hybridizing populations. Thus, the genomic architecture of pollination syndromes in Petunia allows for rapid responses to changing pollinator availability.


Subject(s)
Flowers , Petunia/genetics , Pollination , Cell Division , Chromosomes, Plant , Quantitative Trait Loci , Reproduction , Species Specificity
2.
Plant Cell Environ ; 37(4): 813-826, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24127750

ABSTRACT

Volatile organic compounds (VOCs) released by soil microorganisms influence plant growth and pathogen resistance. Yet, very little is known about their influence on herbivores and higher trophic levels. We studied the origin and role of a major bacterial VOC, 2,3-butanediol (2,3-BD), on plant growth, pathogen and herbivore resistance, and the attraction of natural enemies in maize. One of the major contributors to 2,3-BD in the headspace of soil-grown maize seedlings was identified as Enterobacter aerogenes, an endophytic bacterium that colonizes the plants. The production of 2,3-BD by E. aerogenes rendered maize plants more resistant against the Northern corn leaf blight fungus Setosphaeria turcica. On the contrary, E. aerogenes-inoculated plants were less resistant against the caterpillar Spodoptera littoralis. The effect of 2,3-BD on the attraction of the parasitoid Cotesia marginiventris was more variable: 2,3-BD application to the headspace of the plants had no effect on the parasitoids, but application to the soil increased parasitoid attraction. Furthermore, inoculation of seeds with E. aerogenes decreased plant attractiveness, whereas inoculation of soil with a total extract of soil microbes increased parasitoid attraction, suggesting that the effect of 2,3-BD on the parasitoid is indirect and depends on the composition of the microbial community.


Subject(s)
Bacteria/metabolism , Disease Resistance , Ecosystem , Endophytes/metabolism , Plant Diseases/immunology , Volatile Organic Compounds/metabolism , Zea mays/microbiology , Animals , Butylene Glycols/metabolism , Colony Count, Microbial , Enterobacter aerogenes/growth & development , Gas Chromatography-Mass Spectrometry , Herbivory , Host-Pathogen Interactions/immunology , Molecular Sequence Data , Plant Diseases/microbiology , Plant Diseases/parasitology , Seedlings/microbiology , Soil Microbiology , Spodoptera/physiology , Volatilization , Zea mays/growth & development , Zea mays/parasitology
3.
Curr Biol ; 22(17): 1635-9, 2012 Sep 11.
Article in English | MEDLINE | ID: mdl-22840518

ABSTRACT

Although deception of floral pollinators is well known among orchids, the majority of animal-pollinated plants secure pollination by nectar rewards. The costs and benefits of nectar production remain poorly understood. Here, we developed a crossing design to introgress a low-nectar-volume locus of Petunia integrifolia into the genetic background of P. axillaris. The resulting introgression line resembled P. axillaris but produced only one-third of the nectar volume. When exposed simultaneously to low-nectar and wild-type P. axillaris plants, hawkmoth pollinators reduced their probing duration on low-nectar plants but otherwise did not show any signs of discrimination against these plants. However, reduced probing duration resulted in reduced seed production in the low-nectar plants despite their higher reproductive potential as evidenced by hand pollination. In line with this interpretation, we found a positive correlation between probing duration and seed set, and hawkmoth pollination of low-nectar plants that were manually supplemented with nectar to parental levels yielded seed sets similar to hand pollination. Thus, a simple self-serving pollinator behavior--the adjustment of probing time in response to nectar volume--may select against reducing nectar and protect many plant-pollinator mutualisms against a drift toward parasitism.


Subject(s)
Behavior, Animal , Manduca/physiology , Petunia/physiology , Plant Nectar/biosynthesis , Pollination , Seeds/growth & development , Animals , Feeding Behavior , Petunia/metabolism , Time Factors
4.
Genome ; 54(4): 327-40, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21491975

ABSTRACT

Two linkage maps were constructed for the model plant Petunia. Mapping populations were obtained by crossing the wild species Petunia axillaris subsp. axillaris with Petunia inflata, and Petunia axillaris subsp. parodii with Petunia exserta. Both maps cover the seven chromosomes of Petunia, and span 970 centimorgans (cM) and 700 cM of the genomes, respectively. In total, 207 markers were mapped. Of these, 28 are multilocus amplified fragment length polymorphism (AFLP) markers and 179 are gene-derived markers. For the first time we report on the development and mapping of 83 Petunia microsatellites. The two maps retain the same marker order, but display significant differences of recombination frequencies at orthologous mapping intervals. A complex pattern of genomic rearrangements was detected with the related genome of tomato (Solanum lycopersicum), indicating that synteny between Petunia and other Solanaceae crops has been considerably disrupted. The newly developed markers will facilitate the genetic characterization of mutants and ecological studies on genetic diversity and speciation within the genus Petunia. The maps will provide a powerful tool to link genetic and genomic information and will be useful to support sequence assembly of the Petunia genome.


Subject(s)
Chromosome Mapping/methods , Genome, Plant/genetics , Petunia/genetics , Solanum lycopersicum/genetics , Amplified Fragment Length Polymorphism Analysis , Chromosomes, Plant/genetics , Crosses, Genetic , DNA, Plant/genetics , Genetic Speciation , Genetic Variation , Microsatellite Repeats/genetics , Petunia/classification , Polymorphism, Genetic , Synteny
5.
Curr Opin Plant Biol ; 12(4): 486-90, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19447671

ABSTRACT

We all appreciate the beauty of flowers, but we seldom consider their function in the life cycle of the plant. The function of beautiful flowers is to advertise the presence of nectar. Floral nectar is the key component in the mutualism between flowering plants and their pollinators. Plants offer nectar as a reward for the transport of pollen by animal vectors. Studying nectar is challenging because of its complex physiology, complex polygenetic structure, and strong environmental variability. Recent advances set the stage for exciting future research that combines genetics and physiology to study ecological and evolutionary questions.


Subject(s)
Flowers/physiology , Magnoliopsida/physiology , Pollen/physiology , Pollination/physiology , Animals , Evolution, Molecular , Flowers/metabolism , Flowers/parasitology , Host-Parasite Interactions , Insecta/physiology , Magnoliopsida/metabolism , Magnoliopsida/parasitology , Pollen/metabolism , Pollen/parasitology , Pollination/genetics , Reproduction/genetics , Reproduction/physiology , Research/trends , Research Design
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