Sterility Barriers Research Articles

Genetic differentiation and species cohesion in two widespread Central American Begonia species

Begonia is one of the ten largest plant genera, with over 1500 species. This high species richness may in part be explained by weak species cohesion, which has allowed speciation by divergence in allopatry. In this study, we investigate species cohesion in the widespread Central American Begonia heracleifolia and Begonia nelumbiifolia, by genotyping populations at microsatellite loci. We then test for post-zygotic reproductive barriers using experimental crosses, and assess whether sterility barriers are related to intraspecific changes in genome size, indicating major genome restructuring between isolated populations. Strong population substructure was found for B. heracleifolia (FST=0.364, F'ST=0.506) and B. nelumbiifolia (FST=0.277, F'ST=0.439), and Bayesian admixture analysis supports the division of most populations into discrete genetic clusters. Moderate levels of inferred selfing (B. heracleifolia s=0.40, B. nelumbiifolia s=0.62) and dispersal limitation are likely to have contributed to significant genetic differentiation (B. heracleifolia Jost's D=0.274; B. nelumbiifolia D=0.294). Interpopulation crosses involving a divergent B. heracleifolia population with a genome size ∼10% larger than the species mean had a ∼20% reduction in pollen viability compared with other outcrosses, supporting reproductive isolation being polymorphic within the species. The population genetic data suggest that Begonia populations are only weakly connected by gene flow, allowing reproductive barriers to accumulate between the most isolated populations. This supports allopatric divergence in situ being the precursor of speciation in Begonia, and may also be a common speciation mechanism in other tropical herbaceous plant groups.

Double sterility barrier between Saccharomyces species and its breakdown in allopolyploid hybrids by chromosome loss

The analysis of 57 synthetic interspecies hybrids revealed that Saccharomyces cerevisiae and Saccharomyces uvarum ( Saccharomyces bayanus var. uvarum) are isolated by a double sterility barrier: by hybrid sterility (hybrid cells cannot produce viable spores) operating in allodiploids and by F1 sterility (F1 cells cannot produce viable spores) operating in allopolyploids. F1-sterility is caused by mating-type heterozygosity. It can be overcome by eliminating chromosome 2 of the S.uvarum subgenome that carries a MAT locus. The loss of this MAT gene abolishes the repression of mating activity. In cultures of the resulting fertile alloaneuploid F1 segregants, the cells can conjugate with each other like haploids and form zygotes capable of performing meiotic divisions producing viable and fertile F2 spores. To the best of our knowledge, this is the first report on breaking down interspecies hybrid sterility by chromosome loss in eukaryotic organisms. The filial generations are genetically unstable and can undergo additional changes mainly in the S.uvarum subgenome (directional changes). It is proposed that regaining fertility and subsequent preferential reduction in one of the subgenomes may account for the formation of chimerical ('natural hybrid') genomes found among wine and brewery strains and may also play roles in speciation of hybrid taxa in the Saccharomyces genus.

Determination of nature of polyploidy in Argemone ochroleuca ssp. ochroleuca Sweet

Cytogenetical and molecular studies in Argemone mexicana Lin. (2n = 28) and A.ochroleuca ssp. ochroleuca Sweet. (2n = 56) showed exclusive bivalent pairing at meiois; their triploid hybrid had, univalents, bivalents and trivalents; autotetraploid of diploid A. mexicana had bivalents and quadrivalents and polyhaploid of A. ochroleuca showed bivalency. Random amplified polymorphic DNA analyses did not support the autotetraploid nature of A. ochroleuca. The dendrogram based on pair-wise genetic similarity coefficients showed distinct grouping of two species into two clusters. The conflicting data are resolved by deducing that sufficient similarities existed between one of the ochroleuca and the diploid species genome; the remainder of the ochroleuca genome had homologous chromosomes. Apparently, A. ochroleuca carried enough cryptic intergenomic homologies which ordinarily remained unexposed. In ochroleuca ‘hemizygous-ineffective’ mechanism is suggested. Further a diploidizing genetic mechanism is envisaged. Alternatively an acute propensity to preferential pairing caused bivalent formation. Such a system or systems caused meiotic isolation of various genomes and instituted normal fertility. Thus repression of genetic control is of evolutionary significance in the creation of reproductive isolation and sterility barriers for further speciation. The segmental allotetraploid nature of A. ochroleuca is inferred.

In situ sensor techniques in modern bioprocess monitoring

New reactor concepts as multi-parallel screening systems or disposable bioreactor systems for decentralized and reproducible production increase the need for new and easy applicable sensor technologies to access data for process control. These sophisticated reactor systems require sensors to work with the lowest sampling volumes or, even better, to measure directly in situ, but in situ sensors are directly incorporated into a reactor or fermenter within the sterility barrier and have therefore to stand the sterilization procedures. Consequently, these in situ sensor technologies should enable the measurement of multi-analytes simultaneously online and in real-time at a low price for the robust sensing element. Current research therefore focuses on the implementation of noninvasive spectroscopic and optical technologies, and tries to employ them through fiber optics attached to disposable sensing connectors. Spectroscopic methods reach from ultraviolet to infrared and further comprising fluorescence and Raman spectroscopy. Also, optic techniques like microscopy are adapted for the direct use in bioreactor systems (Ulber et al. in Anal Bioanal Chem 376:342-348, 2003) as well as various electrochemical methods (Joo and Brown in Chem Rev 108:638-651, 2008). This review shows the variety of modern in situ sensing principles in bioprocess monitoring with emphasis on spectroscopic and optical techniques and the progress in the adaption to latest reactor concepts.

High diversity of centric fusions with monobrachial homology in an area of chromosomal polymorphism of Mus musculus domesticus

One of the simplest models of chromosomal speciation is speciation by monobrachial centric fusion. This model is based on the assumption that a sterility barrier can develop between populations, in which fixed centric fusions show monobrachial homology, i.e. share only one chromosome arm. However, studies aimed at delineating intermediate stages of transition to reproductive isolation are lacking. In this paper, we describe a new area of chromosomal polymorphism in the house mouse, Mus musculus domesticus Schwarz and Schwarx, 1943, in Sicily (Italy). We trapped 79 mice at eighteen localities in an area of approximately 500 Km 2 surrounding the largest active European volcano, Mount Etna. Combining G-banding and chromosome painting we identified twelve different Robertsonian (Rb) metacentrics. Considering the high number of Rb fusions, some of them shared with other documented areas, the presently studied area of chromosomal polymorphism is very likely to represent a mixture of allochthonous and autochthonous Rb fusions. The Rb(9.16) is the most widespread metacentric (overall frequency 0.80). Two Rb metacentrics, Rb(4.10) and Rb(5.6), have similar overall frequency, 0.29 and 0.37, respectively, and are narrowly co-distributed in ten populations. Nine fusions – Rb(2.13), Rb(1.3), Rb(12.17), Rb(8.17), Rb(2.14), Rb(10.14), Rb(11.17), Rb(3.15), and Rb(11.14) – show a low frequency (0.04–0.01) and mostly non-overlapping localization, but each of them shares monobrachial homology with at least one other metacentric. The overall geographical distribution of different Rb fusions seems to match an early stage of race formation. The eventual role of the presently studied hybrid zone in the context of chromosomal speciation by monobrachial centric fusions is discussed. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 103, 722–731. ADDITIONAL KEYWORDS: chromosomal speciation – chromosome races – Mus musculus domesticus – population cytogenetics – Robertsonian metacentrics – structural heterozygotes.

Patterns of Sequence Divergence and Evolution of the S1 Orthologous Regions between Asian and African Cultivated Rice Species

A strong postzygotic reproductive barrier separates the recently diverged Asian and African cultivated rice species, Oryza sativa and O. glaberrima. Recently a model of genetic incompatibilities between three adjacent loci: S1A, S1 and S1B (called together the S1 regions) interacting epistatically, was postulated to cause the allelic elimination of female gametes in interspecific hybrids. Two candidate factors for the S1 locus (including a putative F-box gene) were proposed, but candidates for S1A and S1B remained undetermined. Here, to better understand the basis of the evolution of regions involved in reproductive isolation, we studied the genic and structural changes accumulated in the S1 regions between orthologous sequences. First, we established an 813 kb genomic sequence in O. glaberrima, covering completely the S1A, S1 and the majority of the S1B regions, and compared it with the orthologous regions of O. sativa. An overall strong structural conservation was observed, with the exception of three isolated regions of disturbed collinearity: (1) a local invasion of transposable elements around a putative F-box gene within S1, (2) the multiple duplication and subsequent divergence of the same F-box gene within S1A, (3) an interspecific chromosomal inversion in S1B, which restricts recombination in our O. sativa×O. glaberrima crosses. Beside these few structural variations, a uniform conservative pattern of coding sequence divergence was found all along the S1 regions. Hence, the S1 regions have undergone no drastic variation in their recent divergence and evolution between O. sativa and O. glaberrima, suggesting that a small accumulation of genic changes, following a Bateson-Dobzhansky-Muller (BDM) model, might be involved in the establishment of the sterility barrier. In this context, genetic incompatibilities involving the duplicated F-box genes as putative candidates, and a possible strengthening step involving the chromosomal inversion might participate to the reproductive barrier between Asian and African rice species.

Darwin and the Origin of Interspecific Genetic Incompatibilities

Darwin's Origin of Species is often criticized for having little to say about speciation. The complaint focuses in particular on Darwin's supposed failure to explain the evolution of the sterility and inviability of interspecific hybrids. But in his chapter on hybridism, Darwin, working without genetics, got as close to the modern understanding of the evolution of hybrid sterility and inviability as might reasonably be expected. In particular, after surveying what was then known about interspecific crosses and the resulting hybrids, he established two facts that, while now taken for granted, were at the time radical. First, the sterility barriers between species are neither specially endowed by a creator nor directly favored by natural selection but rather evolve as incidental by-products of interspecific divergence. Second, the sterility of species hybrids results when their development is "disturbed by two organizations having been compounded into one." Bateson, Dobzhansky, and Muller later put Mendelian detail to Darwin's inference that the species-specific factors controlling development (i.e., genes) are sometimes incompatible. In this article, I highlight the major developments in our understanding of these interspecific genetic incompatibilities--from Darwin to Muller to modern theory--and review comparative, genetic, and molecular rules that characterize the evolution of hybrid sterility and inviability.

A genetic model for the female sterility barrier between Asian and African cultivated rice species.

S(1) is the most important locus acting as a reproductive barrier between Oryza sativa and O. glaberrima. It is a complex locus, with factors that may affect male and female fertility separately. Recently, the component causing the allelic elimination of pollen was fine mapped. However, the position and nature of the component causing female sterility remains unknown. To fine map the factor of the S(1) locus affecting female fertility, we developed a mapping approach based on the evaluation of the degree of female transmission ratio distortion (fTRD) of markers. Through implementing this methodology in four O. sativa x O. glaberrima crosses, the female component of the S(1) locus was mapped into a 27.8-kb (O. sativa) and 50.3-kb (O. glaberrima) region included within the interval bearing the male component of the locus. Moreover, evidence of additional factors interacting with S(1) was also found. In light of the available data, a model where incompatibilities in epistatic interactions between S(1) and the additional factors are the cause of the female sterility barrier between O. sativa and O. glaberrima was developed to explain the female sterility and the TRD mediated by S(1). According to our model, the recombination ratio and allelic combinations between these factors would determine the final allelic frequencies observed for a given cross.

Identification of a Rice stripe necrosis virus resistance locus and yield component QTLs using Oryza sativa × O. glaberrima introgression lines

BackgroundDeveloping new population types based on interspecific introgressions has been suggested by several authors to facilitate the discovery of novel allelic sources for traits of agronomic importance. Chromosome segment substitution lines from interspecific crosses represent a powerful and useful genetic resource for QTL detection and breeding programs.ResultsWe built a set of 64 chromosome segment substitution lines carrying contiguous chromosomal segments of African rice Oryza glaberrima MG12 (acc. IRGC103544) in the genetic background of Oryza sativa ssp. tropical japonica (cv. Caiapó). Well-distributed simple-sequence repeats markers were used to characterize the introgression events. Average size of the substituted chromosomal segments in the substitution lines was about 10 cM and covered the whole donor genome, except for small regions on chromosome 2 and 4. Proportions of recurrent and donor genome in the substitution lines were 87.59% and 7.64%, respectively. The remaining 4.78% corresponded to heterozygotes and missing data. Strong segregation distortion was found on chromosomes 3 and 6, indicating the presence of interspecific sterility genes. To illustrate the advantages and the power of quantitative trait loci (QTL) detection using substitution lines, a QTL detection was performed for scored traits. Transgressive segregation was observed for several traits measured in the population. Fourteen QTLs for plant height, tiller number per plant, panicle length, sterility percentage, 1000-grain weight and grain yield were located on chromosomes 1, 3, 4, 6 and 9. Furthermore, a highly significant QTL controlling resistance to the Rice stripe necrosis virus was located between SSR markers RM202-RM26406 (44.5-44.8 cM) on chromosome 11.ConclusionsDevelopment and phenotyping of CSSL libraries with entire genome coverage represents a useful strategy for QTL discovery. Mapping of the RSNV locus represents the first identification of a genetic factor underlying resistance to this virus. This population is a powerful breeding tool. It also helps in overcoming hybrid sterility barriers between species of rice.

Hybridization experiments in the genus Luzula IV. Studies with taxa of the campestris-multiflora complex from the Nothern and Southern Hemispheres

Material of the widely distributed campestris-multiflora complex of genus Luzula has been collected from different localities in its areas in Europe, North America, and Japan in the Northern Hemisphere, and in Australia and New Zealand in the Southern Hemisphere. Individuals from these localities have been crossed intra- and inter-regionally, in order to determine the differentiation between the studied populations as expressed in the intensity of crossing barriers. F1-hybrids have been obtained in all tried taxa combinations. The sterility of the hybrids is of the postzygotic type, showing up in F1 and/or F2. The sterility barriers as isolating mechanisms are enhanced, in certain individual combinations, by sub-lethality of F1 or by the occurrence of abnormal segregates in F2. The intensity of the crossing barriers, determined by the mean fertility reduction of the hybrid populations in first and second generations, is approximately proportional to the distance between the geographical origins of the parental populations. The intensity of the sterility barriers is, furthermore, dependent on the effect of the selection pressure brought about by environmental stress and varying with the ecology of the habitats of the crossed populations.

Why are There Indica Type and Japonica Type in Rice? — History of the Studies and a View for Origin of Two Types

On the bases of archaeological discoveries, the earliest domestication of rice has been confirmed in the middle and lower Changjiang River basin, while in the region wild rice populations are found in shallow swamps under a climate with freezing winter cold. These findings lead us re-examine the past ideas about domestication and differentiation of rice. Historically, in 1930s two sub-species, indica and japonica, were proposed on the basis of sterility in F 1 hybrids between them. Soon after that, the two types were classified by the associations of a number of genetically independent traits. The characteristic associations of traits have been explained by the hybrid sterility or reproductive barriers which were assumed to comprise a set of duplicate recessive lethal genes and to be an inner genetic mechanism to lead to the varietal differentiations. In 1980s, the hybrid sterility between Indica and Japonica types was analyzed, and Indica, Japonica, and wide-compatibility type which gives fertile hybrids when cross to Indica and Japonica types, are proved to contain an allele, S 5 i, S 5 j and S 5 n, respectively at a locus on chromosome 6. And those gametes having S 5 j allele are found to be partially aborted in the hybrid genotypes of S 5 i/ S 5 j while no gamete abortion occurs in S 5 i/ S 5 n and S 5 j/ S 5 n genotypes. Since then, the gene S 5 n has been used in hybrid rice breeding to obtain fertile and vigorous hybrids between subspecies, and the long-disputed problem of hybrid sterility has been solved. Also in such studies the characteristic association of traits found in each of varietal groups is better explained by founder effects. On the other hand, a large number of native cultivars of rice were surveyed with enzyme polymorphism in 1980s and later with molecular markers. As a result, profound genetic diversity is found in cultivated rice as well as in wild rice. These findings seem to lead us to the idea of multiple independent domestications of rice. However, before reaching such a conclusion, at least two factors, i.e., long-distance-dissemination of some genotypes and the possibilities of introgression by local wild rice to primitive cultivars need to be examined. Taking the two factors as well as the historical events into consideration, it is considered here that the perennial japonica cultivars which are close to wild rice in the Changjiang River basin were disseminated to East India through Assam or along the Bengal Bay, where they were transformed under the introgressions of local wild rice and formed a secondary center, from which some genotypes seem to be disseminated to colonies in Southeast Asia under the influence of Hinduism. Later some of the genotypes were introduced into China and constituted so called Indica type. This may be a reasonable picture for the varietal differentiation.

Genetic structuring in three closely related circumpolar plant species: AFLP versus microsatellite markers and high-arctic versus arctic–alpine distributions

Genetic structuring in response to the glacial cycles has been investigated for many plant species, but exclusively high-arctic ones have not been studied. Such extremely cold-adapted species have probably experienced range reductions under the present climate. Here we compare three predominantly selfing species of Draba with different distributions and hardiness (D. subcapitata, high-arctic; D. nivalis, arctic to arctic-alpine; D. fladnizensis, arctic-alpine) for genetic structuring on the basis of two different types of molecular markers (10 microsatellite loci and 160 amplified fragment length polymorphisms (AFLPs)). The degree of genetic structuring within these species is of particular interest because it has been shown that they contain many cryptic biological species. The high-arctic D. subcapitata had less phylogeographic structure, less diversity and fewer private alleles than the other two species, suggesting that long-distance dispersal may occur more frequently in the high arctic, that hardy plants may have higher probability for establishment after dispersal under high-arctic conditions and that high-arctic species may have experienced a bottleneck during the present interglacial. In contrast, D. fladnizensis and D. nivalis showed distinct phylogeographic structure and more diversity, suggesting separate long-term refugia in Eurasia and North America/Beringia. The AFLP markers revealed more phylogeographic structuring than the microsatellites, possibly because of the higher number of loci surveyed and/or because structure at very large geographic scales is blurred by high mutation rate leading to homoplasy at microsatellite loci. The number of genetic groups detected was in any case insignificant compared with the numerous cryptic biological species known within these species, supporting rapid development of sterility barriers.

GENETICS OF INTRINSIC POSTZYGOTIC ISOLATION IN A CIRCUMPOLAR PLANT SPECIES,DRABA NIVALIS(BRASSICACEAE)

Sterility barriers, ranging from incomplete to fully developed, were recently demonstrated within taxonomic species of the genus Draba, suggesting the existence of numerous, cryptic biological species. Because these taxa are predominately selfers and of Pleistocene origin, it was concluded that hybrid sterility evolved quickly and possibly by genetic drift. Here we used genetic mapping and QTL analyses to determine the genetic basis of hybrid sterility between geographically distant populations of one of these taxonomic species, Draba nivalis. Fifty microsatellite loci were mapped, and QTL analyses identified five loci underlying seed fertility and two underlying pollen fertility. Four of five seed fertility QTLs reduced fertility in heterozygotes, an observation most consistent with drift-based fixation of underdominant sterility loci. However, several nuclear-nuclear interactions were also found, including two that acted like reciprocal translocations with lowest fitness in double heterozygotes, and two that had a pattern of fitness consistent with Bateson-Dobzhansky-Muller incompatibilities. In contrast, pollen fertility QTLs exhibited additive inheritance, with lowest fertility associated with the paternal allele, a pattern of inheritance suggestive of cytonuclear incompatibilities. The results imply that multiple genetic mechanisms underlie the rapid evolution of reproductive barriers in Draba.

Genome relationships between eight diploid Hordeum species

The eight species included in Hordeum section Anisolepis s. lat., viz. H. pusillum Nutt., H. intercedens Nevski, H. euclaston Steud., H. flexuosum Nees, H. muticum Presl, H. cordobense Bothm. et al., H. stenostachys Godr., and H. chilense Roem. et Schult. were intercrossed in all combinations in order to study the relationships between them. In two combinations, a segregating F2 generation was obtained, otherwise there were strict sterility barriers among the taxa. The meiotic studies revealed that all species have homoto homoeologous chromosome sets, i. e. they have the same ‘basic genome’. Any variation in pairing and occurrence of multivalents was interpreted as indicating that certain populations had undergone structural cytological changes, as these events were not linked to specific taxa. No cytogenetic evidence obtained indicated that some species were more closely related than others.

Global Dissemination of a Single Mutation Conferring White Pericarp in Rice

Here we report that the change from the red seeds of wild rice to the white seeds of cultivated rice (Oryza sativa) resulted from the strong selective sweep of a single mutation, a frame-shift deletion within the Rc gene that is found in 97.9% of white rice varieties today. A second mutation, also within Rc, is present in less than 3% of white accessions surveyed. Haplotype analysis revealed that the predominant mutation originated in the japonica subspecies and crossed both geographic and sterility barriers to move into the indica subspecies. A little less than one Mb of japonica DNA hitchhiked with the rc allele into most indica varieties, suggesting that other linked domestication alleles may have been transferred from japonica to indica along with white pericarp color. Our finding provides evidence of active cultural exchange among ancient farmers over the course of rice domestication coupled with very strong, positive selection for a single white allele in both subspecies of O. sativa.

Frequency and fidelity of alien chromosome transmission inGossypiumhexaploid bridging populations

The Australian diploid Gossypium species possess traits of potential agronomical value, such as gossypol-free seeds and Fusarium wilt resistance. However, they belong to the tertiary germplasm pool, which is the most difficult group of species from which to introgress genes into G. barbadense L. and G. hirsutum L. Interspecific triploid hybrids can be generated but they are sterile. The sterility barrier can be overcome using synthetic polyploids as introgression bridges, but whether there is sufficient homoeologous chromosome interaction at meiosis to allow recombination is still an open question. To ascertain, genetically, observable levels of homoeologous introgression, 2 synthetic hexaploid lines (2x G. hirsutum x G. australe and 2x G. hirsutum x G. sturtianum) were crossed to G. hirsutum to generate pentaploid F1 plants that, in turn, were backcrossed to G. hirsutum to generate BC1 and BC2 multiple alien chromosome addition lines (MACALs). Gossypium australe F. Muell. and G. sturtianum Willis chromosome-specific markers were used to track the frequency and fidelity of chromosome transmission to the BC1 and BC2 MACALs. The chromosomal location of the AFLP markers was determined by their distribution among the MACALs and confirmed in parental F2 families. Roughly half the available chromosomes were transmitted to the G. hirsutum x G. australe (54%) and G. hirsutum x G. sturtianum (52%) BC1 MACALs. The BC2 MACAL families again inherited about half of the available chromosomes. There were, however, notable exceptions for specific chromosomes. Some chromosomes were preferentially eliminated, while others were preferentially transmitted. Consistent with the genomic stability of Gossypium synthetic polyploids, the de novo loss or gain of AFLP fragments was rarely observed. While restructuring of the donor G. australe and G. sturtianum chromosomes was observed, this is more likely the result of chromatin loss, and no clear cases of introgression of donor chromatin into the recipient G. hirsutum genome were observed.

Adaptive radiation of shrubby tarweeds (Deinandra) in the California Islands parallels diversification of the Hawaiian silversword alliance (Compositae–Madiinae)

Phylogenetic analyses of nuclear rDNA transcribed spacers and cytogenetic studies of interspecific hybrids reported here uphold Carlquist's hypothesis (1965, Island Biology) that shrubby tarweeds (Deinandra) of Guadalupe Island, Mexico, are products of in situ radiation in the California Islands, where evidence of plant diversification has been equivocal. Based on the rDNA findings, the Guadalupe Island endemics (D. frutescens, D. greeneana subsp. greeneana, and D. palmeri) constitute a clade that arose since the late Pliocene, well after the origin of Guadalupe Island and diversification of annual, mainland Californian lineages of Deinandra. High interfertility and normal meiosis in F(1) hybrids between the three endemics contrast with reduced interfertility (to complete intersterility) and meiotic irregularities in F(1) hybrids between other, mostly mainland species of Deinandra. Cloned rDNA sequences provided no convincing evidence of introgression among the Guadalupe Island deinandras; morphological, phenological, and/or habitat differences among those taxa indicate ecological barriers to gene flow and a probable role for ecological divergence in diversification. Biosystematic and molecular phylogenetic data for shrubby tarweeds of Guadalupe Island and another secondarily woody, oceanic-island tarweed lineage, the Hawaiian silversword alliance, reveal strikingly similar evolutionary histories. Both groups violate Baker's Rule by stemming from self-incompatible ancestors in western North America, and each has undergone within-island diversification without evolution of strong sterility barriers among lineages. Evolutionary parallels between these Hawaiian and California Island lineages of Madiinae, first suggested by Carlquist, may reflect characteristics of tarweeds that facilitate insular colonization and adaptive radiation.

Extensive Chromosomal Repatterning and the Evolution of Sterility Barriers in Hybrid Sunflower Species

New species may arise via hybridization and without a change in ploidy. This process, termed homoploid hybrid speciation, is theoretically difficult because it requires the development of reproductive barriers in sympatry or parapatry. Theory suggests that isolation may arise through rapid karyotypic evolution and/or ecological divergence of hybrid neospecies. Here, we investigate the role of karyotypic change in homoploid hybrid speciation by generating detailed genetic linkage maps for three hybrid sunflower species, Helianthus anomalus, H. deserticola, and H. paradoxus, and comparing these maps to those previously generated for the parental species, H. annuus and H. petiolaris. We also conduct a quantitative trait locus (QTL) analysis of pollen fertility in a BC2 population between the parental species and assess levels of pollen and seed fertility in all cross-combinations of the hybrid and parental species. The three hybrid species are massively divergent from their parental species in karyotype; gene order differences were observed for between 9 and 11 linkage groups (of 17 total), depending on the comparison. About one-third of the karyoypic differences arose through the sorting of chromosomal rearrangements that differentiate the parental species, but the remainder appear to have arisen de novo (six breakages/six fusions in H. anomalus, four breakages/three fusions in H. deserticola, and five breakages/five fusions in H. paradoxus). QTL analyses indicate that the karyotypic differences contribute to reproductive isolation. Nine of 11 pollen viability QTL occur on rearranged chromosomes and all but one map close to a rearrangement breakpoint. Finally, pollen and seed fertility estimates for F1's between the hybrid and parental species fall below 11%, which is sufficient for evolutionary independence of the hybrid neospecies.

Global dissemination of a single mutation conferring white pericarp in rice

Here we report that the change from the red seeds of wild rice to the white seeds of cultivated rice (Oryza sativa) resulted from the strong selective sweep of a single mutation, a frame-shift deletion within the Rc gene that is found in 97.9% of white rice varieties today. A second mutation, also within Rc, is present in less than 3% of white accessions surveyed. Haplotype analysis revealed that the predominant mutation originated in the japonica subspecies and crossed both geographic and sterility barriers to move into the indica subspecies. A little less than one Mb of japonica DNA hitchhiked with the rc allele into most indica varieties, suggesting that other linked domestication alleles may have been transferred from japonica to indica along with white pericarp color. Our finding provides evidence of active cultural exchange among ancient farmers over the course of rice domestication coupled with very strong, positive selection for a single white allele in both subspecies of O. sativa.

The taxonomic status of the wild rice species Oryza ridleyi Hook. f. and O . longiglumis Jansen (Ser. Ridleyanae Sharma et Shastry) from Southeast Asia

The taxonomic status of the two species O. ridleyi and O. longiglumis in Oryza series Ridleyanae was resolved using morphological and molecular markers. Cluster analysis using a similarity matrix based on 12 qualitative characters separated the O. ridleyi from the O. longiglumis samples and the O. ridleyi samples from Papua New Guinea (PNG). O. ridleyi and O. longiglumis formed distinct groups upon cluster analysis based on 16 quantitative characters. Canonical discriminant analysis showed significant differences between the two species with anther and ligule length and spikelet and leaf dimensions as the most discriminating characters. Cluster analysis based on RAPD markers showed distinct clusters for O. longiglumis and O. ridleyi samples from different geographic origins. Hybridization studies revealed an F1 sterility barrier in interspecific hybrids and those obtained from intraspecific crosses between O. ridleyi from Southeast Asia and PNG.