Speciation history of three closely related pines Pinus mugo (T.), P. uliginosa (N.) and P. sylvestris (L.)

Nucleotide polymorphisms at genomic regions including 17 nuclear loci, two chloroplast and one mitochondrial DNA fragments were used to study the speciation history of three pine species: dwarf mountain pine (Pinus mugo), peat‐bog pine (P. uliginosa) and Scots pine (P. sylvestris). We set out to investigate three specific speciation scenarios: (I) P. uliginosa is a homoploid hybrid between the other two, (II) the species have evolved without gene flow after divergence and (III) there has been substantial gene flow between the species since their divergence. Overall, the genetic data suggest that P. mugo and P. uliginosa share the same gene pool (average net divergence of 0.0001) and that the phenotypic differences (e.g. growth form) are most likely due to very limited areas of the genome. P. mugo and P. uliginosa are more diverged from P. sylvestris than from each other (average net divergence of 0.0027 and 0.0026, respectively). The nucleotide patterns can best be explained by the divergence with migration speciation scenario, although the hybrid speciation scenario with small genomic contribution from P. sylvestris cannot be completely ruled out. We suggest that the large amount of shared polymorphisms between the pine taxa and the lack of monophyly at all loci studied between P. sylvestris and P. mugo–P. uliginosa can largely be explained by relatively recent speciation history and large effective population sizes but also by interspecific gene flow. These closely related pine taxa form an excellent system for searching for loci involved in adaptive variation as they are differentiated in phenotype and ecology but have very similar genetic background.     

Overproduction and secretion of Bacillus circulans endo-β-1,3-1,4-glucanase gene (bglBC1) in B. subtilis and B. megaterium

A gene coding for endo--1,3-1,4-glucanase (lichenase) containing a recombinant plasmid, pLL200K, was transferred from Bacillus circulans into a new shuttle plasmid, pLLS920, by ligating linearized DNAs of pLL200K and pUB110. B. subtilis RM125 and B. megaterium ATCC14945 transformed with pLLS920 produced the endo--1,3-1,4-glucanase. The enzyme was produced during active growth with maximum activity. The B. subtilis (pLLS920) enzyme was 83 times (8522 mU ml^–1) more active than that of the gene donor cells (103 mU ml^–1). The B. megaterium (pLLS920) enzyme was 7 times (735 mU ml^–1) more active than that of the gene donor cells. While E. coli secreted only about 10% of the produced enzyme, B. subtilis excreted the enzyme completely into the medium and B. megaterium by about 98%. The plasmid pLLS920 was stable in B. megaterium (98%), and in B. subtilis (51%) but not in E. coli (29%).     

Phototactic behaviour of Eucryptorrhynchus scrobiculatus and E. brandti (Coleoptera: Curculionidae) adults*

Eucryptorrhynchus scrobiculatus and E. brandti (Coleoptera: Curculionidae) are destructive weevils on Ailanthus altissima in China. This study examined phototactic behaviour of E. scrobiculatus and E. brandti in response to eight light-emitting diodes (LEDs) in the laboratory and field. Effects of gender, starvation, and light and dark experience on the phototactic behaviour of the insects were evaluated. The results demonstrated that, the two species of weevil were phototactic insects and most sensitive to violet light (400–405?nm), followed by blue–violet light (420–430?nm). They were less sensitive to red (655–660?nm), white (6000–6500?k), blue–green (470–480?nm), yellow (590–595?nm), blue (450–455?nm), and green (515–530?nm) light. In the light intensity range of 200–1000?lux, the light intensity had no significant effect on the phototatic behaviour of E. scrobiculatus and E. brandti. Phototactic behaviour of the insects was affected by gender. The phototaxis indices of the two species of weevil increased with starvation, reaching a plateau after 2 or 3?d of starvation. The phototaxis indices of E. scrobiculatus and E. brandti were significantly affected by various wavelengths of light following exposure to the light for 3?h or in different dark experience time. In the mark-release-recapture test, the number of E. scrobiculatus and E. brandti adults trapped by violet (400–405?nm) light traps is the largest. The information provided here provides a basis for survey and control of E. scrobiculatus and E. brandti.     

Analysis of recombinant tagged equilibrative nucleoside transporter 1 (ENT1) expressed in E. coli

Nucleoside transporters (NTs) are integral membrane proteins necessary for the cellular entry of nucleoside analog drugs used in chemotherapeutic treatment of conditions such as cancer and viral or parasitic infections. NTs are also the targets of certain drugs used in the treatment of various cardiovascular conditions. Because of the importance of NTs in drug uptake, determination of the three-dimensional structure of these proteins, particularly hENT1, has the potential to improve these treatments through structure-based design of more specifically targeted and transported drugs. In this paper, we use NMR spectroscopy to investigate the structure of the large intracellular loop between transmembrane domains 6 and 7 and we also describe a method for the successful overexpression of full-length hENT1 in a bacterial system. Recombinant tandem histidine-affinity (HAT) and 3×FLAG tagged hENT1 was overexpressed in E. coli, affinity purified, and functionally characterized by nitrobenzylthioinosine (NBTI) binding. Anti-3×FLAG immunodetection confirmed the expression of N-HAT-3×FLAG-hENT1, while increased NBTI binding (3.2-fold compared with controls) confirmed the conformational integrity of the recombinant hENT1 within the bacterial inner membrane. Yields of recombinant hENT1 using this approach were ~15?μg/L of bacterial culture and this approach provides a basis for large-scale production of protein for a variety of purposes.     

A mitochondrial species identification assay for Australian blacktip sharks (Carcharhinus tilstoni, C. limbatus and C. amblyrhynchoides) using real-time PCR and high-resolution melt analysis

Tropical Australian shark fisheries target two morphologically indistinguishable blacktip sharks, the Australian blacktip (Carcharhinus tilstoni) and the common blacktip (C. limbatus). Their relative contributions to northern and eastern Australian coastal fisheries are unclear because of species identification difficulties. The two species differ in their number of precaudal vertebrae, which is difficult and time consuming to obtain in the field. But, the two species can be distinguished genetically with diagnostic mutations in their mitochondrial DNA ND4 gene. A third closely related sister species, the graceful shark C. amblyrhynchoides, can also be distinguished by species‐specific mutations in this gene. DNA sequencing is an effective diagnostic tool, but is relatively expensive and time consuming. In contrast, real‐time high‐resolution melt (HRM) PCR assays are rapid and relatively inexpensive. These assays amplify regions of DNA with species‐specific genetic mutations that result in PCR products with unique melt profiles. A real‐time HRM PCR species‐diagnostic assay (RT‐HRM‐PCR) has been developed based on the mtDNA ND4 gene for rapid typing of C. tilstoni, C. limbatus and C. amblyrhynchoides. The assay was developed using ND4 sequences from 66 C. tilstoni, 33. C. limbatus and five C. amblyrhynchoides collected from Indonesia and Australian states and territories; Western Australia, the Northern Territory, Queensland and New South Wales. The assay was shown to be 100% accurate on 160 unknown blacktip shark tissue samples by full mtDNA ND4 sequencing.     

Estimating genetic conformity between related ryegrass (Lolium) varieties. 1. Morphology and biochemical characterisation

In this study the morphological and protein diversity of twelve diploid perennial ryegrass accessions (Lolium perenne L.) was examined. These accessions comprised five closely related groups, each containing an `initial variety' (IV) and one or more declared `essentially derived varieties' (EDV), with differing degrees of relatedness. `Essential derivation' is a legal concept relating to intellectual property in plant varieties and is additional to Plant Breeders Rights (PBR). An EDV is defined as clearly distinct from, but conforming in its expression of the essential characteristics of an IV, from which it is found to have been predominantly derived. Where an essential derivation has been confirmed, the breeder of the IV may be entitled to some royalty sharing of the EDV. Clearly, therefore, in any successful EDV claim, evidence of a high degree of conformity in either the phenotype or genotype would be required. Examination of plant morphology indicated that all the EDVs were morphologically distinct from their corresponding IV in one or more morphological characteristic. using a principal co-ordinates analysis to give an overall measure of morphological difference, all twelve accessions were correctly clustered into their related groups and the magnitude of the differences within groups reflected their known breeding histories. Examining protein diversity by methods that targeted single- and multiple-locus genes also clustered the accessions into their correct groups, in most cases. However, only by examining diversity in seed storage proteins were within-group relationships accurately represented. The methods used provided no consistent representation of between-group relationships. It was concluded that the morphological method provided a creditable measure of genetic conformity, but to avoid incurring excessive time, work and cost, results from existing national PBR trials would need to be openly available. Within the limits of the genetic material examined, seed storage protein diversity appeared to provide a suitable combination of accuracy and efficiency on which to base a routine test. However, given more complex breeding relationships than those in this study, methods such as AFLP¹ markers that sample more genetic diversity, may be necessary to maintain this level of accuracy.     

Late Turolian Mesopithecus (Mammalia: Cercopithecidae) from Axios Valley (Macedonia,Greece): earliest presence of M. monspessulanus in Europe

The fossil mammal localities of the Axios Valley (Macedonia, Greece) yielded a rich collection of Mesopithecus remains, which were first described at the beginning of the 1990s. The late Turolian Dytiko localities include several specimens of Mesopithecus, which were originally separated in two size-related forms: the relatively larger-sized M. cf. or aff. pentelicus, and the relatively smaller-sized M. cf. monspessulanus. However, some Dytiko specimens were only partially described, or remained even undescribed because the cranium either was still in connection with the mandible or was markedly deformed. Later, careful cleaning of the materials and their revision based on larger comparative samples indicate that they represent two distinct species: the relatively larger-sized specimens belong to M. pentelicus, while the relatively smaller-sized ones to M. monspessulanus. The Dytiko M. pentelicus has slightly smaller dental dimensions compared to M. pentelicus from Pikermi, indicating a possible trend for size decrease. The Dytiko M. monspessulanus, although close to the typical form of this species, has somewhat larger dimensions. The semi-terrestrial M. pentelicus disappeared at the end of the Miocene, while some of its populations adapted to the wetter and more woody Pliocene habitats, finally giving origin to M. monspessulanus, whose elbow-joint indicates an arboreal lifestyle. M. monspessulanus was widely distributed in Europe, but its remains are very scarce and are all from the Pliocene. Some questionable indications for the presence of M. monspessulanus in the latest Miocene come from some Italian Messinian sites (Gravitelli, Baccinello V3), but this scenario still needs verification. However, even if its presence in some Italian localities was confirmed, the Dytiko M. monspessulanus nonetheless represents the earliest known occurrence of this species in Europe, as the Dytiko fauna is considered as latest Turolian (pre-Messinian, 7.0–6.0 Ma).     

Two new records of ascomycetes from Japan,Pyrenopeziza protrusa and P. nervicola (Helotiales,Dermateaceae sensu lato)

Two Pyrenopeziza species, P. protrusa and P. nervicola known to have similar morphology, were newly reported from Japan. This study clarified that P. protrusa morphologically differs from P. nervicola in (1) more protruded outermost cells in ectal excipulum, (2) smaller ascospores, and (3) longer and thinner asci. Pyrenopeziza protrusa produces chlamydospore-like brown cells under culture while P. nervicola forms more complex, brown bulbils. These species formed distinct clades based on ITS-5.8S rDNA in the phylogenetic analysis. The two species did not share the same host.     

The interplay of hybridization and clonal reproduction in the evolution of willows – Experiments with hybrids of S. eriocephala[R] & S. exigua[X] and S. eriocephala & S. petiolaris[P].

Clonal reproduction may contribute to plant evolution either by affecting population biology or by allowing partially sterile individuals (e.g., hybrids) repeated opportunities to reproduce sexually. The interplay of hybridization and clonal reproduction was first proposed by Stebbins (1950), but previously has not been tested experimentally. Alternative models for the effects of hybridization include speciation, introgression, and swamping. Salix spp. were chosen to test comparatively these hypotheses because they are easily hybridized and cloned. Over 500 separate crosses and backcrosses were made and over 6000 separate plants were measured in field experiments and statistically compared for significance to both evolutionary theory and plant breeding for biomass production. The F₁ hybrids in this study always equalled, and in the case of the hybrid PR, outperformed their parents in vegetative parameters. It seems likely that even without reproducing sexually, these F₁ hybrids could exist as successful individuals (sensu Stebbins 1950). However, it also seems likely that they would sexually reproduce: three of four F₁ hybrids studied (RX, RP, and PR) equalled or surpassed their parents in sexual parameters when crossing with at least one other accession. Of the alternative models, experimental data suggest that introgression would be the most likely outcome of a hybridization event. The hybrid XR, however, was partially sterile and performed poorly when crossing with all other accessions in its group except S. exigua (pistillate parent). Thus, this hybrid may fit Stebbins' model of a partially sterile yet vegetatively vigorous plant that can exist as a successful individual and make some contribution to interspecific gene flow over time. This is the first experimental study to confirm the evolutionary importance of clonal reproduction coupled with hybridization. However, distinguishing any of these evolutionary pathways would be difficult in nature using morphological techniques, as interspecific hybrids tend to resemble their pistillate parents in terms of leaf shape.     

Mapping of within-species segregation distortion in Drosophila persimilis and hybrid sterility between D. persimilis and D. pseudoobscura

In contrast to the prevailing dogma in the 1990s, recent studies have suggested that an evolutionary history of segregation distortion within species may contribute to sterility in species hybrids. However, this recent work identified segregation distortion exclusively in species hybrids that may never have had an evolutionary history of segregation distortion in either parent species. We expand on previous work using a strain of Drosophila persimilis exhibiting segregation distortion within species to generate QTL maps for segregation distortion and hybrid sterility in crosses between D. persimilis and D. pseudoobscura. The maps localize regions along the XR contributing to both phenotypes, and they indicate one region of overlap between the two maps. This overlap could provide preliminary evidence for an association between segregation distortion within species and hybrid sterility, but the localizations are currently too broad to have confidence in this conclusion. This work is a first step towards possibly supporting a genetic conflict model of speciation in this system.     

Evolution of bract development and B-class MADS box gene expression in petaloid bracts of Cornus s. l. (Cornaceae)

? Despite increasing interest in the molecular mechanisms of floral diversity, few studies have investigated the developmental and genetic bases of petaloid bracts. This study examined morphological patterns of bract initiation and expression patterns of B-class MADS-box genes in bracts of several Cornus species. We suggest that petaloid bracts in this genus may not share a single evolutionary origin. ? Developmental pathways of bracts and spatiotemporal expression of B-class genes in bracts and flowers were examined for four closely related dogwood species. ? Divergent morphological progressions and gene expression patterns were found in the two sister lineages with petaloid bracts, represented by Cornus florida and Cornus canadensis. Phylogeny-based analysis identified developmental and gene expression changes that are correlated with the evolution of petaloid bracts in C.?florida and C.?canadensis. ? Our data support the existence of independent evolutionary origins of petaloid bracts in C.?canadensis and C.?florida. Additionally, we suggest that functional transference within B-class gene families may have contributed to the origin of bract petaloidy in C.?florida. However, the underlying mechanisms of petaloid bract development likely differ between C.?florida and C.?canadensis. In the future this hypothesis can be tested by functional analyses of Cornus B-class genes.     

Cytological differentiation between the two subgenomes of the tetraploid Emilia fosbergii Nicolson and its relationship with E. sonchifolia (L.) DC. (Asteraceae)

The diploid Emila sonchifolia (2n = 10) and the tetraploid E. fosbergii (2n = 20) species are widely distributed throughout tropical and subtropical America, and are the only two Emilia species occurring in Brazil. Emilia fosbergii displays two sets of ten chromosomes, one slightly larger than the other. The smaller chromosome set is similar to the chromosome complement of the diploid, which agrees with the suggested participation of E. sonchifolia in the formation of E. fosbergii. To elucidate this hypothesis, the relationship between the genomes of the two species was investigated using chromomycin A3 (CMA)/4’,6-diamidino-2-phenylindole (DAPI) double staining, distribution of 5S and 45S rDNA sites by fluorescence in situ hybridization (FISH) and whole genome comparison by genomic in situ hybridization (GISH). CMA/DAPI staining and FISH revealed the occurrence of one pair of CMA bands in E. sonchifolia and three pairs in E. fosbergii, all of them co-localized with 45S rDNA sites. Additionally, E. fosbergii displayed a fourth, small 45S rDNA site in its larger subgenome which was not detected as CMA band. Surprisingly, the euchromatin of the smaller subgenome of E. fosbergii stained less intensely with CMA than the larger one. The GISH procedure demonstrated the similarity between the genome of E. sonchifolia and the smaller chromosome set of E. fosbergii. GISH and CMA staining clearly demonstrate that E. fosbergii is an allotetraploid species and suggest E. sonchifolia as one of its ancestors. The maintenance of at least one pair of 5S and 45S rDNA sites per subgenome of E. fosbergii and the differentiation between its subgenomes by CMA staining seem to indicate that post-polyploidization changes are still incipient, probably because the polyploidization event and the origin of E. fosbergii were relatively recent.     

Plasticity of the Electrical Connectome of C. elegans

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QTL mapping of black rot (Guignardia bidwellii) resistance in the grapevine rootstock ‘Börner’ (V. riparia Gm183 × V. cinerea Arnold)

Key message

In the grapevine cultivar ‘Börner’ QTLs for black rot resistance were detected consistently in several independent experiments. For one QTL on chromosome 14 closely linked markers were developed and a detailed map provided.

Abstract

Black rot is a serious grapevine disease that causes substantial yield loss under unfavourable conditions. All traditional European grapevine cultivars are susceptible to the causative fungus Guignardia bidwellii which is native to North America. The cultivar ‘Börner’, an interspecific hybrid of V. riparia and V. cinerea, shows a high resistance to black rot. Therefore, a mapping population derived from the cross of the susceptible breeding line V3125 (‘Schiava grossa’ × ‘Riesling’) with ‘Börner’ was used to carry out QTL analysis. A resistance test was established based on potted plants which were artificially inoculated in a climate chamber with in vitro produced G. bidwellii spores. Several rating systems were developed and tested. Finally, a five class scheme was applied for scoring the level of resistance. A major QTL was detected based on a previously constructed genetic map and data from six independent resistance tests in the climate chamber and one rating of natural infections in the field. The QTL is located on linkage group 14 (Rgb1) and explained up to 21.8 % of the phenotypic variation (LOD 10.5). A second stable QTL mapped on linkage group 16 (Rgb2; LOD 4.2) and explained 8.5 % of the phenotypic variation. These two QTLs together with several minor QTLs observed on the integrated map indicate a polygenic nature of the black rot resistance in ‘Börner’. A detailed genetic map is presented for the locus Rgb1 with tightly linked markers valuable for the development for marker-assisted selection for black rot resistance in grapevine breeding.     

Distinct genetic isolation between “Kunimasu” (Oncorhynchus kawamurae) and “Himemasu” (O. nerka) in Lake Saiko, Yamanashi Prefecture, Japan, inferred from microsatellite analysis

The possibility of interspecific hybridization between Kunimasu (Oncorhynchus kawamurae) and Himemasu (Oncorhynchus nerka) was investigated in a large number of specimens, in a search for basic data relevant to conservation needs. A Bayesian-based clustering method using five microsatellite DNA loci separated 144 specimens from Lake Saiko, Yamanashi Prefecture, into two genetically distinct groups, corresponding to Kunimasu and Himemasu. Application of a threshold of individual proportion of membership of 0.90, so as to separate hybrids from purebreds, resulted in all specimens except two having high probability of purebred. These results implied that Kunimasu and Himemasu have been maintained as independent genetic entities in Lake Saiko.     

Advanced backcross-QTL analysis in spring barley (H. vulgare ssp. spontaneum) comparing a REML versus a Bayesian model in multi-environmental field trials

A common difficulty in mapping quantitative trait loci (QTLs) is that QTL effects may show environment specificity and thus differ across environments. Furthermore, quantitative traits are likely to be influenced by multiple QTLs or genes having different effect sizes. There is currently a need for efficient mapping strategies to account for both multiple QTLs and marker-by-environment interactions. Thus, the objective of our study was to develop a Bayesian multi-locus multi-environmental method of QTL analysis. This strategy is compared to (1) Bayesian multi-locus mapping, where each environment is analysed separately, (2) Restricted Maximum Likelihood (REML) single-locus method using a mixed hierarchical model, and (3) REML forward selection applying a mixed hierarchical model. For this study, we used data on multi-environmental field trials of 301 BC₂DH lines derived from a cross between the spring barley elite cultivar Scarlett and the wild donor ISR42-8 from Israel. The lines were genotyped by 98 SSR markers and measured for the agronomic traits “ears per m2,” “days until heading,” “plant height,” “thousand grain weight,” and “grain yield”. Additionally, a simulation study was performed to verify the QTL results obtained in the spring barley population. In general, the results of Bayesian QTL mapping are in accordance with REML methods. In this study, Bayesian multi-locus multi-environmental analysis is a valuable method that is particularly suitable if lines are cultivated in multi-environmental field trials. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Entosis Controls a Developmental Cell Clearance in C. elegans

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Hybridization and introgression in Carex aquatilis and C. paleacea

The diversification and distribution of Abies species throughout the Mediterranean region has led to a complex of species which are difficult to classify. An open question is whether these mainly allopatric taxa have exchanged genetic information via secondary contact. We studied the variation and geographic distribution of paternally inherited chloroplast DNA markers in nine Mediterranean Abies taxa. Markers with high and low mutation rates were applied in order to differentiate among a scenario of secondary genetic contact and a scenario of complete isolation after speciation. The observed molecular variation was analysed using statistical parsimony, geostatistics, and measures of population genetic differentiation. Ancient paternal lineages, represented by markers with low mutation rates, were shared among species. The central and widespread A. alba retained all ancient lineages whereas other species exhibited fewer, down to a single lineage. In contrast, modern lineages, depicted by markers with high mutation rates, were largely separated among species. The western Mediterranean A. pinsapo and A. numidica were clearly separated from each other and from the remaining Abies species. This indicates the absence of secondary contact. The same scenario applies to the eastern Mediterranean Abies species. An exception is the parapatric complex of A. alba, A. cephalonica, and their supposed hybrid A. borisii regis, which exhibited evidence of secondary contact.