Stable Carbon Isotope Discrimination Is under Genetic Control in the C4 Species Maize with Several Genomic Regions Influencing Trait Expression

In plants with C₄ photosynthesis, physiological mechanisms underlying variation in stable carbon isotope discrimination (Δ13C) are largely unknown, and genetic components influencing Δ13C have not been described. We analyzed a maize (Zea mays) introgression library derived from two elite parents to investigate whether Δ13C is under genetic control in this C₄ species. High-density genotyping with the Illumina MaizeSNP50 Bead Chip was used for a detailed structural characterization of 89 introgression lines. Phenotypic analyses were conducted in the field and in the greenhouse for kernel Δ13C as well as plant developmental and photosynthesis-related traits. Highly heritable significant genetic variation for Δ13C was detected under field and greenhouse conditions. For several introgression library lines, Δ13C values consistently differed from the recurrent parent within and across the two phenotyping platforms. Δ13C was significantly associated with 22 out of 164 analyzed genomic regions, indicating a complex genetic architecture of Δ13C. The five genomic regions with the largest effects were located on chromosomes 1, 2, 6, 7, and 9 and explained 55% of the phenotypic variation for Δ13C. Plant development stage had no effect on Δ13C expression, as phenotypic as well as genotypic correlations between Δ13C, flowering time, and plant height were not significant. To our knowledge, this is the first study demonstrating Δ13C to be under polygenic control in the C₄ species maize.During photosynthesis, plants use light energy to convert atmospheric CO₂ and water into carbohydrates. For the element carbon, there are two stable isotopes, ¹²C and ¹³C. Due to the physical and chemical properties of photosynthetic CO₂ fixation, plants are depleted in ¹³C compared with atmospheric CO₂. In C₃ plants, this discrimination of stable carbon isotopes (Δ13C) has long been used to detect genetic differences of water use efficiency and has been shown to be an accurate predictor for yield under drought (Rebetzke et al., 2002). As Δ13C is linearly related to the ratio of intercellular to atmospheric CO₂ partial pressure (Farquhar et al., 1982), stomatal closure under drought stress is associated with reduced Δ13C. For C₄ plants, our knowledge about the mechanisms underlying Δ13C and about its association with water use efficiency is much more limited. Differences in Δ13C between genotypes of C₄ species have been reported, among others, for sorghum (Sorghum bicolor; Hubick et al., 1990) and maize (Zea mays; Monneveux et al., 2007). However, comprehensive studies analyzing the inheritance of Δ13C have not been performed to date.In C₃ plants, the important steps of CO₂ uptake include the diffusion of atmospheric CO₂ through the boundary layer and the stomata. Subsequently, CO₂ is taken up by the cell and enters the chloroplast, where carboxylation by Rubisco takes place. During photosynthetic carbon fixation, the strongest fractionation of carbon isotopes occurs during the carboxylation reaction of Rubisco (Roeske and O’Leary, 1984). A theoretical model of Δ13C in C₃ photosynthesis has been described by Farquhar et al. (1982), in which Δ13C depends linearly on the ratio of intercellular to ambient partial pressure of CO₂ (p_i p_a−1), and thus provides an indication of stomatal conductance and photosynthetic capacity. Additionally, the model includes the dependency of Δ13C on the fractionation of carbon isotopes during CO₂ diffusion in the air and on the enzymatic properties of the Rubisco enzyme.For rice (Oryza sativa), tomato (Solanum lycopersicum), and wheat (Triticum aestivum), it has been shown that genetic variation for Δ13C is quantitative, genotype-by-environment interaction is small, and the trait heritability is high (Condon and Richards, 1992; Rebetzke et al., 2002; Comstock et al., 2005; Impa et al., 2005). Quantitative trait loci (QTL) for Δ13C have been mapped (Handley et al., 1994; Price et al., 2002; Rebetzke et al., 2008), and in the model plant Arabidopsis (Arabidopsis thaliana), four genes have been identified that are associated with Δ13C. Two are involved in stomatal patterning and thus influence stomatal conductance (Masle et al., 2005; Nilson and Assmann, 2010), and one of them influences photosynthetic capacity as well (Masle et al., 2005). One gene plays a role in cuticular wax composition and is also associated with stomatal conductance (Lü et al., 2012), whereas the fourth gene encodes a cellulose synthase subunit, and mutations in this gene lead to decreased Δ13C. Presumably, this is the result of a decreased cell turgor due to a decreased water transport capacity of the xylem (Liang et al., 2010).For C₄ plants, our knowledge about the genetic mechanisms and physiological processes underlying Δ13C is much more limited, due to the more complex mechanism of CO₂ fixation. The first carboxylation step in C₄ plants takes place in mesophyll cells, in which CO₂ is fixed by phosphoenolpyruvate carboxylase (PEPC). During this reaction, combined with the fractionation of carbon isotopes during HCO₃⁻ formation, carbon is actually enriched in ¹³C (Farquhar, 1983). The C₄ organic acid formed by PEPC is transported to the bundle sheath cells, where CO₂ is released to be fixed by Rubisco in the second step. However, a fraction of CO₂ released in the bundle sheath can diffuse back to the mesophyll cells. The proportion of carbon fixed by PEPC that subsequently leaks out of the bundle sheath cells is termed leakiness (ϕ) and reduces the opportunity of Rubisco to discriminate against ¹³C in C₄ plants. According to the theoretical model by Farquhar (1983), Δ13C and p_i p_a−1 are also linearly related in C₄ plants, but the regression slope is determined by ϕ. Consequently, there can be a positive or a negative correlation of Δ13C and p_i p_a−1 depending on ϕ (Hubick et al., 1990). Regarding the entire fixation process, discrimination against ¹³C in C₄ plants is not as strong as in C₃ plants, and so far there have been few studies reporting a genetic variation of Δ13C in C₄ plants. In sorghum, small but significant differences in Δ13C have been observed among 12 cultivars (Hubick et al., 1990), and similar to C₃ plants, Δ13C has been shown to be correlated with transpiration efficiency (Henderson et al., 1998). Additionally, it has been shown for maize and sugarcane (Saccharum officinarum) that stress conditions lead to an increase in Δ13C (Bowman et al., 1989; Meinzer et al., 1994; Ranjith et al., 1995; Buchmann et al., 1996). Experiments under drought and under well-watered conditions showed higher values for Δ13C in drought-tolerant maize hybrids than in susceptible checks (Monneveux et al., 2007).The use of Δ13C as an indirect trait in breeding for drought tolerance in C₄ species would be highly beneficial, given a stable trait expression and high heritability similar to that in C₃ plants. To assess whether Δ13C can also be used in C₄ plants as an indirect selection trait for drought-tolerant lines, it needs to be shown that Δ13C is under genetic control, although the physiology and molecular mechanisms of Δ13C are not yet fully understood. In this study, we used an introgression library (IL; Eshed and Zamir, 1994) derived from two elite parents to analyze the genetic variation in Δ13C under well-watered conditions. ILs have been successfully used in genetics to identify QTL for various qualitatively and quantitatively inherited traits. An IL is a defined set of nearly isogenic inbred lines derived from repeated backcrosses with one of the parents (recurrent parent [RP]) and marker-assisted selection for single fragments (Supplemental Fig. S1). Ideally, each IL line carries a single chromosome fragment of a donor parent (DP) in the genetic background of an RP. Taken together, the different segments cover the whole donor genome, allowing estimation of the effects of single donor fragments in an otherwise identical genetic background (Eshed and Zamir, 1994). The RP of the IL under investigation originates from southeastern Europe and is an elite inbred line of the maize dent pool. As DP, we chose an unrelated maize line representative of the European flint pool. The IL (IL_01–IL_89) was genotyped using the Illumina MaizeSNP50 Bead Chip (Ganal et al., 2011) carrying 56,110 single-nucleotide polymorphism (SNP) markers.Kernel Δ13C of 77 IL lines was measured in the field and in the greenhouse (Δ13C is genetically controlled in the C₄ species maize. Our specific goals were (1) to characterize the genetic architecture of Δ13C (i.e. to determine the number of genomic regions associated with Δ13C), (2) to localize genomic regions influencing Δ13C, and (3) to assess the extent to which genotypic variation in Δ13C might be the result of differences in plant development.

Table I.

Overview of the experiments and experimental designs

Genetic diversity and biogeography of native and introduced populations of Ulva pertusa (Ulvales,Chlorophyta)

Genetic diversity of native and introduced populations of Ulva pertusa (Ulvales, Chlorophyta) was examined using genetic markers of chloroplast, mitochondria and nuclear non‐coding region sequences. In the preliminary investigations to genetically identify the species for further analyses, U. pertusa was found only from temperate coasts of the more extensive collection sites including tropical coasts suggesting that it is a temperate species and basically not distributed in tropical regions. For chloroplast and mitochondrial sequences, repeating patterns of short tandem repeat sequences and nucleotide substitutions were used to recognize the haplotypes (genetic types). A total of 48 haplotypes based on combinations of chloroplast and mitochondrial haplotypes were recognized in the 244 specimens collected in the presumptive native range (Northeast Asia) and introduced populations (North America, Australia, New Zealand, Chile and Europe). Among them, 46 haplotypes (H1–H8 and H11–H48) were recognized in Northeast Asia, whereas only 1–5 haplotypes were recognized in the other areas. Nuclear microsatellite sequences were also analyzed. The lengths of the PCR products including the nuclear microsatellite region of 234 specimens were determined, and a total of 17 genotypes were recognized. Among them, 14 genotypes were found in Northeast Asia, whereas 1–7 genotypes were recognized in the other areas. Based on the results, the hypothesis that the native range of the species is in Northeast Asia was supported, and the populations outside this range were concluded to be non‐indigenous populations.     

Phylogeny reconstruction based on the length distribution of <Emphasis Type="Italic">k</Emphasis>-mismatch common substrings

Background

Various approaches to alignment-free sequence comparison are based on the length of exact or inexact word matches between pairs of input sequences. Haubold et al. (J Comput Biol 16:1487–1500, 2009) showed how the average number of substitutions per position between two DNA sequences can be estimated based on the average length of exact common substrings.

Results

In this paper, we study the length distribution of k-mismatch common substrings between two sequences. We show that the number of substitutions per position can be accurately estimated from the position of a local maximum in the length distribution of their k-mismatch common substrings.

     

Adipose stem cell-derived extracellular matrix represents a promising biomaterial by inducing spontaneous formation of prevascular-like structures by mvECs

Tissue constructs of physiologically relevant scale require a vascular system to maintain cell viability. However, in vitro vascularization of engineered tissues is still a major challenge. Successful approaches are based on a feeder layer (FL) to support vascularization. Here, we investigated whether the supporting effect on the self-assembled formation of prevascular-like structures by microvascular endothelial cells (mvECs) originates from the FL itself or from its extracellular matrix (ECM). Therefore, we compared the influence of ECM, either derived from adipose-derived stem cells (ASCs) or adipogenically differentiated ASCs, with the classical cell-based FL. All cell-derived ECM (cdECM) substrates enabled mvEC growth with high viability. Prevascular-like structures were visualized by immunofluorescence staining of endothelial surface protein CD31 and could be observed on all cdECM and FL substrates but not on control substrate collagen I. On adipogenically differentiated ECM, longer and higher branched structures could be found compared with stem cell cdECM. An increased concentration of proangiogenic factors was found in cdECM substrates and FL approaches compared with controls. Finally, the expression of proteins associated with tube formation (E-selectin and thrombomodulin) was confirmed. These results highlight cdECM as promising biomaterial for adipose tissue engineering by inducing the spontaneous formation of prevascular-like structures by mvECs.     

North American black-fruited hawthorns. I. Variation in floral construction,breeding system correlates,and their possible evolutionary significance inCrataegus sect.Douglasii London

Differences in the numbers of stamens and styles per flower are conspicuous features of variation in North American hawthorns (Crataegus L.). Variation in stamen number between individuals is discontinuous, with modes of approximately 20 and 10 (or fewer). In North American black-fruited sectionDouglasii Loudon the 10-stamen morphotype is exclusively polyploid, whereas the 20-stamen morphotype comprises both diploids and polyploids. Polyploidy is associated with apospory, self-fertility, and varying degrees of pollen sterility. Variation in stamen number may also be correlated with variation in distribution, phenology, leaf shape, and other features of floral morphology, leading to recognition of taxa at the specific or infraspecific level. Comparable variation in stamen number is virtually unknown in Eurasian hawthorns, as in the majority of flowering plants. In sectionDouglasii stamen number morphotypes have been recognized as either varieties or species; although correlations between stamen number and other features are not as straightforward as was previously surmised, the higher rank appears to be appropriate. These data on breeding system and morphological variation may be explainable in terms of hypotheses linking gametophytic apomixis, polyploidization, and optimal strategies for pollen dispersal.     

A comprehensive proteome map of the lipid-requiring nosocomial pathogen Corynebacterium jeikeium K411

Corynebacterium jeikeium is a lipid-requiring pathogen that is considered as part of the normal microflora of the human skin and associated with severe nosocomial infections. Systematic reference maps of the cytoplasmic, cell surface-associated, and extracellular proteome fractions of the clinical isolate C. jeikeium K411 were examined by 2-DE coupled with MALDI-TOF MS. A sum total of 555 protein spots were identified by PMF, corresponding to 358 different proteins that were classified into functional categories and integrated into metabolic pathways. The majority of the proteins were linked to housekeeping functions in energy production and translation and to physiological processes in amino acid, carbohydrate, nucleotide, and lipid metabolism. A complete enzymatic machinery necessary to utilize exogenous fatty acids by beta-oxidation was detected in the cytoplasmic proteome fraction. In addition, several predicted virulence factors of C. jeikeium K411 were identified in the cell surface-associated and extracellular subproteome, including the cell surface proteins SurA and SurB, the surface-anchored pilus subunits SapA and SapB, the surface-anchored collagen adhesin CbpA, the cholesterol esterase Che, and the acid phosphatase AcpA.     

Proteomic response of the marine ammonia-oxidising archaeon Nitrosopumilus maritimus to iron limitation reveals strategies to compensate for nutrient scarcity

Dissolved iron (Fe) is vanishingly low in the oceans, with ecological success conferred to microorganisms that can restructure their biochemistry to maintain high growth rates during Fe scarcity. Chemolithoautotrophic ammonia-oxidising archaea (AOA) are highly abundant in the oceans, constituting ~30% of cells below the photic zone. Here we examine the proteomic response of the AOA isolate Nitrosopumilus maritimus to growth-limiting Fe concentrations. Under Fe limitation, we observed a significant reduction in the intensity of Fe-dense ferredoxins associated with respiratory complex I whilst complex III and IV proteins with more central roles in the electron transport chain remain unchanged. We concomitantly observed an increase in the intensity of Fe-free functional alternatives such as flavodoxin and plastocyanin, thioredoxin and alkyl hydroperoxide which are known to mediate electron transport and reactive oxygen species detoxification, respectively. Under Fe limitation, we found a marked increase in the intensity of the ABC phosphonate transport system (Phn), highlighting an intriguing link between Fe and P cycling in N. maritimus. We hypothesise that an elevated uptake of exogenous phosphonates under Fe limitation may either supplement N. maritimus' endogenous methylphosphonate biosynthesis pathway - which requires Fe - or enhance the production of phosphonate-containing exopolysaccharides known to efficiently bind environmental Fe.     

From Mendelian to molecular genetics: the Xiphophorus melanoma model

In human tumor biopsies it is almost impossible to pinpoint the particular molecular abnormalities that determine neoplasia. In animal models where tumorigenesis is initiated by clearly defined genetic events, it is possible to study the genes and their functions that make a normal cell become a fully malignant cancer cell. In the fish Xiphophorus, melanoma can be initiated by simple crossings, and the signaling pathways that govern tumor growth and progression can be delineated. This model offers the prospect of obtaining a complete picture of the molecular changes and regulatory networks underlying tumor formation, which should contribute to a better understanding of some general principles of cancer biology, and identify new targets for melanoma research in particular.