Physiological studies and determination of chromosome number in Maca,Lepidium Meyenii (Brassicaceae)

Experiments based on four accessions of maca (Lepdium meyenii) disclosed higher developmental rates in plants grown in neutral pH (6.6) soil when compared with those grown in acidic soil (5.3). Photoperiod response studies revealed similar growth rate for plants grown under either long day or short day condition. Plants in the field and growth chambers completed their life cycle in 11 months or less, therefore maca can be considered an annual crop. These results suggest that the range of adaptation of maca is not as narrow as previously believed, and therefore it can be successfully produced outside its natural habitat. Chromosome counts and predominance of bivalents in diakinesis and metaphase I disclosed that maca is a disomic octoploid of 2n=8x=64 chromosomes. Field and growth chamber observations and morphological uniformity of the plants within accessions indicate that maca relies mainly on self-fertilization for its reproduction.     

空间条件对几种粮食作物的同工酶和细胞学特性的影响

搭载１９８７年发射的两颗返地卫星（８月５—１０日和９月９—１７日）的几种小麦、大麦种子,经回收后初步研究表明：（１）对发芽率的影响：空间处理的种子,其发芽率与对照无差别;（２）对茎及生育期的影响：空间处理的种子长成的幼苗比对照强壮,植株高度有些品种明显的矮于对照。生育期有不同程度延长;（３）对染色体结构的影响：花粉母细胞减数分裂观察表明搭载卫星的种子当代可诱导出比地面更多的染色体桥、落后染色体及染色体数目异于正常体细胞数目的现象。小麦品种Ｃｏｃｏｒｉｔ—７１经空间处理后花粉母细胞的染色体数目异常可高达２０．５１％,而地面对照组其花粉母细胞基本正常（２ｎ＝２８）;（４）对同工酶的影响：经空间处理的小麦种子酯酶、过氧化物酶的同工酶谱带空间处理的比地面对照减少。由此可见,空间处理可诱导纯合植物种子发生变异,为农作物育种创造一个新途径。     

Analysis of nutrient components of food for Asian elephants in the wild and in captivity

Thirty-seven wild plants as food for Asian elephants in the field in Simao, Yunnan province, China and five cultivated plants as food for captive elephants in the Beijing Zoo were collected and analyzed for their main nutrient components. Protein, fat, fiber, dry material, ash as well as major microelements: calcium, kalium, zincum, sodium in the food were analyzed by standard methodology. No significant differences were found between the wild plants taken in the field and forage provided in captivity. However, the calcium content in the forage is significantly less than the average of those in the wild plants. It is suggested that the increase in calcium intake may contribute to the relief of low plasma calcium diseases of elephants in captivity. Translated from Journal of Beijing Normal University (Natural Science), 2006, 42(2): 184–188 [译自: 北京师范大学学报 (自然科学版)]     

Analysis of nutrient components of food for Asian elephants in the wild and in captivity

Thirty-seven wild plants as food for Asian elephants in the field in Simao,Yunnan province,China and five cultivated plants as food for captive elephants in the Beijing Zoo were collected and analyzed for their main nutrient components.Protein,fat,fiber,dry material,ash as well as major microelements:calcium,kalium,zincum,sodium in the food were analyzed by standard methodology.No significant differences were found between the wild plants taken in the field and forage provided in captivity.However,the calcium content in the forage is significantly less than the average of those in the wild plants.It is suggested that the increase in calcium intake may contribute to the relief of low plasma calcium diseases of elephants in captivity.     

Genetic characterization and molecular mapping of Hessian fly resistance genes derived from Aegilops tauschii in synthetic wheat

Two synthetic hexaploid wheat lines (×Aegilotriticum spp., 2n = 6x = 42, genomes AABBDD), SW8 and SW34, developed from the crosses of the durum wheat cultivar Langdon (Triticum turgidum L. var. durum, 2n = 4x = 28, genomes AABB) with two Aegilops tauschii Cosson accessions (2n = 2x = 14, genome DD), were determined to carry Hessian fly [Mayetiola destructor (Say)] resistance genes derived from the Ae. tauschii parents. SW8 was resistant to the Hessian fly biotype Great Plains (GP) and strain vH13 (virulent to H13). SW34 was resistant to biotype GP, but susceptible to strain vH13. Allelism tests indicated that resistance genes in SW8 and SW34 may be allelic to H26 and H13 or correspond to paralogs at both loci, respectively. H26 and H13 were localized to chromosome 4D and 6D, respectively, in previous studies. Molecular mapping in the present study, however, assigned the H26 locus to chromosome 3D rather than 4D. On the other hand, mapping of the resistance gene in SW34 verified the previous assignment of the H13 locus to chromosome 6D. Linkage analysis and physical mapping positioned the H26 locus to the chromosomal deletion bin 3DL3-0.81–1.00. A linkage map for each of these two resistance genes was constructed using simple sequence repeat (SSR) and target region amplification polymorphism (TRAP) markers.     

LSGermOPA,a custom OPA of 384 EST-derived SNPs for high-throughput lettuce (<Emphasis Type="Italic">Lactuca sativa</Emphasis> L.) germplasm fingerprinting

To deploy a high-throughput genotyping platform in germplasm management, we designed and tested a custom OPA (Oligo Pool All), LSGermOPA, for assessing the genetic diversity and population structure of the USDA cultivated lettuce (Lactuca sativa L.) germplasm collection using Illumina’s GoldenGate assay. This OPA contains 384 EST (expressed sequence tag)-derived SNP (single nucleotide polymorphism) markers selected from a large set of SNP markers experimentally validated and mapped by the Compositae Genome Project. Used for genotyping were DNA samples prepared from bulked leaves of five randomly-selected seedlings from each of 380 lettuce accessions. High-quality genotype data were obtained from 354 of the 384 SNPs. The reproducibility of automatic genotype calls was 99.8% as calculated from the four pairs of duplicated DNA samples in the assay. An unexpectedly high percentage of heterozygous genotypes at the polymorphic loci for most accessions indicated a high level of heterogeneity within accessions. Only 148 homogenous accessions, collectively comprising all five horticultural types, were used in subsequent analyses to demonstrate the usefulness of LSGermOPA. The results of phylogenetic relationship, population structure and genetic differentiation analyses were consistent with previous reports using other marker systems. This suggests that LSGermOPA is capable of revealing sufficient levels of polymorphism among lettuce cultivars and is appropriate for rapid assessment of genetic diversity and population structure in the lettuce germplasm collection. Challenges and strategies for effective genotyping and managing lettuce germplasm are discussed.     

1H NMR-based metabonomics study on serum of renal interstitial fibrosis rats induced by unilateral ureteral obstruction

Renal fibrosis is the common pathway of progressive renal disease with complex pathogenesis. Investigating the metabolic changes in the evaluation process of renal fibrosis may enhance the understanding of its pathogenesis. In this study, (1)H nuclear magnetic resonance ((1)H NMR) measurements combined with multivariate statistical techniques were performed to study the metabolic changes in serum samples of renal interstitial fibrosis (RIF) rats, induced by unilateral ureteral obstruction (UUO). Partial least squares-discriminant analysis (PLS-DA) showed satisfactory clustering between UUO and sham operation (SO) rats, suggesting that the metabolic profiles of the RIF groups are markedly different from those of the controls. Alterations in the levels of some metabolites such as valine, isoleucine, lactate, 3-hydroxybutyrate, alanine, acetate, acetoacetate, pyruvate, and glutamate, with time dependence in UUO rats, were observed in PLS-DA loading plots. These changed metabolites represent potential metabolic biomarkers and provide clues that can elucidate the mechanisms underlying the generation and development of RIF. Enhanced metabolic pathways of lipid and ketone body synthesis were predominant in RIF rats. Energy metabolism seemed to be impaired at the early stage of fibrosis but enhanced at a late stage. Our results suggest that (1)H NMR-based metabonomics can provide novel insights into the pathogenesis of RIF.     

Mapping one of the 2 genes controlling lemon ray flower color in sunflower (Helianthus annuus L.)

In an F2 population of 120 plants derived from a cross between 2 breeding lines with yellow ray flowers, we observed 111 plants with yellow-colored and 9 plants with lemon-colored ray flowers. The segregation pattern fits a 15:1 (chi2(15:1) = 0.32, P > 0.5) ratio, suggesting that the lemon ray flower color is conditioned by 2 independent recessive genes that had been contributed individually by each of the parents. We sampled 111 plants from the 3 F(2:3) families displaying a 3 to 1 segregating ratio for genotyping with molecular markers. One of the genes, Yf(1), was mapped onto linkage group 11 of the public sunflower map. A targeted region amplified polymorphism marker (B26P17Trap13-68) had a genetic distance of 1.5 cM to Yf(1), and one simple sequence repeat marker (ORS733) and one expressed sequence tag (EST)-based marker (HT167) previously mapped to linkage group 11 were linked to Yf(1) with distances of 9.9 and 2.3 cM, respectively.     

Molecular mapping of an apical branching gene of cultivated sunflower (<Emphasis Type="Italic">Helianthus annuus</Emphasis> L.)

Commercial hybrids of cultivated sunflower (Helianthus annuus L.) are obtained by crossing a cytoplasmic male sterile line (A-line) with a restorer pollinator (R-line). The incorporation of a recessive branching trait to extend the pollination period of R-lines during hybrid seed production is laborious and time-consuming. By using target region polymorphism (TRAP) and bulked segregant analysis (BSA), we identified 15 TRAP markers linked to the b(1) (branching) locus in a population of 229 F(2) plants derived from a cross between nonbranched (HA 234) and branched (RHA 271) lines. TBr4-720 and TBr8-555 markers were linked to the b(1) gene in the coupling phase at 0.5 cM (0.004 recombination frequency). The Tbr20-297 and Tbr20-494 markers flanked the b(1) locus in the repulsion phase at genetic distances of 7.5 and 2.5 cM, respectively. Tbr19-395, also in the repulsion phase, mapped at 3.8 cM from the b(1) locus and on the opposite side of the marker Tbr20-297. The 8A1 and 15B3 restriction fragment length polymorphic (RFLP) markers of linkage group (LG) 16 of the RHA 271 x HA 234 cultivated sunflower map anchored the b(1) LG onto the RFLP map. Polymerase chain reaction (PCR)-based markers tightly linked to the recessive b(1) gene have been developed. Their identification and the incorporation of the LG containing the b(1) locus onto an RFLP map will be useful for marker-assisted selection (MAS) in breeding programs and provide the bases for map-based cloning of this gene.