Phylogenetic analysis of Hordeum marinum Huds. based on nucleotide sequences linked to the vrs1 locus

 More than 100 accessions of Hordeum marinum ssp. marinum, ssp. gussoneanum 2x and ssp. gussoneanum 4x were studied by analyzing the nuclear DNA homologous to the chloroplast translation elongation factor. PCR amplification using the locus-specific primers generated a 932 bp fragment from ssp. marinum, a 915 bp fragment from ssp. gussoneanum 2x, and 915 bp and 931 bp fragments from ssp. gussoneanum 4x. Sequencing of the entire DNAs showed that the 915-bp fragments of diploids and tetraploids are identical, indicating that the diploid probably is the immediate donor of the 915-bp fragment of tetraploids. Although the donor of the 931-bp fragment was not determined, phylogenetic analysis of the data showed that the clade of the 931-bp fragment was included in the H. marinum complex. A MspI site was diagnostic to distinguish ssp. marinum into two clades with disjunct distributions, the Iberian Peninsula (type 2) and other regions (type 1). Nucleotide variation was revealed in the type 2 accessions but all the other clades were highly uniform. Received January 3, 1999 Accepted January 24, 2001     

A new multiflorous species of Leymus (Poaceae: Triticeae) from western China

A new species of Leymus section Racemosus, L. pluriflorus L.B.Cai & T.L.Zhang, is described and illustrated. It grows in the eastern part of Qinghai Province and the southern part of Gansu Province, China. It most closely resembles L. crassiusculus L.B.Cai, from which it differs in having longer rachis internodes, some pedicellate spikelets, more florets per spikelet, glabrous lemmas, shorter paleas and shorter anthers. It differs from all other Chinese species taxa in Leymus with regard to the large number (8–12) of florets in its spikelets, and from all species of Leymus in adjacent countries in having three to four spikelets per node. © 2009 The Linnean Society of London, Botanical Journal of the Linnean Society, 2009, 159 , 343–348.     

Allelic diversity of high-molecular-weight glutenin protein subunits in natural populations of Dasypyrum villosum (L.) Candargy

Dasypyrum villosum (L.) Candargy (2n=14, V genome) is a wild, allogamous, diploid grass species that is a potential genetic resource for wheat improvement. The diversity of high-molecular-weight (HMW) glutenin subunits of the seed storage proteins of this species was examined in populations sampled in their natural habitats in Italy and Yugoslavia where the species is widely distributed. The results of selfed progeny tests confirmed that the allelic variation of HMW-glutenin subunits in D. villosum is controlled by a single locus (Glu-V1). Fourteen alleles at Glu-V1 were found among 982 individuals representing 12 populations from Italy and two from Yugoslavia, with a mean of seven alleles per population. Among the 14 Glu-V1 alleles, one produced no HMW-glutenin subunits, ten coded for a single subunit, and three for two subunits. The mobilities of all the subunits in SDS-PAGE gels were greater than that of reference subunit 7 of Triticum aestivum cv Chinese Spring. Eight of the alleles were relatively abundant (mean frequency over all populations ranged from 0.08 to 0.17) and distributed widely among the 14 populations (8 to 14); five of the alleles were rare (0.003 to 0.021) and found in only 1 to 5 populations. The frequencies of two alleles could not be individually estimated because of the similar electrophoretic mobility of their subunits. The multiple-allelic diversity at Glu-V1 was high (H_e ranged from 0.700 to 0.857) but similar from population to population. Overall, about 7% of the total allelic variation was distributed among populations (G_st=0.072), and more than 90% within populations. Whether the allelic variation at Glu-V1 is subject to natural selection is unknown, but the discovery of the homozygous null Glu-V1 alleles in the present study may be useful in pursuing this question. The multiple-allelic diversity in Glu-V1 presents the plant breeder with an opportunity to evaluate and select the most useful alleles for transfer to wheat. The importance of an evaluation genetic diversity in a wild species before interspecific gene transfers are attempted is well illustrated in this study.     

Est-7, a set of genes controlling green tissue esterases in wheat and related species

Summary Analysis using isoelectric focusing of Chinese Spring wheat genetic stocks revealed a set of coleoptile and leaf esterase loci, designated Est-7, on the long arms of the group 2 chromosomes. A survey of 38 other hexaploid genotypes revealed onyl a single variant, at Est-D7. Homoeoloci were found on chromosome (arm) 2HL of Hordeum vulgare, 2RL of Secale cereale, 2R ^m of S. montanum, 2U of Aegilops umbellulata, 2E of Agropyron elongation and 2V of Dasypyrum villosa.     

麦类作物遗传转化

麦类作物包括小麦(Triticum aestivum L.)、硬粒小麦(Triticum turgidum con v.durum Dest.e.m)、大麦(Hordeum vulgare L.)、黑麦(Secale cereal L.)、燕麦(Avena sativa L.)及小大麦(×Tritordeum Ascherson et Graebuer.).自从基因枪被发明以来,科学家们已经利用来自麦类作物的幼胚、 盾片、成熟种子胚、花粉粒、花药、幼穗、叶基组织、发芽种子幼苗的顶端分生组织及其愈伤组织或培养物作为外植体,通过基因枪、农杆菌介导、 PEG法、电激法、微注射法、硅化纤维素介导、幼穗注射法等技术先后将一些选择标记基因、报告基因和有用的目的基因如抗真菌、抗虫、 籽粒品质、抗干旱基因等转化到麦类作物中.转基因植物表现为抗性增强或籽粒的加工品质提高和营养成份增加.被转化的基因通常以单位点多拷贝的形式随机整合到受体细胞的基因组中,并以孟德尔规律遗传.整合位点一般分布在染色体的近端粒区域,整合的拷贝数大多为5～10个拷贝,最高可达到50个拷贝.在转化过程中,被转化的质粒上的片段包括选择标记基因、目标基因、甚至质粒的抗生素基因和其他无关序列,随机地连接并形成多个分子量大小不等,组成成分不同的分子簇,或首先由其中一个分子簇整合到植物基因组中,这会导致在整合位点附近产生"热点",易于其他分子簇在此处整合,从而完成两期整合;或被转化的质粒上的选择标记基因、目标基因、质粒的抗生素基因和其他无关序列、植物基因组DNA等片段共同形成各种不同类型的分子簇,当植物细胞染色体复制时,在复制叉处整合到植物基因组中.转基因可以在各种水平上表达,也会时常发生基因沉默,这会导致转基因植物DNA水平上表达但在蛋白质水平上不表达,后代偏向分离,沉默的转基因重新表达.转基因的位置效应、甲基化和启动子都会诱发转基因沉默.在麦类作物中,35S启动子易于导致转基因沉默,应尽量减少使用.转基因还导致被转化麦类作物在农艺性状和细胞学上的变异.目前,麦类作物遗传转化已经成为一种常规的技术,转基因麦类作物正开始进入商业应用阶段.相信多种转化新技术的应用和发展将会培育出高产、稳产、优质、低投入的各类品种和种质.     

Variability and structure of natural populations of Hordeum murinum L. based on morphology

Based on a detailed statistical analysis of 19 quantitative and four qualitative characters of 31 samples of Hordeum murinum from Poland, it was stated that the small variability of these characters does not permit to distinguish any intra-specific units. Only a slight geographical differentiation of populations was found. Based on the differences discovered, the populations have been divided into two groups: one with the centre of distribution in the North-East (group E) and the second in South-West Poland (group W). This differentiation might result from the different routes of migration of this species into Poland. The chromosome number (2n = 28) confirms earlier reports from Poland. New data concerning the distribution of H. murinum in north-eastern Poland are also presented. A detailed study on the distribution of H. murinum in Poland is under way. It is the fourth paper from the series: Biodiversity of wild Triticeae (Poaceae) in Poland. The first is: Mizianty M. (2005). Variability and structure of natural populations of Elymus caninus (L.) L. based on morphology. Pl. Syst. Evol 251: 199–216, the second: Mizianty M. et al. (2006). Variability and structure of natural populations of Elymus caninus (L.) L. and their possible relationship with Hordelymus europaeus (L.) Jess. ex Harz as revealed by AFLP analysis. Pl. Syst. Evol. 256: 193–200, the third: Mizianty M. and Szklarczyk M. (2005). Systematic significance of Elymus caninus morphological characters revealed by AFLP analysis. In: Frey L. (red.) Biology of grasses. W. Szafer Institute of Botany, Polish Academy of Sciences. Kraków, pp. 9-21.     

山东小麦族植物叶表皮微形态的研究

利用光学显微镜,对山东小麦族5属9种植物的叶片下表皮微形态特征进行了研究。叶片下表皮微形态在属间差异明显,可作为分属的参考依据;山东5种鹅观草属植物的叶片下表皮微形态可分为两种类型,这与形态上划分的拟披碱草组和犬草组相一致。     

The barley (Hordeum vulgare L.) dehydrin multigene family: sequences, allele types, chromosome assignments, and expression characteristics of 11 Dhn genes of cv Dicktoo

 Dehydrins (LEA D11 proteins) have been identified in both higher and lower plants, and are associated with tolerance to, or response to the onset of, low temperature or dehydration. Several studies have suggested that specific alleles of Dhn genes may contribute to a number of phenotypic traits, including the emergence of seedlings in cool or saline soils and the frost tolerance of more-mature plants. However, an incomplete collection of the Dhn multigene family in any system and nucleic acid cross-hybridization between Dhn gene-family members have limited the precision of these studies. We attempted to overcome these impediments by determining the nucleotide sequences of the entire Dhn multigene family in barley and by developing gene-specific probes. We identified 11 unique Dicktoo Dhn genes. Seven appear to be alleles of Dhn genes identified previously in other barley cultivars. Another, Dhn9, appears to be orthologous to a Triticum durum Dhn gene. A statistical analysis of the total collection of genomic clones brings the estimated size of the barley Dhn gene family to 13. Allelic differences in the protein-coding regions appear to result principally from duplications of entire Φ-segments or single amino-acid substitutions, suggesting that polypeptide structural constraints have been a strong force in the evolution of Dhn alleles. Chromosome mapping by PCR with wheat-barley addition lines established the presence of Dhn genes in four barley chromosomes (3H, 4H, 5H, 6H). RT-PCR demonstrated that the Dhn genes are differentially regulated under dehydration, low temperature and ABA treatment, consistent with putative regulatory elements located upstream of the respective Dhn coding regions. This whole-genome, gene-specific study unifies what previously seemed to be disparate-mapping, expression, and genetic-variation data for Dhn genes in the Triticeae and other plant systems. Received: 23 September 1998 / Accepted: 13 October 1998     

Genetic variation and differentiation in Nordic populations of Elymus alaskanus (Scrib. ex Merr.) Löve (Poaceae)

 To gain information on the extent and nature of genetic variation in Elymus alaskanus, levels and distribution of genetic variation were assessed within and among 13 populations originating from Iceland, Norway, Sweden and Russia using allozymes. The results showed that four (30.7%) of the 13 loci were polymorphic within the species, while the mean percentage of polymorphic loci within the populations was 1.9%. The mean number of alleles per locus for the species was 1.8 and 1.02 across the populations. Genetic diversity at the species level was low (H _es=0.135), and mean population diversity was notably lower (H _ep=0.005). A high degree of genetic differentiation was observed among populations. The salient points emerging from this study are: (1) statistically significant differences were found in allele frequencies among populations for every polymorphic locus (P<0.001), (2) the high mean coefficient of gene differentiation (G _ST) showed that 95% of the total allozyme variation was attributable to differences among populations, and (3) relatively high genetic distances between the populations were obtained (mean D=0.16). The Norwegian populations had the highest genetic diversity as compared with the other populations. Geographical comparisons revealed three different groups of populations clearly differentiated, i.e. Scandinavia (Norway and Sweden), Iceland and Russia. Cluster and principal coordinates analyses revealed the same genetic patterns of relationships among populations. Generally, this study indicates that E. alaskanus contains low allozymic variation in its populations. The implications of these results for the conservation of the species are discussed. Received: 23 October 1998 / Accepted: 19 December 1998