The wheat wcs120 gene family. A useful model to understand the molecular genetics of freezing tolerance in cereals

Winter, as compared with spring cereals, possess better acclimation mechanisms that allow them to overwinter and survive freezing temperatures. This difference is genetically programmed and involves a complex genetic system. To understand the nature of this system and its regulation by low temperature, genes associated with freezing tolerance in wheat ( Triticum aestivum L.) were identified and characterized. Among these, the wcs120 gene family encodes a group of proteins ranging in size from 12 to 200 kDa. As shown by biochemical, immunohistochemical, molecular and genetic analyses, this gene family is specific to the Poaceae, highly abundant and coordinately regulated by low temperature. Furthermore, accumulation of WCS protein is directly correlated with the development of freezing tolerance. These analyses also revealed a regulatory control of the vernalization process over low temperature gene expression in winter cereals. Recent studies suggest that the molecular mechanisms controlling the expression of these genes involve negative regulatory factors that are modulated by phosphorylation.     

Large branchiopod assemblages common to Mexico and the United States

Cu, Cd, Zn and Pb concentrations in both dissolved andparticulate phase were assessed during 1995. DataQuality Assurance was an integral part of this studyand involved all major steps of the analysis proceduresuch as sampling, sample handling, preconcentrationand determination. Desorption and redox processes clearly control thedissolved Cu and Cd profiles. Mobilisation ofdissolved Zn is small and essentially restricted tothe low salinity area and the late spring survey.Dissolved Pb shows the clearest dilution pattern. Theparameters representative of these processes(dissolved oxygen and salinity) also correlate verywell with the particulate metal profiles. In addition, the plankton activity (expressed by thechlorophyll-a levels) may influence the dissolved andparticulate metal profiles. In combination withdesorption and redox processes, seasonal variationswere induced. This revised version was published online in July 2006 with corrections to the Cover Date.     

Demographic variability in tiller populations of two perennial pampa grasses

Abstract. The general objectives of this study were: (1) to investigate the importance of internal influences in regulating the tiller dynamics in natural populations of the warm-season perennial grasses Paspalum dilatatum and Sporobolus indicus, coexisting in Argentine flooded pampa, in as much as they act independently of the underlying external environment, and (2) to evaluate the extent to which interactions between internal and external factors affect the variation in tiller dynamics within such populations. Within-population variation in seasonal development of plants and tillers with different neighbour composition was studied for an annual growth cycle. Tiller survival and tillering were significantly influenced by tiller size. Tiller age influenced tiller fate, as suggested by the additive effects of age and size of tillers. These relationships varied with season and with species. Size and age of tillers showed additive effects with their neighbouring species on the tiller fate of P. dilatatum, but the effects of age and size of S. indicus changed according their neighbourhood. Tiller survival of S. indicus during the early growth season was more size-dependent when the cold-season species Poa lanigera, was the principal neighbour. Flowering and tillering probabilities were positively related through their common positive responses to tiller size. Tiller survival and recruitment between different seasons were strongly related. Independently of neighbour composition, tiller survival was generally inversely related to tiller recruitment in previous seasons. Therefore, significant density-dependent mortality of tillers was found for both species during the early summer when tiller density was expressed by basal area units.     

Differential Staining of Two Subpopulations of Purkinje Neurons in Rat Cerebellum with Acid Dyes

We present a new method that stains differently two subpopulations of Purkinje cells in the adult rat. Deparaffinized sections of cerebella, fixed by perfusion with buffered glutaraldehyde or Bouin's fluid were stained with 0.5% light green in 50% ethanolf 10-30 min). The excess dye was removed with saturated aqueous picric acid (10-30 min). At this point some Purkinje cells appeared as lightly stained neurons, while others were strongly stained. Slides were immersed in 0.5% aqueous acid fuchsin for approximately 1 min until the lightly stained neurons acquired a red color. Following immersion in 1% phosphotungstic acid, slides were rapidly dehydrated in ethanol, passed to xylene and mounted in Canada balsam. Two subpopulations of Purkinje cells differing in their protein content in somata and proximal dendrites stained differentially by this method. They occurred in all coronal and sagittal sections and in patches or stripes. Their relative proportion varied from lobule to lobule. A second staining method used potassium permanganate as the sole staining reagent. The staining reagent can be used on sections previously stained with the acid dyes. Purkinje cells appeared as subsets of brownish to deep brown stained neurons, the latter ones corresponding to green stained cells in the dichromic method. The results obtained indicated that the subpopulations reflect real differences among individual neurons and are not artifacts. The technique holds promise for identifying and localizing subsets of Purkinje cells differing in their protein content under normal and experimental conditions and for their further characterization by combined staining and histochemical procedures.     

Seasonal levels of LH, FSH, testosterone and prolactin in adult male pudu (Pudu puda)

Seasonal levels of LH, FSH, testosterone (T) and prolactin (PRL) were determined in plasma of six captive adult male pudu (Pudu puda) kept in Concepcion, Chile. Average PRL levels exhibited one peak (28 ng/ml) in December (summer); minimal levels (3 to 6 ng/ml) were detected between April and July. FSH concentrations remained at peak levels (54–63 ng/ml) from December until March; minimal values (25–33 ng/ml) were detected from April until October. T levels exhibited two, almost equal peaks; the first peak (2.8 ng/ml) was detected in March (rut) and the second one (2.7 ng/ml) in October (spring). Both T peaks were preceded by an earlier elevation of LH in February and July (both around 1.3 ng/ml). During the fall, only the alpha male exhibited a sharp peak of T (8.4 ng/ml), whereas in the spring five out of six bucks demonstrated an increase of T levels. Two peaks of LH and T and the 4 months of elevated FSH may be related to a long period of spermatogenesis observed in this species.     

Hepatitis B Virus with X Gene Mutation Is Associated with the Majority of Serologically “Silent” Non-B,Non-C Chronic Hepatitis

Hepatitis B virus (HBV) with X gene mutations has been a putative pathogen of chronic hepatitis without serological markers of known hepatitis viruses. The aim of this study was to reconfirm whether the HBV with the X gene mutation is associated with these serologically “silent” non-B, non-C (NBNC) chronic hepatitis, alcoholic liver disease (ALD) and autoimmune hepatitis (AIH). HBV DNA was amplified from serum and sequenced in 30 patients with NBNC chronic hepatitis in comparison with 20 patients with ALD and 5 patients with AIH. HBV DNA was identified in 21 patients (70%) in NBNC chronic hepatitis by nested polymerase chain reaction while only one patient (5%) in ALD and none in AIH showed HBV DNA. Eighteen (85.7%) of the 21 identified HBV DNAs had an identical 8-nucleotide deletion mutation at the distal part of the X region. This mutation affected the core promoter and the enhancer II sequence of HBV DNA and created a translational stop codon which truncated the X protein by 20 amino acids from the C-terminal end. All the HBV DNAs had a precore mutation at the 83rd nucleotide resulting in disruption of HBe antigen synthesis. These results indicate that HBV mutants are closely associated with the majority of serologically “silent” NBNC chronic hepatitis cases and the population of such mutant HBV DNAs is not uniform.     

Effect of 12C+5 ion beam irradiation on cell viability and plant regeneration in callus,protoplasts and cell suspensions of Lavatera thuringiaca

Summary The biological effects of irradiation with¹²C⁺⁵ ion beam on plant cells have been analyzed. Protoplasts and cell suspensions ofLavatera thuringiaca, and a somatic hybrid callus (Hibiscus rosa-sinensis +Lavatera thuringiaca), were irradiated with doses from 0.05 to 50 Gy, and the effects on cell growth, cell division, cell viability and embryogenesis rates were analyzed. Irradiation with¹²C⁺⁵ ion beam at relatively very low doses (5.0 Gy) significantly inhibited cell division, yet the survival rate and regeneration capability of the cells through somatic embryogenesis were conserved in more than 70 and 50 %, respectively. These results indicate that cell division is the most sensitive parameter to irradiation, accounting for the inhibition of colony formation and callus growth. The potential use of the¹²C⁺⁵ ion beam in asymmetric protoplast fusion experiments is discussed.     

A molecular phylogenetic and phylogeographic study of two forms of Calliptamus barbarus (Costa 1836) (Orthoptera: Acrididae,Calliptaminae) from two regions of Algeria

Calliptamus barbarus (Orthoptera: Acrididae) is the most polymorphic species within the genus Calliptamus. It shows a morphological polymorphism (three hind femoral spots, or only one hind femoral spot). Several studies have been made in order to distinguish the two forms: morphometry, number of ovarioles, sound production, protein and enzyme system. The aim of our work is to assess whether the two forms can be considered as different taxa and to perform a molecular phylogenetic study of two populations of C. barbarus collected from two different Algerian localities. No clear genetic differentiation was found between the samples with different morphologies. Additionally, the samples from Algeria do not form a monophyletic sister clade compared to the one formed by the sequences from GenBank from other geographical regions. Despite the morphological differences shown between the two populations, our molecular study indicates that there are no differences at a molecular level using the two mitochondrial genes COI and 16S.