Chromatid Behavior in Late Mitosis: A Scanning Electron Microscopy Analysis of Mammalian Cell Lines with Various Chromosome Numbers

Chromatid activity during the process of nuclear reformation following metaphase is a period of mitosis where little precise information is available. Nuclear reformation requires that chromosomes, at metaphase and chromatids during anaphase and telophase align, position and associate in a clearly defined sequence to insure the specific design of each nucleus. Four cell lines with chromosome numbers ranging from seven to almost seventy were chosen to determine whether the process of nuclear assembly is the same throughout. Chromosomal alignment at metaphase is found to be radial in all four cell lines. Chromosome positioning is essentially the same in all four, where the smaller chromosomes are located centrally and longer ones are positioned peripherally in a radial alignment. Chromosomal association is directly related to chromosome number. The more chromosomes in a one dimensional plane occupying a given area, the closer the association. In comparing the HeLaS3 and muntjac chromatids, the former has the closer association at metaphase. Since association is the most important aspect of chromatid behavior in nuclear reformation, chromatid positioning becomes a vital process during anaphase movement. Chromatid positions established during anaphase determines later positioning in the interphase nucleus because of the subsequent interconnection of adjacent chromatids by the formation of a fibrous meshwork. This fibrous meshwork, formed in anaphase and early telophase, functions to stabilize chromatids following their positioning and it also serves as a substrate or matrix for the assembly of nuclear envelope

A Scanning Electron Microscopic Technique for Three-Dimensional Visualization of the Spatial Arrangement of Metaphase, Anaphase and Telophase Chromatids

Chromosome and chromatid alignment in mitotic configurations remains a topic of interest because there is little precise information. For example, reconstruction of mitotic configurations from serial sections collected with transmission electron microscopy has proven to be neither practical nor a sensitive method for conceptualizing these arrangements. Similarly light microscopy has been even more unsatisfactory because of its limited resolution and lack of three-dimensional capabilities. These limitations conceivably could be overcome by visualization of mitotic configurations by scanning electron microscopy (SEM). However, SEM has its limitations, of which the most obvious with regard to visualization of mitotic configurations, is that such structures in dividing cells are obscured from the beam by membranes, cellular organelles, and the mitotic apparatus. These contaminants, we have found, can be removed by the appropriate procedure such that a direct three-dimensional visualization of intact life-like mitotic configurations of chromatids from mammalian cells is possible. We also demonstrate that these configurations, although some artifacts may exist, retain the same basic shape and chromatid arrangements throughout metaphase, anaphase, and telophase when compared to configurations isolated with a non-ionic detergent and neutral buffers

(3-Anilino-1-phenyl­imino­thio­ureato)chloridodimethyl­tin(IV)

In the title compound, [Sn(CH3)2(C13H11N4S)Cl], the Sn atom is five-coordinated in a distorted trigonal-bipyramidal geometry, with two methyl groups and one S atom in the equatorial plane, and one N atom and the Cl atom occupying the apical positions

Elucidation of the metabolites of the novel psychoactive substance 4-methyl-N-ethyl-cathinone (4-MEC) in human urine and pooled liver microsomes by GC-MS & LC-HR-MS/MS techniques and of its detectability by GC-MS or LC-MS(n) standard screening approaches

4-methyl-N-ethcathinone (4-MEC), the N-ethyl homologue of mephedrone, is a novel psychoactive substance of the beta-keto amphetamine (cathinone) group. The aim of the present work was to study the phase I and phase II metabolism of 4-MEC in human urine as well as in pooled human liver microsome (pHLM) incubations. The urine samples were worked up with and without enzymatic cleavage, the pHLM incubations by simple deproteinization. The metabolites were separated and identified by gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-high resolution-tandem mass spectrometry (LC-HR-MS/MS). Based on the metabolites identified in urine and/or pHLM, the following metabolic pathways could be proposed: reduction of the keto group, N-deethylation, hydroxylation of the 4-methyl group followed by further oxidation to the corresponding 4-carboxy metabolite, and combinations of these steps. Glucuronidation could only be observed for the hydroxy metabolite. These pathways were similar to those described for the N-methyl homologue mephedrone and other related drugs. In pHLM, all phase I metabolites with the exception of the N-deethyl-dihydro isomers and the 4-carboxy-dihydro metabolite could be confirmed. Glucuronides could not be formed under the applied conditions. Although the taken dose was not clear, an intake of 4-MEC should be detectable in urine by the GC-MS and LC-MS(n) standard urine screening approaches at least after overdose

Anthracnose susceptibility for grapevines with resistance loci to downy and powdery mildew in Southern Brazil

Anthracnose, downy and powdery mildew are the principal fungal diseases of grapes in tropical and subtropical regions. The pesticide active ingredients that control downy and powdery mildew diseases provide some protection against anthracnose attack. The release of varieties with resistance alleles to downy and powdery mildew results in less pesticide use that can increase anthracnose attack. Thus, the present work aimed to evaluate anthracnose susceptibility of genotypes with resistance loci to downy and powdery mildew under Southern Brazilian conditions. Genotype susceptibility was tested, as well as the influence of the environment (location and crop season) on increased susceptibility to anthracnose infection. To accomplish the objective, a trifactorial design was established that included 20 genotypes, two locations, and two crop seasons. Anthracnose incidence and severity were evaluated under natural infection in the field. Temperature around 16 °C and relative humidity at 84 % increased susceptibility to anthracnose infection compared to temperature around 20 °C and relative humidity at 75 %. All tested genotypes with resistance alleles to downy and powdery mildew presented symptoms of anthracnose. 'Baron', 'Cabernet Cortis' and 'Calardis Blanc' showed the least susceptibility to anthracnose, whereas 'Aromera', 'Felicia', 'Gf.2004-043-0004' and 'Gf.2004-043-0021' were the most susceptible and bore symptoms of anthracnose. Other genotypes showed variable susceptibility during the evaluation period, depending on environmental conditions. Overall, all interactions among the three tested factors were highly significant

Genetic linkage mapping applied to the generation of tools for breeding purposes and genetic dissection of grapevine agronomical traits at Embrapa Uva e Vinho.

Resumo

Possible pseudogap behavior of electron doped high-temperature superconductors

We have measured the low-energy quasiparticle excitation spectrum of the electron doped high-temperature superconductors (HTS) Nd(1.85)Ce(0.15)CuO(4-y) and Pr(1.85)Ce(0.15)CuO(4-y) as a function of temperature and applied magnetic field using tunneling spectroscopy. At zero magnetic field, for these optimum doped samples no excitation gap is observed in the tunneling spectra above the transition temperature Tc. In contrast, below Tc for applied magnetic fields well above the resistively determined upper critical field, a clear excitation gap at the Fermi level is found which is comparable to the superconducting energy gap below Tc. Possible interpretations of this observation are the existence of a normal state pseudogap in the electron doped HTS or the existence of a spatially non-uniform superconducting state.Comment: 4 pages, 4 ps-figures included, to be published in Phys. Rev. B, Rapid Com

Spin-state driven ferromagnetic and spin glass states in layered LaSrCoO4_4

Famous for its spin-state puzzle, LaSrCoO$_4$ (Co$^{3+}$) is an intermediate between antiferromagnetic (AFM) La$_2$CoO$_4$ (Co$^{2+}$) and ferromagnetic (FM) Sr$_2$CoO$_4$ (Co$^{4+}$). The appearance of the Co$^{3+}$ valence state (not present in the end compounds) is intriguing because of the spin-state transitions associated with it. In this work, we report two magnetic transitions in LaSrCoO$_4$: (i) a transition at T $=$ T$_c$ $\simeq$ 225 K, from the paramagnetic state to a state with an inhomogeneous long-range ferromagnetic (FM) order wherein finite FM clusters coexist with infinite FM matrix in the percolation sense, and (ii) the transition to the cluster spin glass (CSG) state at T $=$ T$_g$ $\simeq$ 8 K. Finite FM clusters (which at low temperatures give rise to the cluster spin glass state) and infinite FM matrix are formed due to the spin-spin interactions brought about by the inhomogeneously distributed Co$^{3+}$ high spin (HS) and Co$^{3+}$ low spin (LS) ions. A firm support to the presence of an unconventional (inhomogeneous) ferromagnetic order comes from the anomalous values of the critical exponents $\beta$, $\gamma$ and $\delta$ for the spontaneous magnetization, `zero-field' magnetic susceptibility and the critical M - H isotherm, while the coexistence of HS Co$^{3+}$ and LS Co$^{3+}$ ions is confirmed by the results of the extended X-ray absorption fine structure spectroscopy.Comment: 18 pages, 6 figure