Circadian Rhythms,Monoamines and Behavior: Introduction and Overview

Predictions for the phase angle differences (ψ) between the activity rhythm and the zeitgeber for different skeleton photoperiods based on the phase response curve (PRC) and the free-running period (τ) of the field mouse Mus booduga were made. These predictions were based on two assumptions: (i) The PRC for light pulses of 1 h duration and ca 45 lx intensity should resemble the PRC for pulses of 15 min duration and 1000 lx intensity. (ii) One of the two light pulses (LP) constituting the skeleton photoperiod should always impinge upon that zone of the PRC which has a slope of < ?2. Experiments were performed to compare ψ under skeleton and complete photoperiods and also to test the assumptions made in predicting ψ. The results show that the basic oscillation underlying the activity rhythm of the field mouse Mus booduga undergoes a “phase-jump” when two brief light pulses (of 1 h duration) were used to mimic a photoperiod of 20 h. The ψ values obtained for skeleton photoperiods closely match the predicted values. Under complete photoperiods, the experimentally obtained values match the predictions only up to 16 h. We conclude therefore that beyond this photoperiod, two discrete light pulses may not be sufficient to simulate the effect of a complete photoperiod.     

Allogromia laticollaris: A Foraminiferan with an Unusual Apogamic Metagenic Life Cycle*

SYNOPSIS. The life cycles of 3 strains of Allogromia laticollaris, a monothalamous foraminiferan, have been studied. Each of the strains had a different, nonclassical, and basically apogamic, life cycle. The Cold Spring Harbor (CSH) strain regularly alternated between 2 agamontic forms: agamont I (uninucleate and diploid) and agamont II (multinucleate and diploid). The complete life cycle took 26 days. Sexual reproduction was rare (0.01%) and autogamous. Small numbers of organisms also underwent budding, binary fission, and cytotomy. The life cycles of the Towd Point (TPA) and Sippewissett (SIP) strains were comparatively abbreviated. Agamont II dominated their typical life cycles, which were completed in 16-18 days. The life cycle of SIP was basically a continuous cycling of the agamont II phase. Approximately 75% of the schizozoites of the TPA strain developed into agamont II. The other 25% alternated between agamont II and agamont I phase. In the CSH strain schizozoites with ～ 8 (range 5-15) nuclei characterized newly formed agamonts II. More nuclei (～ 25) were found in the other 2 strains. The nuclei in young agamonts II underwent rapid morphologic changes leading to a “mushroom-like” chromosome appearance and extensive RNA synthesis. Nucleolar material accumulated at the nuclear periphery and eventually was discharged to the cytoplasm. Karyokinesis took place without the breakdown of the nuclear membrane. The single nucleus of young agamont I forms was proportionally quite large. The S₁ phase occurred quite early (2-5 days) in this part of the life cycle. RNA in the CSH strain formed a compact, subcortical, coarsely granular ring, while in the TPA it was cortical and differentiated into finely granular matrix with randomly distributed coarse granules. During the G₂ phase the nucleus became further enlarged and eventually amoeba-form. Intermediate stages in nuclear breakdown were not found.     

From ecophysiology to phenomics: some implications of photoprotection and shade–sun acclimation in situ for dynamics of thylakoids in vitro

Half a century of research into the physiology and biochemistry of sun–shade acclimation in diverse plants has provided reality checks for contemporary understanding of thylakoid membrane dynamics. This paper reviews recent insights into photosynthetic efficiency and photoprotection from studies of two xanthophyll cycles in old shade leaves from the inner canopy of the tropical trees Inga sapindoides and Persea americana (avocado). It then presents new physiological data from avocado on the time frames of the slow coordinated photosynthetic development of sink leaves in sunlight and on the slow renovation of photosynthetic properties in old leaves during sun to shade and shade to sun acclimation. In so doing, it grapples with issues in vivo that seem relevant to our increasingly sophisticated understanding of ΔpH-dependent, xanthophyll-pigment-stabilized non-photochemical quenching in the antenna of PSII in thylakoid membranes in vitro.     

细胞周期调控的研究进展

细胞周期是一种非常复杂和精细的调节过程,有大量调节蛋白参与其中。此过程的核心是细胞周期依赖性蛋白激酶（CDKs）。CDKs的激活又依赖于另一类呈细胞周期特异性或时相性表达的细胞周期蛋白（cyclins）,而CDKs调节的关键步骤是细胞周期检查点。PLKs是多种细胞周期检查点的主要调节因子,Aurora蛋白激酶主要在细胞有丝分裂期起作用。本文就上述因素在细胞周期进程中的作用作一综述。     

Circadian clock,cell cycle,and breast cancer: an updated review

Some key elements are common to two fundamental periodic regulatory processes; the circadian cycle and the cell cycle. Underlying mechanisms of coordination between the two processes are critical for proper cellular functioning and physiology. Disruption in the mechanisms of one process may affect the role of other that may direct critical physiological changes and may cause severe diseases like cancer, etc. More or less persuasive evidences evolve from the breast cancer research. In this mini review, we highlighted the molecular coordination’s of the elements of circadian cycle and the cell cycle and their altered expressions associated with the genesis and progression of breast cancer.     

Timing the phases of the microtubule cycles involved in cytoplasmic and nuclear divisions in cells of undisturbed onion root meristems

The duration of the different phases of the microtubule and chromosome cycles were estimated in the native diploid cell populations of Allium cepa L root meristems proliferating undisturbed, under steady state conditions, at the physiological temperature of 15°C. The cycles were coupled by considering their fitting in relation to the short process of nuclear envelope breakdown. In the cycle related to cytoplasmic division, the preprophase band which predicts the future position of the phragmoplast made its appearance, as a wide band, 16 mm before the G₂ to prophase transition, ie it was only present during the final 5% of the total G₂ timing (5 h 30 mm). The band became narrow only 6 mm after prophase had started and it was present in this form for the remaining prophase time (2 h 24 mm). Its disappearance occurred strictly coinciding with nuclear envelope breakdown, at the end of prophase. No microtubules related to cytoplasmic division were apparent until 9 mm after telophase had initiated. The two initial stages of phragmoplast formation which followed occupied, respectively, 27 mm and 54.5 mm of the 2-h long telophase. On the other hand, the third and last stage in phragmoplast formation covered both the final 35 mm of mitosis and the 6 initial mm of the G₁ of the next interphase. A very short (less than 4 mm) stage of microtubular nucleation around the nuclear envelope took place immediately afterwards, before the cortical array of microtubules appeared. The microtubule cycle related to nuclear division started with the apparent activation of the future spindle poles 7.4 mm before prophase was over. The mitotic spindle developed in the 5.6 mm long prometaphase. The spindle functioned in metaphase for the 42 mm it lasted, half spindles being separated for the 37 mm anaphase occupied in these cells.     

Astronomical cycles

Abstract

Talorchestia quoyana, a sand beach amphipod, shows a rhythm of locomotor activity controlled by a circadian clock and an inhibitory circatidal clock. This article reports on an investigation of the entrainment of the circadian dock to skeleton photoperiods. Four important mathematical models for circadian rhythms are examined with respect to the results of the entrainment experiments and to predictions from the phase response curve for Talorchestia. Significant differences between the models are described, and properties of circadian rhythms not accounted for by present models are outlined.     

Solar and lunar rhythms in the occurrence of Astronesthes niger (Pisces) at the sea surface

Abstract

The mesopelagic fish Astronesthes niger concentrates in the uppermost centimeters of the sea when both sun and moon are below the horizon. Probability of positive catches increases towards the times of lower culmination of sun and moon and perhaps is highest when both culminations are about synchronous. Positive catches were made only when the moon was near its first or third quarter, but this might be somewhat influenced by the material which was not evenly distributed in relation to moonphases. It is assumed that A. niger needs moonlight for vertical migration, but avoids the surface during illumination.     

Enzymes of the citramalate cycle in <Emphasis Type="Italic">Rhodospirillum rubrum</Emphasis>

Rhodospirillum rubrum is among the bacteria that can assimilate acetate in the absence of isocitrate lyase, the key enzyme of glyoxylate shunt. Previously we have suggested the functioning of a new anaplerotic cycle of acetate assimilation in this bacterium: citramalate cycle, where acetyl-CoA is oxidized to glyoxylate. This work has demonstrated the presence of all the key enzymes of this cycle in R. rubrum extracts: citramalate synthase catalyzing condensation of acetyl-CoA and pyruvate with the formation of citramalate, mesaconase forming mesaconate from L-citramalate, and the enzymes catalyzing transformation of propionyl-CoA + glyoxylate 3-methylmalyl-CoA ? mesaconyl-CoA. At the same time, R. rubrum synthesizes crotonyl-CoA carboxylase/reductase, which is the key enzyme of ethylmalonyl-CoA pathway discovered recently in Rhodobacter sphaeroides. Physiological differences between the citramalate cycle and the ethylmalonyl-CoA pathway are discussed.     

p16Ink4a is overexpressed in H. pylori-associated gastritis and is correlated with increased epithelial apoptosis

Background. Cell cycle regulatory proteins may be critical targets during carcinogenesis. We have previously shown that chronic H. pylori infection is associated with decreased expression of the cyclin dependent kinase inhibitor (CDI) p27^kip1. Loss of p27^kip1 and p16^Ink4a (p16) expression, another CDI, has been reported during the progression of gastric tubular adenomas to advanced gastric cancer. The aim of the current study was to examine whether H. pylori infection also affects the expression of p16 in the gastric mucosa of H. pylori‐infected patients. Methods. p16 expression was evaluated in gastric antral biopsies by immunohistochemistry in 50 patients with nonulcer dyspepsia (n = 18 uninfected, n = 32 H. pylori infected, 24 by cagA⁺ strains). Adjacent sections were stained for proliferating epithelial cells (by Ki67) and for apoptotic cells (by TUNEL assay). Results. Both in H. pylori infected and uninfected patients the expression of p16 was higher in the neck and base of the gland than in the foveolar region. Epithelial staining for p16 was increased with H. pylori infection (31.3% vs. 11.1% in the foveolar region, 68.8% vs. 27.8% in the neck and 75% vs. 50% in the glandular base). There was no correlation between the expression of 16 and proliferation but there was a significant positive correlation between apoptosis and 16 immunostaining. Conclusions. The tumor suppressor gene 16 is over expressed in gastric epithelial cells of H. pylori infected patients and this is associated with an increase in apoptosis. These findings suggest a possible role for this cell cycle regulator in the increase in gastric cell turnover that is associated with H. pylori infection.     

Polo样激酶1在细胞周期及细胞周期监测点中的功能

Plk1（Polo-like kinase 1）是一类从酵母到人类都高度保守的丝氨酸/苏氨酸蛋白激酶,是真核细胞有丝分裂的重要调控因子.Plk1随有丝分裂进程定位于不同位点,调节分裂期进入、纺锤体形成和胞质分裂等过程.Plk1能够与磷酸化的停靠蛋白结合,从而在不同空间被激活以满足其在细胞周期中的不同功能.Plk1还参与G2和M期DNA损伤监测点的调节,对于DNA损伤恢复后重新进入有丝分裂期是必须的.目前,Plk1的重要功能尤其是在DNA损伤监测点中发挥的重要功能正在被广泛研究.Plk1在多种恶性肿瘤中存在过表达且与肿瘤发生密切相关,对于Plk1功能的深入研究为以Plk1为靶的肿瘤治疗提供理论依据     

Retrospective distribution of Trypanosoma cruzi I genotypes in Colombia

Trypanosoma cruzi is the aetiological agent of Chagas disease, which affects approximately eight million people in the Americas. This parasite exhibits genetic variability, with at least six discrete typing units broadly distributed in the American continent. T. cruzi I (TcI) shows remarkable genetic diversity; a genotype linked to human infections and a domestic cycle of transmission have recently been identified, hence, this strain was named TcIDom. The aim of this work was to describe the spatiotemporal distribution of TcI subpopulations across humans, insect vectors and mammalian reservoirs in Colombia by means of molecular typing targeting the spliced leader intergenic region of mini-exon gene. We analysed 101 TcI isolates and observed a distribution of sylvatic TcI in 70% and TcIDom in 30%. In humans, the ratio was sylvatic TcI in 60% and TcIDom in 40%. In mammal reservoirs, the distribution corresponded to sylvatic TcI in 96% and TcIDom in 4%. Among insect vectors, sylvatic TcI was observed in 48% and TcIDom in 52%. In conclusion, the circulation of TcIDom is emerging in Colombia and this genotype is still adapting to the domestic cycle of transmission. The epidemiological and clinical implications of these findings are discussed herein.     

苜蓿银纹夜蛾核型多角体病毒的感染对Sf9细胞周期的影响

病毒的感染导致细胞内部发生一系列变化.应用流式细胞仪FACS的荧光检测,测出Sf9细胞完成整个周期循环大约需要18h,G\-1、S、G\-2/M各时相的时间间隔约为6h;AcNPV感染Sf9细胞12-18h,细胞被抑制于G\-2/M期;Sf9细胞同步于G\-1/S期后释放细胞并用AcNPV感染,12h后,2/3的细胞处于G\-2/M期,1/3的细胞处于S期.     

Calcium, potassium, and magnesium cycling in aMexican tropical dry forest ecosystem

We estimated the fluxes, inputs and outputs of Ca, K,and Mg in a Mexican tropical dry forest. The studywas conducted in five contiguous small watersheds(12–28 ha) gauged for long-term ecosystem research. A total of five 80 × 30 m plots were used for thestudy. We quantified inputs from the atmosphere,dissolved and particulate-bound losses, throughfalland litterfall fluxes, and standing crop litter pools. Mean cation inputs for a six-year period were 3.03 kg/ha for Ca, 1.31 kg/ha for K, and 0.80 kg/ha for Mg. Mean outputs in runoff were 5.24, 2.83, and 1.79 kg/ha, respectively. Calcium, K, and Mgconcentrations increased as rainfall moved through thecanopy. Annual Ca return in the litterfall (11.4 g/m²) was much higher than K (2.3 g/m²)and Mg (1.6 g/m²). Litterfall represented 99%of the Ca, 84% of the Mg, and 53% of the K, totalaboveground return to the soil. Calcium concentrationin standing litter (3.87%) was much higher than K(0.38%) and Mg (0.37%). These concentrations werehigher (Ca), lower (K), or similar (Mg) to those inlitterfall. Residence times on the forest floor were0.86, 1.17, and 1.77 yr for K, Mg, and Carespectively. Compared to the residence time fororganic matter at the site (1.31 yr), these resultssuggest slow mineralization for Ca in this ecosystem. Budget estimates were calculated for a wet and a dryyear. Results indicated that nutrients accumulated inthe dry but that nutrients were lost during the wetyear. Comparison of Ca, K, and Mg losses in streamwater with the input rates from the atmosphere for thesix-year period show that inputs are lower thanoutputs in the Chamela tropical dry forestecosystem.     

Fluorescence kinetics in HeLa cells after treatment with cell cycle arrest inducers visualized with Fucci (fluorescent ubiquitination-based cell cycle indicator)

Fucci (fluorescent ubiquitination-based cell cycle indicator) is able to visualize dynamics of cell cycle progression in live cells; G1- and S-/G2-/M-phase cells expressing Fucci emit red and green fluorescence, respectively. This system could be applied to cell kinetic analysis of tumour cells in the field of cancer therapy; however, it is still unclear how fluorescence kinetics change after various treatments, including exposure to anticancer agents. To explore this, we arrested live HeLa cells expressing the Fucci probes at various cell cycle stages and observed the fluorescence, in conjunction with flow cytometric analysis. X-irradiation, HU (hydroxyurea) and nocodazole arrest cells at G2/M boundary, early S-phase and early M-phase, respectively. Although X-irradiation and HU treatment induced similar accumulation kinetics of green fluorescent cells, nocodazole treatment induced an abnormal red fluorescence at M phase, followed by accumulation of both red and green fluorescent cells with 4N DNA content. We conclude that certain agents that disrupt normal cell cycle regulation could cause unexpected fluorescence kinetics in the Fucci system.     

细胞周期研究的新进展

细胞周期研究的新进展陆长德（中国科学院上海生物化学研究所２０００３１）主要来自三方面的研究以及它们之间的相互交叉对于细胞周期研究的进展起了很大的作用。十多年来酵母分子遗传学的研究鉴定了许多与细胞周期的控制有关的基因,提供了许多突变株（如ＣＤＣ）;１９８８年对蛙卵成熟促进因子ＭＰＦ成分的鉴定和对它生物学功能的确定使人们对细胞周期的认识有了一个飞跃;人类的致癌基因（如Ｔａｇ）,肿瘤抑制基因（如p53,pRB)以及其他一些疾病(如对电离辐射敏感的遗传病,AT的分子机制的研究也大大地促进了细胞周期的研究。