Molecular genetics of cell death in the nematode Caenorhabditis elegans

In C. elegans, cell death can be readily studied at the cellular, genetic, and molecular levels. Two types of death have been characterized in this nematode: (1) programmed cell death, which occurs as a normal component in development; and (2) pathological cell death which occurs aberrantly as a consequence of mutation. Analysis of mutations that disrupt programmed cell death in various ways has defined a genetic pathway for programmed cell death which includes genes that perform such functions as the determination of which cells die, the execution of cell death, the engulfment of cell corpses, and the digestion of DNA from dead cells. Molecular analysis is providing insightinto the nature of the molecules that function in these aspects of programmed cell death. Characterization of some genes that mutate to induce abnormal cell death has defined a novel gene family called degenerins that encode putative membrane proteins. Dominant alleles of at least two degenerin genes, mec-4 and deg-1, can cause cellular swelling and late onset neurodegeneration of specific groups of cells. © 1992 John Wiley & Sons, Inc.     

Primers for the amplification of sequence‐characterized loci in Cryphonectria cubensis populations

We describe the development of DNA markers for the fungal pathogen of Eucalyptus, Cryphonectria cubensis. These markers originated from cloned intershort sequence repeat polymerase chain reactions, which enrich for medium to highly repetitive DNA sequences. In total, 10 markers were isolated, eight of which were polymorphic, and these can subsequently be applied to study populations of C. cubensis.     

Systemic amyloidosis in transgenic mice carrying the human mutant transthyretin (Met 30) gene

To analyze the pathologic processes of amyloid deposition in type I familial amyloidotic polyneuropathy (FAP), mice were made transgenic by introducing the human mutant transthyretin (TTR) gene(MT-hMet 30). An inbred strain of mouse, C57 BL/6, was chosen. Transgenic mice were killed using ether anesthesia at 3-mo intervals up to 24 mo after birth. In these transgenic mice, amyloid deposition started in the gastrointestinal tract, cardiovascular system, and kidneys and extended to various other organs and tissues with advancing age. The pattern of amyloid deposition was similar to that observed in human autopsy cases of FAP, except for its absence in the choroid plexus and in the peripheral and autonomic nervous systems. We extracted the amyloid fibrils from kidneys of these mice with a human mutant TTR gene and analyzed them immunochemically and electronmicroscopically. Deposited amyloid was shown to be composed of human mutant TTR and mouse serum amyloid P component. Amyloid fibril from transgenic mice was morphologically and immunohistochemically similar to that of human FAP. The most striking pathologic feature of the transgenic mice was the absence of amyloid deposition in the peripheral and autonomic nervous tissues. Thus, other intrinsic factors may be involved in amyloid deposition in the nervous tissues of human FAP.     

谷子显性雄性不育基因“Ms~（ch）”的细胞质转换

通过种间杂交和连续置换回交,选育出具有轮生狗尾草（Ｓ,ｖｅｒｔｉｃｉｌｌａｔａ（Ｌ．）Ｂｅａｕｖ．）细胞质的谷子（Ｓｅｔａｒｉａｉｔａｌｉｃａ（Ｌ．）Ｂｅａｕｖ．）核质杂种,以带有上位基因Ｒｆ的显性核不育植株为父本与此核质杂种杂交,已将显性核不育基因导入轮生狗尾草细胞质中,从其分离后代中选出了具有显性核不育基因的新核质杂种,为谷子的三系选育和细胞质研究创造了新工具,也为核互作杂优利用增加了核质互作优势新机制。     

Dominant rotifers of Võrtsjärv (Estonia)

Rotifers form 71% of the zooplankton of the strongly eutrophic (total N 2 g m^–3, total P 53 mg m^–3) Võrtsjärv (Estonia). Altogether 150 taxa of rotifers occur. Species characteristic of oligo- and mesotrophic waters have totally disappeared during the last 30 years, or are disappearing now. Species whose numbers and biomass reached 20% or more of total zooplankton were considered dominants. These were Anuraeopsis fissa, Keratella cochlearis, K. quadrata frenzeli, Polyarthra dolichoptera, P. luminosa, Synchaeta verrucosa and Trichocerca rousseleti. The contribution of dominant rotifers to total zooplankton and its biomass is as follows: S. verrucosa 25% and 39%, P.dolichoptera 34% and 25%, K. cochlearis 25% and 7%, K. quadrata frenzeli 9% and 7%, A. fissa 28% and 0.4%, T. rousseleti 20% and 0.6%, respectively.     

X-linked dominant inheritance of partial phosphorylase kinase deficiency in mice

A new mouse strain, the V strain, with a partial deficiency of phosphorylase kinase has been established. The deficiency is caused by an X-linked dominant gene (Phk ^c ). Muscle extracts of homozygous and heterozygous females and hemizygous males have about 25% of the activity found in extracts of normal (C3H/HeHan) mice. This dominant phosphorylase kinase deficiency of the new V strain is different from that of the I-strain mice with the X-linked recessive deficiency of skeletal muscle phosphorylase kinase. The muscle extracts of V-strain and normal mice contain the same phosphorylase phosphatase activity of about 1 U/mg. Heart and liver extracts from V mice contained about 50% and 66%, respectively, of the phosphorylase kinase activity compared to that found in the same organs from the normal mice. The glycogen content of the skeletal muscle of the V strain was normal, i.e., 0.9 mg/g. Phosphorylase kinase was purified from the skeletal muscle of the V strain by (a) hydrophobic chromatography on methylamine Sepharose, (b) ammonium sulfate precipitation, and (c) gel filtration of Sepharose 4B. The enzyme has a similar structure to the normal murine and rabbit skeletal muscle enzyme, except that the proportion of the subunits differs. The molar ratio of the subunits of the V strain mice is (+)::=0.54:1:1.169, in comparison with that of the rabbit (+)::=1.1:1.0:1.0 and that of normal murine enzyme 0.9:1.0:0.7.This work was supported by the Minister für Wissenschaft und Forschung des Landes Nordrhein-Westfalen, West Germany and of the Fonds der Chemie, West Germany, and forms part of the md thesis of A. Vrbica.     

草地利用方式对温性典型草原优势种植物功能性状的影响

当外界环境发生变化后植物能够改变自身功能性状及时调整适应策略, 因此植物功能性状能够有效地反映植物对草地利用变化的响应, 然而在内蒙古草原从植物功能性状角度开展草地利用方式影响的研究略少。该研究以内蒙古典型草原大针茅(Stipa grandis)、羊草(Leymus chinensis)、糙隐子草(Cleistogenes squarrosa)和冷蒿(Artemisia frigida) 4种主要优势种为研究对象, 探讨在长期自由放牧、割草、短期围封和长期无干扰的影响下优势种植物功能性状的差异, 以期从功能性状视角, 揭示植物在受到外界干扰后的适应策略, 旨为天然草地的可持续管理提供基础数据支持和科学依据。结果表明: 1)除糙隐子草外, 在长期放牧后内蒙古典型草原优势植物植株高度、根长和植物碳氮含量降低, 这些性状的变化能够使植物个体小型化, 适口性降低, 表明植物通过逃避放牧的策略适应长期自由放牧的干扰; 在割草管理方式下, 优势种的高度和比叶面积有增加的趋势, 其中冷蒿的氮含量对割草响应最敏感, 其根、茎、叶中的氮含量均在割草样地最低; 围封和长期无干扰处理下植物的碳氮含量增加, 表明在干扰强度降低后, 植物通过功能性状的改变从资源获取策略向资源储藏策略转变。2)对优势种功能性状集合分析表明, 糙隐子草具有较低的植株高度和较高的比叶面积, 冷蒿具有较高的木质素含量和氮含量, 这些性状能够使两种植物被家畜采食量减少, 并保证其具有较强的再生能力, 这可能是糙隐子草和冷蒿耐牧的原因; 大针茅具有最高的植株高度、最大的叶片干物质含量, 以及最高的茎、叶纤维素含量, 说明大针茅是非常典型的竞争物种, 在干扰较低的条件下, 大针茅采取竞争策略对其他物种产生较大的竞争压力可能是其占优势的重要原因。     

QT interval measurement using RMED curve; a novel approach based on wavelet techniques

Hypothesis/objective: Prolonged QT interval is an index of propensity for dangerous ventricular tachyarrhythmias. The aim of this article is to establish an automatic algorithm for QT interval measurement.

Method: The proposed method is based on the continuous wavelet transform. In this method, the concepts of the rescaled wavelet coefficients and dominant scales of the electrocardiogram (ECG) components are used to perform detection of ECG characteristic points. A new concept of rescaled maximum energy density is introduced so as to perform the estimation of the QT interval.

Results and conclusion: We have applied the algorithm to the PTB database of the Physiobank?Physionet in lead II. Then, the results were evaluated using pertinent reference QT. The criterion used for evaluation of the method's performance is the root mean square (RMS) error. The method approached the RMS error of 27.89 ms for 549 subjects. The proposed method is fast, simple and is applicable to a wide range of ECG cardio cycle morphologies.