Retrograde transport of endocytosed Shiga toxin to the endoplasmic reticulum.

Shiga toxin and some other protein toxins that act on targets in the cytosol have previously been shown to enter the trans-Golgi network. Transport by this route may be necessary for translocation of the toxin to the cytosol and for intoxication, but it is not known whether the enzymatically active part of the toxins actually enters the cytosol from the trans-Golgi network. It has been suggested that such toxins are transported in a retrograde manner to the endoplasmic reticulum and that translocation occurs in this organelle, but retrograde transport of endocytosed material beyond the trans-Golgi network has never been demonstrated. Here we show that in butyric acid-treated A431 cells endocytosed Shiga toxin is not only transported to the trans-Golgi network, but also to all Golgi stacks, to the endoplasmic reticulum and to the nuclear envelope. Furthermore, butyric acid sensitizes the cells to Shiga toxin, which is consistent with the possibility that retrograde transport is required for translocation of the toxin to the cytosol.     

探讨使用野外随机取样推断随机变量概率分布的数学方法--杂草研究作为一个例子

我们在生态学研究中涉及到的大多数变量呈现出随机性，因而可以认为它们就是随机变量。概率分布是研究随机变量变化规律的基础，如何利用野外取样来推断检验随机变量的分布是本文要解决的主要问题。本文扩展了回归方法的应用，使其能用来推断一个随机变量的分布函数。并且该推断还能被统计检验。作为一个应用实例。该方法被用于确定杂草种子在特定条件下扩散的分布函数。在此条件下，该杂草种子扩散为近似的高斯(正态)分布。     

Cell-type-specific replication initiation programs set fragility of the FRA3B fragile site

Common fragile sites have long been identified by cytogeneticists as chromosomal regions prone to breakage upon replication stress. They are increasingly recognized to be preferential targets for oncogene-induced DNA damage in pre-neoplastic lesions and hotspots for chromosomal rearrangements in various cancers. Common fragile site instability was attributed to the fact that they contain sequences prone to form secondary structures that may impair replication fork movement, possibly leading to fork collapse resulting in DNA breaks. Here we show, in contrast to this view, that the fragility of FRA3B--the most active common fragile site in human lymphocytes--does not rely on fork slowing or stalling but on a paucity of initiation events. Indeed, in lymphoblastoid cells, but not in fibroblasts, initiation events are excluded from a FRA3B core extending approximately 700 kilobases, which forces forks coming from flanking regions to cover long distances in order to complete replication. We also show that origins of the flanking regions fire in mid-S phase, leaving the site incompletely replicated upon fork slowing. Notably, FRA3B instability is specific to cells showing this particular initiation pattern. The fact that both origin setting and replication timing are highly plastic in mammalian cells explains the tissue specificity of common fragile site instability we observed. Thus, we propose that common fragile sites correspond to the latest initiation-poor regions to complete replication in a given cell type. For historical reasons, common fragile sites have been essentially mapped in lymphocytes. Therefore, common fragile site contribution to chromosomal rearrangements in tumours should be reassessed after mapping fragile sites in the cell type from which each tumour originates.     

Demography of black-tailed prairie dog populations reoccupying sites treated with rodenticide

Normal 0 false false false EN-US X-NONE X-NONE MicrosoftInternetExplorer4 st1\:*{behavior:url(#ieooui) } /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;} A rodenticide, zinc phosphide, was applied to remove black-tailed prairie dogs ( Cynomys ludovicianus ) from 6 ha of a prairie dog colony in southwestern South Dakota. Another adjacent 6 ha was left untreated. The removal experiment was repeated two consecutive years. Contingency table analysis showed that the resultant population was not homogeneous; age classes by sex of the immigrant and resident subpopulations were different (P     

Trapping methods for rangeland insects in burned and unburned sites: a comparison

Different insect trapping methods were compared weekly on recently burned and nearby unburned rangeland in the Great Basin of western Utah. Flight traps (or wing traps) collected the most specimens (total = 4,916 at burned site, 4,384 at unburned site) but represented the fewest species (no more than 11 spp./wk at either site); this method was not recommended because of difficulty in removing specimens from adhesive. Water traps amassed the next largest number of specimens (￣x ± SE/wk = 150.9 ± 75.3 at burned site, 158.0 ± 66.4 at unburned site) and the most species (￣x ± SE/wk = 21.6 ± 6.4 at burned site, 35. 1 ± 4.5 at unburned site). The weekly collections from pitfall traps between the sites were significantly different (P < .05) in number of specimens (￣x ± SE/wk = 8.1 ± 1.5 at burned site, 19.7 ± 4.8 at unburned site) and species (￣x ± SE/wk = 4.7 ± 0.6 at burned site, 9.5 ± 2.0 at unburned site). Malaise traps were the most convenient. Black Malaise traps collected more specimens (￣x ± SE/wk = 99.8 ± 19.4 at burned site, 90.6 ± 16.4 at unburned site) and species (￣x ± SE/wk = 22.9 ± 3.9 at burned site, 19.4 ± 6.5 at unburned site) than white malaise traps (specimens: ￣x ± SE/wk = 72.1 ± 22.4 at burned site, 87.1 ± 31.2 at unburned site; species: ￣x ± SE/ wk = 19.7 ± 6.6 at burned site, 16.4 ± 5.4 at unburned site), although this difference was not significant.     

Western balsam bark beetle, Dryocoetes confusus Swaine, flight periodicity in northern Utah

The flight periodicity of western balsam bark beetle ( Dryocoetes confusus Swaine) in Big Cottonwood Canyon, Utah, was studied during the summer months of 1992, 1993, and 1994. Contents of baited funnel traps were tallied by species up to 3 times weekly. Two main periods of flight activity were observed each year. The first and, generally, largest occurred in early summer soon after flight was initiated for the season. A 2nd period was observed in late summer, generally August. Timing of the 2 periods was influenced by unusually warm or cool weather in each study year. The 1st period had more males than females while the 2nd period had a majority of females. Except during periods of cool or wet weather, western balsam bark beetles were found to be active at least at minimal levels from June through September.     

Sequence of Plasmodium falciparum chromosomes 2, 10, 11 and 14

The mosquito-borne malaria parasite Plasmodium falciparum kills an estimated 0.7-2.7 million people every year, primarily children in sub-Saharan Africa. Without effective interventions, a variety of factors-including the spread of parasites resistant to antimalarial drugs and the increasing insecticide resistance of mosquitoes-may cause the number of malaria cases to double over the next two decades. To stimulate basic research and facilitate the development of new drugs and vaccines, the genome of Plasmodium falciparum clone 3D7 has been sequenced using a chromosome-by-chromosome shotgun strategy. We report here the nucleotide sequences of chromosomes 10, 11 and 14, and a re-analysis of the chromosome 2 sequence. These chromosomes represent about 35% of the 23-megabase P. falciparum genome.     

Dimethyloxarsylethanol from anaerobic decomposition of brown kelp (Ecklonia radiata): A likely precursor of arsenobetaine in marine fauna

Summary The novel arsenic compound, dimethyloxarsylethanol, has been isolated from anaerobically incubatedEcklonia radiata. It is proposed that this compound has a key position in the biosynthesis of arsenobetaine.C, H microanalyses were performed by the Australian Microanalytical Service.