Diatoms in recent bottom sediments and trophic status of eight lakes and reservoirs in northeastern Utah

Recent bottom sediments of eight lakes and reservoirs in northeastern Utah were examined. One hundred and sixty-four diatom taxa were identified and their relative abundances determined. Seven stand associations were evident by cluster analysis of similarity indices. These association patterns mirrored trophic status of the waters. Shannon-Wiener species diversity values were also determined. The diversities fell in patterns that were similar to the stand associations determined by cluster analysis. The most prevalent diatom taxa encountered in this study were found mostly in eutrophic waters. These taxa included Stephanodiscus astraea, Stephanodiscus astraea var. minutula, Asterionella formosa, and Fragilaria crotonensis. A wide variety of other taxa dominated various mesotrophic and oligotrophic sites.         

Puzzles, promises and a cure for ageing

Recent discoveries in the science of ageing indicate that lifespan in model organisms such as yeast, nematodes, flies and mice is plastic and can be manipulated by genetic, nutritional or pharmacological intervention. A better understanding of the targets of such interventions, as well as the proximate causes of ageing-related degeneration and disease, is essential before we can evaluate if abrogation of human senescence is a realistic prospect.     

Misfolded proteins partition between two distinct quality control compartments

The accumulation of misfolded proteins in intracellular amyloid inclusions, typical of many neurodegenerative disorders including Huntington's and prion disease, is thought to occur after failure of the cellular protein quality control mechanisms. Here we examine the formation of misfolded protein inclusions in the eukaryotic cytosol of yeast and mammalian cell culture models. We identify two intracellular compartments for the sequestration of misfolded cytosolic proteins. Partition of quality control substrates to either compartment seems to depend on their ubiquitination status and aggregation state. Soluble ubiquitinated misfolded proteins accumulate in a juxtanuclear compartment where proteasomes are concentrated. In contrast, terminally aggregated proteins are sequestered in a perivacuolar inclusion. Notably, disease-associated Huntingtin and prion proteins are preferentially directed to the perivacuolar compartment. Enhancing ubiquitination of a prion protein suffices to promote its delivery to the juxtanuclear inclusion. Our findings provide a framework for understanding the preferential accumulation of amyloidogenic proteins in inclusions linked to human disease.     

A nuclear Argonaute promotes multigenerational epigenetic inheritance and germline immortality

Epigenetic information is frequently erased near the start of each new generation. In some cases, however, epigenetic information can be transmitted from parent to progeny (multigenerational epigenetic inheritance). A particularly notable example of this type of epigenetic inheritance is double-stranded RNA-mediated gene silencing in Caenorhabditis elegans. This RNA-mediated interference (RNAi) can be inherited for more than five generations. To understand this process, here we conduct a genetic screen for nematodes defective in transmitting RNAi silencing signals to future generations. This screen identified the heritable RNAi defective 1 (hrde-1) gene. hrde-1 encodes an Argonaute protein that associates with small interfering RNAs in the germ cells of progeny of animals exposed to double-stranded RNA. In the nuclei of these germ cells, HRDE-1 engages the nuclear RNAi defective pathway to direct the trimethylation of histone H3 at Lys?9 (H3K9me3) at RNAi-targeted genomic loci and promote RNAi inheritance. Under normal growth conditions, HRDE-1 associates with endogenously expressed short interfering RNAs, which direct nuclear gene silencing in germ cells. In hrde-1- or nuclear RNAi-deficient animals, germline silencing is lost over generational time. Concurrently, these animals exhibit steadily worsening defects in gamete formation and function that ultimately lead to sterility. These results establish that the Argonaute protein HRDE-1 directs gene-silencing events in germ-cell nuclei that drive multigenerational RNAi inheritance and promote immortality of the germ-cell lineage. We propose that C. elegans use the RNAi inheritance machinery to transmit epigenetic information, accrued by past generations, into future generations to regulate important biological processes.     

xnd-1 regulates the global recombination landscape in Caenorhabditis elegans

Meiotic crossover (CO) recombination establishes physical linkages between homologous chromosomes that are required for their proper segregation into developing gametes, and promotes genetic diversity by shuffling genetic material between parental chromosomes. COs require the formation of double strand breaks (DSBs) to create the substrate for strand exchange. DSBs occur in small intervals called hotspots and significant variation in hotspot usage exists between and among individuals. This variation is thought to reflect differences in sequence identity and chromatin structure, DNA topology and/ or chromosome domain organization. Chromosomes show different frequencies of nondisjunction (NDJ), reflecting inherent differences in meiotic crossover control, yet the underlying basis of these differences remains elusive. Here we show that a novel chromatin factor, X non-disjunction factor 1 (xnd-1), is responsible for the global distribution of COs in C. elegans. xnd-1 is also required for formation of double-strand breaks (DSBs) on the X, but surprisingly XND-1 protein is autosomally enriched. We show that xnd-1 functions independently of genes required for X chromosome-specific gene silencing, revealing a novel pathway that distinguishes the X from autosomes in the germ line, and further show that xnd-1 exerts its effects on COs, at least in part, by modulating levels of H2A lysine 5 acetylation.     

Nitrosamines and other carcinogens as agents of protein denaturation

Résumé Les auteurs montrent que les composés cancérogènes hydrosolubles, l'acide tannique, le phénol, la diéthyl-et diméthylnitrosamine, la thioacétamide, le carbamate d'éthyl et la thiourée sont des agents puissants de dénaturation de protéines. La précipitation produite par ces agents peut être inhibée, inversée ou accrue par divers réactifs de groupes sulfhydryles. Ces recoupements, ainsi que d'autres expériences sur l'effet de l'urée sur la précipitation par la diméthylnitrosamine, indiquent que le mécanisme de la formation des aggrégats moléculaires consiste dans l'établissement de ponts -S-S- intermoléculaires, probablement renforcés par des liaisons intermoléculaires d'hydrogène.

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This work was supported by USPHS Grant CY-4939 at the University of Florida, and by USPHS Grant C-5431 and a Grant-in-aid from the Greater New Orleans Cancer Association and the Cancer Society of Greater Baton Rouge, at Tulane University.

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Presented at the Fifty-second Annual Meeting of the American Association for Cancer Research, Atlantic City, N.J., April, 1961 (Abstr., Proc. Amer. Assoc. Cancer Research3, 206 (1961)).