Nitrogen fixation and diversity of benthic cyanobacterial mats on coral reefs in Curaçao

Coral Reefs - Benthic cyanobacterial mats (BCMs) have increased in abundance on coral reefs worldwide. However, their species diversity and role in nitrogen fixation are poorly understood. We...     

The side-effects of plant protection products used in olive cultivation on the hymenopterous egg parasitoid Trichogramma cacoeciae Marchal

Abstract:  Six insecticides (Malathion, Quik, Cidial, Dimethoate, Actellic, Deltamethrin) and two mineral oils (Super misrona and Kemesol) are currently used to control the most important pests in Mediterranean olive cultivation (olive fly, olive moth and black scale). Potential side-effects of these compounds were tested on the egg parasitoid Trichogramma cacoeciae Marchal, following recommendations of the working group 'Pesticides and Beneficial Organisms' of the International Organization for Biological Control, West Palaearctic Regional Section (IOBC/WPRS). In the present study, three different types of test methods were carried out: (1) initial toxicity dose–response test on adult wasps; (2) initial toxicity test on pupae, using field recommended rates; and (3) persistent test on olive foliage to assess the duration of harmful activity. The six insecticides tested reduced parasitism by 80–95% and rated as moderately harmful at the field recommended doses. The two mineral oils reduced parasitism up to 25% and were therefore rated as harmless to the adult stage of the parasitoid. The results of the pupal test (parasitoid pupa inside the host egg) showed that Malathion was harmless; Quik, Actellic and Cidial were slightly harmful, while Dimethoate and Deltamethrin were moderately harmful. The results of the persistence test on olive foliage showed that Malathion, Quik and Actellic were slightly persistent, while Cidial, Dimethoate and Deltamethrin were moderately persistent.     

Stereochemistry of chapliatrin and its congeners from Liatris gracilis

Re-examination of Liatris gracilis afforded the known sesquiterpene lactones chapliatrin, isochapliatrin, acetlisochapliatrin, five new closely related 5,10-epoxygermacranolides and a new eudesmanolide. The stereochemistry of the 5,10-epoxygermacranolides has been settled by an X-ray analysis of isochapliatrin.     

Flavonoids and eupahakonenin B from Stevia satureiaefolia

Extraction of Stevia satureiaefolia furnished the flavonoids cirsimaritin and eupatorin and the guaianolide eupahakonenin B.     

A new melampolide from Sigesbeckia orientalis

Isolation and structure determination of orientalide, a new melampolide closely related to the acanthospermals, from Sigesbeckia orientalis is reported.     

Light activation of phosphodiesterase activity in retinal rod outer segments

Light “activates” phosphodiesterase activity of bovine rod outer segments in the presence of 0.1 mM ATP. In contrast, no difference in phosphodiesterase activity can be observed between dark-adapted and light-bleached outer segments in the absence of ATP.     

LRP1 controls intracellular cholesterol storage and fatty acid synthesis through modulation of Wnt signaling

The low-density lipoprotein receptor-related protein LRP1 is a cell surface receptor with functions in diverse physiological pathways, including lipid metabolism. Here we show that LRP1-deficient fibroblasts accumulate high levels of intracellular cholesterol and cholesteryl-ester when stimulated for adipocyte differentiation. We demonstrate that LRP1 stimulates a canonical Wnt5a signaling pathway that prevents cholesterol accumulation. Moreover, we show that LRP1 is required for lipolysis and stimulates fatty acid synthesis independently of the noradrenergic pathway, through inhibition of GSK3beta and its previously unknown target acetyl-CoA carboxylase (ACC). As a result of ACC inhibition, mature LRP1-deficient adipocytes of adult mice are hypotrophic, and lower uptake of fatty acids into adipose tissue leads to their redistribution to the liver. These results establish LRP1 as a novel integrator of adipogenic differentiation and fat storage signals.     

Common and Distinct Genetic Properties of ESCRT-II Components in Drosophila

Background

Genetic studies in yeast have identified class E vps genes that form the ESCRT complexes required for protein sorting at the early endosome. In Drosophila, mutations of the ESCRT-II component vps25 cause endosomal defects leading to accumulation of Notch protein and increased Notch pathway activity. These endosomal and signaling defects are thought to account for several phenotypes. Depending on the developmental context, two different types of overgrowth can be detected. Tissue predominantly mutant for vps25 displays neoplastic tumor characteristics. In contrast, vps25 mutant clones in a wild-type background trigger hyperplastic overgrowth in a non-autonomous manner. In addition, vps25 mutant clones also promote apoptotic resistance in a non-autonomous manner.

Principal Findings

Here, we genetically characterize the remaining ESCRT-II components vps22 and vps36. Like vps25, mutants of vps22 and vps36 display endosomal defects, accumulate Notch protein and – when the tissue is predominantly mutant – show neoplastic tumor characteristics. However, despite these common phenotypes, they have distinct non-autonomous phenotypes. While vps22 mutations cause strong non-autonomous overgrowth, they do not affect apoptotic resistance. In contrast, vps36 mutations increase apoptotic resistance, but have little effect on non-autonomous proliferation. Further characterization reveals that although all ESCRT-II mutants accumulate Notch protein, only vps22 and vps25 mutations trigger Notch activity.

Conclusions/Significance

The ESCRT-II components vps22, vps25 and vps36 display common and distinct genetic properties. Our data redefine the role of Notch for hyperplastic and neoplastic overgrowth in these mutants. While Notch is required for hyperplastic growth, it appears to be dispensable for neoplastic transformation.     

Lrp4 Regulates Initiation of Ureteric Budding and Is Crucial for Kidney Formation – A Mouse Model for Cenani-Lenz Syndrome

Background

Development of the kidney is initiated when the ureteric bud (UB) branches from the Wolffian duct and invades the overlying metanephric mesenchyme (MM) triggering the mesenchymal/epithelial interactions that are the basis of organ formation. Multiple signaling pathways must be integrated to ensure proper timing and location of the ureteric bud formation.

Methods and Principal Findings

We have used gene targeting to create an Lrp4 null mouse line. The mutation results in early embryonic lethality with a subpenetrant phenotype of kidney agenesis. Ureteric budding is delayed with a failure to stimulate the metanephric mesenchyme in a timely manner, resulting in failure of cellular differentiation and resulting absence of kidney formation in the mouse as well as comparable malformations in humans with Cenani-Lenz syndrome.

Conclusion

Lrp4 is a multi-functional receptor implicated in the regulation of several molecular pathways, including Wnt and Bmp signaling. Lrp4^−/− mice show a delay in ureteric bud formation that results in unilateral or bilateral kidney agenesis. These data indicate that Lrp4 is a critical regulator of UB branching and lack of Lrp4 results in congenital kidney malformations in humans and mice.