Carcasses increase the probability of predation of ground-nesting birds: a caveat regarding the conservation value of vulture restaurants

Carcasses not only recruit carrion-eaters, but can also attract facultative scavengers which could predate on species living in the surroundings. At supplementary feeding stations ('vulture restaurants') carcasses are available permanently, posing a conservation dilemma: enhancing populations of endangered scavengers might introduce a predation pressure on non-target species. Here, we test if nest predation risk on ground-nesting birds increases near carcasses in Fuerteventura Island (Canary Archipelago). This is an optimal scenario for performing this study because there is a simple community of ground-nesting birds and facultative scavengers; carrion-eaters feed regularly in a unique vulture restaurant but also exploit scattered carcasses of goats. We placed artificial nests along different lines located at variable distances (200 m to 34 km) from the vulture restaurant or from single carcasses. Sixty-seven per cent of lines and up to 90% of nests within lines were predated. Predation risk was higher in lines near carcasses, that is single carcasses or the vulture restaurant. Thus, our study alerts that choosing the location for vulture restaurants may be the key not only for scavengers but also for the conservation of the species living nearby.     

Advances in endophenotyping schizophrenia

The search for the genetic architecture of schizophrenia has employed multiple, often converging strategies. One such strategy entails the use of tracing the heritability and neurobiology of endophenotypes. Endophenotypes are quantifiable traits not visible to the eye, which are thought to reflect an intermediate place on the path from genes to disorder. Endophenotype abnormalities in domains such as neurophysiology or neurocognition occur in schizophrenia patients as well as their clinically “unaffected” relatives, and reflect polymorphisms in the DNA of schizophrenia spectrum subjects which create vulnerability to developing schizophrenia. By identifying the single nucleotide polymorphisms (SNPs) associated with endophenotypes in schizophrenia, psychiatric neuroscientists can select new strong inference based molecular targets for the treatment of schizophrenia.     

Phylogenetic position of a remarkable new fideliine bee from northern Chile (Hymenoptera: Megachilidae)

Fideliine bees are an archaic group with a disjunct distribution mostly restricted to deserts of South America and South Africa. This group was previously thought to be more diverse in Africa than in South America, where only one genus (Neofidelia) comprising five species is known. Here we describe a species belonging to a second South American genus: Xenofidelia colorada Packer gen. et sp.n. , from northern Chile. The species is illustrated and its phylogenetic position within Megachilidae is assessed using morphological, molecular and combined data. The 214 character morphological matrix includes 55 new characters with an additional 16 hitherto unexplored for megachilid phylogeny. The molecular dataset is based upon seven nuclear gene sequences, totalling 6439 bp, many of which are published for the first time for particular megachilid taxa. In all analyses, Xenofidelia was found as sister to Neofidelia (endemic to Chile and Peru). It differs from that genus most notably in its short mouthparts, absence of a glossal rod, unmodified female metabasitarsus and an elongate and horizontal dorsal surface of the metapostnotum. Morphological and combined data support a monophyletic Fideliinae (excluding Pararhophites), while molecular data alone failed to recover fideliine monophyly. Dating analyses suggest that Xenofidelia and Neofidelia diverged 34.3–40.6 Ma, indicating that New World fideliines were probably present in arid habitats of South America during the Eocene. This divergence time predates both the main orogenic events that resulted in the formation of the Andean mountains and the origin of hyperarid conditions in the Atacama Desert; it also corresponds to a period prior to the origin of the summer rainfall area in the far north of Chile where the new genus is found. These results support the view that arid habitats have been present continuously in South America since the Eocene. This published work has been registered in ZooBank, http://zoobank.org/urn:lsid:zoobank.org:pub:EA69BB4A‐6F59‐4A15‐AB44‐2A8949E3CF8F .     

A Single Conserved Residue Mediates Binding of the Ribonucleotide Reductase Catalytic Subunit RRM1 to RRM2 and Is Essential for Mouse Development

The ribonucleotide reductase (RNR) complex, composed of a catalytic subunit (RRM1) and a regulatory subunit (RRM2), is thought to be a rate-limiting enzymatic complex for the production of nucleotides. In humans, the Rrm1 gene lies at 11p15.5, a tumor suppressor region, and RRM1 expression in cancer has been shown to predict responses to chemotherapy. Nevertheless, whether RRM1 is essential in mammalian cells and what the effects of its haploinsufficiency are remain unknown. To model RNR function in mice we used a mutation previously described in Saccharomyces cerevisiae (Rnr1-W688G) which, despite being viable, leads to increased interaction of the RNR complex with its allosteric inhibitor Sml1. In contrast to yeast, homozygous mutant mice carrying the Rrm1 mutation (Rrm1^WG/WG) are not viable, even at the earliest embryonic stages. Proteomic analyses failed to identify proteins that specifically bind to the mutant RRM1 but revealed that, in mammals, the mutation prevents RRM1 binding to RRM2. Despite the impact of the mutation, Rrm1^WG/+ mice and cells presented no obvious phenotype, suggesting that the RRM1 protein exists in excess. Our work reveals that binding of RRM1 to RRM2 is essential for mammalian cells and provides the first loss-of-function model of the RNR complex for genetic studies.     

A Highlights from MBoC Selection: Cell shape impacts on the positioning of the mitotic spindle with respect to the substratum

All known mechanisms of mitotic spindle orientation rely on astral microtubules. We report that even in the absence of astral microtubules, metaphase spindles in MDCK and HeLa cells are not randomly positioned along their x-z dimension, but preferentially adopt shallow β angles between spindle pole axis and substratum. The nonrandom spindle positioning is due to constraints imposed by the cell cortex in flat cells that drive spindles that are longer and/or wider than the cell''s height into a tilted, quasidiagonal x-z position. In rounder cells, which are taller, fewer cortical constraints make the x-z spindle position more random. Reestablishment of astral microtubule–mediated forces align the spindle poles with cortical cues parallel to the substratum in all cells. However, in flat cells, they frequently cause spindle deformations. Similar deformations are apparent when confined spindles rotate from tilted to parallel positions while MDCK cells progress from prometaphase to metaphase. The spindle disruptions cause the engagement of the spindle assembly checkpoint. We propose that cell rounding serves to maintain spindle integrity during its positioning.     

Multifunctional roles of the autoimmune disease-associated tyrosine phosphatase PTPN22 in regulating T cell homeostasis

The non-receptor tyrosine phosphatase PTPN22 has a vital function in inhibiting antigen-receptor signaling in T cells, while polymorphisms in the PTPN22 gene are important risk alleles in human autoimmune diseases. We recently reported that a key physiological function of PTPN22 was to prevent naïve T cell activation and effector cell responses in response to low affinity antigens. PTPN22 also has a more general role in limiting T cell receptor-induced proliferation. Here we present new data emphasizing this dual function for PTPN22 in T cells. Furthermore, we show that T cell activation modulates the expression of PTPN22 and additional inhibitory phosphatases. We discuss the implication of these findings for our understanding of the roles of PTPN22 in regulating T cell responses and in autoimmunity.     

Alterations in the Colonic Microbiota of Pigs Associated with Feeding Distillers Dried Grains with Solubles

In an effort to reduce feed costs, many pork producers have increased their use of coproducts of biofuel production in commercial pig diets, including increased feeding of distiller’s dried grains with solubles (DDGS). The inclusion of DDGS increases the insoluble fiber content in the ration, which has the potential to impact the colonic microbiota considerably as the large intestine contains a dynamic microenvironment with tremendous interplay between microorganisms. Any alteration to the physical or chemical properties of the colonic contents has the potential to impact the resident bacterial population and potentially favor or inhibit the establishment of pathogenic species. In the present study, colonic contents collected at necropsy from pigs fed either 30% or no DDGS were analyzed to examine the relative abundance of bacterial taxa associated with feeding this ingredient. No difference in alpha diversity (richness) was detected between diet groups. However, the beta diversity was significantly different between groups with feeding of DDGS being associated with a decreased Firmicutes:Bacteriodetes ratio (P = .004) and a significantly lower abundance of Lactobacillus spp. (P = .016). Predictive functional profiling of the microbiota revealed more predicted genes associated with carbohydrate metabolism, protein digestion, and degradation of glycans in the microbiota of pigs fed DDGS. Taken together, these findings confirm that alterations in dietary insoluble fiber significantly alter the colonic microbial profile of pigs and suggest the resultant microbiome may predispose to the development of colitis.