Stepwise formation of a SMAD activity gradient during dorsal-ventral patterning of the Drosophila embryo

Genetic evidence suggests that the Drosophila ectoderm is patterned by a spatial gradient of bone morphogenetic protein (BMP). Here we compare patterns of two related cellular responses, both signal-dependent phosphorylation of the BMP-regulated R-SMAD, MAD, and signal-dependent changes in levels and sub-cellular distribution of the co-SMAD Medea. Our data demonstrate that nuclear accumulation of the co-SMAD Medea requires a BMP signal during blastoderm and gastrula stages. During this period, nuclear co-SMAD responses occur in three distinct patterns. At the end of blastoderm, a broad dorsal domain of weak SMAD response is detected. During early gastrulation, this domain narrows to a thin stripe of strong SMAD response at the dorsal midline. SMAD response levels continue to rise in the dorsal midline region during gastrulation, and flanking plateaus of weak responses are detected in dorsolateral cells. Thus, the thresholds for gene expression responses are implicit in the levels of SMAD responses during gastrulation. Both BMP ligands, DPP and Screw, are required for nuclear co-SMAD responses during these stages. The BMP antagonist Short gastrulation (SOG) is required to elevate peak responses at the dorsal midline as well as to depress responses in dorsolateral cells. The midline SMAD response gradient can form in embryos with reduced dpp gene dosage, but the peak level is reduced. These data support a model in which weak BMP activity during blastoderm defines the boundary between ventral neurogenic ectoderm and dorsal ectoderm. Subsequently, BMP activity creates a step gradient of SMAD responses that patterns the amnioserosa and dorsomedial ectoderm.     

Protein associated with SMAD1 (PAWS1/FAM83G) is a substrate for type I bone morphogenetic protein receptors and modulates bone morphogenetic protein signalling

Bone morphogenetic proteins (BMPs) control multiple cellular processes in embryos and adult tissues. BMPs signal through the activation of type I BMP receptor kinases, which then phosphorylate SMADs 1/5/8. In the canonical pathway, this triggers the association of these SMADs with SMAD4 and their translocation to the nucleus, where they regulate gene expression. BMPs can also signal independently of SMAD4, but this pathway is poorly understood. Here, we report the discovery and characterization of PAWS1/FAM83G as a novel SMAD1 interactor. PAWS1 forms a complex with SMAD1 in a SMAD4-independent manner, and BMP signalling induces the phosphorylation of PAWS1 through BMPR1A. The phosphorylation of PAWS1 in response to BMP is essential for activation of the SMAD4-independent BMP target genes NEDD9 and ASNS. Our findings identify PAWS1 as the first non-SMAD substrate for type I BMP receptor kinases and as a novel player in the BMP pathway. We also demonstrate that PAWS1 regulates the expression of several non-BMP target genes, suggesting roles for PAWS1 beyond the BMP pathway.     

Smads基因功能的研究进展

转化生长因子 -β( TGF-β)超家族通过调节细胞的增殖、分化、移行和凋亡而在脊椎动物发育过程中起重要的作用 . SMAD家族是一类新发现的 TGF-β信号的细胞质内介导者 ,它们可将TGF- β信号直接从细胞膜转导入细胞核内 .受体激活的 SMADs被特导性的细胞表面受体磷酸化后 ,与通用介导分子 SMAD4相互作用形成异源三聚体 ,转移至细胞核内并激活靶基因的转录 .抑制型 SMADs通过负反馈途径阻断或减弱 TGF- β信号 .SMADs通过与 TGF- β配体应答的启动子序列及其它转录因子和辅助活化因子相互作用而调节转录 .通过同源重组在小鼠中定位敲除Smads基因的研究已经开始揭示 SMADs分子在脊椎动物发育过程中的功能 .     

Learning and signal copying facilitate communication among bird species

Signals relevant to different sets of receivers in different contexts create a conflict for signal design. A classic example is vocal alarm signals, often used both during intraspecific and interspecific interactions. How can signals alert individuals from a variety of other species in some contexts, while also maintaining efficient communication among conspecifics? We studied heterospecific responses to avian alarm signals that drive the formation of anti-predator groups but are also used during intraspecific interactions. In three species-rich communities in the western Himalayas, alarm signals vary drastically across species. We show that, independently of differences in their calls, birds respond strongly to the alarm signals of other species with which they co-occur and much more weakly to those of species with which they do not co-occur. These results suggest that previous exposure and learning maintain heterospecific responses in the face of widespread signal divergence. At an area where only two species regularly interact, one species'' calls incorporate the call of the other. We demonstrate experimentally that signal copying allows strong responses even without previous exposure and suggest that such hybrid calls may be especially favoured when pairwise interactions between species are strong.     

The highs and lows of theoretical interpretation in animal-metacognition research

Humans feel uncertain. They know when they do not know. These feelings and the responses to them ground the research literature on metacognition. It is a natural question whether animals share this cognitive capacity, and thus animal metacognition has become an influential research area within comparative psychology. Researchers have explored this question by testing many species using perception and memory paradigms. There is an emerging consensus that animals share functional parallels with humans' conscious metacognition. Of course, this research area poses difficult issues of scientific inference. How firmly should we hold the line in insisting that animals' performances are low-level and associative? How high should we set the bar for concluding that animals share metacognitive capacities with humans? This area offers a constructive case study for considering theoretical problems that often confront comparative psychologists. The authors present this case study and address diverse issues of scientific judgement and interpretation within comparative psychology.     

Bringing up small oocytes to eggs in pigs and cows

It has been known that the mammalian ovary contains a huge number of non-growing small oocytes, of which only a small number grow to their final size, mature, and are ovulated. Artificial maturation of small oocytes could provide a new source of mature eggs for livestock production and assisted reproduction in humans and in endangered species. Two methods have been used for oocyte growth, in vitro growth (IVG) culture and xenotransplantation. By these methods, oocytes in some species grow up to their final size and acquire developmental competence, although the methods are still at the experimental stage. The experiments remind us of many basic questions in mammalian oogenesis: Does the oocyte require certain stimuli to initiate growth? How are the few oocytes selected to grow to final size? How do they grow up in follicular units? How do they acquire meiotic competence during the growth phase? This paper will give some clues to answer these questions by presenting our recent data from IVG and xenotransplantation experiments, and by illustrating differences between the oocytes of mice and larger animals.     

Fluid shear stress and the vascular endothelium: for better and for worse

As blood flows, the vascular wall is constantly subjected to physical forces, which regulate important physiological blood vessel responses, as well as being implicated in the development of arterial wall pathologies. Changes in blood flow, thus generating altered hemodynamic forces are responsible for acute vessel tone regulation, the development of blood vessel structure during embryogenesis and early growth, as well as chronic remodeling and generation of adult blood vessels. The complex interaction of biomechanical forces, and more specifically shear stress, derived by the flow of blood and the vascular endothelium raise many yet to be answered questions:How are mechanical forces transduced by endothelial cells into a biological response, and is there a "shear stress receptor"?Are "mechanical receptors" and the final signaling pathways they evoke similar to other stimulus-response transduction systems?How do vascular endothelial cells differ in their response to physiological or pathological shear stresses?Can shear stress receptors or shear stress responsive genes serve as novel targets for the design of diagnostic and therapeutic modalities for cardiovascular pathologies?The current review attempts to bring together recent findings on the in vivo and in vitro responses of the vascular endothelium to shear stress and to address some of the questions raised above.     

Population growth rate as a basis for ecological risk assessment of toxic chemicals

Assessing the ecological risks of toxic chemicals is most often based on individual-level responses such as survival, reproduction or growth. Such an approach raises the following questions with regard to translating these measured effects into likely impacts on natural populations. (i) To what extent do individual-level variables underestimate or overestimate population-level responses? (ii) How do toxicant-caused changes in individual-level variables translate into changes in population dynamics for species with different life cycles? (iii) To what extent are these relationships complicated by population-density effects? These issues go to the heart of the ecological relevance of ecotoxicology and we have addressed them using the population growth rate as an integrating concept. Our analysis indicates that although the most sensitive individual-level variables are likely to be equally or more sensitive to increasing concentrations of toxic chemicals than population growth rate, they are difficult to identify a priori and, even if they could be identified, integrating impacts on key life-cycle variables via population growth rate analysis is nevertheless a more robust approach for assessing the ecological risks of chemicals. Populations living under density-dependent control may respond differently to toxic chemicals than exponentially growing populations, and greater care needs to be given to incorporating realistic density conditions (either experimentally or by simulation) into ecotoxicological test designs. It is impractical to expect full life-table studies, which record changes in survival, fecundity and development at defined intervals through the life cycle of organisms under specified conditions, for all relevant species, so we argue that population growth rate analysis should be used to provide guidance for a more pragmatic and ecologically sound approach to ecological risk assessment.     

Multidecadal changes in functional diversity lag behind the recovery of taxonomic diversity

While there has been increasing interest in how taxonomic diversity is changing over time, less is known about how long‐term taxonomic changes may affect ecosystem functioning and resilience. Exploring long‐term patterns of functional diversity can provide key insights into the capacity of a community to carry out ecological processes and the redundancy of species’ roles. We focus on a protected freshwater system located in a national park in southeast Germany. We use a high‐resolution benthic macroinvertebrate dataset spanning 32 years (1983–2014) and test whether changes in functional diversity are reflected in taxonomic diversity using a multidimensional trait‐based approach and regression analyses. Specifically, we asked: (i) How has functional diversity changed over time? (ii) How functionally distinct are the community''s taxa? (iii) Are changes in functional diversity concurrent with taxonomic diversity? And (iv) what is the extent of community functional redundancy? Resultant from acidification mitigation, macroinvertebrate taxonomic diversity increased over the study period. Recovery of functional diversity was less pronounced, lagging behind responses of taxonomic diversity. Over multidecadal timescales, the macroinvertebrate community has become more homogenous with a high degree of functional redundancy, despite being isolated from direct anthropogenic activity. While taxonomic diversity increased over time, functional diversity has yet to catch up. These results demonstrate that anthropogenic pressures can remain a threat to biotic communities even in protected areas. The differences in taxonomic and functional recovery processes highlight the need to incorporate functional traits in assessments of biodiversity responses to global change.