Several hypotheses are available to predict change in genetic diversity when approaching peripheral populations. We used the eastern spadefoot toad in Israel as a model system to examine these hypotheses using population genetics analyses and network theory. Our results contradicted most of the predictions from the 'abundant centre' model, that edge populations should have lower density and lower genetic diversity than core populations. Furthermore, dispersal rate between core and peripheral populations is expected to be asymmetric, mostly directed outwards from the core population, but we did not detect such a trend. Our data did not support the hypothesis of no change or a non-linear change in genetic diversity towards the range edge. However, our results did fit the Fisher (The Genetical Theory of Natural Selection, Clarendon Press, Oxford, 1930) hypothesis, which predicts increase in genetic variability from core to edge of distribution. We attributed this finding to the much harsher climatic and abiotic conditions at the edge, which must be tolerated over generations by both tadpoles and post-metamorphic individuals in this region. Finally, our results have significant conservation implications for the survival of this species in Israel, where it is critically endangered. We identified two distinct communities, which are genetically linked through two specific rain pools in the Upper Galilee. Details on the spatial subdivision of this species are cardinal for future management and restoration of temporary wetlands in Israel.
Sarcopeniathe accelerated age-related loss of muscle mass and functionis an under-diagnosed condition, and is central to deteriorating mobility, disability and frailty in older age. There is a lack of treatment options for older adults at risk of sarcopenia. Although sarcopenia's pathogenesis is multifactorial, its major phenotypesmuscle mass and muscle strengthare highly heritable. Several genome-wide association studies of musclerelated traits were published recently, providing dozens of candidate genes, many with unknown function. Therefore, animal models are required not only to identify causal mechanisms, but also to clarify the underlying biology and translate this knowledge into new interventions. Over the past several decades, small teleost fishes had emerged as powerful systems for modeling the genetics of human diseases. Owing to their amenability to rapid genetic intervention and the large number of conserved genetic and physiological features, small teleostssuch as zebrafish, medaka and killifishhave become indispensable for skeletal muscle genomic studies. The goal of this Review is to summarize evidence supporting the utility of small fish models for accelerating our understanding of human skeletal muscle in health and disease. We do this by providing a basic foundation of the (zebra)fish skeletal muscle morphology and physiology, and evidence of muscle-related gene homology. We also outline challenges in interpreting zebrafish mutant phenotypes and in translating them to human disease. Finally, we conclude with recommendations on future directions to leverage the large body of tools developed in small fish for the needs of genomic exploration in sarcopenia.
The assessment of the composition and dynamics of endangered populations is crucial for management and conservation, and appropriate genetic markers are critical. The genetic structuring of the Mediterranean green turtle (Chelonia mydas) populations and the origin of the stranded animals found along the Israeli coast was investigated using new highly polymorphic short tandem repeat (STR) markers. The structuring of nesting populations was studied using pairwise genetic distances and a principal coordinates analysis (PCoA). The contribution of the different nesting populations to the stranded sample was assessed by using a mixed‐stock analysis. A clear population genetic structure, not detected before, has been revealed. The four nesting populations are genetically well differentiated, and thus should be considered as different management units. The populations from Turkey and Israel showed higher resemblance, despite residing at opposite ends of the Mediterranean distribution. The Turkish nesting population is the main source of the stranded turtles sampled along the Israeli shore, confirming that individuals from this population migrate from north to south along the eastern shore of the Mediterranean, as previously shown by telemetry studies. The use of a highly polymorphic haplotyping method enabled the detection of a clear genetic structuring of the green turtle populations in the eastern Mediterranean Sea that was not revealed in previous studies, demonstrating the importance of marker selection in population genetics. The analysis of the genetic composition of the stranded turtles allowed us to investigate the migration patterns from nesting to foraging areas, supporting previous satellite‐tracking and stable‐isotope results. These results will help to delineate conservation management units for the species in the Mediterranean, and reveal connectivity among beaches and mixed aggregations.
GNE Myopathy is a rare recessively inherited neuromuscular disorder caused by mutations in the GNE gene, which codes for the key enzyme in the metabolic pathway of sialic acid synthesis. The process by which GNE mutations lead to myopathy is not well understood. By in situ hybridization and gne promoter-driven fluorescent transgenic fish generation, we have characterized the spatiotemporal expression pattern of the zebrafish gne gene and have shown that it is highly conserved compared with the human ortholog. We also show the deposition of maternal gne mRNA and maternal GNE protein at the earliest embryonic stage, emphasizing the critical role of gne in embryonic development. Injection of morpholino (MO)-modified antisense oligonucleotides specifically designed to knockdown gne, into one-cell embryos lead to a variety of phenotypic severity. Characterization of the gne knockdown morphants showed a significantly reduced locomotor activity as well as distorted muscle integrity, including a reduction in the number of muscle myofibers, even in mild or intermediate phenotype morphants. These findings were further confirmed by electron microscopy studies, where large gaps between sarcolemmas were visualized, although normal sarcomeric structures were maintained. These results demonstrate a critical novel role for gne in embryonic development and particularly in myofiber development, muscle integrity and activity.
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