38 research outputs found

    Seismotectonic aspects of the Ms 7.3 1948 October 5 Aşgabat (Ashgabat) earthquake, Türkmenistan: right-lateral rupture across multiple fault segments, and continuing urban hazard

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    The Ms 7.3 1948 Aşgabat earthquake was one of the most devastating earthquakes of the 20th century, yet little is known about its location, style and causative fault. In this study, we bring together new seismic and geomorphic observations with previously published descriptions of surface rupture and damage distributions to determine the likely source of the earthquake. We determine the epicentre and focal mechanism of this earthquake from digitized historical seismograms and the relocation of regional seismicity to show that the earthquake most likely nucleated close to the city of Aşgabat. The earthquake ruptured a right-lateral strike-slip fault to the southeast of the city, which has a clear long-term expression in the landscape, and also likely reactivated a subparallel concealed thrust along the Gyaursdag anticline east of the city. The earthquake potentially also ruptured a right-lateral segment northwest of Aşgabat, which does not have an identifiable expression in the landscape. Using high-resolution satellite imagery and digital elevation models we investigate the geomorphology of active faulting around Aşgabat and adjacent parts of the Köpetdag (Kopeh Dagh) mountain range front, showing that there are significant strike-slip and oblique strike-slip segments adjacent to the city that apparently did not rupture in 1948, and yet show clear geomorphic expression and potential right-lateral displacement of Parthian-era (∼2000 yr) and post-Sassanian era (∼1500 yr) archaeological remains. Luminescence dating of displaced fluvial terraces west of Aşgabat yields a vertical displacement rate of 0.6 mm yr−1, though the strike-slip rate remains undetermined

    A Modular Cloning System for Standardized Assembly of Multigene Constructs

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    The field of synthetic biology promises to revolutionize biotechnology through the design of organisms with novel phenotypes useful for medicine, agriculture and industry. However, a limiting factor is the ability of current methods to assemble complex DNA molecules encoding multiple genetic elements in various predefined arrangements. We present here a hierarchical modular cloning system that allows the creation at will and with high efficiency of any eukaryotic multigene construct, starting from libraries of defined and validated basic modules containing regulatory and coding sequences. This system is based on the ability of type IIS restriction enzymes to assemble multiple DNA fragments in a defined linear order. We constructed a 33 kb DNA molecule containing 11 transcription units made from 44 individual basic modules in only three successive cloning steps. This modular cloning (MoClo) system can be readily automated and will be extremely useful for applications such as gene stacking and metabolic engineering

    The Status of Dosage Compensation in the Multiple X Chromosomes of the Platypus

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    Dosage compensation has been thought to be a ubiquitous property of sex chromosomes that are represented differently in males and females. The expression of most X-borne genes is equalized between XX females and XY males in therian mammals (marsupials and “placentals”) by inactivating one X chromosome in female somatic cells. However, compensation seems not to be strictly required to equalize the expression of most Z-borne genes between ZZ male and ZW female birds. Whether dosage compensation operates in the third mammal lineage, the egg-laying monotremes, is of considerable interest, since the platypus has a complex sex chromosome system in which five X and five Y chromosomes share considerable genetic homology with the chicken ZW sex chromosome pair, but not with therian XY chromosomes. The assignment of genes to four platypus X chromosomes allowed us to examine X dosage compensation in this unique species. Quantitative PCR showed a range of compensation, but SNP analysis of several X-borne genes showed that both alleles are transcribed in a heterozygous female. Transcription of 14 BACs representing 19 X-borne genes was examined by RNA-FISH in female and male fibroblasts. An autosomal control gene was expressed from both alleles in nearly all nuclei, and four pseudoautosomal BACs were usually expressed from both alleles in male as well as female nuclei, showing that their Y loci are active. However, nine X-specific BACs were usually transcribed from only one allele. This suggests that while some genes on the platypus X are not dosage compensated, other genes do show some form of compensation via stochastic transcriptional inhibition, perhaps representing an ancestral system that evolved to be more tightly controlled in placental mammals such as human and mouse

    Medicinal plants – prophylactic and therapeutic options for gastrointestinal and respiratory diseases in calves and piglets? A systematic review

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