Getting around Antarctica: new high-resolution mappings of the grounded and freely-floating boundaries of the Antarctic ice sheet created for the International Polar Year.

The boundary of grounded ice and the location of ice transitioning to a freely floating state are mapped at 15-m resolution around the entire continent of Antarctica. These data products are produced by participants of the International Polar Year project ASAID using customized software combining Landsat-7 imagery and ICESat laser altimetry. The grounded ice boundary is 53 610 km long; 74% of it abuts to floating ice shelves or outlet glaciers, 19% is adjacent to open or sea-ice covered ocean, and 7% of the boundary are land terminations with bare rock. Elevations along each line are selected from 6 candidate digital elevation models: two created from the input ICESat laser altimetry and Landsat data, two from stereo satellite imagery, and two from compilations of primarily radar altimetry. Elevation selection and an assignment of confidence in the elevation value are based on agreement with ICESat elevation values and shape of the surface inferred from the Landsat imagery. Elevations along the freely-floating boundary (called the hydrostatic line) are converted to ice thicknesses by applying a firn-correction factor and a flotation criterion. The relationship between the seaward offset of the hydrostatic line from the grounding line only weakly matches a prediction based on beam theory. Airborne data are used to validate the technique of grounding line mapping, elevation selection and ice thickness derivation. The mapped products along with the customized software to generate them and a variety of intermediate products are available from the National Snow and Ice Data Center

IT-Konzept der Universität Osnabrück

IT-Konzept der Universität Osnabrüc

Bacterial ribosome collision sensing by a MutS DNA repair ATPase paralogue

Ribosome stalling during translation is detrimental to cellular fitness, but how this is sensed and elicits recycling of ribosomal subunits and quality control of associated mRNA and incomplete nascent chains is poorly understood(1,2). Here we uncover Bacillus subtilis MutS2, a member of the conserved MutS family of ATPases that function in DNA mismatch repair(3), as an unexpected ribosome-binding protein with an essential function in translational quality control. Cryo-electron microscopy analysis of affinity-purified native complexes shows that MutS2 functions in sensing collisions between stalled and translating ribosomes and suggests how ribosome collisions can serve as platforms to deploy downstream processes: MutS2 has an RNA endonuclease small MutS-related (SMR) domain, as well as an ATPase/clamp domain that is properly positioned to promote ribosomal subunit dissociation, which is a requirement both for ribosome recycling and for initiation of ribosome-associated protein quality control (RQC). Accordingly, MutS2 promotes nascent chain modification with alanine-tail degrons-an early step in RQC-in an ATPase domain-dependent manner. The relevance of these observations is underscored by evidence of strong co-occurrence of MutS2 and RQC genes across bacterial phyla. Overall, the findings demonstrate a deeply conserved role for ribosome collisions in mounting a complex response to the interruption of translation within open reading frames

Status of the down-regulated canine testis using two different GNRH agonist implants in comparison with the juvenile testis

Testicular function in the dog was down-regulated using two different GNRH agonist implants, with adult and juvenile testes serving as controls. Treatment resulted in an increased percentage of the interstitial area and decreased area of Leydig cell nuclei. Expression of StAR and the steroidogenic enzymes cytochrome P450 side-chain cleavage enzyme (P450scc, CYP11A1) and cytochrome P450 17α-hydroxylase-17,20-lyase (P450c17, CYP17A1) in Leydig cells was blocked at the mRNA and protein level, showing no differences between the two agonists. Staining for androgen receptor (AR) by immunohistochemistry was positive in Sertoli, Leydig and peritubular cells and some spermatogonia, with in situ hybridization confirming expression in Sertoli cells. At the mRNA level, expression of AR was not affected; however, translation was blocked (reduced percentage of AR-positive Sertoli cells), with the number of nuclei in basal position being decreased. In the juvenile testes, mRNA expression of StAR, CYP11A1 and CYP17A1 was higher compared with the other groups but distinctly lower for the AR. At the protein level, the expression was at the limit of detection for StAR; AR-positive Sertoli cells were not detected. Our observations show that the down-regulated testis is different from the juvenile one rather resembling the testicular status in seasonal breeders out of season