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Aim Coralligenous reefs are the main marine bioconstructions in terms of spatial distribution within the Mediterranean basin. Two distinct reef morphologies can be distinguished based on the surface and topographical features of the seafloor: cliffs developing vertical slopes and banks found on gently steep or horizontal bottoms. Despite their importance for monitoring and conservation efforts, observations regarding the variability of biogeographical patterns are scarce. Here, we aimed to assess the differences in the composition and structure of these cliffs across ecoregions and estimate the relative role of abiotic environmental features, geographic location, and connectivity in shaping diversity patterns. Location The study was carried out in the Central‐Western Mediterranean Sea. Samples were collected at 65 sites across the Algero‐Provençal Basin, the Ionian Sea and the Tyrrhenian Sea. Methods We assessed the composition and structure of coralligenous cliffs through photographic samplings collected by scuba divers. Patterns in α‐ and β‐diversity were associated with 9 abiotic environmental variables, latitudinal and longitudinal gradients, and connectivity measures using Generalized Additive (GAM) and Conditional Autoregressive (CAR) models. Results Coralligenous cliffs were primarily composed of algae and displayed a high degree of variability. The Partition Around Medoids (PAM) clustering method successfully delineated seven distinct clusters with a non‐uniform distribution within the studied ecoregions. The α‐diversity increased in eastern and northern sites and with phosphate concentration, while decreased with temperature, chlorophyll and nitrates concentration. β‐diversity at the site level increased with temperature, while it was negatively affected by northward current speed and chlorophyll concentration. Moveover, β‐diversity increased within connected sites. Main Conclusions Coralligenous cliff diversity responds both to the physico‐chemical features of the habitat and between‐habitats connectivity. However, our findings suggest that small‐scale abiotic and biotic processes could contribute to explaining the variability observed. These findings can significantly enhance the monitoring and conservation efforts of this Mediterranean endemic ecosystem.

Prostate cancer is among the most commonly diagnosed male diseases and a leading cause of cancer mortality in men. There is emerging evidence that autophagy plays an important role in malignant cell survival and offers protection from the anti-cancer drugs in prostate cancer cells. AMBRA1 and the autophagic protein sequestosome-1 (SQSTM1; p62) expression were evaluated by immunohistochemistry and western blot on tissue samples from both benign and malignant prostatic lesions. The data reported in this pilot study demonstrated an increased expression of AMBRA1 and SQSTM1, which were also associated with an accumulation of LC3II in prostate cancer but not in benign lesion. In the present study we found that: (i) at variance with benign lesion, prostate cancer cells underwent SQSTM1 accumulation, i.e., clearly displayed a defective autophagic process but, also, (ii) prostate cancer accumulated AMBRA1 and (iii) this increase positively correlated with the Gleason score. These results underscore a possible implication of autophagy in prostate cancer phenotype and of AMBRA1 as possible cancer progression biomarker in this malignancy.

Background Complex chromosomal rearrangements are constitutive structural aberrations involving three or more breaks. They can be balanced or unbalanced and result in different outcomes, depending on deletion/duplication of genomic material, gene disruption, or position effects. Case presentation We report on a patient presenting with severe anemia, splenomegaly, mild intellectual disability and facial dysmorphisms harboring a 4.3 Mb duplication at 1p22.1p21.3 and a 2.1 Mb deletion at 8q21.3q22.1, involving RUNX1T1 gene. The healthy brother presented the same duplication of chromosome 1p as at 1p22.1p21.3. Conclusions The rearrangement found both these siblings resulted from malsegregation in the proband and recombination in her healthy brother of a balanced paternal complex chromosomal rearrangement. These results confirm RUNX1T1 as a causative gene for intellectual disability and suggest the 1p22.1p21.3 duplication is likely benign.