The morphological description is supplemented with 436 sequenced base pairs of the 18S gene (including the V4 region) as well as 1,041 sequenced
base pairs spanning the complete ITS-1, 5.8S, and ITS-2 regions. BLAST (Basic Local Alignment Search Tool) searches failed to provide any close matches for either regions of DNA, with Gyrodactylus colemanensis infecting Salvelinus fontinalis being the most genetically similar for both the 18S (similar to 91%, JF836090) and ITS DMXAA Angiogenesis inhibitor (similar to 84%, JF836142) rDNA regions. Gyrodactylus mediotorus n. sp. has been found infecting spottail shiners in the St. Lawrence River in low prevalence and intensities periodically over the last 15 yr.”
“Crustacean hyperglycemic hormone (CHH) synthesizing cells in
the optic lobe, one of the pacemakers of the circadian system, have been shown to be present in crayfish. However, the presence of CHH in the central brain, another putative pacemaker of the multi-oscillatory circadian system, of this decapod and its circadian transcription in the optic lobe and brain have yet to be explored. Therefore, using qualitative and quantitative PCR, we isolated and cloned a CHH mRNA fragment from two putative pacemakers of the multi-oscillatory circadian system of Procambarus clarkii, the optic lobe and the central Wnt cancer brain. This CHH transcript synchronized to daily light-dark cycles and oscillated under dark, constant conditions demonstrating statistically significant daily and circadian rhythms in both structures. Furthermore, to investigate the Nutlin 3 presence of the peptide in the central brain of this decapod, we used immunohistochemical methods. Confocal microscopy revealed the presence of CHH-IR in fibers and cells of the protocerebral and tritocerebal clusters and neuropiles, particularly in some neurons located in clusters 6, 14, 15 and 17. The presence of CHH positive neurons in structures of P. clarkii where clock proteins have been reported suggests a relationship between the circadian
clockwork and CHH. This work provides new insights into the circadian regulation of CHH, a pleiotropic hormone that regulates many physiological processes such as glucose metabolism and osmoregulatory responses to stress.”
“Human neutrophil antigen 2 (HNA-2) deficiency is a common phenotype as 3-5% humans do not express HNA-2. HNA-2 is coded by CD177 gene that associates with human myeloproliferative disorders. HNA-2 deficient individuals are prone to produce HNA-2 alloantibodies that cause a number of disorders including transfusion-related acute lung injury and immune neutropenia. In addition, the percentages of HNA-2 positive neutrophils vary significantly among individuals and HNA-2 expression variations play a role in human diseases such as myelodysplastic syndrome, chronic myelogenous leukemia, and gastric cancer. The underlying genetic mechanism of HNA-2 deficiency and expression variations has remained a mystery.