GENETIC INTERACTIONS OF FACTORS THAT REGULATE ALTERNATIVE RNA SPLICING IN THE MALE GERM LINE OF DROSOPHILA

Alternative RNA splicing is a critical process that contributes variety to protein functions, and further controls cell differentiation and normal development. Although it is known that most eukaryotic genes produce multiple transcripts in which splice site selection is regulated, how RNA binding proteins cooperate to activate and repress specific splice sites is still poorly understood. In addition how the regulation of alternative splicing affects germ cell development is also not well known. In this study, Drosophila Transformer 2 (Tra2) was used as a model to explore both the mechanism of its repressive function on its own pre-mRNA splicing, and the effect of the splicing regulation on spermatogenesis in testis. Half-pint (Hfp), a protein known as splicing activator, was identified in an S2 cell-based RNAi screen as a co-repressor that functions in combination with Tra2 in the splicing repression of the M1 intron. Its repressive splicing function is found to be sequence specific and is dependent on both the weak 3’ splice site and an intronic splicing silencer within the M1 intron. In addition we found that in vivo, two forms of Hfp are expressed in a cell type specific manner. These alternative forms differ at their amino terminus affecting the presence of a region with four RS dipeptides. Using assays in Drosophila S2 cells, we determined that the alternative N terminal domain is necessary in repression. This difference is probably due to differential localization of the two isoforms in the nucleus and cytoplasm. Our in vivo studies show that both Hfp and Tra2 are required for normal spermatogenesis and cooperate in repression of M1 splicing in spermatocytes. But interestingly, Tra2 and Hfp antagonize each other’s function in regulating germline specific alternative splicing of Taf1 (TBP associated factor 1). Genetic and cytological studies showed that mutants of Hfp and Taf1 both cause similar defects in meiosis and spermatogenesis. These results suggest Hfp regulates normal spermatogenesis partially through the regulation of taf1 splicing. These observations indicate that Hfp regulates tra2 and taf1 activity and play an important role in germ cell differentiation of male flies.

Evaluación de la preferencia de Liriomyza spp. en genotipos diferentes de garbanzo y efecto del extracto de Melia azedarach L. : resultados preliminares

En Argentina se están desarrollando genotipos de garbanzo (Cicer arietinum L.) para adecuarlos a las distintas zonas de producción. Estos presentan diferentes fenotipos lo que podría afectar las preferencias de oviposición de los insectos herbívoros de hábito minador. Los objetivos de este trabajo fueron: 1) determinar si las hembras del género Liriomyza spp. muestran preferencia por algún genotipo de garbanzo, y 2) evaluar el efecto del extracto de Melia azedarach sobre las líneas de garbanzo que resultaran susceptibles. Se sembraron dos líneas selectas y dos cultivares de C. arietinum que presentan hojas unifoliadas enteras o compuestas, en el Campo Experimental de la Facultad de Ciencias Agropecuarias, Universidad Nacional de Córdoba, en bloques al azar con tres repeticiones. Para analizar la preferencia, mediante censos semanales se evaluó la presencia de las larvas de las moscas en el período julio-septiembre. Los dípteros eligieron de manera significativa los genotipos de hoja entera y grande. Posteriormente, las plantas con hojas minadas de las variedades preferidas fueron sometidas a tratamiento con el extracto botánico. Para ello se marcaron cinco plantas de cada bloque: a 15 se les aplicó extracto (10%) y a las otras 15 agua (control). Se observó que el número de hojas minadas, de pupas y adultos emergidos disminuyeron en los tratamientos con el extracto. Estudios complementarios serán necesarios para poder considerar este compuesto natural en un plan de manejo del herbívoro.

Characteristics and stomach contents of Greenland sharks (Somniosus microcephalus) caught in Svalbard during June 2008-2009

Harbour seals in Svalbard have short longevity, despite being protected from human hunting and having limited terrestrial predation at their haulout sites, low contaminant burdens and no fishery by-catch issues. This led us to explore the diet of Greenland sharks (Somniosus microcephalus) in this region as a potential seal predator. We examined gastrointestinal tracts (GITs) from 45 Greenland sharks in this study. These sharks ranged from 229 to 381 cm in fork length and 136-700 kg in body mass; all were sexually immature. Seal and whale tissues were found in 36.4 and 18.2%, respectively, of the GITs that had contents (n = 33). Based on genetic analyses, the dominant seal prey species was the ringed seal (Pusa hispida); bearded seal (Erignathus barbatus) and hooded seal (Cystophora cristata) tissues were each found in a single shark. The sharks had eaten ringed seal pups and adults based on the presence of lanugo-covered prey (pups) and age determinations based on growth rings on claws (<1 year and adults). All of the whale tissue was from minke whale (Balenoptera acutorostrata) offal, from animals that had been harvested in the whale fishery near Svalbard. Fish dominated the sharks' diet, with Atlantic cod (Gadus morhua), Atlantic wolffish (Anarhichas lupus) and haddock (Melanogrammus aeglefinus) being the most important fish species. Circumstantial evidence suggests that these sharks actively prey on seals and fishes, in addition to eating carrion such as the whale tissue. Our study suggests that Greenland sharks may play a significant predatory role in Arctic food webs.