0000000000022621
AUTHOR
Gabriele Stern-schneider
showing 3 related works from this author
Mesadenes maturation and its hormonal control in the milkweed bug, Oncopeltus fasciatus
1993
Abstract Adult maturation of the mesadenia was examined by electron microscopy. The glandular epithelium exhibits only one cell type with a polarity along the haemocoel-lumen axis. In newly emerged males, the glands show little signs of secretory activity although the narrow lumen contains some material. Dramatic changes commence at day 2. The rER increases drastically, and at day 3 cisternae of the rER are considerably distended and include a fine granulated product. The lumen of the gland widens greatly and stores material of the same appearance as in the rER inclusions. The mode of the secretory process is not clear since membrane bound vesicles are not formed. SDS-PAGE of the secretion …
The Leber congenital amaurosis protein AIPL1 and EB proteins co-localize at the photoreceptor cilium.
2015
The aim of this study was to investigate the interaction and co-localization of novel interacting proteins with the Leber congenital amaurosis (LCA) associated protein aryl hydrocarbon receptor interacting protein-like 1 (AIPL1).The CytoTrapXR yeast two-hybrid system was used to screen a bovine retinal cDNA library. A novel interaction between AIPL1 and members of the family of EB proteins was confirmed by directed yeast two-hybrid analysis and co-immunoprecipitation assays. The localization of AIPL1 and the EB proteins in cultured cells and in retinal cryosections was examined by immunofluorescence microscopy and cryo-immunogold electron microscopy.Yeast two-hybrid (Y2H) analysis identifie…
Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa
2013
Retinitis pigmentosa (RP) is a genetically heterogeneous retinal degeneration characterized by photoreceptor death, which results in visual failure. Here, we used a combination of homozygosity mapping and exome sequencing to identify mutations in ARL2BP, which encodes an effector protein of the small GTPases ARL2 and ARL3, as causative for autosomal-recessive RP (RP66). In a family affected by RP and situs inversus, a homozygous, splice-acceptor mutation, c.101−1G>C, which alters pre-mRNA splicing of ARLBP2 in blood RNA, was identified. In another family, a homozygous c.134T>G (p.Met45Arg) mutation was identified. In the mouse retina, ARL2BP localized to the basal body and cilium-associated…