کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1930012 | 1536784 | 2011 | 4 صفحه PDF | دانلود رایگان |
The prion-like protein Shadoo has been suggested to compensate for the lack of PrP in Prnp-knockout mice, explaining their lack of extreme phenotype. In adult mice, both PrP and Shadoo have shown overlapping expression patterns and shared functions [1]. Their expression in the mouse embryo has also been suggested to be complementary, as invalidation of both genes results in embryonic lethality [2]. The developmental expression profile of PrP has been described from post-implantation stages up until birth [3], [4] and [5]. However the spatial expression pattern of Shadoo in the developing mouse embryo is not known. We previously described the expression profile of the prion-like protein Shadoo in adult mice using Sprn reporter mice (Sprn-GFP and Sprn-LacZ). Here we used these mice to describe the developmental expression of Shadoo between 10.5 and 14.5 dpc. The observed pattern in specific embryonic cell lineages and in extra-embryonic tissues is consistent with the previously reported phenotype resulting from its knockdown.
► Regulatory sequences of the Sprn gene (5.3 Kb) were used to drive expression of a LacZ reporter gene in mice.
► Expression of the transgene was detected from 10.5 dpc onwards.
► Extra-embryonic and nerve cell-specific transgene expression was revealed.
► The results suggest a role for Shadoo in mouse embryo development.
Journal: Biochemical and Biophysical Research Communications - Volume 416, Issues 1–2, 9 December 2011, Pages 184–187