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Shadoo 类朊蛋白在发育中鼠胚中的表达。

Expression of the prion-like protein Shadoo in the developing mouse embryo.

机构信息

INRA UMR 1313, Equipe Différenciation et Spécialisation Cellulaires (DISC), Génétique Animale et Biologie Intégrative (GABI), 78350 Jouy-en-Josas, France.

出版信息

Biochem Biophys Res Commun. 2011 Dec 9;416(1-2):184-7. doi: 10.1016/j.bbrc.2011.11.021. Epub 2011 Nov 10.

Abstract

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. Their expression in the mouse embryo has also been suggested to be complementary, as invalidation of both genes results in embryonic lethality. The developmental expression profile of PrP has been described from post-implantation stages up until birth. 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.

摘要

朊病毒样蛋白 Shadoo 被认为可以弥补 Prnp 基因敲除小鼠中 PrP 的缺失,解释了它们缺乏极端表型的原因。在成年小鼠中,PrP 和 Shadoo 的表达模式重叠且具有共同的功能。它们在小鼠胚胎中的表达也被认为是互补的,因为这两种基因的失活都会导致胚胎致死。PrP 的发育表达谱已从着床后阶段描述到出生。然而,Shadoo 在发育中的小鼠胚胎中的空间表达模式尚不清楚。我们之前使用 Sprn 报告小鼠(Sprn-GFP 和 Sprn-LacZ)描述了成年小鼠中朊病毒样蛋白 Shadoo 的表达谱。在这里,我们使用这些小鼠在 10.5 至 14.5 dpc 之间描述 Shadoo 的发育表达。在特定的胚胎细胞谱系和胚胎外组织中观察到的模式与先前报道的因 Shadoo 敲低导致的表型一致。

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