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Ubiquitous expression of Sry induces embryonic lethality related to suppression of Tie2/Tek expression

机译:Sry的普遍表达诱导与抑制Tie2 / Tek表达有关的胚胎致死率

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Sry (sex-determining region on the Y chromosome) is a mammalian sex-determining gene on the Y chromosome. In mice, the transient expression of Sry in supporting cell precursor cells between 10.5 and 12.5 days post-coitus (dpc) triggers the differentiation of Sertoli cells from granulosa cells. The importance of the strict regulation of Sry expression remains unknown. Thus, we attempted to produce a Sry ubiquitous-expressing transgenic (Tg) mouse in which foreign Sry is driven by the CAG (cytomegalovirus immediate-early enhancer, chicken beta-actin promoter, and the fusion intron of chicken beta-actin and rabbit beta-globin)-Sry gene for ubiquitous expressing Sry. A low rate (2/127) of Tg pups was observed, whereas the rate of early-stage transgenic embryos before birth was 19.2% (5/26). The Sry ubiquitous-expressing embryos showed abnormal development. The results suggest that ubiquitous expression of Sry exerts a negative effect on embryonic development. One of the two adult Tg mice showed low levels of Sry expression. The other Tg mouse showed high Sry transgene expression, but was mosaic for the transgene. Developmental analysis of transgenic F1 embryos produced from the mosaic Tg mouse revealed that ubiquitous expression of Sry had a lethal effect on embryonic development around 12.5 dpc. The histological data indicated that ubiquitous expression of Sry induced abnormal cardiovascular development, resulting in embryonic death. Enhanced expression of Sry suppressed endogenous Tie2/Tek (tyrosine kinase with Ig and EGF homology domains 2/tunica interna endothelial cell kinase) expression in Sry-transfected primary cultured cells from wild type embryonic hearts. The results indicate that the tissue-specific and stage-specific expression of Sry is essential for normal embryogenesis.
机译:Sry(Y染色体上的性别决定区)是Y染色体上的哺乳动物性别决定基因。在小鼠中,Sry在性交后10.5至12.5天之间的支持细胞前体细胞中的瞬时表达(dpc)触发了Sertoli细胞与颗粒细胞的分化。严格调控Sry表达的重要性仍然未知。因此,我们试图生产一种表达Sry的泛表达转基因(Tg)小鼠,其中外源Sry由CAG(巨细胞病毒即刻早期增强子,鸡β-肌动蛋白启动子以及鸡β-肌动蛋白和兔β融合内含子)驱动-globin)-Sry基因,用于普遍表达Sry。观察到较低的Tg幼仔比率(2/127),而出生前早期转基因胚胎的比率为19.2%(5/26)。 Sry遍在表达的胚胎显示异常发育。结果表明Sry的普遍表达对胚胎发育产生负面影响。两只成年Tg小鼠之一显示出低水平的Sry表达。另一只Tg小鼠显示出高Sry转基因表达,但为转基因镶嵌。从镶嵌Tg小鼠产生的转基因F1胚胎的发育分析表明,Sry的普遍表达对12.5 dpc左右的胚胎发育具有致死作用。组织学数据表明,Sry的普遍表达诱导心血管异常发育,导致胚胎死亡。 Sry抑制了野生型胚胎心脏Sry转染的原代培养细胞中Sry抑制的内源性Tie2 / Tek(具有Ig和EGF同源结构域2 / tunna内皮细胞激酶的酪氨酸激酶)表达的增强表达。结果表明,Sry的组织特异性和阶段特异性表达对于正常胚胎发生是必不可少的。

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