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首页> 外文期刊>Pigment cell & melanoma research >Inducible expression of ~(V600E)Braf using tyrosinase-driven Cre recombinase results in embryonic lethality
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Inducible expression of ~(V600E)Braf using tyrosinase-driven Cre recombinase results in embryonic lethality

机译:使用酪氨酸酶驱动的Cre重组酶诱导〜(V600E)Braf的表达导致胚胎致死率

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摘要

Summary We recently demonstrated that expression of ~(V600E)Braf in mature mouse melanocytes induces melanoma. Here, we show that expression of ~(V600E)Braf using the tyrosinase promoter leads to an unexpected embryonic lethality, with the animals dying before, at, or shortly after birth. The mice suffer from a range of developmental defects in the skin, the brain, the eyes and the heart, tissues that are normally colonized by melanocytes. We show that the ~(V600E)Braf expressing cells are potential melanocytic precursors that are fully transformed, suggesting that ~(V600E)Braf stimulates proliferation and blocks differentiation of these cells. Our data suggests that the presence of these cells in the organs that are normally occupied by melanocytes leads to severe developmental disruption, resulting in catastrophic defects and leading to death of the individual.
机译:总结我们最近证明了成熟小鼠黑素细胞中〜(V600E)Braf的表达可诱导黑色素瘤。在这里,我们显示使用酪氨酸酶启动子表达〜(V600E)Braf会导致意想不到的胚胎致死性,动物在出生前,出生时或出生后不久死亡。小鼠在皮肤,大脑,眼睛和心脏以及通常由黑素细胞定居的组织中患有一系列发育缺陷。我们显示〜(V600E)Braf表达的细胞是潜在的黑素细胞前体,已被完全转化,表明〜(V600E)Braf刺激了增殖并阻止了这些细胞的分化。我们的数据表明,这些细胞在通常被黑素细胞占据的器官中的存在会导致严重的发育中断,从而导致灾难性的缺陷并导致个体死亡。

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