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使用酪氨酸酶驱动的 Cre 重组酶诱导表达 (V600E) Braf 可导致胚胎致死。

Inducible expression of (V600E) Braf using tyrosinase-driven Cre recombinase results in embryonic lethality.

机构信息

The Institute of Cancer Research, Signal Transduction Team, Cancer Research UK Centre for Cell and Molecular Biology, London, UK.

出版信息

Pigment Cell Melanoma Res. 2010 Feb;23(1):112-20. doi: 10.1111/j.1755-148X.2009.00662.x. Epub 2009 Dec 11.

Abstract

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.

摘要

我们最近证实,(V600E)Braf 在成熟的小鼠黑素细胞中的表达会诱导黑色素瘤。在这里,我们展示了使用酪氨酸酶启动子表达(V600E)Braf 会导致意外的胚胎致死,动物在出生前、出生时或出生后不久死亡。这些小鼠的皮肤、大脑、眼睛和心脏等组织出现多种发育缺陷,这些组织通常被黑素细胞定植。我们发现,表达(V600E)Braf 的细胞是潜在的黑素细胞前体细胞,已完全转化,表明(V600E)Braf 刺激这些细胞的增殖并阻止其分化。我们的数据表明,这些细胞存在于通常由黑素细胞占据的器官中,会导致严重的发育紊乱,导致灾难性的缺陷,并导致个体死亡。

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