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早期胚胎中 LATS 激酶的时间减少可阻止 ICM 谱系分化。

Temporal reduction of LATS kinases in the early preimplantation embryo prevents ICM lineage differentiation.

机构信息

Mammalian Development Laboratory, Institute of Medical Biology, Singapore.

出版信息

Genes Dev. 2013 Jul 1;27(13):1441-6. doi: 10.1101/gad.219618.113.

Abstract

Cellular localization of the Yes-associated protein (YAP) is dependent on large tumor suppressor (LATS) kinase activity and initiates lineage specification in the preimplantation embryo. We temporally reduced LATS activity to disrupt this early event, allowing its reactivation at later stages. This interference resulted in an irreversible lineage misspecification and aberrant polarization of the inner cell mass (ICM). Complementation experiments revealed that neither epiblast nor primitive endoderm can be established from these ICMs. We therefore conclude that precisely timed YAP localization in early morulae is essential to prevent trophectoderm marker expression in, and lineage specification of, the ICM.

摘要

Yes 相关蛋白(YAP)的细胞定位依赖于大肿瘤抑制因子(LATS)激酶活性,并在着床前胚胎中启动谱系特化。我们暂时降低 LATS 活性以破坏这一早期事件,从而使其在后期重新激活。这种干扰导致不可逆转的谱系异常和内细胞团(ICM)的异常极化。补充实验表明,这些 ICM 既不能建立胚外层,也不能建立原始内胚层。因此,我们得出结论,早期桑葚胚中 YAP 定位的精确时间对于防止滋养外胚层标记物在 ICM 中的表达和谱系特化是必不可少的。

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