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Hippo 通路对于 的生长肠中顶底极性的维持是必需的。

The Hippo Pathway Is Essential for Maintenance of Apicobasal Polarity in the Growing Intestine of .

机构信息

Department of Biological Sciences, Seoul National University, Gwanak-gu 08826, Korea.

Department of Biological Sciences, Seoul National University, Gwanak-gu 08826, Korea

出版信息

Genetics. 2019 Oct;213(2):501-515. doi: 10.1534/genetics.119.302477. Epub 2019 Jul 29.

DOI:10.1534/genetics.119.302477
PMID:31358532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6781910/
Abstract

Although multiple determinants for establishing polarity in membranes of epithelial cells have been identified, the mechanism for maintaining apicobasal polarity is not fully understood. Here, we show that the conserved Hippo kinase pathway plays a role in the maintenance of apicobasal polarity in the developing intestine of We screened suppressors of the mutation in -the gene that encodes the LATS kinase homolog, deficiency of which leads to disturbance of the apicobasal polarity of the intestinal cells and to eventual death of the organism. We identified several alleles of and that suppress the effects of this mutation. encodes a homolog of YAP/Yki, and encodes a homolog of TEAD/Sd. WTS-1 bound directly to YAP-1 and inhibited its nuclear accumulation in intestinal cells. We also found that NFM-1, which is a homolog of NF2/Merlin, functioned in the same genetic pathway as WTS-1 to regulate YAP-1 to maintain cellular polarity. Transcriptome analysis identified several target candidates of the YAP-1-EGL-44 complex including TAT-2, which encodes a putative P-type ATPase. In summary, we have delineated the conserved Hippo pathway in consisting of NFM-1-WTS-1-YAP-1-EGL-44 and proved that the proper regulation of YAP-1 by upstream NFM-1 and WTS-1 is essential for maintenance of apicobasal membrane identities of the growing intestine.

摘要

尽管已经确定了多个决定上皮细胞膜极性的因素,但维持顶端基底极性的机制尚未完全了解。在这里,我们显示保守的 Hippo 激酶途径在发育中的肠道中维持顶端基底极性方面起作用。我们筛选了编码 LATS 激酶同源物的基因的突变的抑制子,该突变导致肠细胞的顶端基底极性紊乱,并最终导致生物体死亡。我们鉴定了几种抑制该突变的等位基因。编码 YAP/Yki 的同源物,而编码 TEAD/Sd 的同源物。WTS-1 直接与 YAP-1 结合并抑制其在肠细胞中的核积累。我们还发现,NFM-1,它是 NF2/Merlin 的同源物,与 WTS-1 一样在相同的遗传途径中发挥作用,以调节 YAP-1 来维持细胞极性。转录组分析鉴定了 YAP-1-EGL-44 复合物的几个靶候选物,包括编码假定 P 型 ATP 酶的 TAT-2。总之,我们已经描绘了由 NFM-1-WTS-1-YAP-1-EGL-44 组成的保守 Hippo 途径,并证明了上游 NFM-1 和 WTS-1 对 YAP-1 的适当调节对于维持生长中肠的顶端基底膜特性是必不可少的。

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