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Tulp3 是一个纤毛运输基因,可调节多囊肾病。

Tulp3 Is a Ciliary Trafficking Gene that Regulates Polycystic Kidney Disease.

机构信息

Vertebrate Developmental Biology Program, Department of Pediatrics, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06520, USA.

Vertebrate Developmental Biology Program, Department of Pediatrics, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06520, USA.

出版信息

Curr Biol. 2019 Mar 4;29(5):803-812.e5. doi: 10.1016/j.cub.2019.01.054. Epub 2019 Feb 21.

Abstract

The primary cilium is an organelle essential for cell signaling pathways. One of the most common human genetic diseases is autosomal dominant polycystic kidney disease (ADPKD), which is caused by mutations in the PKD1 or PKD2 genes that encode Polycystin 1 and 2 (PC1/2), transmembrane proteins that translocate to the cilium. Mutations in genes that disrupt ciliogenesis also cause kidney cysts as part of a "ciliopathic" disease spectrum. The molecular mechanisms that link cilia function with renal cystic diseases are not well understood, and the mechanistic relationship between ADPKD and ciliopathic PKD is not known. Here we identify the gene Tubby-like protein-3 (Tulp3) as a key regulator of renal cystic disease from a forward genetic screen in the mouse. Mice homozygous for a hypomorphic missense mutation within the conserved Tubby domain of Tulp3 develop cysts at late embryonic stages, leading to severe postnatal loss of kidney function. In contrast to other ciliopathic disease models, Tulp3 mutations do not affect ciliogenesis. Instead, we demonstrate that Tulp3 is essential for the trafficking of the Joubert syndrome-associated small GTPase Arl13b into kidney cilia. We show that reduction of Pkd1 dosage promotes cystogenesis in the Tulp3 conditional ciliopathic PKD model. However, in an adult model of ADPKD utilizing inducible conditional Pkd1 deletion, concomitant removal of Tulp3 surprisingly ameliorates cystic disease. Therefore, Tulp3 controls distinct ciliary pathways that positively or negatively regulate cystogenesis depending on the cellular context.

摘要

初级纤毛是细胞信号通路所必需的细胞器。最常见的人类遗传疾病之一是常染色体显性多囊肾病(ADPKD),它是由 PKD1 或 PKD2 基因突变引起的,这些基因编码多囊蛋白 1 和 2(PC1/2),它们是跨膜蛋白,可转位到纤毛。破坏纤毛发生的基因突变也会导致肾脏囊肿,这是“纤毛病”疾病谱的一部分。将纤毛功能与肾脏囊性疾病联系起来的分子机制尚不清楚,ADPKD 和纤毛病 PKD 之间的机制关系也不清楚。在这里,我们从小鼠的正向遗传筛选中鉴定出 Tubby 样蛋白 3(Tulp3)基因作为肾脏囊性疾病的关键调节因子。Tulp3 保守的 Tubby 结构域内的纯合隐性错义突变小鼠在胚胎后期会形成囊肿,导致严重的出生后肾功能丧失。与其他纤毛病模型不同,Tulp3 突变不会影响纤毛发生。相反,我们证明 Tulp3 对于与 Joubert 综合征相关的小 GTP 酶 Arl13b 向肾脏纤毛的运输是必需的。我们表明,降低 Pkd1 剂量会促进 Tulp3 条件性纤毛病 PKD 模型中的囊肿发生。然而,在利用诱导型条件性 Pkd1 缺失的 ADPKD 成年模型中,同时去除 Tulp3 出人意料地改善了囊性疾病。因此,Tulp3 控制着不同的纤毛途径,根据细胞环境,这些途径正向或负向调节囊肿发生。

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