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小分子 GTPase RAB-18 通过将肠道胆固醇转运蛋白 NCR-1 招募到线虫的顶端,从而参与调控发育/休眠。

The small GTPase RAB-18 is involved in regulating development/diapause by recruiting the intestinal cholesterol transporter NCR-1 onto the apical side in Caenorhabditis elegans.

机构信息

Department of Bioscience, Biotechnology, and Agrochemistry, Faculty of Agriculture, Tottori University, Tottori, Japan.

Department of Agricultural Science, Graduate School of Sustainability Science, Tottori University, Tottori, Japan.

出版信息

Biochem Biophys Res Commun. 2024 Nov 19;734:150609. doi: 10.1016/j.bbrc.2024.150609. Epub 2024 Aug 30.

Abstract

RAB family proteins, which are small GTPases, are integral to the process of eukaryotic membrane trafficking. In the nematode, Caenorhabditis elegans, 31 RAB proteins have been identified through genome sequencing. Using an RNAi screen specifically targeting C. elegans rab genes, we identified multiple genes that are involved in the regulation of larval development, in particular, the rab-18 gene. Our molecular genetic studies resulted in several findings. First, RAB-18 predominantly functions in the intestine to regulate larval development by modulating steroid hormone signaling. Second, the C. elegans cholesterol transporter NCR-1 is a target of RAB-18 in the intestine. Third, the membrane trafficking of NCR-1 to the apical side in intestinal cells is particularly influenced by RAB-18. Finally, RAB-18 and NCR-1 possibly co-localize on membrane vesicles. Our study is the first to demonstrate the relationship between a RAB protein and a cholesterol transporter, in which the RAB protein probably drives the transporter to the apical membrane in the intestine to regulate cholesterol uptake. This study provides insight into the molecular mechanisms underlying human disease stemming from a transport defect of cholesterol and its derivative.

摘要

RAB 家族蛋白是小 GTP 酶,是真核生物膜运输过程的重要组成部分。在秀丽隐杆线虫中,通过基因组测序已经鉴定出 31 种 RAB 蛋白。通过针对秀丽隐杆线虫 rab 基因的 RNAi 筛选,我们发现了多个参与幼虫发育调控的基因,特别是 rab-18 基因。我们的分子遗传学研究有几个发现。首先,RAB-18 主要在肠道中发挥作用,通过调节类固醇激素信号来调节幼虫发育。其次,秀丽隐杆线虫胆固醇转运蛋白 NCR-1 是肠道中 RAB-18 的靶标。第三,NCR-1 向肠道细胞顶侧的膜运输特别受 RAB-18 影响。最后,RAB-18 和 NCR-1 可能在膜小泡上共定位。我们的研究首次证明了 RAB 蛋白和胆固醇转运蛋白之间的关系,其中 RAB 蛋白可能将转运蛋白驱动到肠道的顶膜以调节胆固醇摄取。这项研究为胆固醇及其衍生物转运缺陷导致的人类疾病的分子机制提供了新的见解。

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