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桥连脂质转移蛋白家族成员 2 抑制纤毛发生。

Bridge-like lipid transfer protein family member 2 suppresses ciliogenesis.

机构信息

Department of Cell Biology, Yale School of Medicine, New Haven, CT 06520.

出版信息

Mol Biol Cell. 2024 May 1;35(5):br11. doi: 10.1091/mbc.E24-02-0065. Epub 2024 Mar 27.

DOI:10.1091/mbc.E24-02-0065
PMID:38536441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11151097/
Abstract

Bridge-like lipid transfer protein family member 2 (BLTP2) is an evolutionary conserved protein with unknown function(s). The absence of BLTP2 in results in impaired cellular secretion and larval death, while in mice (), it causes preweaning lethality. Structural predictions propose that BLTP2 belongs to the repeating β-groove domain-containing (also called the VPS13) protein family, forming a long tube with a hydrophobic core, suggesting that it operates as a lipid transfer protein (LTP). We establish as a negative regulator of ciliogenesis in RPE-1 cells based on a strong genetic interaction with , a gene that also suppresses ciliogenesis. Like WDR44, BLTP2 localizes to membrane contact sites involving the endoplasmic reticulum and the tubular endosome network in HeLa cells and that BLTP2 depletion enhanced ciliogenesis in RPE-1 cells grown in serum-containing medium, a condition where ciliogenesis is normally suppressed. This study establishes human BLTP2 as a putative LTP acting between tubular endosomes and ER that regulates primary cilium biogenesis.

摘要

桥连脂质转移蛋白家族成员 2(BLTP2)是一种进化上保守的蛋白,其功能未知。在 中缺乏 BLTP2 会导致细胞分泌受损和幼虫死亡,而在小鼠()中,它会导致出生前致死。结构预测表明 BLTP2 属于重复β槽结构域(也称为 VPS13)蛋白家族,形成一个带有疏水性核心的长管,表明它作为脂质转移蛋白(LTP)发挥作用。我们基于与 的强烈遗传相互作用,将 确立为 RPE-1 细胞中纤毛发生的负调节剂, 是一个也抑制纤毛发生的基因。与 WDR44 一样,BLTP2 定位于涉及内质网和管状内体网络的膜接触位点,在 HeLa 细胞中,BLTP2 的耗竭增强了在含血清培养基中生长的 RPE-1 细胞中的纤毛发生,纤毛发生通常在这种条件下受到抑制。这项研究确立了人类 BLTP2 作为一种在管状内体和 ER 之间起作用的潜在 LTP,调节初级纤毛生物发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5825/11151097/41953aa90764/mbc-35-br11-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5825/11151097/d033da846d0e/mbc-35-br11-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5825/11151097/74c126f49dab/mbc-35-br11-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5825/11151097/282fe5980da7/mbc-35-br11-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5825/11151097/c5af9d1e67bb/mbc-35-br11-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5825/11151097/41953aa90764/mbc-35-br11-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5825/11151097/d033da846d0e/mbc-35-br11-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5825/11151097/74c126f49dab/mbc-35-br11-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5825/11151097/282fe5980da7/mbc-35-br11-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5825/11151097/c5af9d1e67bb/mbc-35-br11-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5825/11151097/41953aa90764/mbc-35-br11-g005.jpg

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The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease.
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