Suppr超能文献

CLN6-CLN8 复合物将溶酶体酶募集到内质网以进行高尔基体转运。

A CLN6-CLN8 complex recruits lysosomal enzymes at the ER for Golgi transfer.

机构信息

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.

Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas, USA.

出版信息

J Clin Invest. 2020 Aug 3;130(8):4118-4132. doi: 10.1172/JCI130955.

Abstract

Lysosomal enzymes are synthesized in the endoplasmic reticulum (ER) and transferred to the Golgi complex by interaction with the Batten disease protein CLN8 (ceroid lipofuscinosis, neuronal, 8). Here we investigated the relationship of this pathway with CLN6, an ER-associated protein of unknown function that is defective in a different Batten disease subtype. Experiments focused on protein interaction and trafficking identified CLN6 as an obligate component of a CLN6-CLN8 complex (herein referred to as EGRESS: ER-to-Golgi relaying of enzymes of the lysosomal system), which recruits lysosomal enzymes at the ER to promote their Golgi transfer. Mutagenesis experiments showed that the second luminal loop of CLN6 is required for the interaction of CLN6 with the enzymes but dispensable for interaction with CLN8. In vitro and in vivo studies showed that CLN6 deficiency results in inefficient ER export of lysosomal enzymes and diminished levels of the enzymes at the lysosome. Mice lacking both CLN6 and CLN8 did not display aggravated pathology compared with the single deficiencies, indicating that the EGRESS complex works as a functional unit. These results identify CLN6 and the EGRESS complex as key players in lysosome biogenesis and shed light on the molecular etiology of Batten disease caused by defects in CLN6.

摘要

溶酶体酶在粗面内质网(ER)中合成,并通过与巴滕病蛋白 CLN8(神经细胞蜡样脂褐质沉积症,8 号)相互作用转移到高尔基复合体。在这里,我们研究了该途径与 CLN6 的关系,CLN6 是一种 ER 相关蛋白,其功能未知,在另一种巴滕病亚型中存在缺陷。专注于蛋白相互作用和运输的实验确定 CLN6 是 CLN6-CLN8 复合物(以下简称 Egress:溶酶体系统酶的 ER 到高尔基体传递)的必需组成部分,该复合物在 ER 募集溶酶体酶以促进其高尔基体转移。突变实验表明,CLN6 的第二个腔环对于 CLN6 与酶的相互作用是必需的,但对于与 CLN8 的相互作用是可有可无的。体外和体内研究表明,CLN6 缺乏导致溶酶体酶在 ER 中的有效输出减少,溶酶体中的酶水平降低。与单个缺陷相比,缺乏 CLN6 和 CLN8 的小鼠并未显示出加重的病理学,表明 Egress 复合物作为一个功能单位发挥作用。这些结果确定了 CLN6 和 Egress 复合物是溶酶体生物发生的关键参与者,并揭示了 CLN6 缺陷导致的巴滕病的分子病因。

相似文献

引用本文的文献

4
Expanded Phenotype of the Mouse Model.小鼠模型的扩展表型
Cells. 2025 Apr 30;14(9):661. doi: 10.3390/cells14090661.
8
CLN6-related continuum phenotype caused by aberrant splicing.由异常剪接引起的CLN6相关连续表型。
Epilepsia Open. 2025 Feb;10(1):348-354. doi: 10.1002/epi4.13119. Epub 2024 Dec 24.

本文引用的文献

7
Lysosome biogenesis in health and disease.溶酶体的生物发生与健康和疾病。
J Neurochem. 2019 Mar;148(5):573-589. doi: 10.1111/jnc.14564. Epub 2018 Oct 18.
10
Lysosomes and Brain Health.溶酶体与大脑健康。
Annu Rev Neurosci. 2018 Jul 8;41:255-276. doi: 10.1146/annurev-neuro-080317-061804. Epub 2018 Apr 16.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验