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