Chattopadhyay Subrata, Roberts Paul M, Pearce David A
Center for Aging and Developmental Biology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.
Biochem Biophys Res Commun. 2003 Mar 14;302(3):534-8. doi: 10.1016/s0006-291x(03)00209-2.
Btn2p is a novel coiled coil cytosolic protein in Saccharomyces cerevisiae. We report that Btn2p interacts with Yif1p, a component of a protein complex at the Golgi that functions in ER to Golgi transport. Deletion of Btn2p, btn2-delta, results in mis-localiztion of Yif1p to the vacuole. Therefore, Btn2p may have an apparent role in intracellular trafficking of proteins. Btn2p was originally identified as being up-regulated in a btn1-delta strain, which exhibits dysregulation of vacuolar pH, and this up-regulation of Btn2p was presumed to contribute to maintaining a stable vacuolar pH [Pearce et al. Nat. Genet. 22 (1999) 55]. We propose that up-regulation of Btn2p in btn1-delta is an indicator of altered trafficking within the cell, and as btn1-delta serves as a model for the lysosomal storage disorder Batten disease, that altered intracellular trafficking may contribute to some of the cellular pathological hallmarks of this disease.
Btn2p是酿酒酵母中一种新型的卷曲螺旋胞质蛋白。我们报道Btn2p与Yif1p相互作用,Yif1p是高尔基体中一个蛋白质复合体的组成部分,在从内质网到高尔基体的转运过程中发挥作用。Btn2p的缺失(btn2-δ)会导致Yif1p错误定位于液泡。因此,Btn2p可能在蛋白质的细胞内运输中具有明显作用。Btn2p最初被鉴定为在btn1-δ菌株中上调,该菌株表现出液泡pH失调,并且推测Btn2p的这种上调有助于维持稳定的液泡pH [Pearce等人,《自然遗传学》22 (1999) 55]。我们提出,btn1-δ中Btn2p的上调是细胞内运输改变的一个指标,并且由于btn1-δ作为溶酶体贮积症巴滕病的模型,细胞内运输改变可能导致该疾病的一些细胞病理学特征。