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酵母酿酒酵母中与少年型巴顿病缺陷蛋白同源的蛋白的亚细胞定位。

The subcellular location of the yeast Saccharomyces cerevisiae homologue of the protein defective in the juvenile form of Batten disease.

作者信息

Croopnick J B, Choi H C, Mueller D M

机构信息

Department of Biological Chemistry, Chicago Medical School, Illinois 60064, USA.

出版信息

Biochem Biophys Res Commun. 1998 Sep 18;250(2):335-41. doi: 10.1006/bbrc.1998.9272.

Abstract

The mutation responsible for the juvenile form of Batten disease was mapped to a single gene, Cln3 (T. J. Lerner et al. (1995) Cell 82:949-957). Yeast Saccharomyces cerevisiae has an open reading frame, BTN1 (YHC3), that encodes the putative homologue of Cln3p. Primary structure comparison indicates that the human Cln3p and yeast Btn1p are 59% similar and 39% identical and they have similar hydropathy profiles. Gene disruption of BTN1 in yeast has no apparent effect on growth or viability of the cells under a variety of conditions. Gene fusion protein constructs of green fluorescent protein (GFP) and Btn1p, with GFP at the amino and carboxyl ends of Btn1p, localize to the vacuole in yeast. These data indicate that BTN1 is a nonessential gene under most growth conditions which functions in the vacuole in yeast Saccharomyces cerevisiae.

摘要

导致少年型贝敦氏病的突变被定位到一个单一基因,即Cln3(T. J. 勒纳等人,《细胞》,1995年,第82卷,第949 - 957页)。酿酒酵母有一个开放阅读框BTN1(YHC3),它编码推定的Cln3p同源物。一级结构比较表明,人类Cln3p和酵母Btn1p的相似度为59%,一致性为39%,并且它们具有相似的亲水性图谱。在酵母中破坏BTN1基因,在各种条件下对细胞的生长或活力没有明显影响。绿色荧光蛋白(GFP)与Btn1p的基因融合蛋白构建体,GFP位于Btn1p的氨基端和羧基端,定位于酵母的液泡中。这些数据表明,在大多数生长条件下,BTN1是一个非必需基因,在酿酒酵母的液泡中发挥作用。

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