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自噬与细胞质到液泡蛋白靶向途径之间的遗传和表型重叠。

Genetic and phenotypic overlap between autophagy and the cytoplasm to vacuole protein targeting pathway.

作者信息

Harding T M, Hefner-Gravink A, Thumm M, Klionsky D J

机构信息

Section of Microbiology, University of California, Davis, California 95616, USA.

出版信息

J Biol Chem. 1996 Jul 26;271(30):17621-4. doi: 10.1074/jbc.271.30.17621.

Abstract

We have explored the phenotypic and genetic overlap between autophagocytosis and cytoplasm to vacuole targeting in the yeast Saccharomyces cerevisiae. Complementation analysis was performed with mutants in each of these groups (aut and cvt, respectively), and three complementation groups were found to overlap. Also, most of the unique aut mutants accumulated precursor aminopeptidase I in the cytoplasm, while maintaining wild type kinetics and maturation of proteins targeted to the vacuole via the secretory pathway. The majority of the non-overlapping cvt mutants were found to be at least partially defective in autophagy. Some mutants in each group, however, appear to be only marginally affected in the other phenotype, implying that these pathways only partially overlap. We propose that import of aminopeptidase I into the vacuole shares a number of components required for bulk autophagocytosis, but is made specific, saturable, and constitutive by the presence of a receptor or other interacting protein(s).

摘要

我们已经探究了酿酒酵母中自噬作用与细胞质到液泡靶向之间的表型和基因重叠。对这些组(分别为自噬和液泡靶向分选,即aut和cvt)中的每个突变体进行了互补分析,发现有三个互补组存在重叠。此外,大多数独特的自噬突变体在细胞质中积累了前体氨肽酶I,同时维持了野生型动力学以及通过分泌途径靶向液泡的蛋白质的成熟。发现大多数不重叠的液泡靶向分选突变体在自噬方面至少存在部分缺陷。然而,每组中的一些突变体似乎仅在另一种表型中受到轻微影响,这意味着这些途径仅部分重叠。我们提出,氨肽酶I导入液泡共享了大量自噬所需的成分,但通过受体或其他相互作用蛋白的存在使其具有特异性、饱和性和组成性。

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