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酵母KRE9基因编码一种参与细胞表面β-葡聚糖组装的O-糖蛋白。

The yeast KRE9 gene encodes an O glycoprotein involved in cell surface beta-glucan assembly.

作者信息

Brown J L, Bussey H

机构信息

Biology Department, McGill University, Montreal, Quebec, Canada.

出版信息

Mol Cell Biol. 1993 Oct;13(10):6346-56. doi: 10.1128/mcb.13.10.6346-6356.1993.

Abstract

The yeast KRE9 gene encodes a 30-kDa secretory pathway protein involved in the synthesis of cell wall (1-->6)-beta-glucan. Disruption of KRE9 leads to serious growth impairment and an altered cell wall containing less than 20% of the wild-type amount of (1-->6)-beta-glucan. Analysis of the glucan material remaining in a kre9 delta null mutant indicated a polymer with a reduced average molecular mass. kre9 delta null mutants also displayed several additional cell-wall-related phenotypes, including an aberrant multiply budded morphology, a mating defect, and a failure to form projections in the presence of alpha-factor. Double mutants were generated by crossing kre9 delta strains with strains harboring a null mutation in the KRE1, KRE6, or KRE11 gene, and each of these double mutants was found to be inviable in the SEY6210 background. Similar crosses with null mutations in the KRE5 and SKN1 genes indicated that these double mutants were no more severely affected than kre5 delta or kre9 delta single mutants alone. Antibodies were generated against Kre9p and detected an O glycoprotein of approximately 55 to 60 kDa found in the extracellular medium of a strain overproducing Kre9p.

摘要

酵母KRE9基因编码一种30 kDa的分泌途径蛋白,参与细胞壁(1→6)-β-葡聚糖的合成。KRE9基因的破坏会导致严重的生长缺陷,并且细胞壁发生改变,(1→6)-β-葡聚糖的含量不到野生型的20%。对kre9Δ缺失突变体中残留的葡聚糖物质的分析表明,其聚合物的平均分子量降低。kre9Δ缺失突变体还表现出其他几种与细胞壁相关的表型,包括异常的多芽形态、交配缺陷以及在存在α-因子时无法形成突起。通过将kre9Δ菌株与KRE1、KRE6或KRE11基因存在缺失突变的菌株杂交产生双突变体,发现这些双突变体在SEY6210背景下均无法存活。与KRE5和SKN1基因缺失突变体的类似杂交表明,这些双突变体单独受到的影响并不比kre5Δ或kre9Δ单突变体更严重。制备了针对Kre9p的抗体,并在过量表达Kre9p的菌株的细胞外培养基中检测到一种约55至60 kDa的O糖蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9b/364693/903c5f13e4df/molcellb00022-0433-a.jpg

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