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酿酒酵母SSD1基因在HST1/NRC1/BFR1的参与下,参与对高浓度Ca2+的耐受性。

The Saccharomyces cerevisiae SSD1 gene is involved in the tolerance to high concentration of Ca2+ with the participation of HST1/NRC1/BFR1.

作者信息

Tsuchiya E, Matsuzaki G, Kurano K, Fukuchi T, Tsukao A, Miyakawa T

机构信息

Department of Fermentation Technology, Faculty of Engineering, Hiroshima University, Japan.

出版信息

Gene. 1996 Oct 17;176(1-2):35-8. doi: 10.1016/0378-1119(96)00204-1.

Abstract

The SSD1 gene of Saccharomyces (S.) cerevisiae is a polymorphic gene involved in many aspects of the yeast cell growth (Sutton et al., 1991). We found that ssd1 null mutant shows increased sensitivities of growth to trifluoperazine (TFP) and high concentration of Ca2+. A high-copy suppressor gene, HST1, for the TFP and Ca2+ sensitivities of ssd1 null mutant was cloned and sequenced. The HST1 gene encodes a polypeptide of 915 amino acids, and is identical to the NRC1/BRF1 gene in databases. The HST1 disrupted cells were viable, but they grew slowly in the presence of high levels of Ca2+, with notable morphological change. In addition, disruption of the gene in a ssd1 null mutant further increased the sensitivities of the cells to TFP and Ca2+. The results indicated the possibility that the SSD1 gene is involved in the tolerance mechanism to high concentration of Ca2+, and the HST1 gene participates with SSD1 by its functional redundancy in Ca2+ tolerance.

摘要

酿酒酵母(S. cerevisiae)的SSD1基因是一个多态性基因,参与酵母细胞生长的多个方面(Sutton等人,1991年)。我们发现ssd1缺失突变体对三氟拉嗪(TFP)和高浓度Ca2+的生长敏感性增加。克隆并测序了一个高拷贝抑制基因HST1,它可抑制ssd1缺失突变体对TFP和Ca2+的敏感性。HST1基因编码一个由915个氨基酸组成的多肽,在数据库中与NRC1/BRF1基因相同。HST1基因敲除的细胞是存活的,但在高浓度Ca2+存在的情况下生长缓慢,且有明显的形态变化。此外,在ssd1缺失突变体中敲除该基因会进一步增加细胞对TFP和Ca2+的敏感性。结果表明,SSD1基因可能参与了对高浓度Ca2+的耐受机制,而HST1基因通过其在Ca2+耐受方面的功能冗余与SSD1共同发挥作用。

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