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酿酒酵母中高度保守、协同调控的SNO和SNZ基因家族对营养限制作出反应。

The highly conserved, coregulated SNO and SNZ gene families in Saccharomyces cerevisiae respond to nutrient limitation.

作者信息

Padilla P A, Fuge E K, Crawford M E, Errett A, Werner-Washburne M

机构信息

Department of Biology, University of New Mexico, Albuquerque, New Mexico 87131, USA.

出版信息

J Bacteriol. 1998 Nov;180(21):5718-26. doi: 10.1128/JB.180.21.5718-5726.1998.

Abstract

SNZ1, a member of a highly conserved gene family, was first identified through studies of proteins synthesized in stationary-phase yeast cells. There are three SNZ genes in Saccharomyces cerevisiae, each of which has another highly conserved gene, named SNO (SNZ proximal open reading frame), upstream. The DNA sequences and relative positions of SNZ and SNO genes have been phylogenetically conserved. This report details studies of the expression of the SNZ-SNO gene pairs under various conditions and phenotypic analysis of snz-sno mutants. An analysis of total RNA was used to determine that adjacent SNZ-SNO gene pairs are coregulated. SNZ2/3 and SNO2/3 mRNAs are induced prior to the diauxic shift and decrease in abundance during the postdiauxic phase, when SNZ1 and SNO1 are induced. In snz2 snz3 mutants, SNZ1 mRNA is induced prior to the diauxic shift, when SNZ2/3 mRNAs are normally induced. Under nitrogen-limiting conditions, SNZ1 mRNAs accumulate in tryptophan, adenine, and uracil auxotrophs but not in prototrophic strains, indicating that induction occurs in response to the limitation of specific nutrients. Strains carrying deletions in all SNZ-SNO gene pairs are viable, but snz1 and sno1 mutants are sensitive to 6-azauracil (6-AU), an inhibitor of purine and pyrimidine biosynthetic enzymes, and methylene blue, a producer of singlet oxygen. The conservation of sequence and chromosomal position, the coregulation and pattern of expression of SNZ1 and SNO1 genes, and the sensitivity of snz1 and sno1 mutants to 6-AU support the hypothesis that the associated proteins are part of an ancient response to nutrient limitation.

摘要

SNZ1是一个高度保守的基因家族的成员,最初是通过对稳定期酵母细胞中合成的蛋白质进行研究而鉴定出来的。酿酒酵母中有三个SNZ基因,每个基因上游都有另一个高度保守的基因,名为SNO(SNZ近端开放阅读框)。SNZ和SNO基因的DNA序列及相对位置在系统发育上是保守的。本报告详细介绍了在各种条件下SNZ - SNO基因对的表达研究以及snz - sno突变体的表型分析。通过对总RNA的分析确定相邻的SNZ - SNO基因对是共调控的。在双相转变之前诱导SNZ2/3和SNO2/3 mRNA,在双相转变后阶段丰度下降,此时诱导SNZ1和SNO1。在snz2 snz3突变体中,在双相转变之前诱导SNZ1 mRNA,而正常情况下此时诱导SNZ2/3 mRNA。在氮限制条件下,SNZ1 mRNA在色氨酸、腺嘌呤和尿嘧啶营养缺陷型菌株中积累,但在原养型菌株中不积累,这表明诱导是对特定营养物质限制的响应。在所有SNZ - SNO基因对中携带缺失的菌株是有活力的,但snz1和sno1突变体对嘌呤和嘧啶生物合成酶的抑制剂6 - 氮杂尿嘧啶(6 - AU)以及单线态氧的产生剂亚甲蓝敏感。SNZ1和SNO1基因的序列和染色体位置的保守性、共调控和表达模式以及snz1和sno1突变体对6 - AU的敏感性支持了相关蛋白质是古老的营养限制反应一部分的假说。

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