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正负反馈回路影响酿酒酵母减数分裂的正向调节因子IME1的转录。

Positive and negative feedback loops affect the transcription of IME1, a positive regulator of meiosis in Saccharomyces cerevisiae.

作者信息

Shefer-Vaida M, Sherman A, Ashkenazi T, Robzyk K, Kassir Y

机构信息

Department of Biology, Technion-Israel Institute of Technology, Haifa.

出版信息

Dev Genet. 1995;16(3):219-28. doi: 10.1002/dvg.1020160302.

Abstract

The IME1 gene of Saccharomyces cerevisiae encodes a transcription factor that is required for the expression of meiosis-specific genes. Like many of the genes it regulates, IME1 itself is expressed according to the following complex pattern: barely detectable levels during vegetative growth, and high induced levels under starvation conditions, followed by a subsequent decline in the course of meiosis. This report examines the influence of Ime1 protein on its own expression, demonstrating feedback regulation. Disruption of either IME1 or IME2 leads to constantly increasing levels of Ime1-lacZ expression, under meiotic conditions. This apparent negative regulation is due to cis elements in the IME1 upstream region, which confer transient meiotic expression to heterologous promoter-less genes. A specific DNA/protein complex, whose level is transiently increased under meiotic conditions, is detected on this element. In ime1- diploids, the level of this DNA/protein complex increases, without any decline. These results indicate that the transient expression of IME1 is apparently due to transcriptional regulation. This report also presents evidence suggesting that Ime1p is directly responsible for regulating its own transcription. Positive feedback regulation in mitotic conditions is suggested by the observation that overexpression of Ime1p leads to increased levels of IME1-lacZ. Negative autoregulation in meiotic cultures is demonstrated by the observation that a specific point mutation in IME1, ime1-3, permits expression of meiosis-specific genes, as well as induction of meiosis, but is defective in negative-feedback regulation of IME1.

摘要

酿酒酵母的IME1基因编码一种转录因子,该转录因子是减数分裂特异性基因表达所必需的。与它所调控的许多基因一样,IME1自身的表达遵循以下复杂模式:在营养生长期间几乎检测不到,在饥饿条件下诱导水平很高,随后在减数分裂过程中下降。本报告研究了Ime1蛋白对其自身表达的影响,证明了反馈调节。在减数分裂条件下,IME1或IME2的破坏会导致Ime1 - lacZ表达水平持续增加。这种明显的负调控是由于IME1上游区域的顺式元件,该元件赋予无启动子的异源基因瞬时减数分裂表达。在该元件上检测到一种特定的DNA/蛋白质复合物,其水平在减数分裂条件下瞬时增加。在ime1 - 二倍体中,这种DNA/蛋白质复合物的水平增加,且没有任何下降。这些结果表明IME1的瞬时表达显然是由于转录调控。本报告还提供了证据表明Ime1p直接负责调节其自身的转录。Ime1p的过表达导致IME1 - lacZ水平增加,这一观察结果表明在有丝分裂条件下存在正反馈调节。IME1中的一个特定点突变ime1 - 3允许减数分裂特异性基因的表达以及减数分裂的诱导,但在IME1的负反馈调节中存在缺陷,这一观察结果证明了减数分裂培养中的负自调节。

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