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首页> 外文期刊>Developmental genetics >POSITIVE AND NEGATIVE FEEDBACK LOOPS AFFECT THE TRANSCRIPTION OF IME1, A POSITIVE REGULATOR OF MEIOSIS IN SACCHAROMYCES CEREVISIAE
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POSITIVE AND NEGATIVE FEEDBACK LOOPS AFFECT THE TRANSCRIPTION OF IME1, A POSITIVE REGULATOR OF MEIOSIS IN SACCHAROMYCES CEREVISIAE

机译:正反馈环和负反馈环影响IME1的转录,该酶是酿酒酵母中减数分裂的正向调节剂。

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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.
机译:啤酒酵母的IME1基因编码表达减数分裂特异性基因所需的转录因子。像它调控的许多基因一样,IME1本身也按照以下复杂模式表达:在营养生长过程中几乎检测不到水平,在饥饿条件下诱导水平很高,随后减数分裂过程随之下降。该报告研究了Ime1蛋白对其自身表达的影响,证明了反馈调节作用。在减数分裂条件下,IME1或IME2的破坏会导致Ime1-lacZ表达水平不断提高。这种明显的负调控归因于IME1上游区域的顺式元件,这些顺式元件将瞬时减数分裂表达赋予了无异源启动子基因。在该减数分裂条件下检测到一种特定的DNA /蛋白质复合物,其水平在减数分裂条件下会瞬时增加。在ime1(-)二倍体中,此DNA /蛋白质复合物的水平增加,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。该报告还提供了证据表明Ime1p直接负责调节其自身的转录。通过观察到Ime1p的过度表达会导致IME1-lacZ的水平升高,表明有丝分裂条件下的正反馈调节。减数分裂培养物中的负自动调节通过以下观察证明:IME1,ime1-3中的特定点突变允许表达减数分裂特异性基因以及诱导减数分裂,但在IME1的负反馈调节中存在缺陷。

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