Pitkin J, Perriere M, Kanehl A, Ristow J L, Davis R H
Department of Molecular Biology and Biochemistry, University of California, Irvine 92717.
Arch Biochem Biophys. 1994 Nov 15;315(1):153-60. doi: 10.1006/abbi.1994.1484.
Ornithine decarboxylase (ODC) initiates the synthesis of polyamines (putrescine, spermidine, and spermine) and is highly regulated. We wished to know the importance of the control of ODC synthesis to the rates of growth and polyamine synthesis in the fungus, Neurospora crassa. We identified two control sites of the spe-1 gene, encoding ODC. One was an upstream activation region (UAR) and the other was the DNA encoding the long ODC mRNA leader, which governs polyamine-mediated repression of enzyme synthesis. Transformants receiving copies of spe-1 sequences lacking the UAR compensated for the deficiency by derepression or enzyme stabilization; polyamine synthesis was almost normal. A transformant lacking the spe-1 mRNA leader DNA constitutively expressed ODC mRNA and ODC activity, and synthesized excessive putrescine, especially when provided exogenous ornithine. This transformant grew normally and had only mildly elevated pools of spermidine, the major polyamine of this organism. We conclude that ODC activity normally limits polyamine synthesis, and ornithine becomes limiting in the ODC-constitutive strain. In this strain, however, spermidine synthesis remains rigorously limited by another step of the pathway, as yet unidentified. Thus the control of ODC activity in Neurospora is not vital to growth in laboratory culture, and synthesis of toxic levels of spermidine is limited by other mechanisms.
鸟氨酸脱羧酶(ODC)启动多胺(腐胺、亚精胺和精胺)的合成,且受到高度调控。我们想了解控制ODC合成对真菌粗糙脉孢菌生长速率和多胺合成的重要性。我们确定了编码ODC的spe-1基因的两个控制位点。一个是上游激活区域(UAR),另一个是编码长ODC mRNA前导序列的DNA,该序列控制多胺介导的酶合成抑制。接受缺少UAR的spe-1序列拷贝的转化体通过去抑制或酶稳定化来弥补缺陷;多胺合成几乎正常。一个缺少spe-1 mRNA前导序列DNA的转化体组成型表达ODC mRNA和ODC活性,并合成过量的腐胺,尤其是在提供外源性鸟氨酸时。该转化体正常生长,其主要多胺亚精胺的池仅略有升高。我们得出结论,ODC活性通常限制多胺合成,在ODC组成型菌株中鸟氨酸成为限制因素。然而,在该菌株中,亚精胺合成仍然受到该途径中另一个尚未确定的步骤的严格限制。因此,粗糙脉孢菌中ODC活性的控制对实验室培养中的生长并非至关重要,并且有毒水平的亚精胺合成受到其他机制的限制。