Osanai Takashi, Imamura Sousuke, Asayama Munehiko, Shirai Makoto, Suzuki Iwane, Murata Norio, Tanaka Kan
Institute of Molecular and Cellular Biosciences, The University of Tokyo 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan.
DNA Res. 2006 Oct 31;13(5):185-95. doi: 10.1093/dnares/dsl010. Epub 2006 Oct 17.
Nitrogen starvation requires cells to change their transcriptome in order to cope with this essential nutrient limitation. Here, using microarray analysis, we investigated changes in transcript profiles following nitrogen depletion in the unicellular cyanobacterium Synechocystis sp. PCC 6803. Results revealed that genes for sugar catabolic pathways including glycolysis, oxidative pentose phosphate (OPP) pathway, and glycogen catabolism were induced by nitrogen depletion, and activities of glucose-6-phosphate dehydrogenase (G6PD) and 6-phosphogluconate dehydrogenase (6PGD), two key enzymes of the OPP pathway, were demonstrated to increase under this condition. We recently showed that a group 2 sigma factor SigE, which is under the control of the global nitrogen regulator NtcA, positively regulated these sugar catabolic pathways. However, increases of transcript levels of these sugar catabolic genes under nitrogen starvation were still observed even in a sigE-deficient mutant, indicating the involvement of other regulatory element(s) in addition to SigE. Since these nitrogen activations were abolished in an ntcA mutant, and since these genes were not directly included in the NtcA regulon, we suggested that sugar catabolic genes were induced by nitrogen depletion under complex and redundant regulations including SigE and other unknown factor(s) under the control of NtcA.
氮饥饿要求细胞改变其转录组以应对这种必需营养物质的限制。在此,我们使用微阵列分析研究了单细胞蓝藻集胞藻PCC 6803在氮耗尽后转录谱的变化。结果显示,包括糖酵解、氧化戊糖磷酸(OPP)途径和糖原分解代谢在内的糖分解代谢途径的基因在氮耗尽时被诱导,并且OPP途径的两个关键酶葡萄糖-6-磷酸脱氢酶(G6PD)和6-磷酸葡萄糖酸脱氢酶(6PGD)的活性在这种条件下被证明会增加。我们最近表明,受全局氮调节因子NtcA控制的2组sigma因子SigE对这些糖分解代谢途径起正调控作用。然而,即使在sigE缺陷型突变体中,在氮饥饿条件下这些糖分解代谢基因的转录水平仍会增加,这表明除了SigE之外还涉及其他调控元件。由于在ntcA突变体中这些氮激活作用被消除,并且由于这些基因未直接包含在NtcA调控子中,我们认为糖分解代谢基因是在包括SigE和NtcA控制下的其他未知因子在内的复杂且冗余的调控下,由氮耗尽诱导产生的。