López-Gomollón Sara, Hernández José A, Pellicer Silvia, Angarica Vladimir Espinosa, Peleato M Luisa, Fillat María F
Department of Biochemistry and Molecular and Cell Biology, and Biocomputation and Complex Systems Physics Institute (BiFi), University of Zaragoza, Zaragoza, Spain.
J Mol Biol. 2007 Nov 16;374(1):267-81. doi: 10.1016/j.jmb.2007.09.010. Epub 2007 Sep 11.
Nitrogen signalling in cyanobacteria involves a complex network in which the availability of iron plays an important role. In the nitrogen-fixing cyanobacterium Anabaena sp. PCC 7120, iron uptake is controlled by FurA, while NtcA is the master regulator of nitrogen metabolism and shows a mutual dependence with HetR in the first steps of heterocyst development. Expression of FurA is modulated by NtcA and it is enhanced in a hetR(-) background. Iron starvation in cells grown in the presence of combined nitrogen causes a moderate increase in the transcription of glnA that is more evident in a ntcA(-) background. Those results evidence a tight link between the reserves of iron and nitrogen metabolism that leads us to search for target genes potentially co-regulated by FurA and NtcA. Using a bioinformatic approach we have found a significant number of NtcA-regulated genes exhibiting iron boxes in their upstream regions. Our computational predictions have been validated using electrophoretic mobility shift assay (EMSA) analysis. These candidates for dual regulation are involved in different functions such as photosynthesis (i.e. psaL, petH, rbcL, isiA), heterocyst differentiation (i.e. xisA, hanA, prpJ, nifH), transcriptional regulation (several alternative sigma factors) or redox balance (i.e. trxA, ftrC, gor). The identification of common elements overlapping the NtcA and FurA regulons allows us to establish a previously unrecognized transcriptional regulatory connection between iron homeostasis, redox control and nitrogen metabolism.
蓝藻中的氮信号传导涉及一个复杂的网络,其中铁的可用性起着重要作用。在固氮蓝藻鱼腥藻PCC 7120中,铁的摄取由FurA控制,而NtcA是氮代谢的主要调节因子,并且在异形胞发育的第一步中与HetR相互依赖。FurA的表达受NtcA调节,并且在hetR(-)背景中增强。在结合态氮存在下生长的细胞中的铁饥饿会导致glnA转录适度增加,这在ntcA(-)背景中更为明显。这些结果证明了铁储备与氮代谢之间的紧密联系,这促使我们寻找可能由FurA和NtcA共同调节的靶基因。使用生物信息学方法,我们发现大量NtcA调节的基因在其上游区域显示出铁盒。我们的计算预测已通过电泳迁移率变动分析(EMSA)得到验证。这些双重调节的候选基因参与不同的功能,如光合作用(即psaL、petH、rbcL、isiA)、异形胞分化(即xisA、hanA、prpJ、nifH)、转录调节(几种替代的sigma因子)或氧化还原平衡(即trxA、ftrC、gor)。NtcA和FurA调控子重叠的共同元件的鉴定使我们能够在铁稳态、氧化还原控制和氮代谢之间建立以前未被认识的转录调控联系。