Brune Iris, Werner Hendrikje, Hüser Andrea T, Kalinowski Jörn, Pühler Alfred, Tauch Andreas
Institut für Genomforschung, Centrum für Biotechnologie, Universität Bielefeld, Universitätsstrasse 25, D-33615 Bielefeld, Germany.
BMC Genomics. 2006 Feb 9;7:21. doi: 10.1186/1471-2164-7-21.
The knowledge about complete bacterial genome sequences opens the way to reconstruct the qualitative topology and global connectivity of transcriptional regulatory networks. Since iron is essential for a variety of cellular processes but also poses problems in biological systems due to its high toxicity, bacteria have evolved complex transcriptional regulatory networks to achieve an effective iron homeostasis. Here, we apply a combination of transcriptomics, bioinformatics, in vitro assays, and comparative genomics to decipher the regulatory network of the iron-dependent transcriptional regulator DtxR of Corynebacterium glutamicum.
A deletion of the dtxR gene of C. glutamicum ATCC 13032 led to the mutant strain C. glutamicum IB2103 that was able to grow in minimal medium only under low-iron conditions. By performing genome-wide DNA microarray hybridizations, differentially expressed genes involved in iron metabolism of C. glutamicum were detected in the dtxR mutant. Bioinformatics analysis of the genome sequence identified a common 19-bp motif within the upstream region of 31 genes, whose differential expression in C. glutamicum IB2103 was verified by real-time reverse transcription PCR. Binding of a His-tagged DtxR protein to oligonucleotides containing the 19-bp motifs was demonstrated in vitro by DNA band shift assays. At least 64 genes encoding a variety of physiological functions in iron transport and utilization, in central carbohydrate metabolism and in transcriptional regulation are controlled directly by the DtxR protein. A comparison with the bioinformatically predicted networks of C. efficiens, C. diphtheriae and C. jeikeium identified evolutionary conserved elements of the DtxR network.
This work adds considerably to our currrent understanding of the transcriptional regulatory network of C. glutamicum genes that are controlled by DtxR. The DtxR protein has a major role in controlling the expression of genes involved in iron metabolism and exerts a dual regulatory function as repressor of genes participating in iron uptake and utilization and as activator of genes responsible for iron storage and DNA protection. The data suggest that the DtxR protein acts as global regulator by controlling the expression of other regulatory proteins that might take care of an iron-dependent regulation of a broader transcriptional network of C. glutamicum genes.
关于完整细菌基因组序列的知识为重建转录调控网络的定性拓扑结构和全局连通性开辟了道路。由于铁对于多种细胞过程至关重要,但因其高毒性在生物系统中也带来问题,细菌进化出了复杂的转录调控网络以实现有效的铁稳态。在此,我们应用转录组学、生物信息学、体外实验和比较基因组学相结合的方法来解析谷氨酸棒杆菌铁依赖性转录调节因子DtxR的调控网络。
谷氨酸棒杆菌ATCC 13032的dtxR基因缺失导致突变株谷氨酸棒杆菌IB2103,该菌株仅在低铁条件下才能在基本培养基中生长。通过进行全基因组DNA微阵列杂交,在dtxR突变体中检测到了参与谷氨酸棒杆菌铁代谢的差异表达基因。对基因组序列的生物信息学分析在31个基因的上游区域鉴定出一个共同的19碱基基序,其在谷氨酸棒杆菌IB2103中的差异表达通过实时逆转录PCR得到验证。通过DNA条带迁移实验在体外证明了His标签的DtxR蛋白与含有19碱基基序的寡核苷酸结合。至少64个编码铁转运和利用、中心碳水化合物代谢及转录调控等多种生理功能的基因直接受DtxR蛋白控制。与高效棒杆菌、白喉棒杆菌和杰氏棒杆菌的生物信息学预测网络进行比较,确定了DtxR网络的进化保守元件。
这项工作极大地增进了我们目前对受DtxR控制的谷氨酸棒杆菌基因转录调控网络的理解。DtxR蛋白在控制参与铁代谢的基因表达中起主要作用,并发挥双重调节功能,作为参与铁摄取和利用的基因的阻遏物以及负责铁储存和DNA保护的基因的激活物。数据表明,DtxR蛋白通过控制其他调节蛋白的表达作为全局调节因子,这些调节蛋白可能负责对谷氨酸棒杆菌基因更广泛转录网络进行铁依赖性调节。