Campbell Elsie L, Christman Harry, Meeks John C
Department of Microbiology, One Shields Ave., University of California, Davis, CA 95616, USA.
J Bacteriol. 2008 Nov;190(22):7382-91. doi: 10.1128/JB.00990-08. Epub 2008 Sep 12.
Hormogonia are nongrowing filaments, motile by means of a gliding mechanism, that are produced by certain cyanobacteria. Their differentiation is induced by positive and negative factors for growth, such as deprivation of combined nitrogen (nitrogen stress induction [NSI]). In Nostoc punctiforme, they are also induced by the exudate (hormogonium-inducing factor [HIF]) of a symbiotic plant partner. Time course (0.5 to 24 h) transcription profiles were determined by DNA microarray assays for hormogonia of N. punctiforme following induction by HIF and NSI. Clustering analysis revealed both common and distinct transcriptional patterns for the two methods of induction. By 24 h, a common set of 1,328 genes was identified. This 24-h common set of genes arose by the transition of 474 genes from an 819-member common set of genes at 1 h after induction; 405 and 51 genes unique to the HIF and NSI groups at 1 h, respectively; and 398 genes differentially transcribed at later time points. The NSI hormogonia showed a transcriptional checkpoint at 12 h following induction in which up- and downregulated genes were transiently down- or upregulated, respectively. The transient changes in these 1,043 genes appeared to reflect a switch back to a vegetative growth state. Such a checkpoint was not seen in HIF hormogonia. Genes uniquely upregulated in HIF hormogonia included those encoding proteins hypothesized to synthesize a metabolite repressor of hormogonium differentiation. Approximately 34 to 42% of the 6,893 printed genes were differentially transcribed during hormogonium differentiation; about half of those genes were upregulated, and 1,034 genes responded within 0.5 h after induction. These collective results indicate extensive and rapid global changes in the transcription of specific genes during the differentiation of these specialized filaments.
藻殖段是某些蓝细菌产生的不生长的丝状体,通过滑行机制运动。它们的分化由生长的正负因子诱导,如化合态氮的缺乏(氮胁迫诱导[NSI])。在点状念珠藻中,它们也由共生植物伙伴的渗出物(藻殖段诱导因子[HIF])诱导。通过DNA微阵列分析确定了点状念珠藻藻殖段在HIF和NSI诱导后的时间进程(0.5至24小时)转录谱。聚类分析揭示了两种诱导方法的共同和不同转录模式。到24小时时,鉴定出一组共1328个基因。这组24小时的共同基因是由诱导后1小时819个共同基因中的474个基因转变而来;分别有405个和51个基因在1小时时是HIF和NSI组特有的;以及398个基因在后期时间点差异转录。NSI藻殖段在诱导后12小时显示出一个转录检查点,其中上调和下调的基因分别短暂下调或上调。这1043个基因的瞬时变化似乎反映了向营养生长状态的转变。在HIF藻殖段中未观察到这样的检查点。在HIF藻殖段中独特上调的基因包括那些编码假设用于合成藻殖段分化代谢物阻遏物的蛋白质的基因。在藻殖段分化过程中,6893个打印基因中约34%至42%差异转录;其中约一半基因上调,1034个基因在诱导后0.5小时内做出反应。这些总体结果表明,在这些特殊丝状体的分化过程中,特定基因的转录发生了广泛而迅速的全局变化。