Faculty of Biology, University of Freiburg, D-79104 Freiburg, Germany.
Proc Natl Acad Sci U S A. 2011 Dec 13;108(50):20130-5. doi: 10.1073/pnas.1112724108. Epub 2011 Nov 30.
The fixation of atmospheric N(2) by cyanobacteria is a major source of nitrogen in the biosphere. In Nostocales, such as Anabaena, this process is spatially separated from oxygenic photosynthesis and occurs in heterocysts. Upon nitrogen step-down, these specialized cells differentiate from vegetative cells in a process controlled by two major regulators: NtcA and HetR. However, the regulon controlled by these two factors is only partially defined, and several aspects of the differentiation process have remained enigmatic. Using differential RNA-seq, we experimentally define a genome-wide map of >10,000 transcriptional start sites (TSS) of Anabaena sp. PCC7120, a model organism for the study of prokaryotic cell differentiation and N(2) fixation. By analyzing the adaptation to nitrogen stress, our global TSS map provides insight into the dynamic changes that modify the transcriptional organization at a critical step of the differentiation process. We identify >900 TSS with minimum fold change in response to nitrogen deficiency of eight. From these TSS, at least 209 were under control of HetR, whereas at least 158 other TSS were potentially directly controlled by NtcA. Our analysis of the promoters activated during the switch to N(2) fixation adds hundreds of protein-coding genes and noncoding transcripts to the list of potentially involved factors. These data experimentally define the NtcA regulon and the DIF(+) motif, a palindrome at or close to position -35 that seems essential for heterocyst-specific expression of certain genes.
蓝藻固定大气中的 N(2) 是生物圈中氮素的主要来源。在 Nostocales 中,如鱼腥藻,这个过程与产氧光合作用在异形胞中空间分离。在氮素减少时,这些特化细胞在由两个主要调节剂 NtcA 和 HetR 控制的过程中从营养细胞中分化出来。然而,这两个因素控制的调控组仅部分定义,并且分化过程的几个方面仍然是神秘的。通过使用差异 RNA-seq,我们通过实验确定了鱼腥藻 PCC7120 的全基因组 >10000 个转录起始位点(TSS)的图谱,鱼腥藻 PCC7120 是研究原核细胞分化和 N(2) 固定的模式生物。通过分析对氮胁迫的适应,我们的全局 TSS 图谱提供了对在分化过程的关键步骤中改变转录组织的动态变化的深入了解。我们确定了 >900 个 TSS,它们对氮缺乏的响应倍数变化最小,有 8 个。从这些 TSS 中,至少有 209 个受 HetR 控制,而至少有 158 个其他 TSS 可能直接受 NtcA 控制。我们对切换到 N(2) 固定过程中激活的启动子的分析增加了数百个编码蛋白的基因和非编码转录本,使其成为潜在参与因子的列表。这些数据通过实验定义了 NtcA 调控组和 DIF(+) 基序,DIF(+) 基序是位于或接近-35 位的回文序列,似乎对某些基因的异形胞特异性表达是必不可少的。