Department of Biochemistry and Food Science, Plant Physiology and Molecular Biology, University of Turku, Turku FI-20014, Finland.
J Biol Chem. 2012 Sep 28;287(40):33153-62. doi: 10.1074/jbc.M112.391755. Epub 2012 Aug 1.
The functional relevance of natural cis-antisense transcripts is mostly unknown. Here we have characterized the association of three antisense RNAs and one intergenically encoded noncoding RNA with an operon that plays a crucial role in photoprotection of photosystem II under low carbon conditions in the cyanobacterium Synechocystis sp. PCC 6803. Cyanobacteria show strong gene expression dynamics in response to a shift of cells from high carbon to low levels of inorganic carbon (C(i)), but the regulatory mechanisms are poorly understood. Among the most up-regulated genes in Synechocystis are flv4, sll0218, and flv2, which are organized in the flv4-2 operon. The flavodiiron proteins encoded by this operon open up an alternative electron transfer route, likely starting from the Q(B) site in photosystem II, under photooxidative stress conditions. Our expression analysis of cells shifted from high carbon to low carbon demonstrated an inversely correlated transcript accumulation of the flv4-2 operon mRNA and one antisense RNA to flv4, designated as As1_flv4. Overexpression of As1_flv4 led to a decrease in flv4-2 mRNA. The promoter activity of as1_flv4 was transiently stimulated by C(i) limitation and negatively regulated by the AbrB-like transcription regulator Sll0822, whereas the flv4-2 operon was positively regulated by the transcription factor NdhR. The results indicate that the tightly regulated antisense RNA As1_flv4 establishes a transient threshold for flv4-2 expression in the early phase after a change in C(i) conditions. Thus, it prevents unfavorable synthesis of the proteins from the flv4-2 operon.
天然顺式反义转录本的功能相关性大多未知。在这里,我们描述了三个反义 RNA 和一个基因间编码的非编码 RNA 与操纵子的关联,该操纵子在蓝藻集胞藻 PCC 6803 中低碳条件下的光保护中对光系统 II 起着至关重要的作用。蓝藻在响应细胞从高碳向低无机碳 (C(i)) 水平转移时表现出强烈的基因表达动态,但调控机制知之甚少。在集胞藻中上调最明显的基因之一是 flv4、sll0218 和 flv2,它们在 flv4-2 操纵子中组织。该操纵子编码的黄素铁蛋白在光氧化应激条件下打开了一种替代的电子传递途径,可能从光系统 II 的 Q(B) 位点开始。我们对从高碳到低碳转移的细胞进行的表达分析表明,flv4-2 操纵子 mRNA 和一个反义 RNA(命名为 As1_flv4)的转录物积累呈反向相关。As1_flv4 的过表达导致 flv4-2 mRNA 减少。As1_flv4 的启动子活性受到 C(i)限制的瞬时刺激,并受到 AbrB 样转录调节因子 Sll0822 的负调控,而 flv4-2 操纵子受到转录因子 NdhR 的正调控。结果表明,受严格调控的反义 RNA As1_flv4 在 C(i)条件改变后的早期阶段为 flv4-2 表达建立了一个瞬时阈值。因此,它防止了不利的 flv4-2 操纵子蛋白的合成。