Wu Xiaoqiang, Liu Duan, Lee Martin H, Golden James W
Department of Biology, Texas A&M University, College Station, Texas 77843-3258, USA.
J Bacteriol. 2004 Oct;186(19):6422-9. doi: 10.1128/JB.186.19.6422-6429.2004.
The patS gene encodes a small peptide that is required for normal heterocyst pattern formation in the cyanobacterium Anabaena sp. strain PCC 7120. PatS is proposed to control the heterocyst pattern by lateral inhibition. patS minigenes were constructed and expressed by different developmentally regulated promoters to gain further insight into PatS signaling. patS minigenes patS4 to patS8 encode PatS C-terminal 4 (GSGR) to 8 (CDERGSGR) oligopeptides. When expressed by P(petE), P(patS), or P(rbcL) promoters, patS5 to patS8 inhibited heterocyst formation but patS4 did not. In contrast to the full-length patS gene, P(hepA)-patS5 failed to restore a wild-type pattern in a patS null mutant, indicating that PatS-5 cannot function in cell-to-cell signaling if it is expressed in proheterocysts. To establish the location of the PatS receptor, PatS-5 was confined within the cytoplasm as a gfp-patS5 fusion. The green fluorescent protein GFP-PatS-5 fusion protein inhibited heterocyst formation. Similarly, full-length PatS with a C-terminal hexahistidine tag inhibited heterocyst formation. These data indicate that the PatS receptor is located in the cytoplasm, which is consistent with recently published data indicating that HetR is a PatS target. We speculated that overexpression of other Anabaena strain PCC 7120 RGSGR-encoding genes might show heterocyst inhibition activity. In addition to patS and hetN, open reading frame (ORF) all3290 and an unannotated ORF, orf77, encode an RGSGR motif. Overexpression of all3290 and orf77 under the control of the petE promoter inhibited heterocyst formation, indicating that the RGSGR motif can inhibit heterocyst development in a variety of contexts.
patS基因编码一种小肽,它是蓝藻鱼腥藻PCC 7120菌株中正常异形胞模式形成所必需的。有人提出PatS通过侧向抑制来控制异形胞模式。构建了patS小基因,并由不同的发育调控启动子进行表达,以进一步深入了解PatS信号传导。patS小基因patS4至patS8编码PatS的C末端4肽(GSGR)至8肽(CDERGSGR)。当由P(petE)、P(patS)或P(rbcL)启动子表达时,patS5至patS8抑制异形胞形成,但patS4没有。与全长patS基因不同,P(hepA)-patS5未能在patS缺失突变体中恢复野生型模式,这表明如果PatS-5在原异形胞中表达,它不能在细胞间信号传导中发挥作用。为了确定PatS受体的位置,将PatS-5作为gfp-patS5融合蛋白限制在细胞质中。绿色荧光蛋白GFP-PatS-5融合蛋白抑制异形胞形成。同样,带有C末端六组氨酸标签的全长PatS也抑制异形胞形成。这些数据表明PatS受体位于细胞质中,这与最近发表的数据一致,即HetR是PatS的一个靶点。我们推测,其他鱼腥藻PCC 7120菌株中编码RGSGR的基因的过表达可能会显示出异形胞抑制活性。除了patS和hetN外,开放阅读框(ORF)all3290和一个未注释的ORF(orf77)也编码RGSGR基序。在petE启动子控制下,all3290和orf77的过表达抑制了异形胞形成,这表明RGSGR基序在多种情况下都能抑制异形胞发育。