Krupinska Karin, Oetke Svenja, Desel Christine, Mulisch Maria, Schäfer Anke, Hollmann Julien, Kumlehn Jochen, Hensel Götz
Institute of Botany, Christian-Albrechts-University of Kiel Kiel, Germany.
Institute of Botany, Christian-Albrechts-University of Kiel Kiel, Germany ; Central Microscopy of the Center of Biology, Christian-Albrechts-University of Kiel Kiel, Germany.
Front Plant Sci. 2014 Sep 4;5:432. doi: 10.3389/fpls.2014.00432. eCollection 2014.
WHIRLY1 is an abundant protein of chloroplast nucleoids, which has also been named pTAC-1 with regard to its detection in the proteome of transcriptionally active chromosomes (TAC). In barley primary foliage leaves, expression of the WHIRLY1 gene is highest at the base whereas protein accumulation is highest in the middle of the leaf where young developing chloroplasts are found. In order to elucidate the function of WHIRLY1 in chloroplast nucleoids, transgenic barley plants with an RNAi-mediated knock-down of the HvWHIRLY1 gene (RNAi-W1) were generated. The homozygous RNAi-W1-7 plants, barely containing traces of the WHIRLY1 protein, were chosen for detailed analyses of nucleoids. Nucleic acid specific-staining with YO-PRO®-1 revealed that in comparison to wild type chloroplasts, which have multiple small nucleoids attached to thylakoids, chloroplasts of the transgenic plants contain large irregularly formed patches of DNA besides nucleoids that are similar in size and shape to those of wild type chloroplasts. In large electron lucent areas, filamentous structures were detected by conventional transmission electron microscopy. Analyses of ptDNA levels by both DNA dot-blot hybridization and quantitative PCR showed that leaves of the transgenic plants have a two- to three-fold higher level of ptDNA than the wild type. The higher ptDNA level in RNAi-W1 plants coincided with an enhanced expression of the gene encoding a putative organelle targeted DNA polymerase in the mid part of primary foliage leaves. Furthermore, overexpression of the barley WHIRLY1 gene in E. coli cells revealed a higher compaction of bacterial nucleoids. These results suggest that WHIRLY1 belongs to the group of plastid nucleoid associated proteins (ptNAP) having a function in compacting a subpopulation of chloroplast nucleoids thereby affecting DNA replication.
WHIRLY1是叶绿体类核中的一种丰富蛋白质,就其在转录活性染色体(TAC)蛋白质组中的检测而言,它也被命名为pTAC-1。在大麦初生叶中,WHIRLY1基因的表达在基部最高,而蛋白质积累在叶片中部最高,那里有发育中的年轻叶绿体。为了阐明WHIRLY1在叶绿体类核中的功能,构建了通过RNA干扰介导HvWHIRLY1基因敲低的转基因大麦植株(RNAi-W1)。选择几乎不含WHIRLY1蛋白痕迹的纯合RNAi-W1-7植株进行类核的详细分析。用YO-PRO®-1进行核酸特异性染色显示,与野生型叶绿体相比,野生型叶绿体有多个附着在类囊体上的小类核,而转基因植物的叶绿体除了有与野生型叶绿体大小和形状相似的类核外,还含有大的不规则形成的DNA斑块。在大的电子透明区域,通过传统透射电子显微镜检测到丝状结构。通过DNA斑点杂交和定量PCR对ptDNA水平进行分析表明,转基因植物叶片中的ptDNA水平比野生型高两到三倍。RNAi-W1植株中较高的ptDNA水平与初生叶中部编码假定的细胞器靶向DNA聚合酶的基因表达增强相一致。此外,大麦WHIRLY1基因在大肠杆菌细胞中的过表达显示细菌类核的压缩程度更高。这些结果表明,WHIRLY1属于质体类核相关蛋白(ptNAP)组,其功能是压缩叶绿体类核的一个亚群,从而影响DNA复制。