Favory Jean-Jacques, Kobayshi Masanori, Tanaka Kan, Peltier Gilles, Kreis Martin, Valay Jean-Gabriel, Lerbs-Mache Silva
Laboratoire Plastes et différenciation cellulaire, Université Joseph Fourier and Centre National de la Recherche Scientifique, B.P. 53, 38041 Grenoble, France.
Nucleic Acids Res. 2005 Oct 20;33(18):5991-9. doi: 10.1093/nar/gki908. Print 2005.
The complexity of the plastid transcriptional apparatus (two or three different RNA polymerases and numerous regulatory proteins) makes it very difficult to attribute specific function(s) to its individual components. We have characterized an Arabidopsis T-DNA insertion line disrupting the nuclear gene coding for one of the six plastid sigma factors (SIG4) that regulate the activity of the plastid-encoded RNA polymerase PEP. This mutant shows a specific diminution of transcription of the plastid ndhF gene, coding for a subunit of the plastid NDH [NAD(P)H dehydrogenase] complex. The absence of another NDH subunit, i.e. NDHH, and the absence of a chlorophyll fluorescence transient previously attributed to the activity of the plastid NDH complex indicate a strong down-regulation of NDH activity in the mutant plants. Results suggest that plastid NDH activity is regulated on the transcriptional level by an ndhF-specific plastid sigma factor, SIG4.
质体转录装置的复杂性(两种或三种不同的RNA聚合酶以及众多调控蛋白)使得很难确定其各个组件的具体功能。我们对一个拟南芥T-DNA插入系进行了表征,该插入系破坏了编码六种质体sigma因子(SIG4)之一的核基因,SIG4可调节质体编码的RNA聚合酶PEP的活性。该突变体显示质体ndhF基因的转录特异性降低,ndhF基因编码质体NDH [NAD(P)H脱氢酶]复合体的一个亚基。另一个NDH亚基(即NDHH)的缺失,以及先前归因于质体NDH复合体活性的叶绿素荧光瞬变的缺失,表明突变植物中NDH活性强烈下调。结果表明,质体NDH活性在转录水平上受ndhF特异性质体sigma因子SIG4的调控。