Yamazaki Hiroyuki, Tasaka Masao, Shikanai Toshiharu
Graduate School of Biological Sciences, Nara Institute of Science and Technology, Ikoma, Nara 630-0101, Japan.
Plant J. 2004 Apr;38(1):152-63. doi: 10.1111/j.1365-313X.2004.02035.x.
Plastid gene expression is regulated by a variety of nuclear genes. We have isolated Arabidopsis thaliana proton gradient regulation 3 (pgr3) mutants, which display aberrant chlorophyll fluorescence because of defects in chloroplast gene expression. High chlorophyll fluorescence (HCF) because of a reduced level of the cytochrome b6/f complex was observed in two alleles, pgr3-1 and pgr3-2 but not in pgr3-3. In contrast, a transient increase in fluorescence after turning off the actinic light, which was ascribed to chloroplast NADPH dehydrogenase (NDH) activity, was impaired in pgr3-1 and pgr3-3 but not in pgr3-2. Both phenotypes were complemented by the introduction of a single gene, PGR3, encoding a protein containing 27 pentatrico-peptide repeat (PPR) motifs. PPR motifs are present in proteins functioning in the post-transcriptional regulation of organellar gene expression. The conserved threonine in the motif was substituted by isoleucine in the 15th and 12th PPR motifs in pgr3-1 and pgr3-2, respectively, and the conserved leucine by phenylalanine in the final incomplete motif of pgr3-3. We consider that the different domains of the PPR repeats in PGR3 might have different functions in conferring RNA stability and probably allowing translation as well as recognizing at least two distinct target RNAs.
质体基因表达受多种核基因调控。我们分离出了拟南芥质子梯度调节3(pgr3)突变体,这些突变体由于叶绿体基因表达缺陷而表现出异常的叶绿素荧光。在两个等位基因pgr3-1和pgr3-2中观察到由于细胞色素b6/f复合体水平降低导致的高叶绿素荧光(HCF),而在pgr3-3中未观察到。相反,在关闭光化光后荧光的短暂增加(这归因于叶绿体NADPH脱氢酶(NDH)活性)在pgr3-1和pgr3-3中受损,但在pgr3-2中未受损。通过引入单个基因PGR3(编码一种含有27个五肽重复(PPR)基序的蛋白质),这两种表型都得到了互补。PPR基序存在于参与细胞器基因表达转录后调控的蛋白质中。在pgr3-1和pgr3-2的第15个和第12个PPR基序中,该基序中的保守苏氨酸分别被异亮氨酸取代,在pgr3-3的最后一个不完整基序中,保守亮氨酸被苯丙氨酸取代。我们认为PGR3中PPR重复序列的不同结构域在赋予RNA稳定性以及可能允许翻译以及识别至少两种不同的靶RNA方面可能具有不同的功能。