Institute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.
Plant Mol Biol. 2010 Jun;73(3):309-23. doi: 10.1007/s11103-010-9616-5. Epub 2010 Feb 9.
The vanilla cream1 (vac1) albino mutant is defective in a gene encoding a chloroplast-localized pentatricopeptide repeat protein of the DYW subgroup. However, the carboxyl-terminal DYW motif is truncated in VAC1. To identify vac1-specific phenotypes, we compared 34 chloroplast RNA editing sites and approximately 90 chloroplast gene expression patterns among wild type, vac1 and another albino mutant ispH, which is defective in the plastid isoprenoid biosynthesis pathway. We found that the editing of accD and ndhF transcripts is partially affected in vac1. In addition, steady-state levels of chloroplast rRNAs are significantly decreased in vac1. The expression of plastid-encoded RNA polymerase transcribed genes is down-regulated, whereas the expression of nucleus-encoded RNA polymerase transcribed genes is up-regulated in vac1. Although the development and function of mutant chloroplasts are severely impaired, steady-state mRNA levels of nucleus-encoded photosynthetic genes are not affected or are only slightly decreased in vac1. The ZAT10 gene encodes a transcription factor and its expression is down-regulated by norflurazon treatment in wild type. This norflurazon effect was not observed in vac1. These results suggest that the VAC1 protein may be involved in plastid-to-nucleus retrograde signaling in addition to its role in chloroplast RNA editing and gene expression. A defect in a key biosynthetic pathway can have many indirect effects on chloroplast gene expression as is seen in the ispH mutant. Similarly, the vac1 mutant has pleiotropic molecular phenotypes and most of which may be indirect effects.
香草奶油 1(vac1)白化突变体在编码质体定位的五肽重复蛋白 DYW 亚组的基因中存在缺陷。然而,VAC1 中羧基末端的 DYW 基序被截断。为了鉴定 vac1 特异表型,我们比较了野生型、vac1 和另一种白化突变体 ispH 中的 34 个叶绿体 RNA 编辑位点和大约 90 个叶绿体基因表达模式,ispH 是质体异戊二烯生物合成途径的缺陷。我们发现 accD 和 ndhF 转录物的编辑在 vac1 中部分受到影响。此外, vac1 中叶绿体 rRNA 的稳态水平显著降低。质体编码 RNA 聚合酶转录基因的表达下调,而 vac1 中核编码 RNA 聚合酶转录基因的表达上调。尽管突变体叶绿体的发育和功能严重受损,但 vac1 中核编码光合作用基因的稳态 mRNA 水平不受影响或仅略有降低。ZAT10 基因编码转录因子,其表达在野生型中被 norflurazon 处理下调。在 vac1 中未观察到 norflurazon 效应。这些结果表明,除了在叶绿体 RNA 编辑和基因表达中的作用外,VAC1 蛋白可能参与质体到核的逆行信号转导。关键生物合成途径的缺陷会对叶绿体基因表达产生许多间接影响,如在 ispH 突变体中所见。同样,vac1 突变体具有多种表型分子表型,其中大多数可能是间接影响。