State Key Laboratory of Crop Stress Biology for Arid Areas and College of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, People's Republic of China.
State Key Laboratory of Crop Stress Biology for Arid Areas and College of Life Sciences, Northwest A&F University, Yangling, Shaanxi 712100, People's Republic of China
Plant Physiol. 2018 Jan;176(1):804-818. doi: 10.1104/pp.17.00673. Epub 2017 Nov 15.
The development of functional chloroplasts relies on the fine coordination of expressions of both nuclear and chloroplast genomes. We have been using the Arabidopsis () () leaf variegation mutant as a tool to dissect the regulation of chloroplast development. In this work, we screened for genetic enhancer modifiers termed () mutants and report the characterization of the first locus, We showed that encodes the cytosolic 80S ribosome 40S small subunit protein RPS21B and the loss of causes the enhancement of leaf variegation. We further demonstrated that combined S21 activities from EVR1 and its close homolog, EVR1L1, are essential for Arabidopsis, and they act redundantly in regulating leaf development and leaf variegation. Moreover, using additional cytosolic ribosomal protein mutants, we showed that although mutations in cytosolic ribosomal proteins all enhance leaf variegation to varying degrees, the 40S subunit appears to have a more profound role over the 60S subunit in regulating VAR2-mediated chloroplast development. Comprehensive genetic analyses with suppressors that are defective in chloroplast translation established that the enhancement of leaf variegation by cytosolic ribosomal protein mutants is dependent on chloroplast translation. Based on our data, we propose a model that incorporates the suppression and enhancement of leaf variegation, and hypothesize that VAR2/AtFtsH2 may be intimately involved in the balancing of cytosolic and chloroplast translation programs during chloroplast biogenesis.
功能叶绿体的发育依赖于核基因组和叶绿体基因组表达的精细协调。我们一直使用拟南芥()()叶斑变异突变体作为工具来剖析叶绿体发育的调控。在这项工作中,我们筛选了称为()突变体的遗传增强修饰子,并报告了第一个()位点的特征。我们表明,编码细胞质 80S 核糖体 40S 小亚基蛋白 RPS21B,并且()的缺失导致()叶斑变异的增强。我们进一步证明,EVR1 及其近同源物 EVR1L1 的组合 S21 活性对于拟南芥是必需的,它们在调节叶片发育和()叶斑变异中起冗余作用。此外,使用额外的细胞质核糖体蛋白突变体,我们表明,尽管细胞质核糖体蛋白的突变都在不同程度上增强了()叶斑变异,但 40S 亚基在调节 VAR2 介导的叶绿体发育方面似乎比 60S 亚基具有更深远的作用。与叶绿体翻译有缺陷的抑制子进行的综合遗传分析表明,细胞质核糖体蛋白突变体增强()叶斑变异依赖于叶绿体翻译。根据我们的数据,我们提出了一个模型,该模型包含对()叶斑变异的抑制和增强,并假设 VAR2/AtFtsH2 可能在叶绿体生物发生过程中密切参与细胞质和叶绿体翻译程序的平衡。