首页> 外文期刊>Biochimica et biophysica acta. Gene structure and expression >DNA macroarray and real-time PCR analysis of two nuclear photosystem I mutants from Chlamydomonas reinhardtii reveal downregulation of Lhcb genes but different regulation of Lhca genes
【24h】

DNA macroarray and real-time PCR analysis of two nuclear photosystem I mutants from Chlamydomonas reinhardtii reveal downregulation of Lhcb genes but different regulation of Lhca genes

机译:莱茵衣藻的两个核光系统I突变体的DNA宏阵列和实时PCR分析显示Lhcb基因的下调但Lhca基因的不同调节

获取原文
获取原文并翻译 | 示例
       

摘要

In photoautotrophic organisms, the expression of nuclear genes encoding plastid proteins is known to be regulated at various levels. In this study, we present the analysis of two non-photosynthetic mutants (CC1051 and TR72) from the unicellular green alga Chlamydomonas reinhardtii. Both mutant strains show a defect in the processing of chloroplast psaA mRNA, and therefore they are assumed to be defective in photosystem I (PSI) assembly. We have performed macroarray experiments with trans-splicing mutants CC1051 and TR72 in order to analyse putative pleiotropic, effects of nuclear-located mutations leading to a non-functional PSI. To the best of our knowledge, this is the first example of Chlamydomonas cDNA macroarray analysis comparing the transcriptional regulation of nuclear genes in wild-type and photosystem I mutants. The macroarray results demonstrated a transcriptional downregulation of members of the Lhcb gene family more than 2-fold in both mutant strains. In addition, real-time RT-PCR experiments found a 4- to 16-fold reduction in transcript levels of several Lhca genes in TR72; whereas in CC1051, no significant change in transcript levels was observed. Taken together, our data suggest that a signal is transmitted from the chloroplast to the nucleus that serves to regulate the level of light harvesting polypeptides in the organelle. (c) 2005 Elsevier B.V. All rights reserved.
机译:在光合自养生物中,已知编码质体蛋白的核基因表达受到不同水平的调节。在这项研究中,我们目前对单细胞绿藻莱茵衣藻的两个非光合突变体(CC1051和TR72)进行分析。两种突变菌株在叶绿体psaA mRNA的加工中均显示出缺陷,因此,它们被认为在光系统I(PSI)组装中存在缺陷。我们已经用转拼突变体CC1051和TR72进行了宏阵列实验,以分析推定的多效性,即核定位突变导致无功能PSI的影响。据我们所知,这是衣藻属cDNA宏阵列分析的第一个例子,比较了野生型和光系统I突变体中核基因的转录调控。宏阵列结果表明,在两种突变菌株中,Lhcb基因家族成员的转录下调均超过2倍。另外,实时RT-PCR实验发现TR72中几个Lhca基因的转录水平降低了4到16倍。而在CC1051中,转录水平没有明显变化。综上所述,我们的数据表明信号从叶绿体传递到细胞核,该信号用于调节细胞器中光收集多肽的水平。 (c)2005 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号