Hahn D, Bennoun P, Kück U
Lehrstuhl für Allgemeine Botanik, Ruhr-Universität Bochum, Germany.
Mol Gen Genet. 1996 Sep 25;252(4):362-70. doi: 10.1007/BF02173000.
In photoautotrophic organisms it is well documented that the expression of nuclear genes encoding plastid proteins can be regulated at various levels. We present here the analysis of a non-photosynthetic strain (CC1051) of the green unicellular alga Chlamydomonas reinhardtii; this strain carries a mutation in the newly identified Cen gene involved in the co-regulated expression of several different nuclear genes encoding plastid proteins. We performed a differential screening strategy to isolate cDNAs corresponding to genes that are differentially expressed in mutant and wild-type strains. Extensive hybridization experiments revealed that the 15 cDNA clones isolated represent five different mRNAs that fail to accumulate in the non-photosynthetic mutant. Comparative analysis of DNA sequencing data showed that they all code for plastid proteins. In particular, we identified genes for the chlorophyll a/b binding protein of the light-harvesting complex II (LHCII), for subunits II and III of photosystem I (PsaD, PsaF), for pentose-5-phosphate 3-epimerase (PPE), an enzyme of the Calvin cycle, and for an unidentified 7 kDa protein with a suggested lumenal location. With the exception of the gene for LHCII, all proteins are encoded by single-copy genes. Evidence from run-on transcription experiments is presented showing that expression of the above mentioned plastid proteins is affected at the post-transcriptional level in the mutant strain CC1051 with a defect in the Cen gene. Our results suggest that the product of the Cen gene is involved in stabilization and/or processing of transcripts from nuclear genes encoding chloroplast proteins.
在光合自养生物中,有充分的文献记载,编码质体蛋白的核基因的表达可在多个水平上受到调控。我们在此展示了对绿色单细胞藻类莱茵衣藻的非光合菌株(CC1051)的分析;该菌株在新鉴定的Cen基因中发生了突变,该基因参与了几个不同的编码质体蛋白的核基因的共同调控表达。我们采用了差异筛选策略来分离与在突变体和野生型菌株中差异表达的基因相对应的cDNA。广泛的杂交实验表明,分离出的15个cDNA克隆代表了5种不同的mRNA,它们在非光合突变体中无法积累。DNA测序数据的比较分析表明,它们都编码质体蛋白。特别是,我们鉴定出了编码光捕获复合体II(LHCII)的叶绿素a/b结合蛋白、光系统I的亚基II和III(PsaD、PsaF)、戊糖-5-磷酸3-表异构酶(PPE,卡尔文循环中的一种酶)以及一种推测位于类囊体腔的未知7 kDa蛋白的基因。除了LHCII基因外,所有蛋白质均由单拷贝基因编码。本文提供了连续转录实验的证据,表明上述质体蛋白的表达在Cen基因有缺陷的突变体菌株CC1051中受到转录后水平的影响。我们的结果表明,Cen基因的产物参与了编码叶绿体蛋白的核基因转录本的稳定和/或加工。