Felder S, Meierhoff K, Sane A P, Meurer J, Driemel C, Plücken H, Klaff P, Stein B, Bechtold N, Westhoff P
Institut für Entwicklungs-und Molekularbiologie der Pflanzen, Heinrich-Heine-Universität, Universitätstrasse 1, 40225 Düsseldorf, Germany.
Plant Cell. 2001 Sep;13(9):2127-41. doi: 10.1105/tpc.010090.
To understand the functional significance of RNA processing for the expression of plastome-encoded photosynthesis genes, we investigated the nuclear mutation hcf107 of Arabidopsis. The mutation is represented by two alleles, both of which lead to a defective photosystem II (PSII). In vivo protein labeling, in vitro phosphorylation, and immunoblot experiments revealed that the psbB gene product (CP47) and an 8-kD phosphoprotein, the psbH gene product (PsbH), are absent in mutant plants. PsbH and PsbB are essential requirements for PSII assembly in photosynthetic eukaryotes, and their absence in hcf107 is consistent with the PSII-less mutant phenotype. RNA gel blot hybridizations showed that the hcf107 mutation specifically impairs the accumulation of some but not all oligocistronic psbH transcripts that are released from the pentacistronic psbB-psbT-psbH-petB-petD precursor RNA by intergenic endonucleolytic cleavage. In contrast, neither the levels nor the sizes of psbB-containing RNAs are affected. S1 nuclease protection analyses revealed that psbH RNAs are lacking only where psbH is the leading cistron and that they are processed at position -45 in the 5' leader segment of psbH. These data and additional experiments with the cytochrome b(6)f complex mutant hcf152, which is defective in 3' psbH processing, suggest that only those psbH-containing transcripts that are processed at their -45 5' ends can be translated. Secondary structure analysis of the 5' psbH leader predicted the formation of stable stem loops in the nonprocessed transcripts, which are unfolded by processing at the -45 site. We propose that this unfolding of the psbH leader segment as a result of RNA processing is essential for the translation of the psbH reading frame. We suggest further that HCF107 has dual functions: it is involved in intercistronic processing of the psbH 5' untranslated region or the stabilization of 5' processed psbH RNAs, and concomitantly, it is required for the synthesis of CP47.
为了理解RNA加工对质体基因组编码的光合作用基因表达的功能意义,我们研究了拟南芥的核突变体hcf107。该突变由两个等位基因代表,二者均导致光系统II(PSII)缺陷。体内蛋白质标记、体外磷酸化和免疫印迹实验表明,突变植株中不存在psbB基因产物(CP47)和一个8-kD磷蛋白,即psbH基因产物(PsbH)。PsbH和PsbB是光合真核生物中PSII组装的必需条件,它们在hcf107中的缺失与无PSII的突变体表型一致。RNA凝胶印迹杂交表明,hcf107突变特异性地损害了一些(但不是全部)寡顺反子psbH转录本的积累,这些转录本是通过基因间内切核酸酶切割从五顺反子psbB-psbT-psbH-petB-petD前体RNA释放出来的。相反,含psbB的RNA的水平和大小均未受影响。S1核酸酶保护分析表明,只有当psbH是前导顺反子的时候,psbH RNA才会缺失,并且它们在psbH的5'前导序列的-45位被加工。这些数据以及对细胞色素b(6)f复合体突变体hcf152(其在psbH的3'加工中存在缺陷)的额外实验表明,只有那些在其5'端-45位被加工的含psbH的转录本才能被翻译。对psbH 5'前导序列的二级结构分析预测,未加工的转录本中会形成稳定的茎环结构,而在-45位点的加工会使其解折叠。我们提出,由于RNA加工导致的psbH前导序列的这种解折叠对于psbH阅读框的翻译至关重要。我们进一步推测,HCF107具有双重功能:它参与psbH 5'非翻译区的顺反子间加工或5'加工后的psbH RNA的稳定,并且同时,它是CP47合成所必需的。