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光系统II复合物的生物合成:转录、翻译及翻译后调控。

Biogenesis of photosystem II complexes: transcriptional, translational, and posttranslational regulation.

作者信息

Jensen K H, Herrin D L, Plumley F G, Schmidt G W

出版信息

J Cell Biol. 1986 Oct;103(4):1315-25. doi: 10.1083/jcb.103.4.1315.

Abstract

The integral membrane proteins of photosystem II (PS II) reaction center complexes are encoded by chloroplast genomes. These proteins are absent from thylakoids of PS II mutants of algae and vascular plants as a result of either chloroplast or nuclear gene mutations. To resolve the molecular basis for the concurrent absence of the PS II polypeptides, protein synthesis rates and mRNA levels were measured in mutants of Chlamydomonas reinhardtii that lack PS II. The analyses show that one nuclear gene product regulates the levels of transcripts from the chloroplast gene encoding the 51-kD chlorophyll a-binding polypeptide (polypeptide 5) but is not involved in the synthesis of other chloroplast mRNAs. Another nuclear product is specifically required for translation of mRNA encoding the 32-34-kD polypeptide, D1. The absence of either D1 or polypeptide 5 does not eliminate the synthesis and thylakoid insertion of two other integral membrane proteins of PS II, the chlorophyll a-binding polypeptide of 46 kD (polypeptide 6) and the 30-kD "D1-like" protein, D2. However, these two unassembled subunits cannot be properly processed and/or are degraded in the mutants even though they reside in the membrane. In addition, pulse labeling of the nuclear mutants and a chloroplast mutant that does not synthesize D1 mRNA indicates that synthesis of polypeptide 5 and D1 is coordinated at the translational level. A model is presented to explain how absence of one of the two proteins could lead to translational arrest of the other.

摘要

光系统II(PS II)反应中心复合物的整合膜蛋白由叶绿体基因组编码。由于叶绿体或核基因突变,藻类和维管植物的PS II突变体的类囊体中缺少这些蛋白。为了解决PS II多肽同时缺失的分子基础,我们在缺乏PS II的莱茵衣藻突变体中测量了蛋白质合成速率和mRNA水平。分析表明,一种核基因产物调节叶绿体基因转录本的水平,该基因编码51-kD叶绿素a结合多肽(多肽5),但不参与其他叶绿体mRNA的合成。另一种核产物是编码32-34-kD多肽D1的mRNA翻译所特需的。D1或多肽5的缺失并不会消除PS II的另外两种整合膜蛋白的合成和类囊体插入,即46 kD的叶绿素a结合多肽(多肽6)和30-kD的“D1样”蛋白D2。然而,即使这两个未组装的亚基存在于膜中,它们在突变体中也不能被正确加工和/或被降解。此外,对核突变体和不合成D1 mRNA的叶绿体突变体进行脉冲标记表明,多肽5和D1的合成在翻译水平上是协调的。本文提出了一个模型来解释两种蛋白中一种的缺失如何导致另一种的翻译停滞。

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