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2
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本文引用的文献

1
Atrazine, bromacil, and diuron resistance in chlamydomonas: a single non-mendelian genetic locus controls the structure of the thylakoid binding site.衣藻对莠去津、除草定和敌草隆的抗性:一个非孟德尔遗传位点控制类囊体结合位点的结构。
Plant Physiol. 1984 Mar;74(3):469-74. doi: 10.1104/pp.74.3.469.
2
Posttranscriptional Regulation of Ribulose 1,5-bisphosphate Carboxylase Small Subunit Accumulation in Chlamydomonas reinhardtii.莱茵衣藻中核酮糖 1,5-二磷酸羧化酶小亚基积累的转录后调控。
Plant Physiol. 1983 Jul;72(3):847-54. doi: 10.1104/pp.72.3.847.
3
Photosynthesis-deficient Mutants of Chlamydomonas reinhardii with Associated Light-sensitive Phenotypes.莱茵衣藻光合作用缺陷突变体及其相关的光敏感表型。
Plant Physiol. 1981 Mar;67(3):565-9. doi: 10.1104/pp.67.3.565.
4
Light regulation of the synthesis of the large subunit of ribulose-1,5-bisphosphate carboxylase in peas: Evidence for translational control.光对豌豆核酮糖-1,5-二磷酸羧化酶大亚基合成的调控:翻译控制的证据。
Proc Natl Acad Sci U S A. 1985 Sep;82(17):5690-4. doi: 10.1073/pnas.82.17.5690.
5
Primary structure of the M subunit of the reaction center from Rhodopseudomonas sphaeroides.球形红假单胞菌反应中心 M 亚基的一级结构。
Proc Natl Acad Sci U S A. 1983 Nov;80(21):6505-9. doi: 10.1073/pnas.80.21.6505.
6
Rapid degradation of unassembled ribulose 1,5-bisphosphate carboxylase small subunits in chloroplasts.叶绿体中未组装的核酮糖 1,5-二磷酸羧化酶小亚基的快速降解。
Proc Natl Acad Sci U S A. 1983 May;80(9):2632-6. doi: 10.1073/pnas.80.9.2632.
7
Differential transcription in vivo and in vitro of two adjacent maize chloroplast genes: The large subunit of ribulosebisphosphate carboxylase and the 2.2-kilobase gene.体内和体外两种相邻玉米叶绿体基因的差异转录:核酮糖二磷酸羧化酶大亚基和 2.2 千碱基基因。
Proc Natl Acad Sci U S A. 1981 Nov;78(11):6821-5. doi: 10.1073/pnas.78.11.6821.
8
Lithium dodecyl sulfate/polyacrylamide gel electrophoresis of thylakoid membranes at 4 degrees C: Characterizations of two additional chlorophyll a-protein complexes.4℃下类囊体膜的十二烷基硫酸锂/聚丙烯酰胺凝胶电泳:另外两种叶绿素a-蛋白复合物的特性分析
Proc Natl Acad Sci U S A. 1979 Jan;76(1):111-5. doi: 10.1073/pnas.76.1.111.
9
Nuclear mutation leads to an accelerated turnover of chloroplast-encoded 48 kd and 34.5 kd polypeptides in thylakoids lacking photosystem II.核突变导致类囊体中缺乏光系统 II 的叶绿体编码的 48 kd 和 34.5 kd 多肽的周转率加快。
EMBO J. 1985 Jul;4(7):1645-53. doi: 10.1002/j.1460-2075.1985.tb03832.x.
10
Control of psbA gene expression: in mature Spirodela chloroplasts light regulation of 32-kd protein synthesis is independent of transcript level.psbA 基因表达的调控:在成熟的水蕴叶绿体中,32kd 蛋白合成的光调控不依赖于转录水平。
EMBO J. 1985 Feb;4(2):291-5. doi: 10.1002/j.1460-2075.1985.tb03628.x.

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.

DOI:10.1083/jcb.103.4.1315
PMID:3533953
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2114316/
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。