首页> 外文期刊>Journal of the American Society for Horticultural Science >Differential protein expression of two photosystem II subunits, PsbO and PsbP, in an albino mutant of Bambusa edulis with chloroplast DNA aberration
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Differential protein expression of two photosystem II subunits, PsbO and PsbP, in an albino mutant of Bambusa edulis with chloroplast DNA aberration

机译:叶绿体DNA畸变的Bambusa edulis白化突变体中两个光系统II亚基PsbO和PsbP的差异蛋白表达

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The chloroplast genome of an albino mutant isolated from tissue culture of the bamboo Bambusa edulis Munro was examined to identify aberrations. A number of the chloroplast genes encoding ATP synthases, photosystem II subunits, NADH dehydrogenase, and ribosomal proteins had been deleted, at least partially, in the albino mutant. Comparison of the two-dimensional electrophoresis profiles of albino and green bamboos revealed three spots of reduced intensity, indicating repression of these proteins in the albino mutants. Mass spectroscopic analysis subsequently revealed that two of these proteins are 33-kDa subunits of the photosystem II oxygen-evolving protein complex (PsbO) and one is a 23-kDa subunit of photosystem II oxygen-evolving protein complex (PsbP). The genes encoding these two proteins were cloned from B. edulis, and were denoted BePsbO (accession no. EF669513) and BePsbP (accession no. EF669512). Reverse transcription polymerase chain reaction and two-dimensional gel analyses of BePsbO and BePsbP in green and albino bamboos grown in the light or dark revealed that the albino mutant, similar to its green counterpart, sensed the light signal, resulting in the induction of BePsbO and BePsbP transcription, but it did not accumulate the protein products. We conclude that the repression of protein-expressing BePsbO and BePsbP is because of a defect in post-transcriptional regulation in the albino mutant.
机译:检查了从竹子Bambusa edulis Munro的组织培养物中分离出的白化突变体的叶绿体基因组,以鉴定畸变。在白化突变体中,至少部分缺失了许多编码ATP合酶,光系统II亚基,NADH脱氢酶和核糖体蛋白的叶绿体基因。比较白化病和绿色竹子的二维电泳图谱,发现三个强度降低的斑点,表明这些蛋白在白化病突变体中受到抑制。质谱分析随后显示,这些蛋白质中的两个是光系统II释氧蛋白复合物(PsbP)的33 kDa亚基,一个是光系统II释氧蛋白复合物(PsbP)的23 kDa亚基。编码这两种蛋白质的基因从蓝芽孢杆菌中克隆,并命名为BePsbO(登录号EF669513)和BePsbP(登录号EF669512)。在明或暗生长的绿色和白化竹中,BePsbO和BePsbP的逆转录聚合酶链反应和二维凝胶分析表明,与绿色对应物类似的白化突变体感应到光信号,从而诱导了BePsbO和BePsbO的诱导。 BePsbP转录,但没有积聚蛋白质产物。我们得出结论,表达蛋白的BePsbO和BePsbP的抑制是由于白化突变体中转录后调控的缺陷。

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