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通过将rbcS基因导入烟草质体基因组来互补核反义rbcS诱导的光合作用缺陷。

Complementation of the nuclear antisense rbcS-induced photosynthesis deficiency by introducing an rbcS gene into the tobacco plastid genome.

作者信息

Zhang Xing-Hai, Ewy Robert G, Widholm Jack M, Portis Archie R

机构信息

Department of Crop Sciences, University of Illinois, Urbana, IL 61801, U.S.A.

出版信息

Plant Cell Physiol. 2002 Nov;43(11):1302-13. doi: 10.1093/pcp/pcf158.

Abstract

The small subunit (SS) of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) is a nuclear gene-encoded protein that is imported into chloroplasts where it assembles with the large subunit (LS) after removal of the transit peptide to form Rubisco. We have explored the possibility that the severe deficiency in photosynthesis exhibited in nuclear transgenic tobacco (line alpha5) expressing antisense rbcS coding DNA that results in low SS and Rubisco protein content [Rodermel et al. (1988) Cell 55: 673] could be complemented by introducing a copy of the rbcS gene into its plastid genome through chloroplast transformation. Two independent lines of transplastomic plants were generated, in which the tobacco rbcS coding sequence, either with or without the transit sequence, was site-specifically integrated into the plastid genome. We found that compared with the antisense plants, expression of the plastid rbcS gene in the transplastomic plants resulted in very high mRNA abundance but no increased accumulation of the SS and Rubisco protein or improvement in plant growth and photosynthesis. Therefore, there is a limitation in efficient translation of the rbcS mRNA in the plastid or an incorrect processing and modification of the plastid-synthesized SS protein that might cause its rapid degradation.

摘要

1,5 - 二磷酸核酮糖羧化酶/加氧酶(Rubisco)的小亚基(SS)是一种由核基因编码的蛋白质,它被导入叶绿体,在去除转运肽后与大亚基(LS)组装形成Rubisco。我们探讨了通过叶绿体转化将rbcS基因的一个拷贝导入核转基因烟草(α5系)的质体基因组,以弥补该烟草因表达反义rbcS编码DNA而导致光合作用严重缺陷的可能性。该反义DNA导致低水平的SS和Rubisco蛋白含量[罗德梅尔等人(1988年)《细胞》55卷:673页]。我们产生了两个独立的转质体植物株系,其中烟草rbcS编码序列(有或没有转运序列)被定点整合到质体基因组中。我们发现,与反义植物相比,转质体植物中质体rbcS基因的表达导致了非常高的mRNA丰度,但SS和Rubisco蛋白的积累没有增加,植物生长和光合作用也没有改善。因此,质体中rbcS mRNA的有效翻译存在限制,或者质体合成的SS蛋白存在错误的加工和修饰,这可能导致其快速降解。

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