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质体ndhD转录本的惊人特征:非编码核苷酸的添加以及具有未编辑起始密码子的mRNA与多核糖体的关联。

Surprising features of plastid ndhD transcripts: addition of non-encoded nucleotides and polysome association of mRNAs with an unedited start codon.

作者信息

Zandueta-Criado Aitor, Bock Ralph

机构信息

Westfälische Wilhelms-Universität Münster, Institut für Biochemie und Biotechnologie der Pflanzen, Hindenburgplatz 55, D-48143 Münster, Germany.

出版信息

Nucleic Acids Res. 2004 Jan 26;32(2):542-50. doi: 10.1093/nar/gkh217. Print 2004.

Abstract

RNA editing in higher plant plastids is a post- transcriptional RNA maturation process changing single cytidine nucleotides into uridine. In the ndhD transcript of tobacco and several other plant species, editing of an ACG codon to a standard AUG initiator codon is believed to be a prerequisite for translation. In order to test this assumption experimentally, we have analyzed the editing status of ndhD mRNA species in the process of translation. We show that unedited ndhD transcripts are also associated with polysomes in vivo, suggesting that they are translated. This surprising finding challenges the view that ACG to AUG editing is strictly required to make the ndhD message translatable and raises the possibility that ACG can be utilized as an initiator codon in chloroplasts. In addition, we have mapped the termini of the ndhD transcript and discovered a novel form of RNA processing. Unexpectedly, we find that highly specific sequences are added to the 3' end of the ndhD mRNA at high frequency. We propose a model in which these sequences are added by the successive action of a CCA-adding enzyme (tRNA nucleotidyltransferase) and an RNA-dependent RNA polymerase (RdRp) activity. The presence of an RdRp activity may have general implications also for other steps in plastid gene expression.

摘要

高等植物质体中的RNA编辑是一种转录后RNA成熟过程,它将单个胞嘧啶核苷酸转变为尿苷。在烟草和其他几种植物物种的ndhD转录本中,将ACG密码子编辑为标准的AUG起始密码子被认为是翻译的先决条件。为了通过实验验证这一假设,我们分析了翻译过程中ndhD mRNA种类的编辑状态。我们发现,未编辑的ndhD转录本在体内也与多核糖体相关联,这表明它们能够被翻译。这一惊人发现挑战了ACG到AUG的编辑是使ndhD信息可翻译的严格要求这一观点,并提出了ACG可作为叶绿体中起始密码子的可能性。此外,我们绘制了ndhD转录本的末端图谱,并发现了一种新的RNA加工形式。出乎意料的是,我们发现高度特异性序列以高频率添加到ndhD mRNA的3'末端。我们提出了一个模型,其中这些序列是通过添加CCA的酶(tRNA核苷酸转移酶)和RNA依赖性RNA聚合酶(RdRp)活性的连续作用添加的。RdRp活性的存在可能对质体基因表达的其他步骤也有普遍影响。

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