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马铃薯纺锤块茎类病毒由RNA聚合酶II进行的转录主要起始于两个特定位点。

Transcription of potato spindle tuber viroid by RNA polymerase II starts predominantly at two specific sites.

作者信息

Fels A, Hu K, Riesner D

机构信息

Institut für Physikalische Biologie, Heinrich-Heine Universität Düsseldorf, Universitätsstrasse 1, D-40225 Düsseldorf, Germany.

出版信息

Nucleic Acids Res. 2001 Nov 15;29(22):4589-97. doi: 10.1093/nar/29.22.4589.

Abstract

Pospiviroidae, with their main representative potato spindle tuber viroid (PSTVd), are replicated via a rolling circle mechanism by the host-encoded DNA-dependent RNA polymerase II (pol II). In the first step, the (+)-strand circular viroid is transcribed into a (-)-strand oligomer intermediate. As yet it is not known whether transcription is initiated by promotors at specific start sites or is distributed non-specifically over the whole circle. An in vitro transcription extract was prepared from a non-infected potato cell culture which exhibited transcriptional activity using added circular PSTVd (+)-strand RNA as template. In accordance with pol II activity, transcription could be inhibited by alpha-amanitin. RT-PCR revealed the existence of at least two different start sites and primer extension identified these as nucleotides A(111) and A(325). The sequences of the first 7 nt transcribed are very similar, (105)GGAGCGA(111) and (319)GGGGCGA(325). GC-boxes are located at a distance of 15 and 16 nt upstream, respectively, in the native viroid structure, which may act to facilitate initiation. The GC-boxes may have a similar function to the GC-rich hairpin II in the (-)-strand intermediate, as described previously. The results are compared with the corresponding features of avocado sunblotch viroid, which belongs to a different family of viroids and exhibits different transcription initiation properties.

摘要

马铃薯纺锤块茎类病毒科,以其主要代表马铃薯纺锤块茎类病毒(PSTVd)为例,通过宿主编码的DNA依赖性RNA聚合酶II(pol II)以滚环机制进行复制。第一步,正链环状类病毒被转录成负链寡聚体中间体。目前尚不清楚转录是由特定起始位点的启动子启动,还是在整个环上非特异性分布。从未感染的马铃薯细胞培养物中制备了一种体外转录提取物,该提取物以添加的环状PSTVd正链RNA为模板表现出转录活性。与pol II活性一致,转录可被α-鹅膏蕈碱抑制。RT-PCR揭示了至少两个不同的起始位点,引物延伸将这些位点鉴定为核苷酸A(111)和A(325)。转录的前7个核苷酸的序列非常相似,(105)GGAGCGA(111)和(319)GGGGCGA(325)。在天然类病毒结构中,GC框分别位于上游15和16个核苷酸处,可能起到促进起始的作用。如前所述,GC框可能与负链中间体中富含GC的发夹II具有相似的功能。将这些结果与鳄梨日斑类病毒的相应特征进行了比较,鳄梨日斑类病毒属于不同的类病毒家族,具有不同的转录起始特性。

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