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独立调节多组分 DNA 病毒中单个基因组元件的转录和与高转录活性相关的顺式作用元件。

Independent modulation of individual genomic component transcription and a cis-acting element related to high transcriptional activity in a multipartite DNA virus.

机构信息

Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture and Rural Affairs, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101, China.

School of Plant Sciences and BIO5 Institute, University of Arizona, Tucson, 85721, USA.

出版信息

BMC Genomics. 2019 Jul 11;20(1):573. doi: 10.1186/s12864-019-5901-0.

Abstract

BACKGROUND

The genome of Banana bunchy top virus (BBTV) consists of at least six circular, single-stranded DNA components of ~ 1 kb in length. Some BBTV isolates may also carry satellite DNA molecules that are not essential for BBTV infection. The relation between multipartite DNA virus replication and their transcriptional levels and the underlying mechanism remain unclear.

RESULTS

To understand the coordinated replication and transcription of the multiple genomic components, the absolute amounts of each BBTV DNA component were measured by real-time PCR (qPCR), and their transcriptional levels were determined by RNAseq and reverse transcription-qPCR (qRT-PCR). Significant differences were found in the absolute amounts of individual BBTV genomic components. Transcriptional levels of each BBTV genomic component obtained from the RNAseq data matched closely to those obtained from qRT-PCR, but did not correspond to the absolute amount of each DNA component. The ratio of transcript over DNA copies ranged from 46.21 to 1059.44%, which was possibly regulated by the promoter region in the intergenic region of each component. To further determine this speculation, the promoter region of the DNA-S, -M or -N was constructed to the upstream of green fluorescent protein (GFP) gene for transient expression by agrobacterium-mediated transformation method. The qRT-PCR showed the highest transcriptional activity was promoted by DNA-N promoter, about 386.58% activity comparing with CaMV 35S promoter. Confocal microscopy observation showed that the intensity of green fluorescence was corresponding to that of qRT-PCR.

CONCLUSIONS

Our data clearly showed that BBTV was able to control the transcriptional level of each DNA component independently by through the promoter sequences in the intergenic region. Moreover, a cis-acting element from DNA-N component had a high transcriptional activity.

摘要

背景

香蕉束顶病毒(BBTV)的基因组由至少六个环状、单链 DNA 组成,长度约为 1kb。一些 BBTV 分离株还可能携带卫星 DNA 分子,但这些分子对 BBTV 感染不是必需的。多组分 DNA 病毒的复制与其转录水平之间的关系及其潜在机制仍不清楚。

结果

为了了解多个基因组成分的协调复制和转录,我们通过实时 PCR(qPCR)测量了每个 BBTV DNA 成分的绝对量,并通过 RNAseq 和反转录 qPCR(qRT-PCR)确定了它们的转录水平。发现单个 BBTV 基因组成分的绝对量存在显著差异。从 RNAseq 数据获得的每个 BBTV 基因组成分的转录水平与从 qRT-PCR 获得的转录水平非常吻合,但与每个 DNA 成分的绝对量不对应。转录物与 DNA 拷贝的比值范围为 46.21 至 1059.44%,这可能受到每个成分基因间区启动子区域的调节。为了进一步确定这一推测,我们构建了 DNA-S、-M 或 -N 的启动子区域,通过农杆菌介导的转化方法将其上游构建到绿色荧光蛋白(GFP)基因上进行瞬时表达。qRT-PCR 显示,DNA-N 启动子的转录活性最高,与 CaMV 35S 启动子相比,活性约为 386.58%。共聚焦显微镜观察表明,绿色荧光的强度与 qRT-PCR 的结果相对应。

结论

我们的数据清楚地表明,BBTV 能够通过基因间区的启动子序列独立地控制每个 DNA 成分的转录水平。此外,来自 DNA-N 成分的顺式作用元件具有较高的转录活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f73d/6625112/9293b9fc1a19/12864_2019_5901_Fig1_HTML.jpg

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