a College of Life Sciences , Nankai University , Tianjin , P.R.China.
b State Key Laboratory of Veterinary Etiological Biology and Key Laboratory of Veterinary Parasitology of Gansu Province, Lanzhou Veterinary Research Institute , Chinese Academy of Agricultural Science , Lanzhou , P.R.China.
RNA Biol. 2019 Jun;16(6):830-837. doi: 10.1080/15476286.2019.1591035. Epub 2019 Mar 19.
In this study, we used a small RNA sequencing (sRNA-seq) based method to annotate the mitochondrial genome of the insect Erthesina fullo Thunberg at 1 bp resolution. The high-resolution annotations cover both entire strands of the mitochondrial genome without any gaps or overlaps. Most of the new annotations were consistent with the previous annotations which had been obtained using PacBio full-length transcripts. Two important findings were that animals transcribe both entire strands of mitochondrial genomes and the tandem repeats in the control region of the E. fullo mitochondrial genome contains the repeated Transcription Initiation Sites (TISs) of the heavy strand. In addition, we found that the copy numbers of tandem repeats showed a great diversity within an individual, suggesting that mitochondrial DNA recombination occurs in an individual. In conclusion, the sRNA-seq based method uses 5' and 3' end small RNAs to annotate nuclear non-coding and mitochondrial genes at 1 bp resolution, and can be used to identify new steady RNAs, particularly long non-coding RNAs (lncRNAs). The high-resolution annotations of mitochondrial genomes can also be used to study the molecular phylogenetics and evolution of animals or to investigate mitochondrial gene transcription, RNA processing, RNA maturation and several other related topics. The complete mitochondrial genome sequence of E. fullo with the new annotations using the sRNA-seq based method is available at the NCBI GenBank database under the accession number MK374364. We publish our theories, methods, the high quality sRNA-seq and RNA-seq data (SRA: SRP174926) for extensive use.
在本研究中,我们使用基于小 RNA 测序(sRNA-seq)的方法,以 1bp 的分辨率注释昆虫满州黄脊萤的线粒体基因组。高分辨率注释涵盖了线粒体基因组的两条完整链,没有任何间隙或重叠。大多数新注释与之前使用 PacBio 全长转录本获得的注释一致。两个重要的发现是,动物转录两条完整的线粒体基因组链,并且 E. fullo 线粒体基因组控制区的串联重复包含重链的重复转录起始位点(TIS)。此外,我们发现串联重复的拷贝数在个体内表现出很大的多样性,这表明线粒体 DNA 重组发生在个体内。总之,基于 sRNA-seq 的方法使用 5'和 3'端小 RNA 以 1bp 的分辨率注释核非编码和线粒体基因,并可用于鉴定新的稳定 RNA,特别是长非编码 RNA(lncRNA)。线粒体基因组的高分辨率注释也可用于研究动物的分子系统发育和进化,或研究线粒体基因转录、RNA 处理、RNA 成熟和其他几个相关主题。使用基于 sRNA-seq 的方法对 E. fullo 进行注释后的完整线粒体基因组序列可在 NCBI GenBank 数据库中获得,登录号为 MK374364。我们发表了我们的理论、方法、高质量的 sRNA-seq 和 RNA-seq 数据(SRA:SRP174926),以供广泛使用。