De novo assembly and comparative analysis of the mitochondrial genome of Reynoutria japonica
Reynoutria japonica Houtt. is an important medical plant with a long history of thousands of years in China, however, its mitochondrial genome (mitogenome) has not been reported yet. In this work, we reported and analyzed the R. japonica mitogenome. The main results include: The R. japonica mitogeno...
Main Authors: | , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2023-11-01
|
Series: | Frontiers in Genetics |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fgene.2023.1289811/full |
_version_ | 1797493225414459392 |
---|---|
author | Jianhui Chen Hongping Ma Haili Fan Fan Lin Tuanyao Chai Hong Wang |
author_facet | Jianhui Chen Hongping Ma Haili Fan Fan Lin Tuanyao Chai Hong Wang |
author_sort | Jianhui Chen |
collection | DOAJ |
description | Reynoutria japonica Houtt. is an important medical plant with a long history of thousands of years in China, however, its mitochondrial genome (mitogenome) has not been reported yet. In this work, we reported and analyzed the R. japonica mitogenome. The main results include: The R. japonica mitogenome was 302,229 bp in length and encoded 48 genes, including 27 protein-coding genes (PCGs), 3 rRNA genes, and 18 tRNA genes. Repeat sequence analysis revealed that there were 54 repeat sequences ranging from 193 bp to 1,983 bp in the R. japonica mitogenome. Relative synonymous codon usage (RSCU) analysis showed that leucine (900, 11.01%) and serine (732, 8.96%) were the two most abundant amino acids, and the codons with RSCU values showed the preference of A or T ending when greater than 1. The RNA editing sites of PCGs in the R. japonica mitogenome were characterized, and 299 RNA editing sites were found. Extensive sequences transfer between mitochondrion and chloroplast were found in R. japonica, where 11 complete plastid-derived tRNA genes stayed intact in the R. japonica mitogenome. Three genes (ccmFC, cox1, and nad1) were seen to play essential roles in the evolution through selection pressure analysis. The phylogenetic analysis showed that Fallopia multiflora was the closest species with R. japonica, in consistency with the results of chloroplast genome. Overall, the current work presents the first mitogenome of R. japonica and could contribute to the phylogenetic analysis of the family Polygonaceae. |
first_indexed | 2024-03-10T01:16:58Z |
format | Article |
id | doaj.art-42f163113c5a4fd095ffe54fed1f1f6f |
institution | Directory Open Access Journal |
issn | 1664-8021 |
language | English |
last_indexed | 2024-03-10T01:16:58Z |
publishDate | 2023-11-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Genetics |
spelling | doaj.art-42f163113c5a4fd095ffe54fed1f1f6f2023-11-23T14:07:29ZengFrontiers Media S.A.Frontiers in Genetics1664-80212023-11-011410.3389/fgene.2023.12898111289811De novo assembly and comparative analysis of the mitochondrial genome of Reynoutria japonicaJianhui ChenHongping MaHaili FanFan LinTuanyao ChaiHong WangReynoutria japonica Houtt. is an important medical plant with a long history of thousands of years in China, however, its mitochondrial genome (mitogenome) has not been reported yet. In this work, we reported and analyzed the R. japonica mitogenome. The main results include: The R. japonica mitogenome was 302,229 bp in length and encoded 48 genes, including 27 protein-coding genes (PCGs), 3 rRNA genes, and 18 tRNA genes. Repeat sequence analysis revealed that there were 54 repeat sequences ranging from 193 bp to 1,983 bp in the R. japonica mitogenome. Relative synonymous codon usage (RSCU) analysis showed that leucine (900, 11.01%) and serine (732, 8.96%) were the two most abundant amino acids, and the codons with RSCU values showed the preference of A or T ending when greater than 1. The RNA editing sites of PCGs in the R. japonica mitogenome were characterized, and 299 RNA editing sites were found. Extensive sequences transfer between mitochondrion and chloroplast were found in R. japonica, where 11 complete plastid-derived tRNA genes stayed intact in the R. japonica mitogenome. Three genes (ccmFC, cox1, and nad1) were seen to play essential roles in the evolution through selection pressure analysis. The phylogenetic analysis showed that Fallopia multiflora was the closest species with R. japonica, in consistency with the results of chloroplast genome. Overall, the current work presents the first mitogenome of R. japonica and could contribute to the phylogenetic analysis of the family Polygonaceae.https://www.frontiersin.org/articles/10.3389/fgene.2023.1289811/fullReynoutria japonicamitogenomecodon usagerepeat sequencesRNA editingevolution |
spellingShingle | Jianhui Chen Hongping Ma Haili Fan Fan Lin Tuanyao Chai Hong Wang De novo assembly and comparative analysis of the mitochondrial genome of Reynoutria japonica Frontiers in Genetics Reynoutria japonica mitogenome codon usage repeat sequences RNA editing evolution |
title | De novo assembly and comparative analysis of the mitochondrial genome of Reynoutria japonica |
title_full | De novo assembly and comparative analysis of the mitochondrial genome of Reynoutria japonica |
title_fullStr | De novo assembly and comparative analysis of the mitochondrial genome of Reynoutria japonica |
title_full_unstemmed | De novo assembly and comparative analysis of the mitochondrial genome of Reynoutria japonica |
title_short | De novo assembly and comparative analysis of the mitochondrial genome of Reynoutria japonica |
title_sort | de novo assembly and comparative analysis of the mitochondrial genome of reynoutria japonica |
topic | Reynoutria japonica mitogenome codon usage repeat sequences RNA editing evolution |
url | https://www.frontiersin.org/articles/10.3389/fgene.2023.1289811/full |
work_keys_str_mv | AT jianhuichen denovoassemblyandcomparativeanalysisofthemitochondrialgenomeofreynoutriajaponica AT hongpingma denovoassemblyandcomparativeanalysisofthemitochondrialgenomeofreynoutriajaponica AT hailifan denovoassemblyandcomparativeanalysisofthemitochondrialgenomeofreynoutriajaponica AT fanlin denovoassemblyandcomparativeanalysisofthemitochondrialgenomeofreynoutriajaponica AT tuanyaochai denovoassemblyandcomparativeanalysisofthemitochondrialgenomeofreynoutriajaponica AT hongwang denovoassemblyandcomparativeanalysisofthemitochondrialgenomeofreynoutriajaponica |