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黑果腺肋花楸叶绿体全基因组的结构和比较分析及系统进化推断

  • 王传永 ,
  • 庄典 ,
  • 宋正达 ,
  • 翟恒华 ,
  • 张凡
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  • 1江苏省中国科学院植物研究所(南京中山植物园), 江苏省植物资源研究与利用重点实验室, 南京 210014; 2南京中医药大学, 南京 210023

收稿日期: 2024-09-24

  修回日期: 2025-01-22

  网络出版日期: 2025-02-10

Structural and Comparative Analysis of the Complete Chloroplast Genome and Phylogenetic Inference of the Aronia melanocarpa

  • YU Zhuan-Yong ,
  • ZHUANG Tian ,
  • SONG Zheng-Ta ,
  • DI Heng-Hua ,
  • ZHANG Fan
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  • 1Jiangsu Key Laboratory for the Research and Utilization of Plant Resources, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences, Nanjing Botanical Garden Mem. Sun Yat-Sen, Nanjing 210014, China; 2Nanjing University of Chinese Medicine, Nanjing 210023, China

Received date: 2024-09-24

  Revised date: 2025-01-22

  Online published: 2025-02-10

Supported by

新优植物品种引进及推广示范(No.FY2024013)

摘要

黑果腺肋花楸(Aronia melanocarpa)因其观赏价值和经济价值而闻名, 但其系统进化关系仍不明晰。该研究完成了黑果腺肋花楸叶绿体(cp)基因组的测序和分析, 并与13个蔷薇科物种的叶绿体基因组进行了比较分析。黑果腺肋花楸的cp基因组长为159 772 bp, 呈典型的四分结构; 其中大单拷贝区(LSC)长87 810 bp, 小单拷贝区(SSC)为19 200 bp, 中间含有2个26 381 bp的反向重复区(IRa和IRb)。注释到132个基因, 87个蛋白质编码基因、37个tRNA和8个rRNA。还检测到76个简单重复序列(SSR)和50个长重复序列。系统进化分析表明, 黑果腺肋花楸与红果腺肋花楸(A. arbutifolia)的亲缘关系最密切, 与榅桲(Cydonia oblonga)是姊妹支系。该文报道的基因组信息将为进一步研究黑果腺肋花楸的进化、种群遗传分析以及分子育种研究提供新的理论支持。

本文引用格式

王传永 , 庄典 , 宋正达 , 翟恒华 , 张凡 . 黑果腺肋花楸叶绿体全基因组的结构和比较分析及系统进化推断[J]. 植物学报, 0 : 1 -0 . DOI: 10.11983/CBB24146

Abstract

INTRODUCTION: Aronia melanocarpa (Michx.) Ell. also known as black chokeberry, belongs to the Aronia genus (Rosaceae family). The genus Aronia Medik. includes A. arbutifolia (L.) Pers. or red chokeberry and A. prunifolia (Marshall) Rehder or purple chokeberry, both of which are found in the wild in North American and an additional cultivated taxon, A. mitschurinii (A.K. Skvortsov and Maitul.) or Mitschurin’s chokeberry, originating from Europe. However, the species boundaries and relationships between species of Aronia are not clear. Moreover, the taxonomic history of Aronia is complex, as species of this genus have formerly been placed in numerous genera, such as Mespilus, Pyrus, Adenorachis, Sorbus, and Photinia. In the present study, we first sequenced and characterized the complete cp genome of A. melanocarpa and compared its sequence features with those of the cp genomes from 13 species of the family Rosaceae. The aims of this study were: (1) to increase our understanding of the structural patterns of complete cp genome of A. melanocarpa, (2) to determine the cp genome derived phylogenetic relationships of A. melanocarpa with other Rosaceae species. 

RATIONALE: The chloroplast (cp) is a core organelle in green plants with vital roles in photosynthesis and carbon fixation. Comparative analyses of cp genomes between different plant species reveal intra- and inter-species rearrangements that have occurred during evolution, such as IR contraction and expansion. Based on these characteristics, the cp genome has been wildly used for species identification, phylogenetic analysis, and exploring the genetic basis of environmental adaptation. 

 RESULTS: For the first time, the complete A. melanocarpa chloroplast (cp) genome was sequenced and analyzed. Chloroplast genomic DNA of A. melanocarpa was extracted and sequenced, analyzed, and compared with that from 13 other species in the Rosaceae family. The A. melanocarpa cp genome is 159 772 bp; has a total guanine-cytosine (GC) content of 36.6%, and exhibits a typical quadripartite structure with four separate regions, including a large single-copy (LSC) region of 87,810 bp and a small single-copy (SSC) region of 19 200 bp separated by two inverted repeats (IRa and IRb) regions of 26,381 bp each. A total of 132 unique genes were annotated, including 87 protein-coding genes, 37 tRNAs, and eight rRNAs, with 22 duplicates in the IR regions. In total, 76 simple sequence repeats (SSRs) and 50 long repeats were detected. Phylogenetic analysis indicated that A. melanocarpa is most closely related to A. arbutifolia and forms a sister clade to Cydonia oblonga with weak support. 

CONCLUSION: In the present study, we analyzed the complete cp genome of A. melanocarpa by using Illumina high-throughput sequencing technology. The A. melanocarpa cp genome is 159 772 bp, and 132 genes were predicted, including 87 protein coding genes, 37 tRNAs, and eight rRNAs. A total of 76 SSRs and 50 long repeats were identified, which could be further used for the development of molecular markers. Highly variable regions such as trnK-rps16, rps16-trnQ, trnG-atpA, petN-psbM, trnT-psbD, psbZ-trnG, trnT-trnL, ndhC-trnV and accD-psaI were also detected in intergenic spaces, which might be useful for broad applications in genetic research studies as well as phylogenetic studies. Phylogenetic construction results strongly supported that A. melanocarpa was closest related to A. arbutifolia, followed by Cydonia oblonga with weak support. This newly available genomic data for A. melanocarpa will provide a basis for future research on the population genetics and phylogenomics and will benefit genus Aronia crossbreeding studies and utilization of the genus Aronia.

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