Evidence map›Paper›PMID 42469633›Full record

ArticleBMC plant biology2026

Comparative analysis of the complete mitochondrial and chloroplast genomes of Krascheninnikovia arborescens reveals its evolutionary features in Amaranthaceae.

Mingliang Wang, Mengyue Wang, Jialu Liang, Yuying Han, Ruifeng Yang, Meilin Yang, Dongyi Ma, Jinglong Li, Chien-Hsun Huang

Abstract readComparative Study
In one paragraph

Article in BMC plant biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Mingliang WangState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, Key Laboratory of Herbage & Endemic Crop Biology, Ministry of Education, Inner Mongolia Engineering Technology Research Center of Germplasm Resources Conservation and Utilization, School of Life Sciences, Inner Mongolia University, Hohhot, 010000, China.
Mengyue WangState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, Key Laboratory of Herbage & Endemic Crop Biology, Ministry of Education, Inner Mongolia Engineering Technology Research Center of Germplasm Resources Conservation and Utilization, School of Life Sciences, Inner Mongolia University, Hohhot, 010000, China.
Jialu LiangInner Mongolia Key Laboratory of Grassland Ecology and the Candidate State Key Laboratory of Ministry of Science and Technology, Inner Mongolia University, Hohhot, 010010, China.
Yuying HanState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, Key Laboratory of Herbage & Endemic Crop Biology, Ministry of Education, Inner Mongolia Engineering Technology Research Center of Germplasm Resources Conservation and Utilization, School of Life Sciences, Inner Mongolia University, Hohhot, 010000, China.
Ruifeng YangState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, Key Laboratory of Herbage & Endemic Crop Biology, Ministry of Education, Inner Mongolia Engineering Technology Research Center of Germplasm Resources Conservation and Utilization, School of Life Sciences, Inner Mongolia University, Hohhot, 010000, China.
Meilin YangState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, Key Laboratory of Herbage & Endemic Crop Biology, Ministry of Education, Inner Mongolia Engineering Technology Research Center of Germplasm Resources Conservation and Utilization, School of Life Sciences, Inner Mongolia University, Hohhot, 010000, China.
Dongyi MaState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, Key Laboratory of Herbage & Endemic Crop Biology, Ministry of Education, Inner Mongolia Engineering Technology Research Center of Germplasm Resources Conservation and Utilization, School of Life Sciences, Inner Mongolia University, Hohhot, 010000, China.
Jinglong LiState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, Key Laboratory of Herbage & Endemic Crop Biology, Ministry of Education, Inner Mongolia Engineering Technology Research Center of Germplasm Resources Conservation and Utilization, School of Life Sciences, Inner Mongolia University, Hohhot, 010000, China. ljl6528@163.com.
Chien-Hsun HuangState Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, Key Laboratory of Herbage & Endemic Crop Biology, Ministry of Education, Inner Mongolia Engineering Technology Research Center of Germplasm Resources Conservation and Utilization, School of Life Sciences, Inner Mongolia University, Hohhot, 010000, China. chhuang1981@139.com.ORCID http://orcid.org/0000-0002-4331-9041

Funding

the National Natural Science Foundation of China 32270232, 31970224, 31770242the Natural Science Foundation of Inner Mongolia Autonomous Region 2025MS03078
6 · The paper itself

Abstract

backgroundKrascheninnikovia arborescens is a drought-tolerant subshrub of the Amaranthaceae family that is endemic to China and plays an important role in desert ecosystems. However, little is known about the structure and evolutionary dynamics of its organellar genomes. In this study, we assembled and characterized the mitochondrial and chloroplast genomes of K. arborescens using long-read sequencing data.

resultsThe mitochondrial genome was assembled as a master circular genome representation of 387,891 bp and contains 62 annotated genes, whereas the chloroplast genome exhibits a typical quadripartite structure of 152,039 bp with 90 genes. The mitochondrial genome harbors abundant repetitive sequences and multiple plastid-derived insertions, indicating a dynamic structural organization. In contrast, gene content remains highly conserved, and all core protein-coding genes show signatures of purifying selection, particularly those involved in ATP synthesis and respiratory metabolism. Predicted RNA editing sites differ substantially between the two organelles, suggesting distinct post-transcriptional modification patterns. Phylogenetic analyses based on shared organellar genes consistently place K. arborescens within Amaranthaceae and support its evolutionary relationships within Caryophyllales. These results reveal a combination of structural dynamism and functional conservation in the organellar genomes of K. arborescens.

conclusionThis study provides a foundation for future comparative and evolutionary studies of Amaranthaceae and expands genomic resources for this family.

Indexed as

AmaranthaceaeEvolution, MolecularGenome, ChloroplastGenome, MitochondrialPhylogenyRNA EditingChloroplast genomeDNA transferKrascheninnikovia arborescensMitochondrial genomePhylogenetic evolution

Identifiers

PMID42469633
PMCPMC13659944

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