Evidence map›Paper›PMID 33547390›Full record

ArticleScientific reports2021

Complete chloroplast genomes shed light on phylogenetic relationships, divergence time, and biogeography of Allioideae (Amaryllidaceae).

Ju Namgung, Hoang Dang Khoa Do, Changkyun Kim, Hyeok Jae Choi, Joo-Hwan Kim

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Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

24 citing papers in PubMed.

  1. Article
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  3. Review
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  8. Decoding the Chloroplast Genome ofInternational journal of molecular sciences · 2024
    Article
  9. Article
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  11. Article
  12. The complete chloroplast genomes ofMitochondrial DNA. Part B, Resources · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Comparative chloroplast genome analysis ofFrontiers in plant science · 2023
    Article
  17. Article
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ju Namgung *Department of Life Science, Gachon University, Seongnam, 13120, Republic of Korea.
Hoang Dang Khoa Do *Department of Life Science, Gachon University, Seongnam, 13120, Republic of Korea.
Changkyun KimDepartment of Life Science, Gachon University, Seongnam, 13120, Republic of Korea.
Hyeok Jae ChoiDepartment of Biology and Chemistry, Changwon National University, Gyeongsangnamdo, 51140, Republic of Korea.
Joo-Hwan KimDepartment of Life Science, Gachon University, Seongnam, 13120, Republic of Korea. kimjh2009@gachon.ac.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allioideae includes economically important bulb crops such as garlic, onion, leeks, and some ornamental plants in Amaryllidaceae. Here, we reported the complete chloroplast genome (cpDNA) sequences of 17 species of Allioideae, five of Amaryllidoideae, and one of Agapanthoideae. These cpDNA sequences represent 80 protein-coding, 30 tRNA, and four rRNA genes, and range from 151,808 to 159,998 bp in length. Loss and pseudogenization of multiple genes (i.e., rps2, infA, and rpl22) appear to have occurred multiple times during the evolution of Alloideae. Additionally, eight mutation hotspots, including rps15-ycf1, rps16-trnQ-UUG, petG-trnW-CCA, psbA upstream, rpl32-trnL-UAG, ycf1, rpl22, matK, and ndhF, were identified in the studied Allium species. Additionally, we present the first phylogenomic analysis among the four tribes of Allioideae based on 74 cpDNA coding regions of 21 species of Allioideae, five species of Amaryllidoideae, one species of Agapanthoideae, and five species representing selected members of Asparagales. Our molecular phylogenomic results strongly support the monophyly of Allioideae, which is sister to Amaryllioideae. Within Allioideae, Tulbaghieae was sister to Gilliesieae-Leucocoryneae whereas Allieae was sister to the clade of Tulbaghieae- Gilliesieae-Leucocoryneae. Molecular dating analyses revealed the crown age of Allioideae in the Eocene (40.1 mya) followed by differentiation of Allieae in the early Miocene (21.3 mya). The split of Gilliesieae from Leucocoryneae was estimated at 16.5 mya. Biogeographic reconstruction suggests an African origin for Allioideae and subsequent spread to Eurasia during the middle Eocene. Cool and arid conditions during the late Eocene led to isolation between African and Eurasian species. African Allioideae may have diverged to South American taxa in the late Oligocene. Rather than vicariance, long-distance dispersal is the most likely explanation for intercontinental distribution of African and South American Allioideae species.

Indexed as

Genome, ChloroplastAmaryllidaceaeDNA, PlantEvolution, MolecularPhylogenyRNA, PlantDNA, PlantRNA, Plant

Identifiers

PMID33547390
PMCPMC7865063

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