Plastome phylogeography in two African rain forest legume trees reveals that Dahomey Gap populations originate from the Cameroon volcanic line.

African rain forest Cameroon volcanic line Colonization origin Dahomey gap Phylogeography Plastid genome sequencing

Journal

Molecular phylogenetics and evolution
ISSN: 1095-9513
Titre abrégé: Mol Phylogenet Evol
Pays: United States
ID NLM: 9304400

Informations de publication

Date de publication:
09 2020
Historique:
received: 02 10 2019
revised: 08 05 2020
accepted: 13 05 2020
pubmed: 23 5 2020
medline: 18 11 2020
entrez: 23 5 2020
Statut: ppublish

Résumé

Paleo-environmental data show that the distribution of African rain forests was affected by Quaternary climate changes. In particular, the Dahomey Gap (DG) - a 200 km wide savanna corridor currently separating the West African and Central African rain forest blocks and containing relict rain forest fragments - was forested during the mid-Holocene and possibly during previous interglacial periods, whereas it was dominated by open vegetation (savanna) during glacial periods. Genetic signatures of past population fragmentation and demographic changes have been found in some African forest plant species using nuclear markers, but such events appear not to have been synchronous or shared across species. To better understand the colonization history of the DG by rain forest trees through seed dispersal, the plastid genomes of two widespread African forest legume trees, Anthonotha macrophylla and Distemonanthus benthamianus, were sequenced in 47 individuals for each species, providing unprecedented phylogenetic resolution of their maternal lineages (857 and 115 SNPs, respectively). Both species exhibit distinct lineages separating three regions: 1. Upper Guinea (UG, i.e. the West African forest block), 2. the area ranging from the DG to the Cameroon volcanic line (CVL), and 3. Lower Guinea (LG, the western part of the Central African forest block) where three lineages co-occur. In both species, the DG populations (including southern Nigeria west of Cross River) exhibit much lower genetic diversity than UG and LG populations, and their plastid lineages originate from the CVL, confirming the role of the CVL as an ancient forest refuge. Despite the similar phylogeographic structures displayed by A. macrophylla and D. benthamianus, molecular dating indicates very contrasting ages of lineage divergence (UG diverged from LG since c. 7 Ma and 0.7 Ma, respectively) and DG colonization (probably following the Mid Pleistocene Transition and the Last Glacial Maximum, respectively). The stability of forest refuge areas and repeated similar forest shrinking/expanding events during successive glacial periods might explain why similar phylogeographic patterns can be generated over contrasting timescales.

Identifiants

pubmed: 32439485
pii: S1055-7903(20)30126-3
doi: 10.1016/j.ympev.2020.106854
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

106854

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Boris B Demenou (BB)

Evolution Biologique et Ecologie, Université Libre de Bruxelles, Faculté des Sciences, CP160/12, Av. F. D. Roosevelt 50, BE-1050 Brussels, Belgium. Electronic address: bdemenou@ulb.ac.be.

Jérémy Migliore (J)

Evolution Biologique et Ecologie, Université Libre de Bruxelles, Faculté des Sciences, CP160/12, Av. F. D. Roosevelt 50, BE-1050 Brussels, Belgium.

Myriam Heuertz (M)

BIOGECO, INRA, Univ. Bordeaux, F-33610 Cestas, France.

Franck K Monthe (FK)

Evolution Biologique et Ecologie, Université Libre de Bruxelles, Faculté des Sciences, CP160/12, Av. F. D. Roosevelt 50, BE-1050 Brussels, Belgium.

Dario I Ojeda (DI)

Evolution Biologique et Ecologie, Université Libre de Bruxelles, Faculté des Sciences, CP160/12, Av. F. D. Roosevelt 50, BE-1050 Brussels, Belgium; Norwegian Institute of Bioeconomy Research, Høgskoleveien 8, 1433 Ås, Norway.

Jan J Wieringa (JJ)

Naturalis Biodiversity Center, National Herbarium of the Netherlands, Darwinweg 2, 2300 RA Leiden, the Netherlands; Wageningen University & Research, Biosystematics Group, Droevendaalsesteeg 1, 6708 PB Wageningen, the Netherlands.

Gilles Dauby (G)

Evolution Biologique et Ecologie, Université Libre de Bruxelles, Faculté des Sciences, CP160/12, Av. F. D. Roosevelt 50, BE-1050 Brussels, Belgium; AMAP Lab, IRD, CNRS, INRA, Univ Montpellier, Montpellier, France.

Laura Albreht (L)

Evolution Biologique et Ecologie, Université Libre de Bruxelles, Faculté des Sciences, CP160/12, Av. F. D. Roosevelt 50, BE-1050 Brussels, Belgium.

Arthur Boom (A)

Evolution Biologique et Ecologie, Université Libre de Bruxelles, Faculté des Sciences, CP160/12, Av. F. D. Roosevelt 50, BE-1050 Brussels, Belgium.

Olivier J Hardy (OJ)

Evolution Biologique et Ecologie, Université Libre de Bruxelles, Faculté des Sciences, CP160/12, Av. F. D. Roosevelt 50, BE-1050 Brussels, Belgium.

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