TY - JOUR
T1 - Plastome Structural Evolution and Homoplastic Inversions in Neo-Astragalus (Fabaceae)
AU - Charboneau, Joseph L.M.
AU - Cronn, Richard C.
AU - Liston, Aaron
AU - Wojciechowski, Martin F.
AU - Sanderson, Michael J.
N1 - Funding Information:
This work was supported by the National Science Foundation (DEB 1601329 to J.L.M.C. and M.J.S.), the University of Arizona College of Science Galileo Circle (to J.L.M.C.), the American Philosophical Society Lewis and Clark Fund (to J.L.M.C.), the Botanical Society of America (to J.L.M.C.), Arizona State University (to M.F.W.), and the University of Arizona (to M.J.S.). Collecting permits were issued by the Bureau of Land Management (AZ, CA, ID, NV-Elko, UT, WY-Lander), the US Forest Service Southwestern Region, the Navajo Natural Heritage Program, and Zion National Park. Astragalus ampullarioides tissue was collected under a USFWS Permit issued to Zion NP. Michael Moore, Hilda Flores Olvera, Hilda Ochoterena, Ya Yang, Aaron Peretz, Emma Stewart, and Laura Schrage provided assistance in the field. We thank the herbarium staff of ARIZ, MIN, OSC, RM/USFS, and RSA for allowing destructive sampling of specimens. Lynna Nguyen and Wesley Wilcoxen provided assistance with the lab work, and J.L.M.C. wishes to thank Kristen Finch, Laura Hauck, Lucas Longway for their advice in the lab. Stephen Meyers provided the sequence data from A. agnicidus. We also thank Jason Steel and Joy Blain at the Arizona State University Genomic Facility and Mark Dasenko of the Oregon State University Center for Genome Research and Biocomputing. Some of this work was submitted by J.L.M.C. in partial fulfillment of the requirements for the Ph.D. at the University of Arizona, and he wishes to thank committee members Michael Barker, Mark Beilstein, Michelle McMahon, and John Wiens for their suggestions in shaping the study. We also thank two anonymous reviewers for their helpful comments on the manuscript.
Publisher Copyright:
© The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.
PY - 2021/10/1
Y1 - 2021/10/1
N2 - The plastid genomes of photosynthetic green plants have largely maintained conserved gene content and order as well as structure over hundreds of millions of years of evolution. Several plant lineages, however, have departed from this conservation and contain many plastome structural rearrangements, which have been associated with an abundance of repeated sequences both overall and near rearrangement endpoints. We sequenced the plastomes of 25 taxa of Astragalus L. (Fabaceae), a large genus in the inverted repeat-lacking clade of legumes, to gain a greater understanding of the connection between repeats and plastome inversions. We found plastome repeat structure has a strong phylogenetic signal among these closely related taxa mostly in the New World clade of Astragalus called Neo-Astragalus. Taxa without inversions also do not differ substantially in their overall repeat structure from four taxa each with one large-scale inversion. For two taxa with inversion endpoints between the same pairs of genes, differences in their exact endpoints indicate the inversions occurred independently. Our proposed mechanism for inversion formation suggests the short inverted repeats now found near the endpoints of the four inversions may be there as a result of these inversions rather than their cause. The longer inverted repeats now near endpoints may have allowed the inversions first mediated by shorter microhomologous sequences to propagate, something that should be considered in explaining how any plastome rearrangement becomes fixed regardless of the mechanism of initial formation.
AB - The plastid genomes of photosynthetic green plants have largely maintained conserved gene content and order as well as structure over hundreds of millions of years of evolution. Several plant lineages, however, have departed from this conservation and contain many plastome structural rearrangements, which have been associated with an abundance of repeated sequences both overall and near rearrangement endpoints. We sequenced the plastomes of 25 taxa of Astragalus L. (Fabaceae), a large genus in the inverted repeat-lacking clade of legumes, to gain a greater understanding of the connection between repeats and plastome inversions. We found plastome repeat structure has a strong phylogenetic signal among these closely related taxa mostly in the New World clade of Astragalus called Neo-Astragalus. Taxa without inversions also do not differ substantially in their overall repeat structure from four taxa each with one large-scale inversion. For two taxa with inversion endpoints between the same pairs of genes, differences in their exact endpoints indicate the inversions occurred independently. Our proposed mechanism for inversion formation suggests the short inverted repeats now found near the endpoints of the four inversions may be there as a result of these inversions rather than their cause. The longer inverted repeats now near endpoints may have allowed the inversions first mediated by shorter microhomologous sequences to propagate, something that should be considered in explaining how any plastome rearrangement becomes fixed regardless of the mechanism of initial formation.
KW - chloroplast
KW - inverted repeat-lacking clade
KW - legumes
KW - microhomology-mediated rearrangements
KW - plastid genome
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U2 - 10.1093/gbe/evab215
DO - 10.1093/gbe/evab215
M3 - Article
C2 - 34534296
AN - SCOPUS:85118096461
SN - 1759-6653
VL - 13
JO - Genome Biology and Evolution
JF - Genome Biology and Evolution
IS - 10
M1 - evab215
ER -