Structural plastome evolution in holoparasitic Hydnoraceae with special focus on inverted and direct repeats.

Plastome condensation during adaptation to a heterotrophic lifestyle is generally well understood and lineage-independent models have been derived. However, understanding the evolutionary trajectories of comparatively old heterotrophic lineages, that are on the cusp of a minimal plastomes, is essential to complement and expand current knowledge. We study Hydnoraceae, one of the oldest and least investigated parasitic angiosperm lineages. Plastome comparative genomics, using seven out of eight known species of the genus Hydnora and three species of Prosopanche, reveal a high degree of structural similarity and shared gene content; contrasted by striking dissimilarities with respect to repeat content (inverted and direct repeats). We identified varying IR content and positions, likely resulting from multiple, independent evolutionary events and a direct repeat gain in Prosopanche. Considering different evolutionary trajectories and based on a fully resolved and supported species-level phylogenetic hypothesis, we describe three possible, distinct models to explain the Hydnoraceae plastome states. For comparative purposes we also report the first plastid genomes for the closely related autotrophic genera Lactoris (Lactoridaceae) and Thottea (Aristolochiaceae).

[1]  J. Mariath,et al.  Prosopanche cocuccii (Hydnoraceae): a new species from Southern Brazil , 2021, Phytotaxa.

[2]  Shuang Wu,et al.  Extensive genomic rearrangements mediated by repetitive sequences in plastomes of Medicago and its relatives , 2021, BMC plant biology.

[3]  S. Graham,et al.  Discordant Phylogenomic Placement of Hydnoraceae and Lactoridaceae Within Piperales Using Data From All Three Genomes , 2021, Frontiers in Plant Science.

[4]  H. T. Luu,et al.  Comparative Analysis of Plastid Genomes in the Non-photosynthetic Genus Thismia Reveals Ongoing Gene Set Reduction , 2021, Frontiers in Plant Science.

[5]  Timothy B Sackton,et al.  Deeply Altered Genome Architecture in the Endoparasitic Flowering Plant Sapria himalayana Griff. (Rafflesiaceae) , 2021, Current Biology.

[6]  Jun-bo Yang,et al.  The Loss of the Inverted Repeat in the Putranjivoid Clade of Malpighiales , 2020, Frontiers in Plant Science.

[7]  M. Jost,et al.  The First Plastid Genome of the Holoparasitic Genus Prosopanche (Hydnoraceae) , 2020, Plants.

[8]  T. Yi,et al.  Plastome Reduction in the Only Parasitic Gymnosperm Parasitaxus Is Due to Losses of Photosynthesis but Not Housekeeping Genes and Apparently Involves the Secondary Gain of a Large Inverted Repeat , 2019, Genome biology and evolution.

[9]  F. González,et al.  Plastome reduction and gene content in New World Pilostyles (Apodanthaceae) unveils high similarities to African and Australian congeners. , 2019, Molecular phylogenetics and evolution.

[10]  Patricia P. Chan,et al.  tRNAscan-SE 2.0: improved detection and functional classification of transfer RNA genes , 2019, bioRxiv.

[11]  R. Bock,et al.  OrganellarGenomeDRAW (OGDRAW) version 1.3.1: expanded toolkit for the graphical visualization of organellar genomes , 2019, bioRxiv.

[12]  Jeffrey P. Mower,et al.  Lycophyte plastid genomics: extreme variation in GC, gene and intron content and multiple inversions between a direct and inverted orientation of the rRNA repeat , 2019, The New phytologist.

[13]  J. Palmer,et al.  Novel genetic code and record-setting AT-richness in the highly reduced plastid genome of the holoparasitic plant Balanophora , 2018, Proceedings of the National Academy of Sciences of the United States of America.

[14]  G. Petersen,et al.  Genome Reports: Contracted Genes and Dwarfed Plastome in Mycoheterotrophic Sciaphila thaidanica (Triuridaceae, Pandanales) , 2018, Genome biology and evolution.

[15]  J. Bolin,et al.  Hydnora arabica (Aristolochiaceae), a new species from the Arabian Peninsula and a key to Hydnora. , 2018 .

[16]  Jeffrey P. Mower,et al.  Structural Diversity Among Plastid Genomes of Land Plants , 2018 .

[17]  Uwe Scholz,et al.  MISA-web: a web server for microsatellite prediction , 2017, Bioinform..

[18]  Tracey A Ruhlman,et al.  Expansion of inverted repeat does not decrease substitution rates in Pelargonium plastid genomes. , 2017, The New phytologist.

[19]  S. Graham,et al.  Plastomes on the edge: the evolutionary breakdown of mycoheterotroph plastid genomes. , 2017, The New phytologist.

[20]  Robert Lanfear,et al.  PartitionFinder 2: New Methods for Selecting Partitioned Models of Evolution for Molecular and Morphological Phylogenetic Analyses. , 2016, Molecular biology and evolution.

[21]  Chung-Shien Wu,et al.  Large-Scale Comparative Analysis Reveals the Mechanisms Driving Plastomic Compaction, Reduction, and Inversions in Conifers II (Cupressophytes) , 2016, Genome biology and evolution.

[22]  P. Taberlet,et al.  Understanding the evolution of holoparasitic plants: the complete plastid genome of the holoparasite Cytinus hypocistis (Cytinaceae). , 2016, Annals of botany.

[23]  C. dePamphilis,et al.  Mechanistic model of evolutionary rate variation en route to a nonphotosynthetic lifestyle in plants , 2016, Proceedings of the National Academy of Sciences.

[24]  H. Daniell,et al.  Chloroplast genomes: diversity, evolution, and applications in genetic engineering , 2016, Genome Biology.

[25]  Jerrold I. Davis,et al.  Drastic reduction of plastome size in the mycoheterotrophic Thismia tentaculata relative to that of its autotrophic relative Tacca chantrieri. , 2016, American journal of botany.

[26]  Jeffrey P. Mower,et al.  Variable presence of the inverted repeat and plastome stability in Erodium. , 2016, Annals of botany.

[27]  Jeffrey P. Mower,et al.  Evolutionary dynamics of the plastid inverted repeat: the effects of expansion, contraction, and loss on substitution rates. , 2016, The New phytologist.

[28]  Sarah T. Wagner,et al.  Detecting and Characterizing the Highly Divergent Plastid Genome of the Nonphotosynthetic Parasitic Plant Hydnora visseri (Hydnoraceae) , 2016, Genome biology and evolution.

[29]  Susanne S. Renner,et al.  The Plastomes of Two Species in the Endoparasite Genus Pilostyles (Apodanthaceae) Each Retain Just Five or Six Possibly Functional Genes , 2015, Genome biology and evolution.

[30]  M. Sanderson,et al.  Exceptional reduction of the plastid genome of saguaro cactus (Carnegiea gigantea): Loss of the ndh gene suite and inverted repeat. , 2015, American journal of botany.

[31]  M. Logacheva,et al.  Exploring the Limits for Reduction of Plastid Genomes: A Case Study of the Mycoheterotrophic Orchids Epipogium aphyllum and Epipogium roseum , 2015, Genome biology and evolution.

[32]  Anders Larsson,et al.  AliView: a fast and lightweight alignment viewer and editor for large datasets , 2014, Bioinform..

[33]  Rachel S. Meyer,et al.  Possible Loss of the Chloroplast Genome in the Parasitic Flowering Plant Rafflesia lagascae (Rafflesiaceae) , 2014, Molecular biology and evolution.

[34]  Alexandros Stamatakis,et al.  RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies , 2014, Bioinform..

[35]  R. Lanfear,et al.  Selecting optimal partitioning schemes for phylogenomic datasets , 2014, BMC Evolutionary Biology.

[36]  C. Neinhuis,et al.  Single-Copy Nuclear Genes Place Haustorial Hydnoraceae within Piperales and Reveal a Cretaceous Origin of Multiple Parasitic Angiosperm Lineages , 2013, PloS one.

[37]  Yan Zhang,et al.  Mechanisms of Functional and Physical Genome Reduction in Photosynthetic and Nonphotosynthetic Parasitic Plants of the Broomrape Family[W][OPEN] , 2013, Plant Cell.

[38]  Paul D. Shaw,et al.  Using Tablet for visual exploration of second-generation sequencing data , 2013, Briefings Bioinform..

[39]  K. Katoh,et al.  MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability , 2013, Molecular biology and evolution.

[40]  Jerrold I. Davis,et al.  The plastid genome of the mycoheterotrophic Corallorhiza striata (Orchidaceae) is in the relatively early stages of degradation. , 2012, American journal of botany.

[41]  Gaurav Vaidya,et al.  SequenceMatrix: concatenation software for the fast assembly of multi‐gene datasets with character set and codon information , 2011, Cladistics : the international journal of the Willi Hennig Society.

[42]  Kai F. Müller,et al.  The evolution of the plastid chromosome in land plants: gene content, gene order, gene function , 2011, Plant Molecular Biology.

[43]  Ching-Ping Lin,et al.  Comparative Chloroplast Genomes of Pinaceae: Insights into the Mechanism of Diversified Genomic Organizations , 2011, Genome biology and evolution.

[44]  Mitchell J. Sullivan,et al.  Easyfig: a genome comparison visualizer , 2011, Bioinform..

[45]  Mark A. Miller,et al.  Creating the CIPRES Science Gateway for inference of large phylogenetic trees , 2010, 2010 Gateway Computing Environments Workshop (GCE).

[46]  N. Brisson,et al.  Recombination and the maintenance of plant organelle genome stability. , 2010, The New phytologist.

[47]  Ben C. Stöver,et al.  TreeGraph 2: Combining and visualizing evidence from different phylogenetic analyses , 2010, BMC Bioinformatics.

[48]  J. Leebens-Mack,et al.  Parallel Loss of Plastid Introns and Their Maturase in the Genus Cuscuta , 2009, PloS one.

[49]  J. Bolin Ecology and molecular phylogenetics of Hydnora (Hydnoraceae) in southern Africa , 2009 .

[50]  R. Jansen,et al.  Complete plastid genome sequence of the chickpea (Cicer arietinum) and the phylogenetic distribution of rps12 and clpP intron losses among legumes (Leguminosae). , 2008, Molecular phylogenetics and evolution.

[51]  James Leebens-Mack,et al.  Analysis of 81 genes from 64 plastid genomes resolves relationships in angiosperms and identifies genome-scale evolutionary patterns , 2007, Proceedings of the National Academy of Sciences.

[52]  J. Leebens-Mack,et al.  Complete plastid genome sequences of Drimys, Liriodendron, and Piper: implications for the phylogenetic relationships of magnoliids , 2006, BMC Evolutionary Biology.

[53]  M. Chase,et al.  Parallel Loss of a Slowly Evolving Intron from Two Closely Related Families in Asparagales , 2004 .

[54]  J. Palmer,et al.  Chloroplast DNA evolution among legumes: Loss of a large inverted repeat occurred prior to other sequence rearrangements , 2004, Current Genetics.

[55]  K. Katoh,et al.  MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform. , 2002, Nucleic acids research.

[56]  G. Benson,et al.  Tandem repeats finder: a program to analyze DNA sequences. , 1999, Nucleic acids research.

[57]  S. Downie,et al.  Multiple Independent Losses of the rpoC1 Intron in Angiosperm Chloroplast DNA's , 1996 .

[58]  G. Link,et al.  RNA-binding activity of the matK protein encoded by the chloroplast trnK intron from mustard (Sinapis alba L.). , 1995, Nucleic acids research.

[59]  J. B. Walsh,et al.  Biased gene conversion, copy number, and apparent mutation rate differences within chloroplast and bacterial genomes. , 1992, Genetics.

[60]  D. Soltis,et al.  SIX INDEPENDENT LOSSES OF THE CHLOROPLAST DNA rpl2 INTRON IN DICOTYLEDONS: MOLECULAR AND PHYLOGENETIC IMPLICATIONS , 1991, Evolution; international journal of organic evolution.

[61]  J. Palmer,et al.  EVOLUTIONARY SIGNIFICANCE OF THE LOSS OF THE CHLOROPLAST‐DNA INVERTED REPEAT IN THE LEGUMINOSAE SUBFAMILY PAPILIONOIDEAE , 1990, Evolution; international journal of organic evolution.

[62]  L. Musselman,et al.  Taxonomy and Natural History of Hydnora (Hydnoraceae) , 1989 .

[63]  J. Palmer,et al.  Comparative organization of chloroplast genomes. , 1985, Annual review of genetics.

[64]  J. Palmer,et al.  Chloroplast DNA rearrangements are more frequent when a large inverted repeat sequence is lost , 1982, Cell.

[65]  P. LuisD.Gómez,et al.  A new species of Prosopanche (Hydnoraceae) from Costa Rica , 1981 .

[66]  E. Pahlich,et al.  A rapid DNA isolation procedure for small quantities of fresh leaf tissue , 1980 .