scholarly journals Whole Genome Shotgun Phylogenomics Resolves the Pattern and Timing of Swallowtail Butterfly Evolution

2019 ◽  
Vol 69 (1) ◽  
pp. 38-60 ◽  
Author(s):  
Rémi Allio ◽  
Céline Scornavacca ◽  
Benoit Nabholz ◽  
Anne-Laure Clamens ◽  
Felix AH Sperling ◽  
...  

Abstract Evolutionary relationships have remained unresolved in many well-studied groups, even though advances in next-generation sequencing and analysis, using approaches such as transcriptomics, anchored hybrid enrichment, or ultraconserved elements, have brought systematics to the brink of whole genome phylogenomics. Recently, it has become possible to sequence the entire genomes of numerous nonbiological models in parallel at reasonable cost, particularly with shotgun sequencing. Here, we identify orthologous coding sequences from whole-genome shotgun sequences, which we then use to investigate the relevance and power of phylogenomic relationship inference and time-calibrated tree estimation. We study an iconic group of butterflies—swallowtails of the family Papilionidae—that has remained phylogenetically unresolved, with continued debate about the timing of their diversification. Low-coverage whole genomes were obtained using Illumina shotgun sequencing for all genera. Genome assembly coupled to BLAST-based orthology searches allowed extraction of 6621 orthologous protein-coding genes for 45 Papilionidae species and 16 outgroup species (with 32% missing data after cleaning phases). Supermatrix phylogenomic analyses were performed with both maximum-likelihood (IQ-TREE) and Bayesian mixture models (PhyloBayes) for amino acid sequences, which produced a fully resolved phylogeny providing new insights into controversial relationships. Species tree reconstruction from gene trees was performed with ASTRAL and SuperTriplets and recovered the same phylogeny. We estimated gene site concordant factors to complement traditional node-support measures, which strengthens the robustness of inferred phylogenies. Bayesian estimates of divergence times based on a reduced data set (760 orthologs and 12% missing data) indicate a mid-Cretaceous origin of Papilionoidea around 99.2 Ma (95% credibility interval: 68.6–142.7 Ma) and Papilionidae around 71.4 Ma (49.8–103.6 Ma), with subsequent diversification of modern lineages well after the Cretaceous-Paleogene event. These results show that shotgun sequencing of whole genomes, even when highly fragmented, represents a powerful approach to phylogenomics and molecular dating in a group that has previously been refractory to resolution.

2021 ◽  
Vol 160 (6) ◽  
pp. S-569
Author(s):  
Manoj Dadlani ◽  
Kelly Moffat ◽  
Huai Li ◽  
Xin Zhou ◽  
Rita Colwell

2011 ◽  
Vol 193 (19) ◽  
pp. 5553-5554 ◽  
Author(s):  
W. Ghosh ◽  
A. George ◽  
A. Agarwal ◽  
P. Raj ◽  
M. Alam ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (5) ◽  
pp. e0155362 ◽  
Author(s):  
Emily Vogtmann ◽  
Xing Hua ◽  
Georg Zeller ◽  
Shinichi Sunagawa ◽  
Anita Y. Voigt ◽  
...  

2012 ◽  
Vol 194 (5) ◽  
pp. 1264-1265 ◽  
Author(s):  
J. B. Prajapati ◽  
C. D. Khedkar ◽  
J. Chitra ◽  
S. Suja ◽  
V. Mishra ◽  
...  

F1000Research ◽  
2015 ◽  
Vol 4 ◽  
pp. 170 ◽  
Author(s):  
Ted Kalbfleisch ◽  
Pamela Brock ◽  
Angela Snow ◽  
Deborah Neklason ◽  
Gordon Gowans ◽  
...  

Recently, deletions have been identified and published as causal for Familial Adenomatous Polyposis in the 1B promoter region of the APC gene.  Those deletions were measured using multiplex ligation-dependent probe amplification.  Here, we present and characterize an ~11kb deletion identified by whole genome shotgun sequencing.  The deletion occurred in a patient diagnosed with Familial Adenomatous Polyposis, and was located on chr5, between bases 112,034,824 and 112,045,845, fully encompassing the 1B promoter region of the APC gene.   Results are presented here that include the sequence evidence supporting the presence of the deletion as well as base level characterization of the deletion site.  These results demonstrate the capacity of whole genome sequencing for the detection of large structural variants in single individuals.


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