TY - JOUR
T1 - Chromosomal speciation in the genomics era: disentangling phylogenetic evolution of rock-wallabies
AU - Potter, Sally
AU - Bragg, Jason
AU - Blom, Moses
AU - DEAKIN, Janine
AU - Kirkpatrick, Mark
AU - Eldridge, Mark
AU - Moritz, Craig
N1 - Funding Information:
This research was supported by an Australian Research Council Discovery Grant (DP160100187) as well as and ARC Laureate Fellowship awarded to CM (ARC FL110100104). We would like to thank the Australian Museum and South Australian Museum for samples. In addition, we would like to thank all the individuals that contributed tissues that were used in this study. We would like to thank Rachel O'Neill for access to the tammar wallaby genome. We thank Maxine Piggott for assistance with laboratory work. We would also like to thank members of the Moritz and Kirkpatrick labs for ongoing discussions relating to this study, in particular Josh Penalba and Ana Silva for advice on analyses. We thank Ke Bi and Sonal Singhal for providing scripts and for discussions. This work used the ACRF Biomolecular Resource Facility at ANU.
Publisher Copyright:
© 2017 Potter, Bragg, Blom, Deakin, Kirkpatrick, Eldridge and Moritz.
PY - 2017/2/10
Y1 - 2017/2/10
N2 - The association of chromosome rearrangements (CRs) with speciation is well established, and there is a long history of theory and evidence relating to "chromosomal speciation." Genomic sequencing has the potential to provide new insights into how reorganization of genome structure promotes divergence, and in model systems has demonstrated reduced gene flow in rearranged segments. However, there are limits to what we can understand from a small number of model systems, which each only tell us about one episode of chromosomal speciation. Progressing from patterns of association between chromosome (and genic) change, to understanding processes of speciation requires both comparative studies across diverse systems and integration of genome-scale sequence comparisons with other lines of evidence. Here, we showcase a promising example of chromosomal speciation in a non-model organism, the endemic Australian marsupial genus Petrogale. We present initial phylogenetic results from exon-capture that resolve a history of divergence associated with extensive and repeated CRs. Yet it remains challenging to disentangle gene tree heterogeneity caused by recent divergence and gene flow in this and other such recent radiations. We outline a way forward for better integration of comparative genomic sequence data with evidence from molecular cytogenetics, and analyses of shifts in the recombination landscape and potential disruption of meiotic segregation and epigenetic programming. In all likelihood, CRs impact multiple cellular processes and these effects need to be considered together, along with effects of genic divergence. Understanding the effects of CRs together with genic divergence will require development of more integrative theory and inference methods. Together, new data and analysis tools will combine to shed light on long standing questions of how chromosome and genic divergence promote speciation.
AB - The association of chromosome rearrangements (CRs) with speciation is well established, and there is a long history of theory and evidence relating to "chromosomal speciation." Genomic sequencing has the potential to provide new insights into how reorganization of genome structure promotes divergence, and in model systems has demonstrated reduced gene flow in rearranged segments. However, there are limits to what we can understand from a small number of model systems, which each only tell us about one episode of chromosomal speciation. Progressing from patterns of association between chromosome (and genic) change, to understanding processes of speciation requires both comparative studies across diverse systems and integration of genome-scale sequence comparisons with other lines of evidence. Here, we showcase a promising example of chromosomal speciation in a non-model organism, the endemic Australian marsupial genus Petrogale. We present initial phylogenetic results from exon-capture that resolve a history of divergence associated with extensive and repeated CRs. Yet it remains challenging to disentangle gene tree heterogeneity caused by recent divergence and gene flow in this and other such recent radiations. We outline a way forward for better integration of comparative genomic sequence data with evidence from molecular cytogenetics, and analyses of shifts in the recombination landscape and potential disruption of meiotic segregation and epigenetic programming. In all likelihood, CRs impact multiple cellular processes and these effects need to be considered together, along with effects of genic divergence. Understanding the effects of CRs together with genic divergence will require development of more integrative theory and inference methods. Together, new data and analysis tools will combine to shed light on long standing questions of how chromosome and genic divergence promote speciation.
KW - Chromosome rearrangement
KW - Divergence
KW - Genomics
KW - Rock-wallaby
KW - Speciation
UR - http://www.scopus.com/inward/record.url?scp=85014608614&partnerID=8YFLogxK
U2 - 10.3389/fgene.2017.00010
DO - 10.3389/fgene.2017.00010
M3 - Article
SN - 1664-8021
VL - 8
SP - 1
EP - 18
JO - Frontiers in Genetics
JF - Frontiers in Genetics
IS - FEB
M1 - 10
ER -