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Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate evolution

Rhesus macaque is an Old World monkey that shared a common ancestor with human ∼25 Myr ago and is an important animal model for human disease studies. A deep understanding of its genetics is therefore required for both biomedical and evolutionary studies. Among structural variants, inversions repres...

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Published in:Genome research 2020-11, Vol.30 (11), p.1680-1693
Main Authors: Maggiolini, Flavia Angela Maria, Sanders, Ashley D, Shew, Colin James, Sulovari, Arvis, Mao, Yafei, Puig, Marta, Catacchio, Claudia Rita, Dellino, Maria, Palmisano, Donato, Mercuri, Ludovica, Bitonto, Miriana, Porubský, David, Cáceres, Mario, Eichler, Evan E, Ventura, Mario, Dennis, Megan Y, Korbel, Jan O, Antonacci, Francesca
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cited_by cdi_FETCH-LOGICAL-c415t-b5a4cfaf2b747336a02eec7a6db9937d724cfdd6a758f9cfd0318d5e0058215a3
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container_title Genome research
container_volume 30
creator Maggiolini, Flavia Angela Maria
Sanders, Ashley D
Shew, Colin James
Sulovari, Arvis
Mao, Yafei
Puig, Marta
Catacchio, Claudia Rita
Dellino, Maria
Palmisano, Donato
Mercuri, Ludovica
Bitonto, Miriana
Porubský, David
Cáceres, Mario
Eichler, Evan E
Ventura, Mario
Dennis, Megan Y
Korbel, Jan O
Antonacci, Francesca
description Rhesus macaque is an Old World monkey that shared a common ancestor with human ∼25 Myr ago and is an important animal model for human disease studies. A deep understanding of its genetics is therefore required for both biomedical and evolutionary studies. Among structural variants, inversions represent a driving force in speciation and play an important role in disease predisposition. Here we generated a genome-wide map of inversions between human and macaque, combining single-cell strand sequencing with cytogenetics. We identified 375 total inversions between 859 bp and 92 Mbp, increasing by eightfold the number of previously reported inversions. Among these, 19 inversions flanked by segmental duplications overlap with recurrent copy number variants associated with neurocognitive disorders. Evolutionary analyses show that in 17 out of 19 cases, the Hominidae orientation of these disease-associated regions is always derived. This suggests that duplicated sequences likely played a fundamental role in generating inversions in humans and great apes, creating architectures that nowadays predispose these regions to disease-associated genetic instability. Finally, we identified 861 genes mapping at 156 inversions breakpoints, with some showing evidence of differential expression in human and macaque cell lines, thus highlighting candidates that might have contributed to the evolution of species-specific features. This study depicts the most accurate fine-scale map of inversions between human and macaque using a two-pronged integrative approach, such as single-cell strand sequencing and cytogenetics, and represents a valuable resource toward understanding of the biology and evolution of primate species.
doi_str_mv 10.1101/gr.265322.120
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source Freely Accessible Science Journals - check A-Z of ejournals; PubMed Central
subjects Animal models
Breakpoints
Cell lines
Cognition
Copy number
Cytogenetics
Evolution
Gene mapping
Genomes
Genomic instability
Resource
Speciation
title Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate evolution
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