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

Abstract:

: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.

journal_name

Genome Res

journal_title

Genome research

authors

Maggiolini FAM,Sanders AD,Shew CJ,Sulovari A,Mao Y,Puig M,Catacchio CR,Dellino M,Palmisano D,Mercuri L,Bitonto M,Porubský D,Cáceres M,Eichler EE,Ventura M,Dennis MY,Korbel JO,Antonacci F

doi

10.1101/gr.265322.120

subject

Has Abstract

pub_date

2020-11-01 00:00:00

pages

1680-1693

issue

11

eissn

1088-9051

issn

1549-5469

pii

gr.265322.120

journal_volume

30

pub_type

杂志文章
  • Alterations in TCF7L2 expression define its role as a key regulator of glucose metabolism.

    abstract::Genome-wide association studies (GWAS) have consistently implicated noncoding variation within the TCF7L2 locus with type 2 diabetes (T2D) risk. While this locus represents the strongest genetic determinant for T2D risk in humans, it remains unclear how these noncoding variants affect disease etiology. To test the hyp...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.123745.111

    authors: Savic D,Ye H,Aneas I,Park SY,Bell GI,Nobrega MA

    更新日期:2011-09-01 00:00:00

  • Discovery of high-confidence human protein-coding genes and exons by whole-genome PhyloCSF helps elucidate 118 GWAS loci.

    abstract::The most widely appreciated role of DNA is to encode protein, yet the exact portion of the human genome that is translated remains to be ascertained. We previously developed PhyloCSF, a widely used tool to identify evolutionary signatures of protein-coding regions using multispecies genome alignments. Here, we present...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.246462.118

    authors: Mudge JM,Jungreis I,Hunt T,Gonzalez JM,Wright JC,Kay M,Davidson C,Fitzgerald S,Seal R,Tweedie S,He L,Waterhouse RM,Li Y,Bruford E,Choudhary JS,Frankish A,Kellis M

    更新日期:2019-12-01 00:00:00

  • Fourfold faster rate of genome rearrangement in nematodes than in Drosophila.

    abstract::We compared the genome of the nematode Caenorhabditis elegans to 13% of that of Caenorhabditis briggsae, identifying 252 conserved segments along their chromosomes. We detected 517 chromosomal rearrangements, with the ratio of translocations to inversions to transpositions being approximately 1:1:2. We estimate that t...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.172702

    authors: Coghlan A,Wolfe KH

    更新日期:2002-06-01 00:00:00

  • Biological data sciences in genome research.

    abstract::The last 20 years have been a remarkable era for biology and medicine. One of the most significant achievements has been the sequencing of the first human genomes, which has laid the foundation for profound insights into human genetics, the intricacies of regulation and development, and the forces of evolution. Incred...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.191684.115

    authors: Schatz MC

    更新日期:2015-10-01 00:00:00

  • An abundance of bidirectional promoters in the human genome.

    abstract::The alignment of full-length human cDNA sequences to the finished sequence of the human genome provides a unique opportunity to study the distribution of genes throughout the genome. By analyzing the distances between 23,752 genes, we identified a class of divergently transcribed gene pairs, representing more than 10%...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.1982804

    authors: Trinklein ND,Aldred SF,Hartman SJ,Schroeder DI,Otillar RP,Myers RM

    更新日期:2004-01-01 00:00:00

  • Modeling of epigenome dynamics identifies transcription factors that mediate Polycomb targeting.

    abstract::Although changes in chromatin are integral to transcriptional reprogramming during cellular differentiation, it is currently unclear how chromatin modifications are targeted to specific loci. To systematically identify transcription factors (TFs) that can direct chromatin changes during cell fate decisions, we model t...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.142661.112

    authors: Arnold P,Schöler A,Pachkov M,Balwierz PJ,Jørgensen H,Stadler MB,van Nimwegen E,Schübeler D

    更新日期:2013-01-01 00:00:00

  • Ancestral grass karyotype reconstruction unravels new mechanisms of genome shuffling as a source of plant evolution.

    abstract::The comparison of the chromosome numbers of today's species with common reconstructed paleo-ancestors has led to intense speculation of how chromosomes have been rearranged over time in mammals. However, similar studies in plants with respect to genome evolution as well as molecular mechanisms leading to mosaic synten...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.109744.110

    authors: Murat F,Xu JH,Tannier E,Abrouk M,Guilhot N,Pont C,Messing J,Salse J

    更新日期:2010-11-01 00:00:00

  • Distinct transcription factor complexes act on a permissive chromatin landscape to establish regionalized gene expression in CNS stem cells.

    abstract::Spatially distinct gene expression profiles in neural stem cells (NSCs) are a prerequisite to the formation of neuronal diversity, but how these arise from the regulatory interactions between chromatin accessibility and transcription factor activity has remained unclear. Here, we demonstrate that, despite their distin...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.203513.115

    authors: Hagey DW,Zaouter C,Combeau G,Lendahl MA,Andersson O,Huss M,Muhr J

    更新日期:2016-07-01 00:00:00

  • Sequence diversity and genomic organization of vomeronasal receptor genes in the mouse.

    abstract::The vomeronasal system of mice is thought to be specialized in the detection of pheromones. Two multigene families have been identified that encode proteins with seven putative transmembrane domains and that are expressed selectively in subsets of neurons of the vomeronasal organ. The products of these vomeronasal rec...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.10.12.1958

    authors: Del Punta K,Rothman A,Rodriguez I,Mombaerts P

    更新日期:2000-12-01 00:00:00

  • From first base: the sequence of the tip of the X chromosome of Drosophila melanogaster, a comparison of two sequencing strategies.

    abstract::We present the sequence of a contiguous 2.63 Mb of DNA extending from the tip of the X chromosome of Drosophila melanogaster. Within this sequence, we predict 277 protein coding genes, of which 94 had been sequenced already in the course of studying the biology of their gene products, and examples of 12 different tran...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.173801

    authors: Benos PV,Gatt MK,Murphy L,Harris D,Barrell B,Ferraz C,Vidal S,Brun C,Demaille J,Cadieu E,Dreano S,Gloux S,Lelaure V,Mottier S,Galibert F,Borkova D,Miñana B,Kafatos FC,Bolshakov S,Sidén-Kiamos I,Papagiannakis G,S

    更新日期:2001-05-01 00:00:00

  • Copy number variation at the breakpoint region of isochromosome 17q.

    abstract::Isochromosome 17q, or i(17q), is one of the most frequent nonrandom changes occurring in human neoplasia. Most of the i(17q) breakpoints cluster within a approximately 240-kb interval located in the Smith-Magenis syndrome common deletion region in 17p11.2. The breakpoint cluster region is characterized by a complex ar...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.080697.108

    authors: Carvalho CM,Lupski JR

    更新日期:2008-11-01 00:00:00

  • Models of human core transcriptional regulatory circuitries.

    abstract::A small set of core transcription factors (TFs) dominates control of the gene expression program in embryonic stem cells and other well-studied cellular models. These core TFs collectively regulate their own gene expression, thus forming an interconnected auto-regulatory loop that can be considered the core transcript...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.197590.115

    authors: Saint-André V,Federation AJ,Lin CY,Abraham BJ,Reddy J,Lee TI,Bradner JE,Young RA

    更新日期:2016-03-01 00:00:00

  • Genomic organization of the sex-determining and adjacent regions of the sex chromosomes of medaka.

    abstract::Sequencing of the human Y chromosome has uncovered the peculiarities of the genomic organization of a heterogametic sex chromosome of old evolutionary age, and has led to many insights into the evolutionary changes that occurred during its long history. We have studied the genomic organization of the medaka fish Y chr...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5016106

    authors: Kondo M,Hornung U,Nanda I,Imai S,Sasaki T,Shimizu A,Asakawa S,Hori H,Schmid M,Shimizu N,Schartl M

    更新日期:2006-07-01 00:00:00

  • SNP-based quantitative deconvolution of biological mixtures: application to the detection of cows with subclinical mastitis by whole-genome sequencing of tank milk.

    abstract::Biological products of importance in food (e.g., milk) and medical (e.g., donor blood-derived products) sciences often correspond to mixtures of samples contributed by multiple individuals. Identifying which individuals contributed to the mixture and in what proportions may be of interest in several circumstances. We ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.256172.119

    authors: Coppieters W,Karim L,Georges M

    更新日期:2020-08-01 00:00:00

  • Genome-wide identification of conserved regulatory function in diverged sequences.

    abstract::Plasticity of gene regulatory encryption can permit DNA sequence divergence without loss of function. Functional information is preserved through conservation of the composition of transcription factor binding sites (TFBS) in a regulatory element. We have developed a method that can accurately identify pairs of functi...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.119016.110

    authors: Taher L,McGaughey DM,Maragh S,Aneas I,Bessling SL,Miller W,Nobrega MA,McCallion AS,Ovcharenko I

    更新日期:2011-07-01 00:00:00

  • Topologically associating domains and their long-range contacts are established during early G1 coincident with the establishment of the replication-timing program.

    abstract::Mammalian genomes are partitioned into domains that replicate in a defined temporal order. These domains can replicate at similar times in all cell types (constitutive) or at cell type-specific times (developmental). Genome-wide chromatin conformation capture (Hi-C) has revealed sub-megabase topologically associating ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.183699.114

    authors: Dileep V,Ay F,Sima J,Vera DL,Noble WS,Gilbert DM

    更新日期:2015-08-01 00:00:00

  • Deep sequencing of tomato short RNAs identifies microRNAs targeting genes involved in fruit ripening.

    abstract::In plants there are several classes of 21-24-nt short RNAs that regulate gene expression. The most conserved class is the microRNAs (miRNAs), although some miRNAs are found only in specific species. We used high-throughput pyrosequencing to identify conserved and nonconserved miRNAs and other short RNAs in tomato frui...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.080127.108

    authors: Moxon S,Jing R,Szittya G,Schwach F,Rusholme Pilcher RL,Moulton V,Dalmay T

    更新日期:2008-10-01 00:00:00

  • Evolution and multilevel optimization of the genetic code.

    abstract::The discovery of the genetic code was one of the most important advances of modern biology. But there is more to a DNA code than protein sequence; DNA carries signals for splicing, localization, folding, and regulation that are often embedded within the protein-coding sequence. In this issue, Itzkovitz and Alon show t...

    journal_title:Genome research

    pub_type: 评论,杂志文章,评审

    doi:10.1101/gr.6144007

    authors: Bollenbach T,Vetsigian K,Kishony R

    更新日期:2007-04-01 00:00:00

  • A novel testis ubiquitin-binding protein gene arose by exon shuffling in hominoids.

    abstract::Most new genes arise by duplication of existing gene structures, after which relaxed selection on the new copy frequently leads to mutational inactivation of the duplicate; only rarely will a new gene with modified function emerge. Here we describe a unique mechanism of gene creation, whereby new combinations of funct...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6252107

    authors: Babushok DV,Ohshima K,Ostertag EM,Chen X,Wang Y,Mandal PK,Okada N,Abrams CS,Kazazian HH Jr

    更新日期:2007-08-01 00:00:00

  • Schizosaccharomyces pombe essential genes: a pilot study.

    abstract::After completion of the Schizosaccharomyces pombe genome sequence, we have carried out a pilot gene deletion project to assess the feasibility of a genome-wide deletion project and to estimate the percentage of essential genes. Using a PCR-based gene deletion procedure, we investigated 100 genes within a 253-kb region...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.636103

    authors: Decottignies A,Sanchez-Perez I,Nurse P

    更新日期:2003-03-01 00:00:00

  • Reconstructing complex regions of genomes using long-read sequencing technology.

    abstract::Obtaining high-quality sequence continuity of complex regions of recent segmental duplication remains one of the major challenges of finishing genome assemblies. In the human and mouse genomes, this was achieved by targeting large-insert clones using costly and laborious capillary-based sequencing approaches. Sanger s...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.168450.113

    authors: Huddleston J,Ranade S,Malig M,Antonacci F,Chaisson M,Hon L,Sudmant PH,Graves TA,Alkan C,Dennis MY,Wilson RK,Turner SW,Korlach J,Eichler EE

    更新日期:2014-04-01 00:00:00

  • Evaluation of predicted network modules in yeast metabolism using NMR-based metabolite profiling.

    abstract::Genome-scale metabolic models promise important insights into cell function. However, the definition of pathways and functional network modules within these models, and in the biochemical literature in general, is often based on intuitive reasoning. Although mathematical methods have been proposed to identify modules,...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5662207

    authors: Bundy JG,Papp B,Harmston R,Browne RA,Clayson EM,Burton N,Reece RJ,Oliver SG,Brindle KM

    更新日期:2007-04-01 00:00:00

  • The extensive and condition-dependent nature of epistasis among whole-genome duplicates in yeast.

    abstract::Since complete redundancy between extant duplicates (paralogs) is evolutionarily unfavorable, some degree of functional congruency is eventually lost. However, in budding yeast, experimental evidence collected for duplicated metabolic enzymes and in global physical interaction surveys had suggested widespread function...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.076174.108

    authors: Musso G,Costanzo M,Huangfu M,Smith AM,Paw J,San Luis BJ,Boone C,Giaever G,Nislow C,Emili A,Zhang Z

    更新日期:2008-07-01 00:00:00

  • X chromosome cDNA microarray screening identifies a functional PLP2 promoter polymorphism enriched in patients with X-linked mental retardation.

    abstract::X-linked Mental Retardation (XLMR) occurs in 1 in 600 males and is highly genetically heterogeneous. We used a novel human X chromosome cDNA microarray (XCA) to survey the expression profile of X-linked genes in lymphoblasts of XLMR males. Genes with altered expression verified by Northern blot and/or quantitative PCR...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5336307

    authors: Zhang L,Jie C,Obie C,Abidi F,Schwartz CE,Stevenson RE,Valle D,Wang T

    更新日期:2007-05-01 00:00:00

  • A network of transcriptionally coordinated functional modules in Saccharomyces cerevisiae.

    abstract::Recent computational and experimental work suggests that functional modules underlie much of cellular physiology and are a useful unit of cellular organization from the perspective of systems biology. Because interactions among modules can give rise to higher-level properties that are essential to cellular function, a...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.3847105

    authors: Petti AA,Church GM

    更新日期:2005-09-01 00:00:00

  • The first five years of single-cell cancer genomics and beyond.

    abstract::Single-cell sequencing (SCS) is a powerful new tool for investigating evolution and diversity in cancer and understanding the role of rare cells in tumor progression. These methods have begun to unravel key questions in cancer biology that have been difficult to address with bulk tumor measurements. Over the past five...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.191098.115

    authors: Navin NE

    更新日期:2015-10-01 00:00:00

  • Comparative genomics of the Archaea (Euryarchaeota): evolution of conserved protein families, the stable core, and the variable shell.

    abstract::Comparative analysis of the protein sequences encoded in the four euryarchaeal species whose genomes have been sequenced completely (Methanococcus jannaschii, Methanobacterium thermoautotrophicum, Archaeoglobus fulgidus, and Pyrococcus horikoshii) revealed 1326 orthologous sets, of which 543 are represented in all fou...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:

    authors: Makarova KS,Aravind L,Galperin MY,Grishin NV,Tatusov RL,Wolf YI,Koonin EV

    更新日期:1999-07-01 00:00:00

  • The (r)evolution of SINE versus LINE distributions in primate genomes: sex chromosomes are important.

    abstract::The densities of transposable elements (TEs) in the human genome display substantial variation both within individual chromosomes and among chromosome types (autosomes and the two sex chromosomes). Finding an explanation for this variability has been challenging, especially in light of genome landscapes unique to the ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.099044.109

    authors: Kvikstad EM,Makova KD

    更新日期:2010-05-01 00:00:00

  • HD-Marker: a highly multiplexed and flexible approach for targeted genotyping of more than 10,000 genes in a single-tube assay.

    abstract::Targeted genotyping of transcriptome-scale genetic markers is highly attractive for genetic, ecological, and evolutionary studies, but achieving this goal in a cost-effective manner remains a major challenge, especially for laboratories working on nonmodel organisms. Here, we develop a high-throughput, sequencing-base...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.235820.118

    authors: Lv J,Jiao W,Guo H,Liu P,Wang R,Zhang L,Zeng Q,Hu X,Bao Z,Wang S

    更新日期:2018-12-01 00:00:00

  • An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS data.

    abstract::Next-generation sequencing is a powerful approach for discovering genetic variation. Sensitive variant calling and haplotype inference from population sequencing data remain challenging. We describe methods for high-quality discovery, genotyping, and phasing of SNPs for low-coverage (approximately 5×) sequencing of po...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.146084.112

    authors: Wang Y,Lu J,Yu J,Gibbs RA,Yu F

    更新日期:2013-05-01 00:00:00