A chromosome-level assembly of the Atlantic herring genome-detection of a supergene and other signals of selection.

Abstract:

:The Atlantic herring is a model species for exploring the genetic basis for ecological adaptation, due to its huge population size and extremely low genetic differentiation at selectively neutral loci. However, such studies have so far been hampered because of a highly fragmented genome assembly. Here, we deliver a chromosome-level genome assembly based on a hybrid approach combining a de novo Pacific Biosciences (PacBio) assembly with Hi-C-supported scaffolding. The assembly comprises 26 autosomes with sizes ranging from 12.4 to 33.1 Mb and a total size, in chromosomes, of 726 Mb, which has been corroborated by a high-resolution linkage map. A comparison between the herring genome assembly with other high-quality assemblies from bony fishes revealed few inter-chromosomal but frequent intra-chromosomal rearrangements. The improved assembly facilitates analysis of previously intractable large-scale structural variation, allowing, for example, the detection of a 7.8-Mb inversion on Chromosome 12 underlying ecological adaptation. This supergene shows strong genetic differentiation between populations. The chromosome-based assembly also markedly improves the interpretation of previously detected signals of selection, allowing us to reveal hundreds of independent loci associated with ecological adaptation.

journal_name

Genome Res

journal_title

Genome research

authors

Pettersson ME,Rochus CM,Han F,Chen J,Hill J,Wallerman O,Fan G,Hong X,Xu Q,Zhang H,Liu S,Liu X,Haggerty L,Hunt T,Martin FJ,Flicek P,Bunikis I,Folkvord A,Andersson L

doi

10.1101/gr.253435.119

subject

Has Abstract

pub_date

2019-11-01 00:00:00

pages

1919-1928

issue

11

eissn

1088-9051

issn

1549-5469

pii

gr.253435.119

journal_volume

29

pub_type

杂志文章
  • A contiguous 66-kb barley DNA sequence provides evidence for reversible genome expansion.

    abstract::Organisms with large genomes contain vast amounts of repetitive DNA sequences, much of which is composed of retrotransposons. Amplification of retrotransposons has been postulated to be a major mechanism increasing genome size and leading to "genomic obesity." To gain insights into the relation between retrotransposon...

    journal_title:Genome research

    pub_type: 评论,杂志文章

    doi:10.1101/gr.10.7.908

    authors: Shirasu K,Schulman AH,Lahaye T,Schulze-Lefert P

    更新日期:2000-07-01 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

  • Pathway Processor: a tool for integrating whole-genome expression results into metabolic networks.

    abstract::We have developed a new tool to visualize expression data on metabolic pathways and to evaluate which metabolic pathways are most affected by transcriptional changes in whole-genome expression experiments. Using the Fisher Exact Test, the method scores biochemical pathways according to the probability that as many or ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.226602

    authors: Grosu P,Townsend JP,Hartl DL,Cavalieri D

    更新日期:2002-07-01 00:00:00

  • The distribution of variation in regulatory gene segments, as present in MHC class II promoters.

    abstract::Diversity in the antigen-binding receptors of the immune system has long been a primary interest of biologists. Recently it has been suggested that polymorphism in regulatory (noncoding) gene segments is of substantial importance as well. Here, we survey the level of variation in MHC class II gene promoters in man and...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.8.2.124

    authors: Cowell LG,Kepler TB,Janitz M,Lauster R,Mitchison NA

    更新日期:1998-02-01 00:00:00

  • The multicomparative 2-n-way genome suite.

    abstract::To effectively analyze the increasing amounts of available genomic data, improved comparative analytical tools that are accessible to and applicable by a broad scientific community are essential. We built the "2-n-way" software suite to provide a fundamental and innovative processing framework for revealing and compar...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.262261.120

    authors: Churakov G,Zhang F,Grundmann N,Makalowski W,Noll A,Doronina L,Schmitz J

    更新日期:2020-10-01 00:00:00

  • Yeast genetic interaction screen of human genes associated with amyotrophic lateral sclerosis: identification of MAP2K5 kinase as a potential drug target.

    abstract::To understand disease mechanisms, a large-scale analysis of human-yeast genetic interactions was performed. Of 1305 human disease genes assayed, 20 genes exhibited strong toxicity in yeast. Human-yeast genetic interactions were identified by en masse transformation of the human disease genes into a pool of 4653 homozy...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.211649.116

    authors: Jo M,Chung AY,Yachie N,Seo M,Jeon H,Nam Y,Seo Y,Kim E,Zhong Q,Vidal M,Park HC,Roth FP,Suk K

    更新日期:2017-09-01 00:00:00

  • Accumulation of RNA on chromatin disrupts heterochromatic silencing.

    abstract::Long noncoding RNAs (lncRNAs) play a conserved role in regulating gene expression, chromatin dynamics, and cell differentiation. They serve as a platform for RNA interference (RNAi)-mediated heterochromatin formation or DNA methylation in many eukaryotic organisms. We found in Schizosaccharomyces pombe that heterochro...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.216986.116

    authors: Brönner C,Salvi L,Zocco M,Ugolini I,Halic M

    更新日期:2017-07-01 00:00:00

  • The landscape of histone modifications across 1% of the human genome in five human cell lines.

    abstract::We generated high-resolution maps of histone H3 lysine 9/14 acetylation (H3ac), histone H4 lysine 5/8/12/16 acetylation (H4ac), and histone H3 at lysine 4 mono-, di-, and trimethylation (H3K4me1, H3K4me2, H3K4me3, respectively) across the ENCODE regions. Studying each modification in five human cell lines including th...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5704207

    authors: Koch CM,Andrews RM,Flicek P,Dillon SC,Karaöz U,Clelland GK,Wilcox S,Beare DM,Fowler JC,Couttet P,James KD,Lefebvre GC,Bruce AW,Dovey OM,Ellis PD,Dhami P,Langford CF,Weng Z,Birney E,Carter NP,Vetrie D,Dunham I

    更新日期:2007-06-01 00:00:00

  • The mRNA-bound proteome of the early fly embryo.

    abstract::Early embryogenesis is characterized by the maternal to zygotic transition (MZT), in which maternally deposited messenger RNAs are degraded while zygotic transcription begins. Before the MZT, post-transcriptional gene regulation by RNA-binding proteins (RBPs) is the dominant force in embryo patterning. We used two mRN...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.200386.115

    authors: Wessels HH,Imami K,Baltz AG,Kolinski M,Beldovskaya A,Selbach M,Small S,Ohler U,Landthaler M

    更新日期:2016-07-01 00:00:00

  • Arabidopsis-rice: will colinearity allow gene prediction across the eudicot-monocot divide?

    abstract::With the genomic sequencing of Arabidopsis nearing completion and rice sequencing very much in its infancy, a key question is whether we can exploit the Arabidopsis sequence to identify candidate genes for traits in cereal crops using a map-based approach. This requires the existence of colinearity between the Arabido...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.9.9.825

    authors: Devos KM,Beales J,Nagamura Y,Sasaki T

    更新日期:1999-09-01 00:00:00

  • Abundance and length of simple repeats in vertebrate genomes are determined by their structural properties.

    abstract::Microsatellites are abundant in vertebrate genomes, but their sequence representation and length distributions vary greatly within each family of repeats (e.g., tetranucleotides). Biophysical studies of 82 synthetic single-stranded oligonucleotides comprising all tetra- and trinucleotide repeats revealed an inverse co...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.078303.108

    authors: Bacolla A,Larson JE,Collins JR,Li J,Milosavljevic A,Stenson PD,Cooper DN,Wells RD

    更新日期:2008-10-01 00:00:00

  • Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping.

    abstract::Chromosome 21 represents approximately 1% of the human genome, and its long arm has been estimated to contain 600-1000 genes. A dense linkage map and almost complete physical maps based on yeast artificial chromosomes (YACs) and cosmids have been developed. We have used exon trapping to identify portions of genes from...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6.8.747

    authors: Chen H,Chrast R,Rossier C,Morris MA,Lalioti MD,Antonarakis SE

    更新日期:1996-08-01 00:00:00

  • Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion.

    abstract::Large copy number variants (CNVs) have been recently found as structural polymorphisms of the human genome of still unknown biological significance. CNVs are significantly enriched in regions with segmental duplications or low-copy repeats (LCRs). Williams-Beuren syndrome (WBS) is a neurodevelopmental disorder caused ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.073197.107

    authors: Cuscó I,Corominas R,Bayés M,Flores R,Rivera-Brugués N,Campuzano V,Pérez-Jurado LA

    更新日期:2008-05-01 00:00:00

  • End Sequence Analysis Toolkit (ESAT) expands the extractable information from single-cell RNA-seq data.

    abstract::RNA-seq protocols that focus on transcript termini are well suited for applications in which template quantity is limiting. Here we show that, when applied to end-sequencing data, analytical methods designed for global RNA-seq produce computational artifacts. To remedy this, we created the End Sequence Analysis Toolki...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.207902.116

    authors: Derr A,Yang C,Zilionis R,Sergushichev A,Blodgett DM,Redick S,Bortell R,Luban J,Harlan DM,Kadener S,Greiner DL,Klein A,Artyomov MN,Garber M

    更新日期:2016-10-01 00:00:00

  • Copy-number-aware differential analysis of quantitative DNA sequencing data.

    abstract::Developments in microarray and high-throughput sequencing (HTS) technologies have resulted in a rapid expansion of research into epigenomic changes that occur in normal development and in the progression of disease, such as cancer. Not surprisingly, copy number variation (CNV) has a direct effect on HTS read densities...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.139055.112

    authors: Robinson MD,Strbenac D,Stirzaker C,Statham AL,Song J,Speed TP,Clark SJ

    更新日期:2012-12-01 00:00:00

  • Birth and expression evolution of mammalian microRNA genes.

    abstract::MicroRNAs (miRNAs) are major post-transcriptional regulators of gene expression, yet their origins and functional evolution in mammals remain little understood due to the lack of appropriate comparative data. Using RNA sequencing, we have generated extensive and comparable miRNA data for five organs in six species tha...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.140269.112

    authors: Meunier J,Lemoine F,Soumillon M,Liechti A,Weier M,Guschanski K,Hu H,Khaitovich P,Kaessmann H

    更新日期:2013-01-01 00:00:00

  • The marine bacterium Pseudoalteromonas haloplanktis has a complex genome structure composed of two separate genetic units.

    abstract::The genome size of Pseudoalteromonas haloplanktis, a ubiquitous and easily cultured marine bacterium, was measured as a step toward estimating the genome complexity of marine bacterioplankton. To determine total genome size, we digested P. haloplanktis DNA with the restriction endonucleases Notl and Sfil, separated th...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6.12.1160

    authors: Lanoil BD,Ciuffetti LM,Giovannoni SJ

    更新日期:1996-12-01 00:00:00

  • The genome sequence of Mycoplasma mycoides subsp. mycoides SC type strain PG1T, the causative agent of contagious bovine pleuropneumonia (CBPP).

    abstract::Mycoplasma mycoides subsp. mycoidesSC (MmymySC)is the etiological agent of contagious bovine pleuropneumonia (CBPP), a highly contagious respiratory disease in cattle. The genome of Mmymy SC type strain PG1(T) has been sequenced to map all the genes and to facilitate further studies regarding the cell function of the ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.1673304

    authors: Westberg J,Persson A,Holmberg A,Goesmann A,Lundeberg J,Johansson KE,Pettersson B,Uhlén M

    更新日期:2004-02-01 00:00:00

  • Multiplex mapping of chromatin accessibility and DNA methylation within targeted single molecules identifies epigenetic heterogeneity in neural stem cells and glioblastoma.

    abstract::Human tumors are comprised of heterogeneous cell populations that display diverse molecular and phenotypic features. To examine the extent to which epigenetic differences contribute to intratumoral cellular heterogeneity, we have developed a high-throughput method, termed MAPit-patch. The method uses multiplexed ampli...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.161737.113

    authors: Nabilsi NH,Deleyrolle LP,Darst RP,Riva A,Reynolds BA,Kladde MP

    更新日期:2014-02-01 00:00:00

  • Gene expression profiling in human fetal liver and identification of tissue- and developmental-stage-specific genes through compiled expression profiles and efficient cloning of full-length cDNAs.

    abstract::Fetal liver intriguingly consists of hepatic parenchymal cells and hematopoietic stem/progenitor cells. Human fetal liver aged 22 wk of gestation (HFL22w) corresponds to the turning point between immigration and emigration of the hematopoietic system. To gain further molecular insight into its developmental and functi...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.175501

    authors: Yu Y,Zhang C,Zhou G,Wu S,Qu X,Wei H,Xing G,Dong C,Zhai Y,Wan J,Ouyang S,Li L,Zhang S,Zhou K,Zhang Y,Wu C,He F

    更新日期:2001-08-01 00:00:00

  • Prokaryotic phylogenies inferred from protein structural domains.

    abstract::The determination of the phylogenetic relationships among microorganisms has long relied primarily on gene sequence information. Given that prokaryotic organisms often lack morphological characteristics amenable to phylogenetic analysis, prokaryotic phylogenies, in particular, are often based on sequence data. In this...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.3033805

    authors: Deeds EJ,Hennessey H,Shakhnovich EI

    更新日期:2005-03-01 00:00:00

  • Large-scale mapping of gene regulatory logic reveals context-dependent repression by transcriptional activators.

    abstract::Transcription factors (TFs) are key mediators that propagate extracellular and intracellular signals through to changes in gene expression profiles. However, the rules by which promoters decode the amount of active TF into target gene expression are not well understood. To determine the mapping between promoter DNA se...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.212316.116

    authors: van Dijk D,Sharon E,Lotan-Pompan M,Weinberger A,Segal E,Carey LB

    更新日期:2017-01-01 00:00:00

  • Phenotypically distinct female castes in honey bees are defined by alternative chromatin states during larval development.

    abstract::The capacity of the honey bee to produce three phenotypically distinct organisms (two female castes; queens and sterile workers, and haploid male drones) from one genotype represents one of the most remarkable examples of developmental plasticity in any phylum. The queen-worker morphological and reproductive divide is...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.236497.118

    authors: Wojciechowski M,Lowe R,Maleszka J,Conn D,Maleszka R,Hurd PJ

    更新日期:2018-10-01 00:00:00

  • A Plasmodium gene family encoding Maurer's cleft membrane proteins: structural properties and expression profiling.

    abstract::Upon invasion of the erythrocyte cell, the malaria parasite remodels its environment; in particular, it establishes a complex membrane network, which connects the parasitophorous vacuole to the host plasma membrane and is involved in protein transport and trafficking. We have identified a novel subtelomeric gene famil...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.2126104

    authors: Sam-Yellowe TY,Florens L,Johnson JR,Wang T,Drazba JA,Le Roch KG,Zhou Y,Batalov S,Carucci DJ,Winzeler EA,Yates JR 3rd

    更新日期:2004-06-01 00:00:00

  • Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay.

    abstract::Large-scale genetic studies are highly dependent on efficient and scalable multiplex SNP assays. In this study, we report the development of Molecular Inversion Probe technology with four-color, single array detection, applied to large-scale genotyping of up to 12,000 SNPs per reaction. While generating 38,429 SNP ass...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.3185605

    authors: Hardenbol P,Yu F,Belmont J,Mackenzie J,Bruckner C,Brundage T,Boudreau A,Chow S,Eberle J,Erbilgin A,Falkowski M,Fitzgerald R,Ghose S,Iartchouk O,Jain M,Karlin-Neumann G,Lu X,Miao X,Moore B,Moorhead M,Namsaraev E,

    更新日期:2005-02-01 00:00:00

  • Probing genomic diversity and evolution of Escherichia coli O157 by single nucleotide polymorphisms.

    abstract::Infections by Shiga toxin-producing Escherichia coli O157:H7 (STEC O157) are the predominant cause of bloody diarrhea and hemolytic uremic syndrome in the United States. In silico comparison of the two complete STEC O157 genomes (Sakai and EDL933) revealed a strikingly high level of sequence identity in orthologous pr...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.4759706

    authors: Zhang W,Qi W,Albert TJ,Motiwala AS,Alland D,Hyytia-Trees EK,Ribot EM,Fields PI,Whittam TS,Swaminathan B

    更新日期:2006-06-01 00:00:00

  • DNA enrichment by allele-specific hybridization (DEASH): a novel method for haplotyping and for detecting low-frequency base substitutional variants and recombinant DNA molecules.

    abstract::Detecting rare sequence variants in genomic DNA is central to the analysis of de novo mutation and recombination events and the detection of rare pathological mutations in mixed cell populations. Current PCR techniques suffer from noise that limits detection to variants present at a frequency of at least 10(-4)-10(-5)...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.1214603

    authors: Jeffreys AJ,May CA

    更新日期:2003-10-01 00:00:00

  • A comprehensive transcript map of the mouse Gnas imprinted complex.

    abstract::The recent publication of the FANTOM mouse transcriptome has provided a unique opportunity to study the diversity of transcripts arising from a single gene locus. We have focused on the Gnas complex, as imprinting loci themselves provide unique insights into transcriptional regulation. Thirteen full-length cDNAs from ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.955503

    authors: Holmes R,Williamson C,Peters J,Denny P,Wells C,RIKEN GER Group.,GSL Members.

    更新日期:2003-06-01 00:00:00

  • A generic, cost-effective, and scalable cell lineage analysis platform.

    abstract::Advances in single-cell genomics enable commensurate improvements in methods for uncovering lineage relations among individual cells. Current sequencing-based methods for cell lineage analysis depend on low-resolution bulk analysis or rely on extensive single-cell sequencing, which is not scalable and could be biased ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.202903.115

    authors: Biezuner T,Spiro A,Raz O,Amir S,Milo L,Adar R,Chapal-Ilani N,Berman V,Fried Y,Ainbinder E,Cohen G,Barr HM,Halaban R,Shapiro E

    更新日期:2016-11-01 00:00:00

  • Functional DNA methylation differences between tissues, cell types, and across individuals discovered using the M&M algorithm.

    abstract::DNA methylation plays key roles in diverse biological processes such as X chromosome inactivation, transposable element repression, genomic imprinting, and tissue-specific gene expression. Sequencing-based DNA methylation profiling provides an unprecedented opportunity to map and compare complete DNA methylomes. This ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.156539.113

    authors: Zhang B,Zhou Y,Lin N,Lowdon RF,Hong C,Nagarajan RP,Cheng JB,Li D,Stevens M,Lee HJ,Xing X,Zhou J,Sundaram V,Elliott G,Gu J,Shi T,Gascard P,Sigaroudinia M,Tlsty TD,Kadlecek T,Weiss A,O'Geen H,Farnham PJ,Maire

    更新日期:2013-09-01 00:00:00