Capture of a functionally active methyl-CpG binding domain by an arthropod retrotransposon family.

Abstract:

:The repressive capacity of cytosine DNA methylation is mediated by recruitment of silencing complexes by methyl-CpG binding domain (MBD) proteins. Despite MBD proteins being associated with silencing, we discovered that a family of arthropod Copia retrotransposons have incorporated a host-derived MBD. We functionally show how retrotransposon-encoded MBDs preferentially bind to CpG-dense methylated regions, which correspond to transposable element regions of the host genome, in the myriapod Strigamia maritima Consistently, young MBD-encoding Copia retrotransposons (CopiaMBD) accumulate in regions with higher CpG densities than other LTR-retrotransposons also present in the genome. This would suggest that retrotransposons use MBDs to integrate into heterochromatic regions in Strigamia, avoiding potentially harmful insertions into host genes. In contrast, CopiaMBD insertions in the spider Stegodyphus dumicola genome disproportionately accumulate in methylated gene bodies compared with other spider LTR-retrotransposons. Given that transposons are not actively targeted by DNA methylation in the spider genome, this distribution bias would also support a role for MBDs in the integration process. Together, these data show that retrotransposons can co-opt host-derived epigenome readers, potentially harnessing the host epigenome landscape to advantageously tune the retrotransposition process.

journal_name

Genome Res

journal_title

Genome research

authors

de Mendoza A,Pflueger J,Lister R

doi

10.1101/gr.243774.118

subject

Has Abstract

pub_date

2019-08-01 00:00:00

pages

1277-1286

issue

8

eissn

1088-9051

issn

1549-5469

pii

gr.243774.118

journal_volume

29

pub_type

杂志文章
  • Rapid evolution of mouse Y centromere repeat DNA belies recent sequence stability.

    abstract::The Y centromere sequence of house mouse, Mus musculus, remains unknown despite our otherwise significant knowledge of the genome sequence of this important mammalian model organism. Here, we report the complete molecular characterization of the C57BL/6J chromosome Y centromere, which comprises a highly diverged minor...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.092080.109

    authors: Pertile MD,Graham AN,Choo KH,Kalitsis P

    更新日期:2009-12-01 00:00:00

  • DNA methylation at hepatitis B viral integrants is associated with methylation at flanking human genomic sequences.

    abstract::Integration of DNA viruses into the human genome plays an important role in various types of tumors, including hepatitis B virus (HBV)-related hepatocellular carcinoma. However, the molecular details and clinical impact of HBV integration on either human or HBV epigenomes are unknown. Here, we show that methylation of...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.175240.114

    authors: Watanabe Y,Yamamoto H,Oikawa R,Toyota M,Yamamoto M,Kokudo N,Tanaka S,Arii S,Yotsuyanagi H,Koike K,Itoh F

    更新日期:2015-03-01 00:00:00

  • The TAGteam motif facilitates binding of 21 sequence-specific transcription factors in the Drosophila embryo.

    abstract::Highly overlapping patterns of genome-wide binding of many distinct transcription factors have been observed in worms, insects, and mammals, but the origins and consequences of this overlapping binding remain unclear. While analyzing chromatin immunoprecipitation data sets from 21 sequence-specific transcription facto...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.130682.111

    authors: Satija R,Bradley RK

    更新日期:2012-04-01 00:00:00

  • A transposon-based strategy for sequencing repetitive DNA in eukaryotic genomes.

    abstract::Repetitive DNA is a significant component of eukaryotic genomes. We have developed a strategy to efficiently and accurately sequence repetitive DNA in the nematode Caenorhabditis elegans using integrated artificial transposons and automated fluorescent sequencing. Mapping and assembly tools represent important compone...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.7.5.551

    authors: Devine SE,Chissoe SL,Eby Y,Wilson RK,Boeke JD

    更新日期:1997-05-01 00:00:00

  • Optical mapping of BAC clones from the human Y chromosome DAZ locus.

    abstract::The accurate mapping of clones derived from genomic regions containing complex arrangements of repeated elements presents special problems for DNA sequencers. Recent advances in the automation of optical mapping have enabled us to map a set of 16 BAC clones derived from the DAZ locus of the human Y chromosome long arm...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.112100

    authors: Giacalone J,Delobette S,Gibaja V,Ni L,Skiadas Y,Qi R,Edington J,Lai Z,Gebauer D,Zhao H,Anantharaman T,Mishra B,Brown LG,Saxena R,Page DC,Schwartz DC

    更新日期:2000-09-01 00:00:00

  • General gene movement off the X chromosome in the Drosophila genus.

    abstract::In Drosophila melanogaster, there is an excess of genes duplicated by retroposition from the X chromosome to the autosomes. Most of those retrogenes that originated on the X chromosome have testis expression pattern. These observations could be explained by natural selection favoring genes that avoided spermatogenesis...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.088609.108

    authors: Vibranovski MD,Zhang Y,Long M

    更新日期:2009-05-01 00:00:00

  • Decrypting noncoding RNA interactions, structures, and functional networks.

    abstract::The world of noncoding RNAs (ncRNAs) is composed of an enormous and growing number of transcripts, ranging in length from tens of bases to tens of kilobases, involved in all biological processes and altered in expression and/or function in many types of human disorders. The premise of this review is the concept that n...

    journal_title:Genome research

    pub_type: 杂志文章,评审

    doi:10.1101/gr.247239.118

    authors: Fabbri M,Girnita L,Varani G,Calin GA

    更新日期:2019-09-01 00:00:00

  • Genome-wide map of regulatory interactions in the human genome.

    abstract::Increasing evidence suggests that interactions between regulatory genomic elements play an important role in regulating gene expression. We generated a genome-wide interaction map of regulatory elements in human cells (ENCODE tier 1 cells, K562, GM12878) using Chromatin Interaction Analysis by Paired-End Tag sequencin...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.176586.114

    authors: Heidari N,Phanstiel DH,He C,Grubert F,Jahanbani F,Kasowski M,Zhang MQ,Snyder MP

    更新日期:2014-12-01 00:00:00

  • Genomic analysis of primordial dwarfism reveals novel disease genes.

    abstract::Primordial dwarfism (PD) is a disease in which severely impaired fetal growth persists throughout postnatal development and results in stunted adult size. The condition is highly heterogeneous clinically, but the use of certain phenotypic aspects such as head circumference and facial appearance has proven helpful in d...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.160572.113

    authors: Shaheen R,Faqeih E,Ansari S,Abdel-Salam G,Al-Hassnan ZN,Al-Shidi T,Alomar R,Sogaty S,Alkuraya FS

    更新日期:2014-02-01 00:00:00

  • CG dinucleotides enhance promoter activity independent of DNA methylation.

    abstract::Most mammalian RNA polymerase II initiation events occur at CpG islands, which are rich in CpGs and devoid of DNA methylation. Despite their relevance for gene regulation, it is unknown to what extent the CpG dinucleotide itself actually contributes to promoter activity. To address this question, we determined the tra...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.241653.118

    authors: Hartl D,Krebs AR,Grand RS,Baubec T,Isbel L,Wirbelauer C,Burger L,Schübeler D

    更新日期:2019-04-01 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

  • 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

  • Integrative analysis of genome-wide loss of heterozygosity and monoallelic expression at nucleotide resolution reveals disrupted pathways in triple-negative breast cancer.

    abstract::Loss of heterozygosity (LOH) and copy number alteration (CNA) feature prominently in the somatic genomic landscape of tumors. As such, karyotypic aberrations in cancer genomes have been studied extensively to discover novel oncogenes and tumor-suppressor genes. Advances in sequencing technology have enabled the cost-e...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.137570.112

    authors: Ha G,Roth A,Lai D,Bashashati A,Ding J,Goya R,Giuliany R,Rosner J,Oloumi A,Shumansky K,Chin SF,Turashvili G,Hirst M,Caldas C,Marra MA,Aparicio S,Shah SP

    更新日期:2012-10-01 00:00:00

  • Comparative gene mapping: a fine-scale survey of chromosome rearrangements between ruminants and humans.

    abstract::A total of 202 genes were cytogenetically mapped to goat chromosomes, multiplying by five the total number of regional gene localizations in domestic ruminants (255). This map encompasses 249 and 173 common anchor loci regularly spaced along human and murine chromosomes, respectively, which makes it possible to perfor...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.8.9.901

    authors: Schibler L,Vaiman D,Oustry A,Giraud-Delville C,Cribiu EP

    更新日期:1998-09-01 00:00:00

  • Evolution of a genomic regulatory domain: the role of gene co-option and gene duplication in the Enhancer of split complex.

    abstract::The Drosophila Enhancer of split complex [E(spl)-C] is a remarkable complex of genes many of which are effectors or modulators of Notch signaling. The complex contains different classes of genes including four bearded genes and seven basic helix-loop-helix (bHLH) genes. We examined the evolution of this unusual comple...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.104794.109

    authors: Duncan EJ,Dearden PK

    更新日期:2010-07-01 00:00:00

  • Screening of gene-associated polymorphisms by use of in-gel competitive reassociation and EST (cDNA) array hybridization.

    abstract::In-gel competitive reassociation (IGCR) is a method of differential subtraction to enrich polymorphic DNA restriction fragments between two DNA samples without probes or specific sequence information. Here, we show that by combining IGCR and expressed sequence tags (EST) array hybridization, polymorphic DNA fragments ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.434103

    authors: Gotoh K,Oishi M

    更新日期:2003-03-01 00:00:00

  • A simplified procedure for developing multiplex PCRs.

    abstract::We have developed a simplified method for multiplex PCR based on the use of chimeric primers. Each primer contains a 3' region complementary to sequence-specific recognition sites and a 5' region made up of an unrelated 20-nucleotide sequence. Identical reaction conditions, cycling times, and annealing temperatures ha...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5.5.488

    authors: Shuber AP,Grondin VJ,Klinger KW

    更新日期:1995-12-01 00:00:00

  • Dynamic building of a BAC clone tiling path for the Rat Genome Sequencing Project.

    abstract::CLONEPICKER is a software pipeline that integrates sequence data with BAC clone fingerprints to dynamically select a minimal overlapping clone set covering the whole genome. In the Rat Genome Sequencing Project (RGSP), a hybrid strategy of "clone by clone" and "whole genome shotgun" approaches was used to maximize the...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.2171704

    authors: Chen R,Sodergren E,Weinstock GM,Gibbs RA

    更新日期:2004-04-01 00:00:00

  • A computational genomics approach to identify cis-regulatory modules from chromatin immunoprecipitation microarray data--a case study using E2F1.

    abstract::Advances in high-throughput technologies, such as ChIP-chip, and the completion of human and mouse genomic sequences now allow analysis of the mechanisms of gene regulation on a systems level. In this study, we have developed a computational genomics approach (termed ChIPModules), which begins with experimentally dete...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5520206

    authors: Jin VX,Rabinovich A,Squazzo SL,Green R,Farnham PJ

    更新日期:2006-12-01 00:00:00

  • Caenorhabditis elegans has scores of hedgehog-related genes: sequence and expression analysis.

    abstract::Previously, we have described novel families of genes, warthog (wrt) and groundhog (grd), in Caenorhabditis elegans. They are related to Hedgehog (Hh) through the carboxy-terminal autoprocessing domain (called Hog or Hint). A comprehensive survey revealed 10 genes with Hog/Hint modules in C. elegans. Five of these are...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.9.10.909

    authors: Aspöck G,Kagoshima H,Niklaus G,Bürglin TR

    更新日期:1999-10-01 00:00:00

  • A fine scale phenotype-genotype virulence map of a bacterial pathogen.

    abstract::A large fraction of the genes from sequenced organisms are of unknown function. This limits biological insight, and for pathogenic microorganisms hampers the development of new approaches to battle infections. There is thus a great need for novel strategies that link genotypes to phenotypes for microorganisms. We desc...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.137430.112

    authors: van Opijnen T,Camilli A

    更新日期:2012-12-01 00:00:00

  • Genetic analysis of complex traits in the emerging Collaborative Cross.

    abstract::The Collaborative Cross (CC) is a mouse recombinant inbred strain panel that is being developed as a resource for mammalian systems genetics. Here we describe an experiment that uses partially inbred CC lines to evaluate the genetic properties and utility of this emerging resource. Genome-wide analysis of the incipien...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.111310.110

    authors: Aylor DL,Valdar W,Foulds-Mathes W,Buus RJ,Verdugo RA,Baric RS,Ferris MT,Frelinger JA,Heise M,Frieman MB,Gralinski LE,Bell TA,Didion JD,Hua K,Nehrenberg DL,Powell CL,Steigerwalt J,Xie Y,Kelada SN,Collins FS,Yang IV

    更新日期:2011-08-01 00:00:00

  • A scalable high-throughput chemical synthesizer.

    abstract::A machine that employs a novel reagent delivery technique for biomolecular synthesis has been developed. This machine separates the addressing of individual synthesis sites from the actual process of reagent delivery by using masks placed over the sites. Because of this separation, this machine is both cost-effective ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.359002

    authors: Livesay EA,Liu YH,Luebke KJ,Irick J,Belosludtsev Y,Rayner S,Balog R,Johnston SA

    更新日期:2002-12-01 00:00:00

  • Comparative analysis of mammalian Y chromosomes illuminates ancestral structure and lineage-specific evolution.

    abstract::Although more than thirty mammalian genomes have been sequenced to draft quality, very few of these include the Y chromosome. This has limited our understanding of the evolutionary dynamics of gene persistence and loss, our ability to identify conserved regulatory elements, as well our knowledge of the extent to which...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.154286.112

    authors: Li G,Davis BW,Raudsepp T,Pearks Wilkerson AJ,Mason VC,Ferguson-Smith M,O'Brien PC,Waters PD,Murphy WJ

    更新日期:2013-09-01 00:00:00

  • Physicochemical constraint violation by missense substitutions mediates impairment of protein function and disease severity.

    abstract::We find that the degree of impairment of protein function by missense variants is predictable by comparative sequence analysis alone. The applicable range of impairment is not confined to binary predictions that distinguish normal from deleterious variants, but extends continuously from mild to severe effects. The acc...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.3804205

    authors: Stone EA,Sidow A

    更新日期:2005-07-01 00:00:00

  • Exploring the human genome with functional maps.

    abstract::Human genomic data of many types are readily available, but the complexity and scale of human molecular biology make it difficult to integrate this body of data, understand it from a systems level, and apply it to the study of specific pathways or genetic disorders. An investigator could best explore a particular prot...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.082214.108

    authors: Huttenhower C,Haley EM,Hibbs MA,Dumeaux V,Barrett DR,Coller HA,Troyanskaya OG

    更新日期:2009-06-01 00:00:00

  • Strategies for mutational analysis of the large multiexon ATM gene using high-density oligonucleotide arrays.

    abstract::Mutational analysis of large genes with complex genomic structures plays an important role in medical genetics. Technical limitations associated with current mutation screening protocols have placed increased emphasis on the development of new technologies to simplify these procedures. High-density arrays of >90,000-o...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.8.12.1245

    authors: Hacia JG,Sun B,Hunt N,Edgemon K,Mosbrook D,Robbins C,Fodor SP,Tagle DA,Collins FS

    更新日期:1998-12-01 00:00:00

  • Eukaryotic regulatory element conservation analysis and identification using comparative genomics.

    abstract::Comparative genomics is a promising approach to the challenging problem of eukaryotic regulatory element identification, because functional noncoding sequences may be conserved across species from evolutionary constraints. We systematically analyzed known human and Saccharomyces cerevisiae regulatory elements and disc...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.1327604

    authors: Liu Y,Liu XS,Wei L,Altman RB,Batzoglou S

    更新日期:2004-03-01 00:00:00

  • Genome-reconstruction for eukaryotes from complex natural microbial communities.

    abstract::Microbial eukaryotes are integral components of natural microbial communities, and their inclusion is critical for many ecosystem studies, yet the majority of published metagenome analyses ignore eukaryotes. In order to include eukaryotes in environmental studies, we propose a method to recover eukaryotic genomes from...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.228429.117

    authors: West PT,Probst AJ,Grigoriev IV,Thomas BC,Banfield JF

    更新日期:2018-04-01 00:00:00

  • Exploring expression data: identification and analysis of coexpressed genes.

    abstract::Analysis procedures are needed to extract useful information from the large amount of gene expression data that is becoming available. This work describes a set of analytical tools and their application to yeast cell cycle data. The components of our approach are (1) a similarity measure that reduces the number of fal...

    journal_title:Genome research

    pub_type: 杂志文章,评审

    doi:10.1101/gr.9.11.1106

    authors: Heyer LJ,Kruglyak S,Yooseph S

    更新日期:1999-11-01 00:00:00