Centromere repositioning.

Abstract:

:Primate pericentromeric regions recently have been shown to exhibit extraordinary evolutionary plasticity. In this paper we report an additional peculiar feature of these regions that we discovered while analyzing, by FISH, the evolutionary conservation of primate phylogenetic chromosome IX. If the position of the centromere is not taken into account, a relatively small number of rearrangements must be invoked to account for interspecific differences. Conversely, if the centromere is included, a paradox emerges: The position of the centromere seems to have undergone, in some species, an evolutionary history independent from the surrounding markers. A significant number of additional rearrangements must be proposed to reconcile the order of the markers with centromere position. Alternatively, the evolutionary emergence of neocentromeres can be postulated.

journal_name

Genome Res

journal_title

Genome research

authors

Montefalcone G,Tempesta S,Rocchi M,Archidiacono N

doi

10.1101/gr.9.12.1184

subject

Has Abstract

pub_date

1999-12-01 00:00:00

pages

1184-8

issue

12

eissn

1088-9051

issn

1549-5469

journal_volume

9

pub_type

杂志文章
  • A recombination hotspot leads to sequence variability within a novel gene (AK005651) and contributes to type 1 diabetes susceptibility.

    abstract::More than 25 loci have been linked to type 1 diabetes (T1D) in the nonobese diabetic (NOD) mouse, but identification of the underlying genes remains challenging. We describe here the positional cloning of a T1D susceptibility locus, Idd11, located on mouse chromosome 4. Sequence analysis of a series of congenic NOD mo...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.101881.109

    authors: Tan IK,Mackin L,Wang N,Papenfuss AT,Elso CM,Ashton MP,Quirk F,Phipson B,Bahlo M,Speed TP,Smyth GK,Morahan G,Brodnicki TC

    更新日期:2010-12-01 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

  • Software for automated analysis of DNA fingerprinting gels.

    abstract::Here we describe software tools for the automated detection of DNA restriction fragments resolved on agarose fingerprinting gels. We present a mathematical model for the location and shape of the restriction fragments as a function of fragment size, with model parameters determined empirically from "marker" lanes cont...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.904303

    authors: Fuhrmann DR,Krzywinski MI,Chiu R,Saeedi P,Schein JE,Bosdet IE,Chinwalla A,Hillier LW,Waterston RH,McPherson JD,Jones SJ,Marra MA

    更新日期:2003-05-01 00:00:00

  • Genome-wide patterns of natural variation reveal strong selective sweeps and ongoing genomic conflict in Drosophila mauritiana.

    abstract::Although it is well understood that selection shapes the polymorphism pattern in Drosophila, signatures of classic selective sweeps are scarce. Here, we focus on Drosophila mauritiana, an island endemic, which is closely related to Drosophila melanogaster. Based on a new, annotated genome sequence, we characterized th...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.139873.112

    authors: Nolte V,Pandey RV,Kofler R,Schlötterer C

    更新日期:2013-01-01 00:00:00

  • Structured nucleosome fingerprints enable high-resolution mapping of chromatin architecture within regulatory regions.

    abstract::Transcription factors canonically bind nucleosome-free DNA, making the positioning of nucleosomes within regulatory regions crucial to the regulation of gene expression. Using the assay of transposase accessible chromatin (ATAC-seq), we observe a highly structured pattern of DNA fragment lengths and positions around n...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.192294.115

    authors: Schep AN,Buenrostro JD,Denny SK,Schwartz K,Sherlock G,Greenleaf WJ

    更新日期:2015-11-01 00:00:00

  • Introgression maintains the genetic integrity of the mating-type determining chromosome of the fungus Neurospora tetrasperma.

    abstract::Genome evolution is driven by a complex interplay of factors, including selection, recombination, and introgression. The regions determining sexual identity are particularly dynamic parts of eukaryotic genomes that are prone to molecular degeneration associated with suppressed recombination. In the fungus Neurospora t...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.197244.115

    authors: Corcoran P,Anderson JL,Jacobson DJ,Sun Y,Ni P,Lascoux M,Johannesson H

    更新日期:2016-04-01 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

  • Distinct contributions of DNA methylation and histone acetylation to the genomic occupancy of transcription factors.

    abstract::Epigenetic modifications on chromatin play important roles in regulating gene expression. Although chromatin states are often governed by multilayered structure, how individual pathways contribute to gene expression remains poorly understood. For example, DNA methylation is known to regulate transcription factor bindi...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.257576.119

    authors: Cusack M,King HW,Spingardi P,Kessler BM,Klose RJ,Kriaucionis S

    更新日期:2020-10-01 00:00:00

  • Meiotic recombination generates rich diversity in NK cell receptor genes, alleles, and haplotypes.

    abstract::Natural killer (NK) cells contribute to the essential functions of innate immunity and reproduction. Various genes encode NK cell receptors that recognize the major histocompatibility complex (MHC) Class I molecules expressed by other cells. For primate NK cells, the killer-cell immunoglobulin-like receptors (KIR) are...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.085738.108

    authors: Norman PJ,Abi-Rached L,Gendzekhadze K,Hammond JA,Moesta AK,Sharma D,Graef T,McQueen KL,Guethlein LA,Carrington CV,Chandanayingyong D,Chang YH,Crespí C,Saruhan-Direskeneli G,Hameed K,Kamkamidze G,Koram KA,Layrisse Z,Ma

    更新日期:2009-05-01 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

  • Selective enrichment of damaged DNA molecules for ancient genome sequencing.

    abstract::Contamination by present-day human and microbial DNA is one of the major hindrances for large-scale genomic studies using ancient biological material. We describe a new molecular method, U selection, which exploits one of the most distinctive features of ancient DNA--the presence of deoxyuracils--for selective enrichm...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.174201.114

    authors: Gansauge MT,Meyer M

    更新日期:2014-09-01 00:00:00

  • The identification and functional annotation of RNA structures conserved in vertebrates.

    abstract::Structured elements of RNA molecules are essential in, e.g., RNA stabilization, localization, and protein interaction, and their conservation across species suggests a common functional role. We computationally screened vertebrate genomes for conserved RNA structures (CRSs), leveraging structure-based, rather than seq...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.208652.116

    authors: Seemann SE,Mirza AH,Hansen C,Bang-Berthelsen CH,Garde C,Christensen-Dalsgaard M,Torarinsson E,Yao Z,Workman CT,Pociot F,Nielsen H,Tommerup N,Ruzzo WL,Gorodkin J

    更新日期:2017-08-01 00:00:00

  • Deterministic protein inference for shotgun proteomics data provides new insights into Arabidopsis pollen development and function.

    abstract::Pollen, the male gametophyte of flowering plants, represents an ideal biological system to study developmental processes, such as cell polarity, tip growth, and morphogenesis. Upon hydration, the metabolically quiescent pollen rapidly switches to an active state, exhibiting extremely fast growth. This rapid switch req...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.089060.108

    authors: Grobei MA,Qeli E,Brunner E,Rehrauer H,Zhang R,Roschitzki B,Basler K,Ahrens CH,Grossniklaus U

    更新日期:2009-10-01 00:00:00

  • The functional genomic distribution of protein divergence in two animal phyla: coevolution, genomic conflict, and constraint.

    abstract::We compare the functional spectrum of protein evolution in two separate animal lineages with respect to two hypotheses: (1) rates of divergence are distributed similarly among functional classes within both lineages, indicating that selective pressure on the proteome is largely independent of organismic-level biologic...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.2195604

    authors: Castillo-Davis CI,Kondrashov FA,Hartl DL,Kulathinal RJ

    更新日期:2004-05-01 00:00:00

  • A virome-wide clonal integration analysis platform for discovering cancer viral etiology.

    abstract::Oncoviral infection is responsible for 12%-15% of cancer in humans. Convergent evidence from epidemiology, pathology, and oncology suggests that new viral etiologies for cancers remain to be discovered. Oncoviral profiles can be obtained from cancer genome sequencing data; however, widespread viral sequence contaminat...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.242529.118

    authors: Chen X,Kost J,Sulovari A,Wong N,Liang WS,Cao J,Li D

    更新日期:2019-05-01 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

  • Extensive variation and low heritability of DNA methylation identified in a twin study.

    abstract::Disturbance of DNA methylation leading to aberrant gene expression has been implicated in the etiology of many diseases. Whereas variation at the genetic level has been studied extensively, less is known about the extent and function of epigenetic variation. To explore variation and heritability of DNA methylation, we...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.119685.110

    authors: Gervin K,Hammerø M,Akselsen HE,Moe R,Nygård H,Brandt I,Gjessing HK,Harris JR,Undlien DE,Lyle R

    更新日期:2011-11-01 00:00:00

  • Computational and experimental identification of mirtrons in Drosophila melanogaster and Caenorhabditis elegans.

    abstract::Mirtrons are intronic hairpin substrates of the dicing machinery that generate functional microRNAs. In this study, we describe experimental assays that defined the essential requirements for entry of introns into the mirtron pathway. These data informed a bioinformatic screen that effectively identified functional mi...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.113050.110

    authors: Chung WJ,Agius P,Westholm JO,Chen M,Okamura K,Robine N,Leslie CS,Lai EC

    更新日期:2011-02-01 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

  • Dynamic effects of interacting genes underlying rice flowering-time phenotypic plasticity and global adaptation.

    abstract::The phenotypic variation of living organisms is shaped by genetics, environment, and their interaction. Understanding phenotypic plasticity under natural conditions is hindered by the apparently complex environment and the interacting genes and pathways. Herein, we report findings from the dissection of rice flowering...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.255703.119

    authors: Guo T,Mu Q,Wang J,Vanous AE,Onogi A,Iwata H,Li X,Yu J

    更新日期:2020-05-01 00:00:00

  • Inferring tumor progression from genomic heterogeneity.

    abstract::Cancer progression in humans is difficult to infer because we do not routinely sample patients at multiple stages of their disease. However, heterogeneous breast tumors provide a unique opportunity to study human tumor progression because they still contain evidence of early and intermediate subpopulations in the form...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.099622.109

    authors: Navin N,Krasnitz A,Rodgers L,Cook K,Meth J,Kendall J,Riggs M,Eberling Y,Troge J,Grubor V,Levy D,Lundin P,Månér S,Zetterberg A,Hicks J,Wigler M

    更新日期:2010-01-01 00:00:00

  • Determinants of CpG islands: expression in early embryo and isochore structure.

    abstract::In an attempt to understand the origin of CpG islands (CGIs) in mammalian genomes, we have studied their location and structure according to the expression pattern of genes and to the G + C content of isochores in which they are embedded. We show that CGIs located over the transcription start site (named start CGIs) a...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.174501

    authors: Ponger L,Duret L,Mouchiroud D

    更新日期:2001-11-01 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

  • Functional conservation of Rel binding sites in drosophilid genomes.

    abstract::Evolutionary constraints on gene regulatory elements are poorly understood: Little is known about how the strength of transcription factor binding correlates with DNA sequence conservation, and whether transcription factor binding sites can evolve rapidly while retaining their function. Here we use the model of the NF...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6490707

    authors: Copley RR,Totrov M,Linnell J,Field S,Ragoussis J,Udalova IA

    更新日期:2007-09-01 00:00:00

  • The repetitive landscape of the chicken genome.

    abstract::Cot-based cloning and sequencing (CBCS) is a powerful tool for isolating and characterizing the various repetitive components of any genome, combining the established principles of DNA reassociation kinetics with high-throughput sequencing. CBCS was used to generate sequence libraries representing the high, middle, an...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.2438004

    authors: Wicker T,Robertson JS,Schulze SR,Feltus FA,Magrini V,Morrison JA,Mardis ER,Wilson RK,Peterson DG,Paterson AH,Ivarie R

    更新日期:2005-01-01 00:00:00

  • Genomics and hearing impairment.

    abstract::Hearing impairment is clinically and genetically heterogeneous. There are >400 disorders in which hearing impairment is a characteristic of the syndrome, and family studies demonstrate that there are at least 30 autosomal loci for nonsyndromic hearing impairment. The genes that have been identified encode diaphanous (...

    journal_title:Genome research

    pub_type: 历史文章,杂志文章,评审

    doi:

    authors: Keats BJ,Berlin CI

    更新日期:1999-01-01 00:00:00

  • Next-generation sequencing identifies the natural killer cell microRNA transcriptome.

    abstract::Natural killer (NK) cells are innate lymphocytes important for early host defense against infectious pathogens and surveillance against malignant transformation. Resting murine NK cells regulate the translation of effector molecule mRNAs (e.g., granzyme B, GzmB) through unclear molecular mechanisms. MicroRNAs (miRNAs)...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.107995.110

    authors: Fehniger TA,Wylie T,Germino E,Leong JW,Magrini VJ,Koul S,Keppel CR,Schneider SE,Koboldt DC,Sullivan RP,Heinz ME,Crosby SD,Nagarajan R,Ramsingh G,Link DC,Ley TJ,Mardis ER

    更新日期:2010-11-01 00:00:00

  • Ancestry-agnostic estimation of DNA sample contamination from sequence reads.

    abstract::Detecting and estimating DNA sample contamination are important steps to ensure high-quality genotype calls and reliable downstream analysis. Existing methods rely on population allele frequency information for accurate estimation of contamination rates. Correctly specifying population allele frequencies for each indi...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.246934.118

    authors: Zhang F,Flickinger M,Taliun SAG,InPSYght Psychiatric Genetics Consortium.,Abecasis GR,Scott LJ,McCaroll SA,Pato CN,Boehnke M,Kang HM

    更新日期:2020-02-01 00:00:00

  • Gene expression profiling of single cells from archival tissue with laser-capture microdissection and Smart-3SEQ.

    abstract::RNA sequencing (RNA-seq) is a sensitive and accurate method for quantifying gene expression. Small samples or those whose RNA is degraded, such as formalin-fixed paraffin-embedded (FFPE) tissue, remain challenging to study with nonspecialized RNA-seq protocols. Here, we present a new method, Smart-3SEQ, that accuratel...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.234807.118

    authors: Foley JW,Zhu C,Jolivet P,Zhu SX,Lu P,Meaney MJ,West RB

    更新日期:2019-11-01 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