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 X inactivation or by sexual antagonistic effects favoring the fixation of male beneficial mutations on the autosomes. If natural selection played the essential role in distributing male-related genes, then the out-of-the-X chromosomal gene movement should not be limited to retrogenes. Here, we studied DNA-based interchromosome gene movement patterns by analyzing relocated genes that were previously identified in 12 Drosophila genome sequences. We found a significant excess of gene movement out of the X chromosome. In addition, we were able to extend previous retrogene movement analysis to species and branches other than those involving D. melanogaster, confirming the pervasiveness of gene movement out of the X chromosome. Also, for X chromosome-to-autosome (X-->A) movement, we observed high testis expression of relocated genes as opposed to the low testis expression of parental genes, corroborating the involvement of the male germ line on the gene movement process. These analyses of both DNA-based and RNA-based gene relocations reveal that the out-of-the-X movement of testis-expressed genes is a general pattern in the Drosophila genus.

journal_name

Genome Res

journal_title

Genome research

authors

Vibranovski MD,Zhang Y,Long M

doi

10.1101/gr.088609.108

subject

Has Abstract

pub_date

2009-05-01 00:00:00

pages

897-903

issue

5

eissn

1088-9051

issn

1549-5469

pii

gr.088609.108

journal_volume

19

pub_type

杂志文章
  • High mutational rates of large-scale duplication and deletion in Daphnia pulex.

    abstract::Knowledge of the genome-wide rate and spectrum of mutations is necessary to understand the origin of disease and the genetic variation driving all evolutionary processes. Here, we provide a genome-wide analysis of the rate and spectrum of mutations obtained in two Daphnia pulex genotypes via separate mutation-accumula...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.191338.115

    authors: Keith N,Tucker AE,Jackson CE,Sung W,Lucas Lledó JI,Schrider DR,Schaack S,Dudycha JL,Ackerman M,Younge AJ,Shaw JR,Lynch M

    更新日期:2016-01-01 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

  • 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...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.265322.120

    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

    更新日期:2020-11-01 00:00:00

  • Accurate detection and genotyping of SNPs utilizing population sequencing data.

    abstract::Next-generation sequencing technologies have made it possible to sequence targeted regions of the human genome in hundreds of individuals. Deep sequencing represents a powerful approach for the discovery of the complete spectrum of DNA sequence variants in functionally important genomic intervals. Current methods for ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.100040.109

    authors: Bansal V,Harismendy O,Tewhey R,Murray SS,Schork NJ,Topol EJ,Frazer KA

    更新日期:2010-04-01 00:00:00

  • Comprehensive genome sequence analysis of a breast cancer amplicon.

    abstract::Gene amplification occurs in most solid tumors and is associated with poor prognosis. Amplification of 20q13.2 is common to several tumor types including breast cancer. The 1 Mb of sequence spanning the 20q13.2 breast cancer amplicon is one of the most exhaustively studied segments of the human genome. These studies h...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.gr1743r

    authors: Collins C,Volik S,Kowbel D,Ginzinger D,Ylstra B,Cloutier T,Hawkins T,Predki P,Martin C,Wernick M,Kuo WL,Alberts A,Gray JW

    更新日期:2001-06-01 00:00:00

  • Species-specific class I gene expansions formed the telomeric 1 mb of the mouse major histocompatibility complex.

    abstract::We have determined the complete sequence of 951,695 bp from the class I region of H2, the mouse major histocompatibility complex (Mhc) from strain 129/Sv (haplotype bc). The sequence contains 26 genes. The sequence spans from the last 50 kb of the H2-T region, including 2 class I genes and 3 class I pseudogenes, and i...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.975303

    authors: Takada T,Kumánovics A,Amadou C,Yoshino M,Jones EP,Athanasiou M,Evans GA,Fischer Lindahl K

    更新日期:2003-04-01 00:00:00

  • A platform for curated products from novel open reading frames prompts reinterpretation of disease variants.

    abstract::Recent evidence from proteomics and deep massively parallel sequencing studies have revealed that eukaryotic genomes contain substantial numbers of as-yet-uncharacterized open reading frames (ORFs). We define these uncharacterized ORFs as novel ORFs (nORFs). nORFs in humans are mostly under 100 codons and are found in...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.263202.120

    authors: Neville MDC,Kohze R,Erady C,Meena N,Hayden M,Cooper DN,Mort M,Prabakaran S

    更新日期:2021-01-19 00:00:00

  • GrapeTree: visualization of core genomic relationships among 100,000 bacterial pathogens.

    abstract::Current methods struggle to reconstruct and visualize the genomic relationships of large numbers of bacterial genomes. GrapeTree facilitates the analyses of large numbers of allelic profiles by a static "GrapeTree Layout" algorithm that supports interactive visualizations of large trees within a web browser window. Gr...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.232397.117

    authors: Zhou Z,Alikhan NF,Sergeant MJ,Luhmann N,Vaz C,Francisco AP,Carriço JA,Achtman M

    更新日期:2018-09-01 00:00:00

  • Arboretum: reconstruction and analysis of the evolutionary history of condition-specific transcriptional modules.

    abstract::Comparative functional genomics studies the evolution of biological processes by analyzing functional data, such as gene expression profiles, across species. A major challenge is to compare profiles collected in a complex phylogeny. Here, we present Arboretum, a novel scalable computational algorithm that integrates e...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.146233.112

    authors: Roy S,Wapinski I,Pfiffner J,French C,Socha A,Konieczka J,Habib N,Kellis M,Thompson D,Regev A

    更新日期:2013-06-01 00:00:00

  • Time series community genomics analysis reveals rapid shifts in bacterial species, strains, and phage during infant gut colonization.

    abstract::The gastrointestinal microbiome undergoes shifts in species and strain abundances, yet dynamics involving closely related microorganisms remain largely unknown because most methods cannot resolve them. We developed new metagenomic methods and utilized them to track species and strain level variations in microbial comm...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.142315.112

    authors: Sharon I,Morowitz MJ,Thomas BC,Costello EK,Relman DA,Banfield JF

    更新日期:2013-01-01 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

  • Copy number variation, chromosome rearrangement, and their association with recombination during avian evolution.

    abstract::Chromosomal rearrangements and copy number variants (CNVs) play key roles in genome evolution and genetic disease; however, the molecular mechanisms underlying these types of structural genomic variation are not fully understood. The availability of complete genome sequences for two bird species, the chicken and the z...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.103663.109

    authors: Völker M,Backström N,Skinner BM,Langley EJ,Bunzey SK,Ellegren H,Griffin DK

    更新日期:2010-04-01 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

  • Evolution of transcript modification by N6-methyladenosine in primates.

    abstract::Phenotypic differences within populations and between closely related species are often driven by variation and evolution of gene expression. However, most analyses have focused on the effects of genomic variation at cis-regulatory elements such as promoters and enhancers that control transcriptional activity, and lit...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.212563.116

    authors: Ma L,Zhao B,Chen K,Thomas A,Tuteja JH,He X,He C,White KP

    更新日期:2017-03-01 00:00:00

  • Nucleosome occupancy as a novel chromatin parameter for replication origin functions.

    abstract::Eukaryotic DNA replication initiates from multiple discrete sites in the genome, termed origins of replication (origins). Prior to S phase, multiple origins are poised to initiate replication by recruitment of the pre-replicative complex (pre-RC). For proper replication to occur, origin activation must be tightly regu...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.209940.116

    authors: Rodriguez J,Lee L,Lynch B,Tsukiyama T

    更新日期:2017-02-01 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

  • The pig X and Y Chromosomes: structure, sequence, and evolution.

    abstract::We have generated an improved assembly and gene annotation of the pig X Chromosome, and a first draft assembly of the pig Y Chromosome, by sequencing BAC and fosmid clones from Duroc animals and incorporating information from optical mapping and fiber-FISH. The X Chromosome carries 1033 annotated genes, 690 of which a...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.188839.114

    authors: Skinner BM,Sargent CA,Churcher C,Hunt T,Herrero J,Loveland JE,Dunn M,Louzada S,Fu B,Chow W,Gilbert J,Austin-Guest S,Beal K,Carvalho-Silva D,Cheng W,Gordon D,Grafham D,Hardy M,Harley J,Hauser H,Howden P,Howe K,

    更新日期:2016-01-01 00:00:00

  • Prioritizing candidate disease genes by network-based boosting of genome-wide association data.

    abstract::Network "guilt by association" (GBA) is a proven approach for identifying novel disease genes based on the observation that similar mutational phenotypes arise from functionally related genes. In principle, this approach could account even for nonadditive genetic interactions, which underlie the synergistic combinatio...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.118992.110

    authors: Lee I,Blom UM,Wang PI,Shim JE,Marcotte EM

    更新日期:2011-07-01 00:00:00

  • The human homolog T of the mouse T(Brachyury) gene; gene structure, cDNA sequence, and assignment to chromosome 6q27.

    abstract::We have cloned the human gene encoding the transcription factor T. T protein is vital for the formation of posterior mesoderm and axial development in all vertebrates. Brachyury mutant mice, which lack T protein, die in utero with abnormal notochord, posterior somites, and allantois. We have identified human T genomic...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6.3.226

    authors: Edwards YH,Putt W,Lekoape KM,Stott D,Fox M,Hopkinson DA,Sowden J

    更新日期:1996-03-01 00:00:00

  • Accurate gene-tree reconstruction by learning gene- and species-specific substitution rates across multiple complete genomes.

    abstract::Comparative genomics provides a general methodology for discovering functional DNA elements and understanding their evolution. The availability of many related genomes enables more powerful analyses, but requires rigorous phylogenetic methods to resolve orthologous genes and regions. Here, we use 12 recently sequenced...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.7105007

    authors: Rasmussen MD,Kellis M

    更新日期:2007-12-01 00:00:00

  • Systematic identification of novel protein domain families associated with nuclear functions.

    abstract::A systematic computational analysis of protein sequences containing known nuclear domains led to the identification of 28 novel domain families. This represents a 26% increase in the starting set of 107 known nuclear domain families used for the analysis. Most of the novel domains are present in all major eukaryotic l...

    journal_title:Genome research

    pub_type: 信件

    doi:10.1101/gr.203201

    authors: Doerks T,Copley RR,Schultz J,Ponting CP,Bork P

    更新日期:2002-01-01 00:00:00

  • Genomic localization of RNA binding proteins reveals links between pre-mRNA processing and transcription.

    abstract::Pre-mRNA processing often occurs in coordination with transcription thereby coupling these two key regulatory events. As such, many proteins involved in mRNA processing associate with the transcriptional machinery and are in proximity to DNA. This proximity allows for the mapping of the genomic associations of RNA bin...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5211806

    authors: Swinburne IA,Meyer CA,Liu XS,Silver PA,Brodsky AS

    更新日期:2006-07-01 00:00:00

  • The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine.

    abstract::ClinSeq is a pilot project to investigate the use of whole-genome sequencing as a tool for clinical research. By piloting the acquisition of large amounts of DNA sequence data from individual human subjects, we are fostering the development of hypothesis-generating approaches for performing research in genomic medicin...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.092841.109

    authors: Biesecker LG,Mullikin JC,Facio FM,Turner C,Cherukuri PF,Blakesley RW,Bouffard GG,Chines PS,Cruz P,Hansen NF,Teer JK,Maskeri B,Young AC,NISC Comparative Sequencing Program.,Manolio TA,Wilson AF,Finkel T,Hwang P,Arai A

    更新日期:2009-09-01 00:00:00

  • Integrated annotations and analyses of small RNA-producing loci from 47 diverse plants.

    abstract::Plant endogenous small RNAs (sRNAs) are important regulators of gene expression. There are two broad categories of plant sRNAs: microRNAs (miRNAs) and endogenous short interfering RNAs (siRNAs). MicroRNA loci are relatively well-annotated but compose only a small minority of the total sRNA pool; siRNA locus annotation...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.256750.119

    authors: Lunardon A,Johnson NR,Hagerott E,Phifer T,Polydore S,Coruh C,Axtell MJ

    更新日期:2020-03-01 00:00:00

  • Phenotypic diversity and genotypic flexibility of Burkholderia cenocepacia during long-term chronic infection of cystic fibrosis lungs.

    abstract::Chronic bacterial infections of the lung are the leading cause of morbidity and mortality in cystic fibrosis patients. Tracking bacterial evolution during chronic infections can provide insights into how host selection pressures-including immune responses and therapeutic interventions-shape bacterial genomes. We carri...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.213363.116

    authors: Lee AH,Flibotte S,Sinha S,Paiero A,Ehrlich RL,Balashov S,Ehrlich GD,Zlosnik JE,Mell JC,Nislow C

    更新日期:2017-04-01 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

  • 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

  • Phylogeny-wide analysis of social amoeba genomes highlights ancient origins for complex intercellular communication.

    abstract::Dictyostelium discoideum (DD), an extensively studied model organism for cell and developmental biology, belongs to the most derived group 4 of social amoebas, a clade of altruistic multicellular organisms. To understand genome evolution over long time periods and the genetic basis of social evolution, we sequenced th...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.121137.111

    authors: Heidel AJ,Lawal HM,Felder M,Schilde C,Helps NR,Tunggal B,Rivero F,John U,Schleicher M,Eichinger L,Platzer M,Noegel AA,Schaap P,Glöckner G

    更新日期:2011-11-01 00:00:00

  • Conservation of regulatory sequences and gene expression patterns in the disintegrating Drosophila Hox gene complex.

    abstract::Homeotic (Hox) genes are usually clustered and arranged in the same order as they are expressed along the anteroposterior body axis of metazoans. The mechanistic explanation for this colinearity has been elusive, and it may well be that a single and universal cause does not exist. The Hox-gene complex (HOM-C) has been...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.3468605

    authors: Negre B,Casillas S,Suzanne M,Sánchez-Herrero E,Akam M,Nefedov M,Barbadilla A,de Jong P,Ruiz A

    更新日期:2005-05-01 00:00:00

  • Fusion of the human gene for the polyubiquitination coeffector UEV1 with Kua, a newly identified gene.

    abstract::UEV proteins are enzymatically inactive variants of the E2 ubiquitin-conjugating enzymes that regulate noncanonical elongation of ubiquitin chains. In Saccharomyces cerevisiae, UEV is part of the RAD6-mediated error-free DNA repair pathway. In mammalian cells, UEV proteins can modulate c-FOS transcription and the G2-M...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.gr-1405r

    authors: Thomson TM,Lozano JJ,Loukili N,Carrió R,Serras F,Cormand B,Valeri M,Díaz VM,Abril J,Burset M,Merino J,Macaya A,Corominas M,Guigó R

    更新日期:2000-11-01 00:00:00