A biometrical genome search in rats reveals the multigenic basis of blood pressure variation.

Abstract:

:A genome-wide search for multiple loci influencing salt-loaded systolic blood pressure (NaSBP) variation among 188 F2 progeny from a cross between the Brown-Norway and spontaneously hypertensive rat strains was pursued in an effort to gain insight into the polygenic basis of blood pressure regulation. The results suggest that loci within five to six genomic regions collectively explain approximately 43% of the total NaSBP variation exhibited among the 188 F2 progeny. Many of these loci are in regions that previous studies have not implicated in blood pressure regulation. Ultimately, however, this study not only sheds light on the multigenic basis of blood pressure but provides further evidence that the identification of the genetic determinants of polygenic traits in mammals is possible with modern biometrical and molecular genetic tools in controlled settings (i.e., breeding paradigm and model organism).

journal_name

Genome Res

journal_title

Genome research

authors

Schork NJ,Krieger JE,Trolliet MR,Franchini KG,Koike G,Krieger EM,Lander ES,Dzau VJ,Jacob HJ

doi

10.1101/gr.5.2.164

subject

Has Abstract

pub_date

1995-09-01 00:00:00

pages

164-72

issue

2

eissn

1088-9051

issn

1549-5469

journal_volume

5

pub_type

杂志文章
  • 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

  • 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

  • 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

  • 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

  • Genome-scale cloning and expression of individual open reading frames using topoisomerase I-mediated ligation.

    abstract::The in vitro cloning of DNA molecules traditionally uses PCR amplification or site-specific restriction endonucleases to generate linear DNA inserts with defined termini and requires DNA ligase to covalently join those inserts to vectors with the corresponding ends. We have used the properties of Vaccinia DNA topoisom...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:

    authors: Heyman JA,Cornthwaite J,Foncerrada L,Gilmore JR,Gontang E,Hartman KJ,Hernandez CL,Hood R,Hull HM,Lee WY,Marcil R,Marsh EJ,Mudd KM,Patino MJ,Purcell TJ,Rowland JJ,Sindici ML,Hoeffler JP

    更新日期:1999-04-01 00:00:00

  • Identification and analysis of internal promoters in Caenorhabditis elegans operons.

    abstract::The current Caenorhabditis elegans genomic annotation has many genes organized in operons. Using directionally stitched promoterGFP methodology, we have conducted the largest survey to date on the regulatory regions of annotated C. elegans operons and identified 65, over 25% of those studied, with internal promoters. ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6824707

    authors: Huang P,Pleasance ED,Maydan JS,Hunt-Newbury R,O'Neil NJ,Mah A,Baillie DL,Marra MA,Moerman DG,Jones SJ

    更新日期:2007-10-01 00:00:00

  • 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 ch...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.253435.119

    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

    更新日期:2019-11-01 00:00:00

  • Gene and alternative splicing annotation with AIR.

    abstract::Designing effective and accurate tools for identifying the functional and structural elements in a genome remains at the frontier of genome annotation owing to incompleteness and inaccuracy of the data, limitations in the computational models, and shifting paradigms in genomics, such as alternative splicing. We presen...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.2889405

    authors: Florea L,Di Francesco V,Miller J,Turner R,Yao A,Harris M,Walenz B,Mobarry C,Merkulov GV,Charlab R,Dew I,Deng Z,Istrail S,Li P,Sutton G

    更新日期:2005-01-01 00:00:00

  • BLAT--the BLAST-like alignment tool.

    abstract::Analyzing vertebrate genomes requires rapid mRNA/DNA and cross-species protein alignments. A new tool, BLAT, is more accurate and 500 times faster than popular existing tools for mRNA/DNA alignments and 50 times faster for protein alignments at sensitivity settings typically used when comparing vertebrate sequences. B...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.229202

    authors: Kent WJ

    更新日期:2002-04-01 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

  • 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

  • Rapid molecular assays to study human centromere genomics.

    abstract::The centromere is the structural unit responsible for the faithful segregation of chromosomes. Although regulation of centromeric function by epigenetic factors has been well-studied, the contributions of the underlying DNA sequences have been much less well defined, and existing methodologies for studying centromere ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.219709.116

    authors: Contreras-Galindo R,Fischer S,Saha AK,Lundy JD,Cervantes PW,Mourad M,Wang C,Qian B,Dai M,Meng F,Chinnaiyan A,Omenn GS,Kaplan MH,Markovitz DM

    更新日期:2017-12-01 00:00:00

  • A large database of chicken bursal ESTs as a resource for the analysis of vertebrate gene function.

    abstract::Chicken B cells create their immunoglobulin repertoire within the Bursa of Fabricius by gene conversion. The high homologous recombination activity is shared by the bursal B-cell-derived DT40 cell line, which integrates transfected DNA constructs at high rates into its endogenous loci. Targeted integration in DT40 is ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.10.12.2062

    authors: Abdrakhmanov I,Lodygin D,Geroth P,Arakawa H,Law A,Plachy J,Korn B,Buerstedde JM

    更新日期:2000-12-01 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

  • 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

  • CBX3 regulates efficient RNA processing genome-wide.

    abstract::CBX5, CBX1, and CBX3 (HP1α, β, and γ, respectively) play an evolutionarily conserved role in the formation and maintenance of heterochromatin. In addition, CBX5, CBX1, and CBX3 may also participate in transcriptional regulation of genes. Recently, CBX3 binding to the bodies of a subset of genes has been observed in hu...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.124818.111

    authors: Smallwood A,Hon GC,Jin F,Henry RE,Espinosa JM,Ren B

    更新日期:2012-08-01 00:00:00

  • 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 ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.243774.118

    authors: de Mendoza A,Pflueger J,Lister R

    更新日期:2019-08-01 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

  • Genomic evolution, patterns of global dissemination, and interspecies transmission of human and simian T-cell leukemia/lymphotropic viruses.

    abstract::Using both env and long terminal repeat (LTR) sequences, with maximal representation of genetic diversity within primate strains, we revise and expand the unique evolutionary history of human and simian T-cell leukemia/lymphotropic viruses (HTLV/STLV). Based on the robust application of three different phylogenetic al...

    journal_title:Genome research

    pub_type: 杂志文章,评审

    doi:

    authors: Slattery JP,Franchini G,Gessain A

    更新日期:1999-06-01 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

  • Detecting genetic variation in microarray expression data.

    abstract::The use of high-density oligonucleotide arrays to measure the expression levels of thousands of genes in parallel has become commonplace. To take further advantage of the growing body of data, we developed a method, termed "GeSNP," to mine the detailed hybridization patterns in oligonucleotide array expression data fo...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6307307

    authors: Greenhall JA,Zapala MA,Cáceres M,Libiger O,Barlow C,Schork NJ,Lockhart DJ

    更新日期:2007-08-01 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

  • Cell-type, allelic, and genetic signatures in the human pancreatic beta cell transcriptome.

    abstract::Elucidating the pathophysiology and molecular attributes of common disorders as well as developing targeted and effective treatments hinges on the study of the relevant cell type and tissues. Pancreatic beta cells within the islets of Langerhans are centrally involved in the pathogenesis of both type 1 and type 2 diab...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.150706.112

    authors: Nica AC,Ongen H,Irminger JC,Bosco D,Berney T,Antonarakis SE,Halban PA,Dermitzakis ET

    更新日期:2013-09-01 00:00:00

  • Transcriptional alterations in glioma result primarily from DNA methylation-independent mechanisms.

    abstract::In cancer cells, aberrant DNA methylation is commonly associated with transcriptional alterations, including silencing of tumor suppressor genes. However, multiple epigenetic mechanisms, including polycomb repressive marks, contribute to gene deregulation in cancer. To dissect the relative contribution of DNA methylat...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.249219.119

    authors: Court F,Le Boiteux E,Fogli A,Müller-Barthélémy M,Vaurs-Barrière C,Chautard E,Pereira B,Biau J,Kemeny JL,Khalil T,Karayan-Tapon L,Verrelle P,Arnaud P

    更新日期:2019-10-01 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

  • 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

  • Sequences of 95 human MHC haplotypes reveal extreme coding variation in genes other than highly polymorphic HLA class I and II.

    abstract::The most polymorphic part of the human genome, the MHC, encodes over 160 proteins of diverse function. Half of them, including the HLA class I and II genes, are directly involved in immune responses. Consequently, the MHC region strongly associates with numerous diseases and clinical therapies. Notoriously, the MHC re...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.213538.116

    authors: Norman PJ,Norberg SJ,Guethlein LA,Nemat-Gorgani N,Royce T,Wroblewski EE,Dunn T,Mann T,Alicata C,Hollenbach JA,Chang W,Shults Won M,Gunderson KL,Abi-Rached L,Ronaghi M,Parham P

    更新日期:2017-05-01 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

  • A periodic pattern of SNPs in the human genome.

    abstract::By surveying a filtered, high-quality set of SNPs in the human genome, we have found that SNPs positioned 1, 2, 4, 6, or 8 bp apart are more frequent than SNPs positioned 3, 5, 7, or 9 bp apart. The observed pattern is not restricted to genomic regions that are known to cause sequencing or alignment errors, for exampl...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6223207

    authors: Madsen BE,Villesen P,Wiuf C

    更新日期:2007-10-01 00:00:00

  • A general approach for identifying distant regulatory elements applied to the Gdf6 gene.

    abstract::Regulatory sequences in higher genomes can map large distances from gene coding regions, and cannot yet be identified by simple inspection of primary DNA sequence information. Here we describe an efficient method of surveying large genomic regions for gene regulatory information, and subdividing complex sets of distan...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.1306003

    authors: Mortlock DP,Guenther C,Kingsley DM

    更新日期:2003-09-01 00:00:00