Thursday, 25 February 2010

What's new for 'JKB_daily1' in PubMed

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Sender's message: Sepsis or genomics or altitude: JKB_daily1

Sent on Thursday, 2010 Feb 25
Search (sepsis[MeSH Terms] OR septic shock[MeSH Terms] OR altitude[MeSH Terms] OR genomics[MeSH Terms] OR genetics[MeSH Terms] OR retrotransposons[MeSH Terms] OR macrophage[MeSH Terms]) AND ("2009/8/8"[Publication Date] : "3000"[Publication Date]) AND (("Science"[Journal] OR "Nature"[Journal] OR "The New England journal of medicine"[Journal] OR "Lancet"[Journal] OR "Nature genetics"[Journal] OR "Nature medicine"[Journal]) OR (Hume DA[Author] OR Baillie JK[Author] OR Faulkner, Geoffrey J[Author]))
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PubMed Results
Items 1 -5 of 5

1. Science. 2010 Feb 5;327(5966):682-5.

Flight orientation behaviors promote optimal migration trajectories in high-flying insects.

Chapman JW, Nesbit RL, Burgin LE, Reynolds DR, Smith AD, Middleton DR, Hill JK.

Plant and Invertebrate Ecology Department, Rothamsted Research, Harpenden, Hertfordshire AL5 2JQ, UK. jason.chapman@bbsrc.ac.uk

Many insects undertake long-range seasonal migrations to exploit temporary breeding sites hundreds or thousands of kilometers apart, but the behavioral adaptations that facilitate these movements remain largely unknown. Using entomological radar, we showed that the ability to select seasonally favorable, high-altitude winds is widespread in large day- and night-flying migrants and that insects adopt optimal flight headings that partially correct for crosswind drift, thus maximizing distances traveled. Trajectory analyses show that these behaviors increase migration distances by 40% and decrease the degree of drift from seasonally optimal directions. These flight behaviors match the sophistication of those seen in migrant birds and help explain how high-flying insects migrate successfully between seasonal habitats.

PMID: 20133570 [PubMed - indexed for MEDLINE]
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Publication Types:

  • Research Support, Non-U.S. Gov't

MeSH Terms:

  • Altitude
  • Animal Migration*
  • Animals
  • Butterflies/physiology*
  • Computer Simulation
  • Flight, Animal*
  • Moths/physiology*
  • Orientation
  • Radar
  • Seasons
  • Wind*

Grant Support:

  • Biotechnology and Biological Sciences Research Council/United Kingdom
2. Science. 2010 Feb 5;327(5966):656-61.

Development of monocytes, macrophages, and dendritic cells.

Geissmann F, Manz MG, Jung S, Sieweke MH, Merad M, Ley K.

Centre for Molecular and Cellular Biology of Inflammation, Division of Immunology, Infection, and Inflammatory Diseases, King's College London, Great Maze Pond, London SE1 1UL, UK. frederic.geissmann@kcl.ac.uk

Monocytes and macrophages are critical effectors and regulators of inflammation and the innate immune response, the immediate arm of the immune system. Dendritic cells initiate and regulate the highly pathogen-specific adaptive immune responses and are central to the development of immunologic memory and tolerance. Recent in vivo experimental approaches in the mouse have unveiled new aspects of the developmental and lineage relationships among these cell populations. Despite this, the origin and differentiation cues for many tissue macrophages, monocytes, and dendritic cell subsets in mice, and the corresponding cell populations in humans, remain to be elucidated.

PMID: 20133564 [PubMed - indexed for MEDLINE]
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Publication Types:

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH Terms:

  • Animals
  • Cell Lineage
  • Cell Proliferation
  • Cytokines/metabolism
  • Dendritic Cells/cytology
  • Dendritic Cells/immunology
  • Dendritic Cells/physiology*
  • Homeostasis
  • Humans
  • Inflammation/immunology
  • Macrophages/cytology
  • Macrophages/immunology
  • Macrophages/physiology*
  • Mice
  • Monocytes/cytology
  • Monocytes/immunology
  • Monocytes/physiology*
  • Myeloid Progenitor Cells/cytology
  • Myeloid Progenitor Cells/physiology
  • Myelopoiesis*
  • Phagocytosis
  • Transcription, Genetic

Substances:

  • Cytokines

Grant Support:

  • G0900867/Medical Research Council/United Kingdom
  • R01 HL058108/HL/NHLBI NIH HHS/United States
3. Nature. 2010 Jan 14;463(7278):237-40.

KAP1 controls endogenous retroviruses in embryonic stem cells.

Rowe HM, Jakobsson J, Mesnard D, Rougemont J, Reynard S, Aktas T, Maillard PV, Layard-Liesching H, Verp S, Marquis J, Spitz F, Constam DB, Trono D.

School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland.

More than forty per cent of the mammalian genome is derived from retroelements, of which about one-quarter are endogenous retroviruses (ERVs). Some are still active, notably in mice the highly polymorphic early transposon (ETn)/MusD and intracisternal A-type particles (IAP). ERVs are transcriptionally silenced during early embryogenesis by histone and DNA methylation (and reviewed in ref. 7), although the initiators of this process, which is essential to protect genome integrity, remain largely unknown. KAP1 (KRAB-associated protein 1, also known as tripartite motif-containing protein 28, TRIM28) represses genes by recruiting the histone methyltransferase SETDB1, heterochromatin protein 1 (HP1) and the NuRD histone deacetylase complex, but few of its physiological targets are known. Two lines of evidence suggest that KAP1-mediated repression could contribute to the control of ERVs: first, KAP1 can trigger permanent gene silencing during early embryogenesis, and second, a KAP1 complex silences the retrovirus murine leukaemia virus in embryonic cells. Consistent with this hypothesis, here we show that KAP1 deletion leads to a marked upregulation of a range of ERVs, in particular IAP elements, in mouse embryonic stem (ES) cells and in early embryos. We further demonstrate that KAP1 acts synergistically with DNA methylation to silence IAP elements, and that it is enriched at the 5' untranslated region (5'UTR) of IAP genomes, where KAP1 deletion leads to the loss of histone 3 lysine 9 trimethylation (H3K9me3), a hallmark of KAP1-mediated repression. Correspondingly, IAP 5'UTR sequences can impose in cis KAP1-dependent repression on a heterologous promoter in ES cells. Our results establish that KAP1 controls endogenous retroelements during early embryonic development.

PMID: 20075919 [PubMed - indexed for MEDLINE]
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Publication Types:

  • Research Support, Non-U.S. Gov't

MeSH Terms:

  • 5' Untranslated Regions/genetics
  • Acetylation
  • Animals
  • DNA Methylation
  • Embryo, Mammalian/metabolism
  • Embryo, Mammalian/virology
  • Embryonic Stem Cells/metabolism*
  • Embryonic Stem Cells/virology
  • Endogenous Retroviruses/genetics*
  • Fibroblasts
  • Gene Silencing*
  • Genes, Intracisternal A-Particle/genetics*
  • Genes, Reporter
  • Green Fluorescent Proteins/genetics
  • Green Fluorescent Proteins/metabolism
  • Histones/metabolism
  • Leukemia Virus, Murine/genetics
  • Leukemia Virus, Murine/physiology
  • Lysine/metabolism
  • Methylation
  • Mice
  • Nuclear Proteins/deficiency
  • Nuclear Proteins/genetics
  • Nuclear Proteins/metabolism*
  • Promoter Regions, Genetic/genetics
  • Repressor Proteins/deficiency
  • Repressor Proteins/genetics
  • Repressor Proteins/metabolism*

Substances:

  • 5' Untranslated Regions
  • Histones
  • Nuclear Proteins
  • Repressor Proteins
  • Trim28 protein, mouse
  • Green Fluorescent Proteins
  • Lysine
4. Nature. 2010 Jan 14;463(7278):178-83.

Genome sequence of the palaeopolyploid soybean.

Schmutz J, Cannon SB, Schlueter J, Ma J, Mitros T, Nelson W, Hyten DL, Song Q, Thelen JJ, Cheng J, Xu D, Hellsten U, May GD, Yu Y, Sakurai T, Umezawa T, Bhattacharyya MK, Sandhu D, Valliyodan B, Lindquist E, Peto M, Grant D, Shu S, Goodstein D, Barry K, Futrell-Griggs M, Abernathy B, Du J, Tian Z, Zhu L, Gill N, Joshi T, Libault M, Sethuraman A, Zhang XC, Shinozaki K, Nguyen HT, Wing RA, Cregan P, Specht J, Grimwood J, Rokhsar D, Stacey G, Shoemaker RC, Jackson SA.

HudsonAlpha Genome Sequencing Center, 601 Genome Way, Huntsville, Alabama 35806, USA.

Soybean (Glycine max) is one of the most important crop plants for seed protein and oil content, and for its capacity to fix atmospheric nitrogen through symbioses with soil-borne microorganisms. We sequenced the 1.1-gigabase genome by a whole-genome shotgun approach and integrated it with physical and high-density genetic maps to create a chromosome-scale draft sequence assembly. We predict 46,430 protein-coding genes, 70% more than Arabidopsis and similar to the poplar genome which, like soybean, is an ancient polyploid (palaeopolyploid). About 78% of the predicted genes occur in chromosome ends, which comprise less than one-half of the genome but account for nearly all of the genetic recombination. Genome duplications occurred at approximately 59 and 13 million years ago, resulting in a highly duplicated genome with nearly 75% of the genes present in multiple copies. The two duplication events were followed by gene diversification and loss, and numerous chromosome rearrangements. An accurate soybean genome sequence will facilitate the identification of the genetic basis of many soybean traits, and accelerate the creation of improved soybean varieties.

PMID: 20075913 [PubMed - indexed for MEDLINE]
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Publication Types:

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH Terms:

  • Arabidopsis/genetics
  • Breeding
  • Chromosomes, Plant/genetics
  • Evolution, Molecular
  • Gene Duplication
  • Genes, Duplicate/genetics
  • Genes, Plant/genetics
  • Genome, Plant/genetics*
  • Genomics*
  • Molecular Sequence Data
  • Multigene Family/genetics
  • Phylogeny
  • Plant Root Nodulation/genetics
  • Polyploidy*
  • Quantitative Trait Loci/genetics
  • Recombination, Genetic
  • Repetitive Sequences, Nucleic Acid/genetics
  • Soybean Oil/biosynthesis
  • Soybeans/genetics*
  • Synteny/genetics
  • Transcription Factors/genetics

Substances:

  • Transcription Factors
  • Soybean Oil

Secondary Source ID:

  • GENBANK/ACUP00000000
  • GENBANK/ACUP01000000
5. Nature. 2010 Jan 14;463(7278):157.

Spanish cuts could do lasting damage to biomedical research.

Albar JP.

Comment on:

PMID: 20075897 [PubMed - indexed for MEDLINE]
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Publication Types:

  • Comment
  • Letter

MeSH Terms:

  • Biomedical Research/economics*
  • Biomedical Research/trends
  • Budgets*
  • Federal Government
  • Genomics/economics
  • Spain
  • Technology Transfer

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