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Article Released Sun-10th-December-2006 19:33 GMT
Contact: Ruth Institution: Nature Publishing Group
 Malaria parasite diversity

Summaries of newsworthy papers published online on 10 December 2006 in Nature and Nature Research Journals. Lightning strikes twice for milk drinkers, How shigella causes dysentery, Sensing fungal infections, and Improving metagenomics efforts.

NATURE AND THE NATURE RESEARCH JOURNALS PRESS RELEASE

For papers that will be published online on 10 December 2006

This press release is copyrighted to the Nature journals mentioned below.

This press release contains:

Summaries of newsworthy papers:
- Malaria parasite diversity – Nature Genetics
- Lightning strikes twice for milk drinkers – Nature Genetics
- How shigella causes dysentery – Nature Immunology
- Sensing fungal infections – Nature Immunology
- Improving metagenomics efforts – Nature Methods

Mention of papers to be published at the same time with the same embargo
Geographical listing of authors

PDFs of all the papers mentioned on this release can be found in the relevant journal’s section of http://press.nature.com. Press contacts for the Nature journals are listed at the end of this release.

Warning: This document, and the Nature journal papers to which it refers, may contain information that is price sensitive (as legally defined, for example, in the UK Criminal Justice Act 1993 Part V) with respect to publicly quoted companies. Anyone dealing in securities using information contained in this document, or in advance copies of a Nature journal’s content, may be guilty of insider trading under the US Securities Exchange Act of 1934.

PICTURES: To obtain artwork from any of the journals, you must first obtain permission from the copyright holder (if named) or author of the research paper in question (if not).

NOTE: Once a paper is published, the digital object identifier (DOI) number can be used to retrieve the abstract and full text from the journal web site (abstracts are available to everyone, full text is available only to subscribers). To do this, add the DOI to the following URL: http://dx.doi.org/ (For example, http://dx.doi.org/10.1038/ng730). For more information about DOIs and Advance Online Publication, see http://www.nature.com/ng/aop/

PLEASE CITE THE SPECIFIC NATURE JOURNAL AND WEBSITE AS THE SOURCE OF THE FOLLOWING ITEMS. IF PUBLISHING ONLINE, PLEASE CARRY A HYPERLINK TO THE APPROPRIATE JOURNAL’S WEBSITE.

********************NATURE GENETICS *********************
(http://www.nature.com/naturegenetics)

[1], [2] & [3] Malaria parasite diversity

DOI: 10.1038/ng1930
DOI: 10.1038/ng1924
DOI: 10.1038/ng1931

Three studies independently characterize the genetic diversity of the parasite that causes malaria in the January issue of Nature Genetics.

Two of the studies focus on Plasmodium falciparum, the most deadly of the Plasmodium species known to cause human malaria, while one study also compares it to the related Plasmodium reichenowi, which infects chimpanzees. Overall, these data constitute a valuable resource that should improve understanding of drug resistance in malaria, as well as identifying candidate targets for vaccines.

Dyann Wirth and colleagues present a genome-wide map of diversity in P. falciparum, including full genome sequencing of 16 new and geographically diverse strains, and targeted sequencing of an additional 54 worldwide isolates. In an accompanying study, Xin-zhuan Su, Philip Awadalla and colleagues focus on sequencing of genomic regions coding for proteins within 4 P. falciparum isolates. They sequenced approximately 3,500 genes, representing about 19% of the genome, develop a high-resolution map of genetic variation, and report 7 new candidate targets for vaccines. In the third study, Manolis Dermitzakis, Matthew Berriman and colleagues provide the first sequence of the P. reichenowi strain, as well as the sequence of two P. falciparum strains, and examine the evolutionary differences between the two. One of the P. falciparum strains, a new uncultured clinical isolate from an individual from Ghana, may provide a better model than strains cultured in the laboratory.

Author contacts:

Dyann Wirth (Harvard School of Public Health, Boston, MA, USA)
Tel: +1 617 432 1563; E-mail: dfwirth@hsph.harvard.edu
[Author paper 1]

Xin-zhuan Su (National Institutes of Health, Rockville, MD, USA)
Tel: +1 301 402 0876; E-mail: xsu@niaid.nih.gov
[Author paper 2]

Emmanouil Dermitzakis (Wellcome Trust Sanger Institute, Hinxton, UK)
Tel: +44 1223 494866; E-mail: md4@sanger.ac.uk
[Author paper 3]

Additional contact for comment on the papers:

Jane Carlton (New York University School of Medicine, NY, USA)
Tel: +1 212 263 4377; E-mail: jane.carlton@med.nyu.edu


[4] Lightning strikes twice for milk drinkers

DOI: 10.1038/ng1946

The ability of Africans and Europeans to digest milk as adults is a textbook example of a trait arising independently in two populations in response to the same strong selective pressure. This ability - known as lactase persistence - is analyzed in the January issue of Nature Genetics.

Lactase persistence is frequent in Northern European populations, but much lower elsewhere, and may have become established as a consequence of cattle domestication and a pastoralist lifestyle. Previous work had shown that genetically, it could be attributed to variants that control the expression of the gene encoding the enzyme lactase-phlorizin hydrolase (LPH). This enzyme breaks down lactose into more easily absorbed sugars such as glucose and galactose.

Sarah Tishkoff and colleagues asked whether the genetic basis of lactase persistence in certain pastoralist populations in East Africa might be attributed to the same variants. They studied 470 lactase-persistent and lactase non-persistent individuals from Kenya, Tanzania and Sudan and found a significant association between lactase persistence and one variant that is very close in location to the LPH variant previously associated with the trait in Europeans. Because other genetic markers in the region differed between the two populations, the authors conclude that the lactase persistent-associated LPH variants arose independently.

Author contact:

Sarah Tishkoff (University of Maryland, College Park, MD, USA)
Tel: +1 301 405 6038; E-mail: tishkoff@umd.edu


Other papers from Nature Genetics to be published online at the same time and with the same embargo:

[5] Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia
DOI: 10.1038/ng1927


******************* NATURE IMMUNOLOGY *******************
(http://www.nature.com/natureimmunology)

[6] How shigella causes dysentery

DOI: 10.1038/ni1423

A report in the January issue of Nature Immunology explores how shigella bacteria survives and spreads in the gut to cause dysentery — a severe infection of the gastrointestinal tract that affects millions of people worldwide. The report finds that a protein produced by shigella is injected into host cells and blocks the production of immune signals required for preventing disease.

Laurence Arbibe and colleagues studied Shigella flexneri infection of human colon cells to understand the bacterial factors required to initiate disease. Shigella bacteria are known to inject up to 20 proteins into gut intestinal cells for the purpose of promoting infection and for dampening immune responses.

They found that one of the injected proteins from Shigella flexneri, called OpsF, could prevent gut cells from switching on genes involved in immune responses. As a consequence of OspF function, Shigella flexneri avoids being killed by immune cells of their host and is thus able to spread throughout the gut and cause disease.

This study highlights the precision with which pathogens such as shigella can dramatically alter host cells. It also suggests that blocking OspF may provide a therapeutic target for treating bacterial dysentery that kills hundreds of thousands of people annually.

Author contact:

Laurence Arbibe (Pasteur Institut, Paris, France)
Tel: +33 1 40 61 32 47; E-mail: arbibe@pasteur.fr

Additional comment on the paper:

B. Brett Finlay (University of British Columbia, Vancouver, Canada)
Tel: + 1 604 822 2210; E-mail: bfinlay@interchange.ubc.ca


[7] & [8] Sensing fungal infections

DOI: 10.1038/ni1408
DOI: 10.1038/ni1425

Two studies in the January issue of Nature Immunology demonstrate the importance of a host protein in recognizing the presence of fungal infections. Pathogenic fungi can cause life-threatening infections in individuals with immunodeficiencies, such as those with advanced HIV disease.

Two independent groups, led by Gordon Brown and Yoichiro Iwakura, produced mice that lack the protein Dectin-1, a cell-surface protein implicated in immune responses to fungal infections. Both groups show that mice that lack Dectin-1 are relatively normal except when infected with fungi, which causes more lethality in the mutant mice. The authors also evaluated the types of blunted immune responses that occur in the mutant mice and show that only specific immune functions are defective.

These studies substantially extend our understanding of how pathogenic fungi affect host tissues and the requirement of Dectin-1 in those processes.

Author contact:

Gordon Brown (University of Cape Town, South Africa)
Tel: +27 21 406 6684; E-mail: gordon.brown@mweb.co.za
[Author Paper 7]

Yoichiro Iwakura (University of Tokyo, Japan)
Tel: + 81 3 5449 5536; E-mail: iwakura@ims.u-tokyo.ac.jp
[Author Paper 8]

Additional comment on the paper:

Jürg Tschopp (University of Lausanne, Epalinges, Switzerland)
Tel: + 41 21 692 57 38; E-mail: jurg.tschopp@unil.ch


*********************NATURE METHODS**********************
(http://www.nature.com/nmeth)

[9] Improving metagenomics efforts
DOI: 10.1038/nmeth976

A novel technique for simplifying the study of important ecosystems is described in the January issue of Nature Methods.

Shotgun sequencing methods used in metagenomics efforts to study microbial communities produce massive collections of sequence fragments that are very difficult to analyze. A number of methods have been used to attempt to assemble and classify these sequences but they generally fail for highly complex samples and short fragments. Isidore Rigoutsos and colleagues describe a new sequence classification method that uses information from 340 completed genomes to classify and assemble sequence fragments from complex communities that have been resistant to previous efforts.

Author contact:

Isidore Rigoutsos (IBM Thomas J Watson Research Center, Yorktown Heights, NY, USA)
Tel: +1 914 945 1384; E-mail: rigoutso@us.ibm.com


Other papers from Nature Methods to be published online at the same time and with the same embargo:

[10] Disentangling conformational states of macromolecules in 3D-EM through likelihood optimization
DOI: 10.1038/nmeth992

[11] Retrograde neuronal tracing with a deletion-mutant rabies virus
DOI: 10.1038/nmeth999

[12] Major signal increase in fluorescence microscopy through dark-state relaxation
DOI: 10.1038/nmeth986


************************************************************

Items from other Nature journals to be published online at the same time and with the same embargo:

Nature (http://www.nature.com/nature)

[13] Hsp70 regulates erythropoiesis by preventing caspase-3-mediated cleavage of GATA-1
DOI: 10.1038/nature05378

[14] A prokaryotic proton-gated ion channel from the nicotinic acetylcholine receptor family
DOI: 10.1038/nature05371


Nature PHYSICS (http://www.nature.com/naturephysics)

[15] Scaling of proton acceleration driven by petawatt-laser–plasma interactions
DOI: 10.1038/nphys476

[16] Controllable valley splitting in silicon quantum devices
DOI: 10.1038/nphys475

[17] Quasiparticle dynamics in graphene
DOI:10.1038/nphys477


NATURE MATERIALS (http://www.nature.com/naturematerials)

[18] Atomic structure of the binary icosahedral Yb–Cd quasicrystal
DOI: 10.1038/nmat1799

[19] Six-fold coordinated carbon dioxide VI
DOI: 10.1038/nmat1800

[20] A rack-and-pinion device at the molecular scale
DOI: 10.1038/nmat1802

[21] Triggering dynamics of the high-pressure benzene amorphization
DOI: 10.1038/nmat1803


Nature MEDICINE (http://www.nature.com/naturemedicine)

[22] NF-kappaB in breast cancer cells promotes osteolytic bone metastasis by inducing osteoclastogenesis via GM-CSF
DOI: 10.1038/nm1519

[23] Loss of tumor suppressor PTEN function increases B7-H1 expression and immunoresistance in glioma
DOI: 10.1038/nm1517

[24] Chromosome 5q deletion and epigenetic suppression of the gene encoding alpha-catenin (CTNNA1) in myeloid cell transformation
DOI: 10.1038/nm1512

[25] Lactobacillus acidophilus modulates intestinal pain and induces opioid and cannabinoid receptors
DOI: 10.1038/nm1521


Nature NEUROSCIENCE (http://www.nature.com/natureneuroscience)

[26] A new naturally occurring GABAA receptor subunit partnership with high sensitivity to ethanol
DOI: 10.1038/nn1813

[27] Attractive axon guidance involves metric membrane transport and exocytosis in the growth cone
DOI: 10.1038/nn1814

[28] Representation of body identity and body actions in extrastriate body area and ventral premotor cortex
DOI: 10.1038/nn1815

[29] Essential function of HIPK2 in TGFbeta-dependent survival of midbrain dopamine neurons
DOI: 10.1038/nn1816


NATURE CELL BIOLOGY (http://www.nature.com/naturecellbiology)

[30] Regulation of protein tyrosine phosphatase (PTP) 1B by sumoylation
DOI: 10.1038/ncb1522

[31] H3K9 methylation and RNA interference regulate nucleolar organization and repeated DNA stability
DOI: 10.1038/ncb1514

[32] Basal-to-apical cadherin flow at cell junctions
DOI: 10.1038/ncb1520

[33] Triggering neural differentiation of ES cells by subtype switching of importin-alpha
DOI: 10.1038/ncb1521


Nature STRUCTURAL & MOLECULAR BIOLOGY (http://www.nature.com/natstructmolbiol)

[34] Structural insight into the substrate specificity of DNA Polymerase mu
DOI: 10.1038/nsmb1180

[35] Heme is involved in microRNA processing
DOI: 10.1038/nsmb1182

[36] Mutational analysis reveals two independent molecular requirements during transfer RNA selection on the ribosome
DOI: 10.1038/nsmb1183


*************************************************************

GEOGRAPHICAL LISTING OF AUTHORS

The following list of places refers to the whereabouts of authors on the papers numbered in this release. The listing may be for an author's main affiliation, or for a place where they are working temporarily. Please see the PDF of the paper for full details.

BELGIUM
Leuven: 25

CANADA:
Burnaby: 16
Montreal: 5
Quebec City: 5

CHINA
Shanghai: 24, 27

DENMARK
Copenhagen: 13

FRANCE
Aubiere: 25
Clermont-Ferrand: 25
Lille: 25
Palaiseau: 15
Paris: 6, 13, 14, 25
Saint Martin d’Heres: 18
Toulouse: 20

GERMANY
Berlin: 17, 20
Erlangen: 17
Goettingen: 12
Greifswald-Insel Riems: 11
Muenchen: 11

INDIA
Karnataka: 30

ITALY
Chieti Scalo: 28
Ferrara: 4
Florence: 21
Pordenone: 28
Rome: 13, 21, 28
Trieste: 21

JAPAN
Kyoto: 32
Miyagi: 8
Okinawa: 8
Osaka: 8, 33
Saitama: 18, 27
Sapporo: 18
Sendai: 18
Tokyo: 8
Tsukuba: 18

KENYA
Nairobi: 4

KOREA
Seoul: 6

NETHERLANDS
Rijswijk: 3

SENEGAL
Dakar: 1

SOUTH AFRICA
Cape Town: 7

SPAIN
Derio-Bizkaia: 10
Madrid: 10

SUDAN
Khartoum: 4

SWEDEN
Lund: 15

TANZANIA
Dar es Salaam: 4

UNITED KINGDOM
Belfast: 15
Cambridge: 16
Didcot: 15
Glasgow: 15
Hinxton: 3, 4
London: 3, 7, 30
Oxford: 2, 3, 7
Reading: 15

UNITED STATES OF AMERICA
California
Berkeley: 17, 31
Davis: 30
Duarte: 23
La Jolla: 11, 27
Livermore: 19
Los Angeles: 22, 23, 26, 30, 35
Palo Alto: 24
San Francisco: 29
Walnut Creek: 9
Delaware:
Newark: 10
Illinois
Chicago: 4, 24
Maryland
Baltimore: 36
Bethesda: 2
College Park: 4
Massachusetts
Boston: 1, 24, 30
Cambridge: 1, 5
Michigan
Ann Arbor: 22
New York
Albany: 10
New York: 3, 10, 16
Rochester: 24
Yorktown Heights: 9
North Carolina
Chapel Hill: 34
Durham: 4
Raleigh: 2
Research Triangle Park: 34
Pennsylvania
Philadelphia: 30
Pittsburgh: 7, 26
Texas
Houston: 24
Wisconsin
Madison: 16


PRESS CONTACTS…

For media inquiries relating to embargo policy for all the Nature Research Journals:

Katherine Anderson (Nature, London)
Tel: +44 20 7843 4502; E-mail: k.anderson@nature.com

Ruth Francis (Senior Press Officer, Nature, London)
Tel: +44 20 7843 4562; E-mail: r.francis@nature.com

For media inquiries relating to editorial content/policy for the Nature Research Journals, please contact the journals individually:

Nature Cell Biology (London)
Bernd Pulverer
Tel: +44 20 7843 4892; E-mail: cellbio@nature.com

Nature Genetics (New York)
Orli Bahcall
Tel: +1 212 726 9311; E-mail: natgen@natureny.com

Nature Immunology (New York)
Laurie Dempsey
Tel: +1 212 726 9372; E-mail: immunology@natureny.com

Nature Materials (London)
Maria Bellantone
Tel: +44 20 7843 4556; E-mail: materials@nature.com

Nature Medicine (New York)
Juan Carlos Lopez
Tel: +1 212 726 9325; E-mail: medicine@natureny.com

Nature Methods (New York)
Allison Doerr
Tel: +1 212 726 9393; E-mail: methods@natureny.com

Nature Neuroscience (New York)
Sandra Aamodt (based in California)
Tel: +1 530 795 3256; E-mail: neurosci@natureny.com

Nature Physics (London)
Alison Wright
Tel: +44 20 7843 4555; E-mail: a.wright@nature.com

Nature Structural & Molecular Biology (New York)
Michelle Montoya
Tel: +1 212 726 9326; E-mail: nsmb@natureny.com

About Nature Publishing Group

Nature Publishing Group (NPG) is a division of Macmillan Publishers Ltd, dedicated to serving the academic, professional scientific and medical communities. NPG's flagship title, Nature, was first published in 1869. Other publications include Nature research journals, Nature Reviews, Nature Clinical Practice and a range of prestigious academic journals including society-owned publications. NPG also provides news content through news@nature.com and scientific career information through Naturejobs.

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Associated links

Journal information

NATURE Genetics, NATURE Immunology, NATURE Methods, NATURE

Keywords associated to this article: Malaria, Lactase persistence, dysentry, shigella, fungal infections, metagenomics
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