Monday, 26 May 2008

Weekly BioNews 19 - 26 May 2008


- Scientists 'paint' viruses to track their fate in the body

May 20, 2008 05:40 PM

Biologists from Austria and Singapore developed a technique that adds a new twist on the relationship between biology and art. In an article recently published online in The FASEB Journal (http://www.fasebj.org) and scheduled for the August 2008 print issue, these researchers describe how they were able to coat—or paint—viruses with proteins.

This breakthrough should give a much-needed boost to the efficiency of some forms of gene therapy, help track and treat viral disease and evolution, improve the efficiency of vaccines, and ultimately allow health care professionals track the movement of viral infections within the body. Specifically, the new method should make it easier to track and treat infectious diseases such as HIV/AIDS, influenza, hepatitis C, and dengue fever. And because viruses can also be used to introduce biotechnology drugs and replacement genes, and act as vaccines, this research should lead to new treatments for cancer, cardiovascular, metabolic and inherited disorders.....

- Fluorescent nano-barcodes could revolutionize diagnostics

May 22, 2008 07:31 PM

A new technology with research and clinical application including the early detection of disease has been invented and developed by University of Queensland researchers.

Dr Krassen Dimitrov, from UQ's Australian Institute for Bioengineering & Nanotechnology, has developed fluorescent “barcodes” called nanostrings, offers greater sensitivity and accuracy than current detection methods.

The research has been published the prestigious international journal Nature Biotechnology.

Dr Dimitrov said nanostrings bind to RNA molecules for digital gene expression analysis.

“Because this system can count the exact number of biomolecules present we can get an extremely accurate and sensitive picture of gene expression at a particular point in time,” Dr Dimitrov said.

“This quantitative data is superior to other gene expression systems such as microarrays, which rely on the analogue measurement of fluorescence and therefore are less accurate and have a limited range.

“The nanostring is an important technological development in both clinical and research settings. We will be able to more accurately detect molecules associated with particular diseases and in the research arena, we will be able to identify new molecules associated with diseases and trace these back to the genes responsible."


- Plant Flavonoid In Celery And Green Peppers Found To Reduce Inflammatory Response In The Brain

ScienceDaily (May 23, 2008)

Researchers at the University of Illinois report that a plant compound found in abundance in celery and green peppers can disrupt a key component of the inflammatory response in the brain. The findings have implications for research on aging and diseases such as Alzheimer's and multiple sclerosis.

Inflammation can be a blessing or a blight. It is a critical part of the body's immune response that in normal circumstances reduces injury and promotes healing. When it goes awry, however, the inflammatory response can lead to serious physical and mental problems.

Inflammation plays a key role in many neurodegenerative diseases and also is implicated in the cognitive and behavioral impairments seen in aging.

The new study looked at luteolin (LOO-tee-OH-lin), a plant flavonoid known to impede the inflammatory response in several types of cells outside the central nervous system. The purpose of the study was to determine if luteolin could also reduce inflammation the brain, said animal sciences professor and principal investigator Rodney Johnson....

- Many Paths, Few Destinations: How Stem Cells Decide What They'll Become

ScienceDaily (May 24, 2008)

How does a stem cell decide what specialized identity to adopt -- or simply to remain a stem cell? A new study suggests that the conventional view, which assumes that cells are "instructed" to progress along prescribed signaling pathways, is too simplistic. Instead, it supports the idea that cells differentiate through the collective behavior of multiple genes in a network that ultimately leads to just a few endpoints -- just as a marble on a hilltop can travel a nearly infinite number of downward paths, only to arrive in the same valley.

When exposed to a growth factor, a blood stem cell, represented by a blue marble, falls into a new "attractor state," depicted as a valley in a landscape, to become a red blood cell. Different influences, such as differentiation factors, can lead stem cells to the same attractor state, but each cell can take very different paths though the landscape to get there (just as a marble might take a different path each time it rolls down a hill). (Credit: Children's Hospital Boston)

The findings, published in the May 22 issue of Nature, give a glimpse into how that collective behavior works, and show that cell populations maintain a built-in variability that nature can harness for change under the right conditions. The findings also help explain why the process of differentiating stem cells into specific lineages in the laboratory has been highly inefficient.

Led by Sui Huang, MD, PhD, a Visiting Associate Professor in the Children's Hospital Boston Vascular Biology Program (now also on the faculty of the University of Calgary), and Hannah Chang, an MD/PhD student in Children's Vascular Biology Program, the researchers examined how blood stem cells "decide" to become white blood cell progenitors or red blood cell progenitors......

Scientists Back The Use Of Maize As An Efficient 'Factory' For Protein-based Pharmaceutical Products
ScienceDaily (May 25, 2008)
Scientists from the Universidad de Lleida (University of Lleida) have published a study supporting the argument that maize seeds are an effective and sure platform within molecular agriculture to alleviate diseases. Over the next few years AIDS could be one of the first diseases to benefit from these results, although regulations for this technology are being developed at the same time as research is being undertaken.

Maize, the third most important cereal in the world, has a great number of advantages for molecular agriculture. Among these are its physiology, its capacity to express recombinant proteins in the seeds, its widespread cultivation and its genetic diversity, as well as being anti-allergenic and non-toxic.

Last March, transgenic maize became the first plant to be developed commercially for medical use. The PNAS review published the following findings: a maize seed with genes from the 2G12 antibody (already known for its capacity to neutralise infection from the virus) could produce antibodies against the transmission of HIV. Researchers from the Departamento de Producción Vegetal y Ciencia Forestal [Department of Plant Production and Forest Science] at the Universidad de Lleida, were those who actually designed this drug during an international project known as Pharma-Planta (made up of 39 European and South African teams), and headed by the British man Paul Christou...


- Real-time Observation Of DNA-repair Mechanism

ScienceDaily (May 25, 2008)

For the first time, researchers at Delft University of Technology have witnessed the spontaneous repair of damage to DNA molecules in real time. They observed this at the level of a single DNA molecule. Insight into this type of repair mechanism is essential as errors in this process can lead to the development of cancerous cells.

Researchers from the Kavli Institute of Nanoscience Delft are to publish an article on this in the journal Molecular Cell.

Cells have mechanisms for repairing the continuous accidental damage occurring in DNA. These damages can vary from a change to a single part of the DNA to a total break in the DNA structure. These breaks can, for instance, be caused by ultraviolet light or X-rays, but also occur during cell division, when DNA molecules split and form two new DNA molecules. If this type of break is not properly repaired it can be highly dangerous to the functioning of the cell and lead to the creation of a cancerous cell.

One major DNA-repair mechanism involved in repairing these breaks is known as homologous recombination. This mechanism has been observed for the first time by Delft University of Technology researchers in real time and at the level of a single DNA molecule....

- Seasonal patterns of flu

Date: 21/05/2008

Outbreaks of the most common type of influenza virus, A (H3N2), are seeded by viruses that originate in East and Southeast Asia and migrate around the world, new research has found. This discovery may help to further improve flu vaccines and make the evolution of the virus more predictable.Scientists at the University of Cambridge, in collaboration with scientists from the World Health Organisation (WHO) Global Influenza Surveillance Network, found that each year since 2002 influenza A (H3N2) viruses have migrated out of what the authors call the 'East and Southeast Asian circulation network' (which includes tropical, subtropical, and temperate countries) and spread throughout the world. Their findings are reported in the current edition of Science.

Annual influenza epidemics are thought to infect 5 - 15 per cent of the world population each year, cause 3 to 5 million cases of severe illness, and between 250000 and 500 000 deaths, according to the WHO. The flu vaccine protects the 300 million people vaccinated each year.

Because the flu virus evolves so quickly, there are a number of challenges involved in making the vaccine.

In order to create an effective vaccine, each year in February and September a WHO committee meets to select the strains of flu to use in the influenza virus vaccine.

These scientists (many of whom are co-authors on this study) decide which strains pose the greatest threat for the next flu season.....

- Turning back the clock

Date: 19/05/2008

Myelin-making Schwann cells have an ability every ageing Hollywood star would envy: they can become young again. According to a study appearing in the May 19 issue of the Journal of Cell Biology, David B. Parkinson (University College London, London, UK) and colleagues have pinned down a protein that returns the cells to their youth, a finding that might help researchers understand why myelin production falters in some diseases.Wrapped around neurons in the peripheral nervous system, Schwann cells can "dedifferentiate" into a state in which they can't manufacture myelin. Reverting to an immature type of cell speeds healing of injured nerves. Researchers knew that the protein Krox-20 pushes immature Schwann cells to specialise and form myelin, but they didn't know what prompts the reversal. One suspect was a protein called c-Jun, which youthful Schwann cells make but Krox-20 blocks.

Parkinson et al. cultured neurons with Schwann cells whose c-Jun gene they could activate. Turning on the gene curbed myelination, suggesting that c-Jun prevents young Schwann cells from growing up. c-Jun also prodded mature Schwann cells to become youthful again, the researchers discovered. Schwann cells that are separated from neurons normally dedifferentiate, but the team found that the cells remained specialised if c-Jun was missing. They suspect that c-Jun works in part by activating Sox-2, as this protein also inhibits myelination.....

Wednesday, 21 May 2008

Monkeys genetically modified to have Huntington's

Sun May 18, 2008 4:10pm EDT

By Will Dunham

WASHINGTON (Reuters) - Scientists have created monkeys genetically modified to have Huntington's disease in an effort to gain a deeper understanding of the fatal ailment and uncover clues to possible new treatments.

In the journal Nature on Sunday, the researchers said one of two surviving rhesus macaque monkeys engineered to have the defective gene that causes Huntington's in humans already is showing tell-tale symptoms at age 10 months.

Huntington's -- incurable and hereditary -- is caused by a single abnormal gene in which certain nerve cells in the brain waste away. People are born with the gene but symptoms typically do not appear until middle age.

Researchers often study laboratory animals such as mice to get insights into the underlying biology of diseases. But monkeys and other primates are more similar to people than rodents in physiological, neurological and genetic features.

The scientists at Emory University's Yerkes National Primate Research Center in Atlanta said the monkeys are the first primates genetically modified to have a human disease.
They hope studying the monkeys will allow for greater knowledge of Huntington's and ideas for new drugs.
"Rodent species can capture some of the characteristics of the disease, but they have not been satisfactory in being able to really capture the essence of the disease," Stuart Zola, head of the Yerkes center, said in a telephone interview.

"Now we have a genetically modified nonhuman primate that really has captured the clinical signs that we see in patients with Huntington's disease."
Those with the progressive, degenerative disease experience uncontrolled movements, emotional disturbances and mental deterioration.

Drugs can help manage symptoms but do not stop the physical and mental decline. People typically die within 10 to 15 years after symptoms arise.

The researchers said they chose Huntington's as the disease for creating the genetically modified monkeys with an eye toward simplicity -- because it is linked to mutations in a single gene rather than multiple genes.

Zola said the achievement could pave the way for creating genetically modified primates with other neurodegenerative ailments such as Parkinson's disease and Alzheimer's disease.

"This research allows scientists to advance beyond mouse models, which do not replicate all of the changes in the brain and behavior that humans with Huntington's disease experience," said John Harding, a primate resources official at the National Institutes of Health, which funded the study.

Using so-called viral vector technology, the researchers transferred the Huntington's gene into a monkey egg cell. After using in vitro fertilization, the egg grew into a four-cell embryo and was then placed in the womb of a female monkey acting as a surrogate mother.

Of the five baby monkeys born using this process, two died within about a day, another one died in about a month and two are still living at age 10 months, according to Anthony Chan of the Yerkes center and Emory University School of Medicine.

One of the two surviving monkeys has developed symptoms including involuntary movements of the hands and face, Chan said. The other has no symptoms of the disease yet but may develop them later, he added.

(Editing by John O'Callaghan)

Tuesday, 20 May 2008

MPs back hybrid embyro research

BBC Page last updated at 21:57 GMT, Monday, 19 May 2008 22:57 UK
The government has survived two big challenges to its controversial plans to change the law on embryo research for the first time in 20 years.

A cross-party attempt to ban hybrid human animal embryos was defeated on a free vote, by 336 to 176.

Catholic cabinet ministers Ruth Kelly, Des Browne and Paul Murphy voted for a ban. PM Gordon Brown and Tory leader David Cameron both opposed it.

A bid to ban "saviour siblings" was voted down by 342 votes to 163.

The votes followed two impassioned debates in the committee stage of the Human Fertilisation and Embryology Bill, aimed at updating laws from 1990 in line with scientific advances.

'Ethically wrong'

On Tuesday, MPs have a further free vote on the emotive issue of cutting the abortion time limit.

Mr Cameron, along with Mr Brown, has backed the use of hybrid embryos as a means to develop treatments for cancer and conditions such as Parkinson's and Alzheimer's disease. They also both support the creation of "saviour siblings".
However, the majority of the Tory shadow cabinet, including shadow foreign secretary William Hague and shadow home secretary David Davis, backed the unsuccessful attempt to ban hybrids.

A human embryo

Critics say tinkering with human embryos is 'immoral'


Ex-minister Edward Leigh, who led the fight against the creation of hybrid "admixed" embryos, said they were "ethically wrong and almost certainly medically useless".

He said there was "no evidence yet to substantiate" claims the work could lead to treatment for degenerative diseases like Parkinson's and Alzheimer's.

The bill would allow regulated research using hybrid or "admix" embryos, where the nuclei of human cells are inserted into animal eggs. The resulting embryos would be kept for up to 14 days to harvest stem cells.

Health Minister Dawn Primarolo says any research done using human embryos "must satisfy the Human Fertilisation and Embryology Authority that it was necessary or desirable".

No human "admix" embryo would be implanted into a woman or animal, she says.

'Too human'?

But Mr Leigh said: "We do not believe that regulation is enough. We believe this is a step too far and therefore should be banned.

"In embryos, we do have the genetic make up of a complete human being and we could not and should not be spliced together with the animal kingdom."

And ex-Labour minister Sir Gerald Kaufman, agreed, adding: "How far do you go? Where do you stop? What are the limits and what are the boundaries?

"If you permit the creation of hybrid embryos now, what will you seek to permit next time, even if you have no idea where it will lead?"
Labour's Chris Bryant, a former Anglican curate, said Mr Leigh's arguments were like those used by church leaders against the smallpox vaccine.

"They were wrong and I think you are wrong today," he said.

Liberal Democrat Evan Harris criticised those who argued hybrid embryos were too human.

"If it's ethically acceptable to use up and destroy fully human embryos with all the potential they have, how is it right to provide for hybrid embryos, with less potential of viability, greater protection?" he said.

A separate attempt to ban "pure" hybrid embryos, that would mix a human egg with animal sperm or vice versa, was also defeated in the Commons by 286 votes to 223, a government majority of 63.

Tory David Burrowes' attempt to stop parents having so-called "saviour siblings" - babies selected to provide genetic material for seriously ill relatives - also suffered defeat.

The Bill would allow the selection of embryos that are a tissue match for a sick older brother or sister.

But Mr Burrowes said it was wrong to create a child for the benefit of another, regardless of "the need".

MPs are being given a free vote on four controversial parts of the bill. The other two areas are:
Role of fathers in fertility treatment: Would end the requirement for IVF clinics to consider the "welfare" of any child created in terms of need for a father. Debate from 1530 BST Tuesday, with vote at about 1830 BST.

The upper limit for abortion: Amendments have been put down to the bill to cut from 24 weeks the time limit for abortions. Debate on Tuesday from 1830 BST, with votes at about 2200 BST.
The Roman Catholic Church has branded the use of hybrid embryos as "monstrous" and says tinkering with life in this way is immoral.

Catholic bishops in Britain and the Irish Republic have given £25,000 to scientists using adult stem cells, which is less controversial than using immature ones.
Such cells can be used to create brain, skin, heart and other tissue for treating diseases.
But Sir Leszek Borysiewicz, chief executive of the Medical Research Council, said the result would keep the UK at the forefront of embryo research.

Conservative leader David Cameron, along with Mr Brown, has backed the use of hybrid embryos as a means to develop treatments for cancer and conditions such as Parkinson's and Alzheimer's disease. They also both support the creation of "saviour siblings".

Scientists at Newcastle University announced last month that they had created the first part-human, part-animal hybrid embryos in the UK.

They were created by injecting DNA derived from human skin cells into eggs taken from cows' ovaries which had had virtually all their genetic material removed.

Researchers say these human-animal "admixed" embryos could help solve the current problem of the lack of human eggs from which to generate embryos.

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Article

Monday, 19 May 2008

Weekly BioNews 12 - 19 May 2008

- Spotlight On A Key Player In The Dance Of Chromosomes

ScienceDaily (May 16, 2008)

Cell division is essential to life, but the mechanism by which emerging daughter cells organize and divvy up their genetic endowments is little understood. In a new study, researchers at the University of Illinois and Columbia University report on how a key motor protein orchestrates chromosome movements at a critical stage of cell division.

Within the complex world of the cell, motor proteins function as a kind of postal service. These proteins carry cargo from one location to another in the cell, a job that requires precision, in both the location and the timing of delivery. They are fueled by a small molecule, adenosine tri-phosphate (ATP).

Some motor proteins are essential to mitosis – the process by which cell division occurs in higher organisms. During cell division it is important for chromosomes to line up at the middle of the parent cell allowing for their separation between the two daughter cells.

Motor proteins play a key role in the movement of chromosomes to and from the poles of the cell. Should any of these processes lose coordination, it could result in disease or cell death....

- First Transgenic Monkey Model Of Huntington's Disease Developed

ScienceDaily (May 19, 2008)

Scientists have developed the first genetically altered monkey model that replicates some symptoms observed in patients with Huntington's disease, according to a new study funded by the National Institutes of Health. Researchers are now able to better understand this complex, devastating and incurable genetic disorder affecting the brain. This advance, reported in the May 18 advance of online publication edition of Nature, could lead to major breakthroughs in the effort to develop new treatments for a range of neurological diseases.

Huntington's is an inherited disease caused by a defective gene that triggers certain nerve cells in the brain to die. Symptoms may include uncontrolled movements, mood swings, cognitive decline, balance problems, and eventually losing the ability to walk, talk or swallow. It affects five to 10 people in every 100,000. There is no known treatment to halt progression of the disease, only medications to relieve symptoms. Death typically occurs 15 to 20 years after onset.
This study marks the first time that researchers have developed a rhesus macaque model of a specific human disease using transgenic technologies, a marked improvement over mouse models. Transgenic animals are created using a recombinant DNA method to modify a genome...

- Deep Sea Methane Scavengers Captured

ScienceDaily (May 16, 2008)

Scientists of the Helmholtz Centre for Environmental Research (UFZ) in Leipzig and the California Institute of Technology (Caltech) in Pasadena succeeded in capturing syntrophic (means "feeding together") microorganisms that are known to dramatically reduce the oceanic emission of methane into the atmosphere. These microorganisms that oxidize methane anaerobically are an important component of the global carbon cycle and a major sink for methane on Earth. Methane - a more than 20 times stronger greenhouse gas than carbon dioxide - constantly seeps out large methane hydrate reservoirs in the ocean floors, but 80 percent of it are immediately consumed by these microorganisms.

The importance of the anaerobic oxidation of methane for the Earth’s climate is known since 1999 and various international research groups work on isolating the responsible microorganisms, so far with little success. Pernthaler and co-workers developed a new molecular technique to selectively separate these microorganisms from their natural complex community, and subsequently sequenced their genome. The findings were exciting: Besides identifying all genes responsible for the anaerobic oxidation of methane, new bacterial partners of this syntrophic association were discovered and the ability to fix N2 could be demonstrated....

- DNA fingerprinting simplified

May 13, 2008 11:52 PM

Agarose gel electrophoresis" Most teenagers wouldn’t have a clue what this scientific term means, but middle school student Andrew Trigiano knows the protocol inside and out. When Andrew was 12, his father Robert Trigiano, a professor at the University of Tennessee, was looking for an interesting science project for his son. Setting out to compare differences in popular brands of Easter egg dyes, Trigiano’s project soon grew into a full-blown scientific study and set of replicable classroom experiments.

One of the most frequently used tools in biochemistry and biotechnology, agarose gel electrophoresis is a common forensic technique often used in genetic or DNA fingerprinting. The procedure is achieved by moving negatively charged nucleic acid molecules through a gelatinous substance known as agarose by using an electric field.

Andrew, in collaboration with his father and other researchers, completed the study, which is published in the January 2008 issue the American Society of Horticultural Science’s journal HortTechnology. The youngest author ever to publish in an ASHS journal, Andrew was only 12 when he began the research project and 14 when the study was published.

- MIT crafts bacteria-resistant films

May 15, 2008 09:28 PM

Having found that whether bacteria stick to surfaces depends partly on how stiff those surfaces are, MIT engineers have created ultrathin films made of polymers that could be applied to medical devices and other surfaces to control microbe accumulation.

The inexpensive, easy-to-produce films could provide a valuable layer of protection for the health care industry by helping to reduce the spread of hospital-acquired infections, which take the lives of 100,000 people and cost the United States an estimated $4.5 billion annually.

The researchers, who describe their work in an upcoming issue of the journal Biomacromolecules, found they could control the extent of bacterial adhesion to surfaces by manipulating the mechanical stiffness of polymer films called polyelectrolyte multilayers. Thus, the films could be designed to prevent accumulation of hazardous bacteria or promote growth of desirable bacteria.

“All other factors being equal, mechanical stiffness of material surfaces increases bacterial adhesion,” said Krystyn Van Vliet, the Thomas Lord Assistant Professor of Materials Science and Engineering and the paper's anchor author....

- Biosensor for measuring stress in cells

May 17, 2008 03:11 PM

Cancer, nervous system disorders such as Parkinson’s disease, cardiovascular disorders and old age have one thing in common: Both in afflicted tissue and in aging cells, scientists have observed oxidative changes in important biomolecules. These are caused by reactive oxygen molecules, including the notorious “free radicals” that are formed as a by-product of cellular respiration and attack cellular proteins, nucleic and fatty acids.

Today, reactive oxygen molecules are no longer regarded by and large as culprits, since it has turned out that they are also involved in regulating major life processes such as growth and cell death. The right balance between oxidation and the reverse reaction, reduction, makes the difference between health and disease. “Oxidative stress” arises when this balance shifts towards oxidation-promoting processes.

So far, it has hardly been possible for scientists to measure the level of oxidation and, thus, the stress status of living cells. This will now be feasible thanks to a highly sensitive biomarker presented in the journal Nature Methods by Dr. Tobias Dick and co-workers of the German Cancer Research Center, jointly with colleagues from the University of Heidelberg.

Tuesday, 13 May 2008

Monsanto Patent for a Pig

After getting involved in the Soya controversies, Monsanto found itself in the midst of another controversy with its "Pig Patent". In 2005, Monsanto had filed two patents for processes which controlled the breeding and the herds of pigs. This resulted in Monsanto being under scrutiny for ownership rights over pigs and their offspring. Many commentators felt that Monsanto was planning to create improved designer animals for human consumption using special breeding techniques. Monsanto was able to control breeds with specific characteristics as per the patent, and disallowing other breeders and farmers from doing so. The patent, being broad, remained unclear about the ownership of the proceeds from the sale of the pigs by farmers. It did not mention about the royalties involved when a food producer produces sausages (as an example) using those pigs which are bred using Monsanto’s process. This was a source of royalty for Monsanto. Monsanto wanted to cash in on the growing consumer demand for meat products globally and many activists question the ethics of Monsanto’s actions.

The filing of the patents also raises questions about the livelihood of all the pig breeders – those who use Monsanto process on the ownership and those who use traditional methods of pig rearing accused of patent infringement. As like the earlier seed controversy and the Canadian incident, the farmers are afraid of losing their livelihood due to Monsanto’s breeding technique. They fear that Monsanto would also file lawsuits against them like they did to the soya and corn farmers. This stems from the fact that the patent filed by Monsanto is quite broad and the interpretation would lead to them owning not just the breeding process, but also the pigs which are bred from this method.

However, there is no evidence of any addition in the nutritional value and fat content lowering which has been claimed by Monsanto. On its part, Monsanto claims that it is not trying to patent pigs; it wants the ability to track which animals come from its system. Advocates of genetically modified foods stress that this scientific process is one of the ways of increasing food production in a world where the demand for food is ever increasing. It brings about an increase in supply and is beneficial to the community. Hundreds of patents on animals have been granted over the years, including salmon, shrimps and mice. But most are Genetically Modified creatures used in laboratory research, not common farm animals which are a source of income for people.

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Part 5

From: sowhtttt

Monday, 12 May 2008

Weekly BioNews 05 - 12 May 2008

- Surprising Discovery: Multicellular Response Is 'All For One'

ScienceDaily (May 10, 2008)

Real or perceived threats can trigger the well-known "fight or flight response" in humans and other animals. Adrenaline flows, and the stressed individual's heart pumps faster, the muscles work harder, the brain sharpens and non-essential systems shut down. The whole organism responds in concert in order to survive.

At the molecular level, it has been widely assumed that, in single-celled organisms, each cell perceives its environment -- and responds to stress conditions -- individually, each on its own to protect itself. Likewise, it had been thought that cells in multicellular organisms respond the same way, but a new study by scientists at Northwestern University reports otherwise.

The Northwestern researchers demonstrated something very unexpected in their studies of the worm C. elegans: Authority is taken away from individual cells and given to two specialized neurons to sense temperature stress and organize an integrated molecular response for the entire organism.

The study, with results that show a possible parallel with the orchestrated "fight or flight response," will be published in the May 9 issue of the journal Science....


- Bread Mold May Unlock Secret To Eliminating Disease-causing Genes

ScienceDaily (May 11, 2008)

When most people discover mold on their bread, they immediately throw it out. Others see a world of possibilities in the tiny fungus. A University of Missouri scientist, along with a collaborative research team, has examined a new mechanism in the reproductive cycle of a certain species of mold. This mechanism protects the organism from genetic abnormalities by "silencing" unmatched genes during meiosis (sexual reproduction). The finding could have implications for higher organisms and may lead to precise "targeting" of unwanted genes, such as those from the HIV virus.

"Meiotic silencing also occurs in worms, mice and human beings," said Patrick Shiu, assistant professor of biological sciences in the MU College of Arts and Science. "It's unlikely that all share the same mechanism, but the principle of targeting unpaired DNA for silencing seems to be found in both simple and complex organisms. Knowing the process of how DNA in molds is targeted for silencing could be important for silencing genes you don't want to be expressed, like disease-causing genes."

Shiu and his colleagues discovered that each sexual cell in mold has an internal mechanism that "scans" paired chromosomes for anomalies. The researchers found that when one chromosome in a pair carries an extra copy of a gene not found in its partner chromosome, it is a good indication of an intruder and the fungus will "turn off" all copies of that gene during meiosis. The researchers call this process "meiotic silencing by unpaired DNA," or MSUD.....

- Magnet Lab Researchers Make Observing Cell Functions Easier

ScienceDaily (May 12, 2008)

Now that the genome (DNA) of humans and many other organisms have been sequenced, biologists are turning their attention to discovering how the many thousands of structural and control genes -- the "worker bees" of living cells that can turn genes on and off -- function.

To do that, they need to develop new techniques and tools. Scientists in the Optical Microscopy group at the National High Magnetic Field Laboratory at Florida State University, working in collaboration with researchers from the University of Alberta in Canada and the University of California, San Diego, have done just that, and in the process have produced back-to-back articles in the journal Nature Methods.

In the first paper, magnet-lab biologists Michael Davidson and Kristen Hazelwood worked with researchers from the University of Alberta to create two new fluorescent-protein biosensors, molecular "beacons" that can tell if there is activity within a cell. The biosensors can be used simultaneously to monitor two separate dynamic functions in a single cell -- a key to understanding how different proteins and enzymes (the biomolecules that cause chemical reactions) work together to complete the daily chores that help cells grow and divide. Knowing how cells work together can help researchers learn a great deal more about tumors and developmental biology, among many other things.

- Human Aging Gene Found In Flies

ScienceDaily (May 12, 2008)

Scientists funded by the Biotechnology and Biological Sciences Research Council (BBSRC) have found a fast and effective way to investigate important aspects of human aging. Working at the University of Oxford and The Open University, Dr Lynne Cox and Dr Robert Saunders have discovered a gene in fruit flies that means flies can now be used to study the effects aging has on DNA. In new work published today in the journal Aging Cell, the researchers demonstrate the value of this model in helping us to understand the aging process. This exciting study demonstrates that fruit flies can be used to study critical aspects of human aging at cellular, genetic and biochemical levels.

Dr Lynne Cox from the University of Oxford said: "We study a premature human aging disease called Werner syndrome to help us understand normal aging. The key to this disease is that changes in a single gene (called WRN) mean that patients age very quickly. Scientists have made great progress in working out what this gene does in the test tube, but until now we haven’t been able to investigate the gene to look at its effect on development and the whole body. By working on this gene in fruit flies, we can model human aging in a powerful experimental system."

Dr Robert Saunders from The Open University added: "This work shows for the first time that we can use the short-lived fruit fly to investigate the function of an important human aging gene. We have opened up the exciting possibility of using this model system to analyse the way that such genes work in a whole organism, not just in single cells.”

Friday, 9 May 2008

GM food and you

From: gert3d

Opinions – Suggestions - Remarks