Saturday, December 31, 2011

Changes In The Path Of Brain Development Make Human Brains Unique

How the human brain and human cognitive abilities evolved in less than six million years has long puzzled scientists. A new study conducted by scientists in China and Germany, and published December 6 in the online, open-access journal PLoS Biology, now provides a possible explanation by showing that activity levels of genes in the human brain during development changed substantially compared to chimpanzees and macaques. What’s more, these changes might be caused by a handful of key regulatory molecules called microRNAs.

Credit; CAS

The authors studied gene activity in human, chimpanzee and macaque brains across their lifetimes. Starting from newborns, they investigated two brain regions, the cerebellum, which is responsible for motor activity, and the prefrontal cortex, which has roles in more complex behavior such as social interactions or abstract thinking. They first studied the simple gene activity differences between species that are seen at all ages. Although many genes show such simple differences, there was no disparity in numbers of these differences between the human and the chimpanzee evolutionary lineages. 

Moreover, most of these differences were observed in both of the brain regions studied, and the genes involved are not thought to be specifically involved in brain function. In the opinion of Mehmet Somel (CAS-MPG Partner Institute for Computational Biology (PICB), Shanghai Institutes for Biological Sciences), the lead author of the study, these differences represent evolutionary “white noise” and have little importance for human brain evolution.

The authors then looked for changes in gene activity during development, comparing the activity of genes in newborns and adults. In general, brain developmental patterns tend to be quite similar in humans, other primate species, and even mice. Nevertheless, the authors found that for hundreds of genes, humans display unique developmental patterns, with profiles that were different in shape and/or timing from those found in chimpanzees and macaques. 

Such human-specific developmental gene activity patterns were particularly widespread in the prefrontal cortex, where genes showing human-specific changes outnumbered genes showing chimpanzee-specific changes by four-fold. Developmental patterns in the cerebellum, by contrast, were much less human-specific. Furthermore, many genes displaying these human-specific patterns in the prefrontal cortex were known to have specific neural functions, implying roles in human cognitive development.

Looking for possible causes of this widespread developmental remodeling in the human prefrontal cortex, the authors stumbled upon an unexpected signal. Developmental patterns of genes that encode microRNAs (tiny but powerful regulators that target many other genes and processes) showed even greater excess of human-specific changes in the prefrontal cortex than those of ordinary genes did. Several of these changes in microRNA activity could be directly linked to human-specific changes in activity of their target genes. Since each microRNA may regulate the activity of hundreds of other genes, this finding provides a possible explanation to how hundreds of genes changed their activity patterns (in a coordinated way) during human brain development.

This result further implies that the evolution of human cognitive abilities might be traced back to a small number of mutations in key developmental regulators. Philipp Khaitovich, the senior author of the study, suggests that "identifying the exact genetic changes that made us think and act like humans might be easier than we previously imagined”. This said it is likely to require much more work with a focus on the dynamics of brain development and wider use of transgenic mice, and even primate models.

Further to this, the authors point out that identification of the key human-specific DNA mutations could help us to determine how close the Neanderthals’ cognitive abilities were to ours. “If Neanderthals’ brain development was similar to that of chimpanzees and macaques, it would be no wonder that they became extinct when confronted by Modern Humans,” says Mehmet Somel.


Contacts and sources:
Philipp Khaitovich
CAS-MPG Partner Institute for Computational Biology, Shanghai Institutes for Biological Sciences,
Chinese Academy of Sciences, Shanghai, China
PLoS Biology



New Report Highlights Need For Action On Health In The Aftermath Of War

Issue of noncommunicable diseases in post-conflict countries must be addressed

Countries recovering from war are at risk of being left to their own devices in tackling non communicable diseases, leaving an "open door" for exploitation by alcohol, tobacco and food companies, health experts warn.

Writing in the Bulletin of the World Health Organization, Bayard Roberts and Martin McKee, of the London School of Hygiene & Tropical Medicine, and Preeti Patel, of King's College London, argue that the post-conflict environment risks increases of mental health problems and other NCDs, such as high blood pressure, diabetes and cancer.

After exposure to violent and traumatic events, people may be prone to developing harmful health behaviours, such as excessive drinking and smoking, which exacerbate the problem of NCDs in the long-term. This is why the lack of a strong will from the authorities to restore the health system leaves an open door for commercial ventures to influence health policy to their advantage.

The authors write: "This toxic combination of stress, harmful health behaviours and aggressive marketing by multinational companies in transitional settings requires an effective policy response but often the state has limited capacity to do this."

Afghanistan has no national policy or strategy towards NCDs and, apart from the European Commission, none of its partners has given priority to introduce and support them. High blood pressure is largely untreated in Iraq, three times as many people die prematurely from NCDs in Libya than from infectious diseases and similar patterns can be found in other countries recovering from conflict.

"This policy vacuum provides an open door for multinational companies to influence policies in ways that undermine efforts to control tobacco and alcohol use or improve unhealthy diets in transitional countries," the experts say.

Little attention is paid in reconstruction and humanitarian efforts to helping countries emerging from conflict deal with their present or future burden of NCDs – with the topic virtually ignored during the United Nations high-level meeting on NCDs in September 2011. The authors argue that this gap must be filled, pointing out that the post-conflict period can provide an opportunity to completely rewrite strategies and undertake reforms to better address the health needs of a population and lay the foundations for a more efficient health system.

Dr Roberts, a lecturer in the European Centre on Health of Societies in Transition at LSHTM, says: "While great attention is rightly paid to infectious diseases, noncommunicable diseases should also be given attention –especially as the post-conflict environment can provide the perfect breeding ground for unhealthy activities like smoking, drinking and poor diet. We are making the argument that if the authorities do not step up to lead the way in developing policies which will benefit public health, then they leave the route clear for companies to step in and serve their own interests."

Contacts and sources:
Paula Fentiman
London School of Hygiene & Tropical Medicine

Citation: Noncommunicable diseases and post-conflict countries – Bulletin of the World Health Organization, January 2012http://www.who.int/bulletin/volumes/90/1/11-098863

First Of NASA's GRAIL Spacecraft Enters Moon Orbit

The first of two NASA spacecraft to study the moon in unprecedented detail has entered lunar orbit.

NASA's Gravity Recovery And Interior Laboratory (GRAIL)-A spacecraft successfully completed its planned main engine burn at 2 p.m. PST (5 p.m. EST) today. As of 3 p.m. PST (6 p.m. EST), GRAIL-A is in a 56-mile (90-kilometer) by 5,197-mile (8,363-kilometer) orbit around the moon that takes approximately 11.5 hours to complete.

Artist concept of GRAIL mission.
Artist's concept of GRAIL missionImage credit: NASA/JPL-Caltech

"My resolution for the new year is to unlock lunar mysteries and understand how the moon, Earth and other rocky planets evolved," said Maria Zuber, GRAIL principal investigator at the Massachusetts Institute of Technology in Cambridge. "Now, with GRAIL-A successfully placed in orbit around the moon, we are one step closer to achieving that goal."

The next mission milestone occurs tomorrow when GRAIL-A's mirror twin, GRAIL-B, performs its own main engine burn to place it in lunar orbit. At 3 p.m. PST (6 p.m. EST) today, GRAIL-B was 30,018 miles (48,309 kilometers) from the moon and closing at a rate of 896 mph (1,442 kph). GRAIL-B’s insertion burn is scheduled to begin tomorrow at 2:05 p.m. PST (5:05 p.m. EST) and will last about 39 minutes.

"With GRAIL-A in lunar orbit we are halfway home," said David Lehman, GRAIL project manager at NASA's Jet Propulsion Laboratory (JPL) in Pasadena, Calif. "Tomorrow may be New Year's everywhere else, but it's another work day around the moon and here at JPL for the GRAIL team."

Once both spacecraft are confirmed in orbit and operating, science work will begin in March. The spacecraft will transmit radio signals precisely defining the distance between them as they orbit the moon in formation. As they fly over areas of greater and lesser gravity caused by both visible features, such as mountains and craters, and masses hidden beneath the lunar surface, the distance between the two spacecraft will change slightly.

Scientists will translate this information into a high-resolution map of the moon's gravitational field. The data will allow scientists to understand what goes on below the lunar surface. This information will increase knowledge of how Earth and its rocky neighbors in the inner solar system developed into the diverse worlds we see today.

After firing its main engine for 39 minutes, the GRAIL-A spacecraft was captured into lunar orbit.

Credit: NASA

JPL manages the GRAIL mission for NASA's Science Mission Directorate at the agency's headquarters in Washington. The GRAIL mission is part of the Discovery Program managed at NASA's Marshall Space Flight Center in Huntsville, Ala. Lockheed Martin Space Systems in Denver built the spacecraft.

Source:
NASA

For more information about GRAIL, visit:



http://www.nasa.gov/grail