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THE NASSL HAS MOVED TO THE GROUND FLOOR OF THE SLAAS HEADQUARTERS BUILDING AND WILL SHARE THE PREMISES WITH THE INSTITUTE OF CHEMISTRY   ::::      THE COUNCIL HAS CALLED FOR SUGGESTIONS FOR ACTIVITIES TO BE INCLUDED IN THE PROGRAMME FOR THE COMING YEAR. FELLOWS COULD SEND IN THEIR PROPOSALS TO THE GENERAL SECRETARY (SEE CONTACT DETAILS BELOW)   ::::    THE COUNCIL HAS DECIDED TO PUBLISH A BRIEF NEWSLETTER INDICATING THE ONGOING AND PLANNED ACTIVITIES OF NASSL

Welcome to the Home Page of the National Academy of Sciences of Sri Lanka (NASSL). The NASSL is a non-governmental body of eminent scientists of Sri Lanka that provides independent advice on policy matters to the Government and the public in general on all matters of national importance relating to science and technology. The NASSL also promotes the advancement and dissemination of scientific knowledge.

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Researchers shake out basis for rice domestication

Pepper Triggers Suicide in Prostate Cancer Cells

Minor Mutations In Avian Flu Virus Increase .....

'Yanking' Chemical Bonds with Molecular Wires ....

Doodle Search

Cancer Scientists call for Human Epigenome Project

A Key That Opens Cells to Deadly Malaria Parasite

The World's largest DNA model

On 9 March 2002 the world's largest model of DNA, the molecule that contains all our genetic information, was built in The Potteries Shopping Centre, Stoke-on-Trent, UK, by teams from Keele University and CCLRC Daresbury Laboratory.

Clickable image with caption
The model is 10.78 metres tall and contains over 1500 atoms!

EDITORIAL

The 27th Annual General Meeting of the Academy was reasonably well attended and witnessed some lively contributions from Fellows, including some criticism of the Council's performance. After some discussion, it was evident, that much of this criticism arose from a lack of information among members of actions that the Council had already taken in regard to many of the issues raised. Obviously, there is a need for better communication between the Council and Fellows.

Suggestions which were made during the meeting included:

  • keeping the NASSL office open one day in the week for members to meet and discuss matters of interest to them and

  • publishing a periodic newsletter informing Fellows of  actions taken by the Council  from time to time - especially for Fellows who do not visit our website.

Another excellent suggestion made by the Immediate Past President after the meeting was to invite members to attend Council meetings if they so desired.

It is up to concerned Fellows to make further suggestions to be taken up at the next Council meeting (or to give their comments on those already made). We need more inputs from Fellows, including letters (see below)!  

 

LETTERS

 

We once again appeal to Fellows to express their views on matters of national urgency (e.g. on the subject of the Avian Flu threat, the break-up of the Indian tectonic plate and its impact on Sri Lanka, or a national S&T policy for Sri Lanka) have not drawn any response. Now, we are calling for letters on ANY subject of your choice, as long as it is relevant to NASSL and/or S&T. This is your chance to let off steam or bring something to the notice of relevant authorities. Controversies are encouraged!

Our Mission

The Mission of the National Academy of Sciences of Sri Lanka is to be the foremost resource in the country for expert advice on matters of national importance involving science and technology.


Profile

The National Academy of Sciences of Sri Lanka (NASSL) is a high level, non-governmental scientific body, established in 1976 and incorporated by an Act of Parliament in 1988.  Scientists who have achieved excellence in their respective scientific / technological fields are nominated by Fellows of the Academy to be considered for membership.  Admission to the Academy is by election following nomination and evaluation of the nominees. The membership of the NASSL was 110 (90 men and 20 women) in February 2004.

The objectives of the organization include:

 Ø  promoting the dissemination of scientific knowledge,

Ø  recognizing outstanding contributions to the advancement of science and

Ø  acting as a consultative body to the Government of Sri Lanka on all matters and activities related to the application of science and technology in national development. In addition, the NASSL reports on the rational utilization of Sri Lanka’s natural resources consistent with the sustainable use of the biosphere.


NEW FELLOWS

 

The following persons were elected as Fellows of the National Academy of Sciences at the 27 the Annual General Meeting of the Academy.

 

Prof. R. Hewamanne

Prof. N. E. Gunawardene

Prof. M. H. R. Sheriff

Dr. D. S. A. Wijesundara

Prof. J. P. Edirisinghe

Prof. S. H. P. P. Karunaratne

Dr. Saman Kelegama


 Newsfeeds


Cancer Scientists Call for a Large-scale Human Epigenome Project


December 15, 2005

PHILADELPHIA – A vast code, invisible to the DNA sequencing effort that constituted the Human Genome Project, is rapidly being shown to play a direct role in human health. This “epigenome” - from the Greek epi, meaning “in addition to” - consists of chemical “amendments” that dangle like charms on a bracelet from the linear string of letters that spell out the genetic code.

 Now, an international group of 40 leading cancer scientists says the time is ripe to undertake a large-scale international “Human Epigenome Project” designed to map the chemical modifications to DNA that comprise the epigenetic code. Their proposal, “A Blueprint for a Human Epigenome Project” -- published in the December 15, 2005 issue of Cancer Research -- summarizes the findings of an AACR-sponsored workshop held June 15-18, 2005, in Lansdowne, Va.

 “Definition of the human epigenome and its application to developing diagnostic, prognostic and therapeutic tools will likely produce some of the earliest translational research benefits flowing from large-scale genome initiatives to the bedside,” said Frank Rauscher, III, Ph.D., editor-in-chief of Cancer Research. “It is time to create a concerted international effort to unlock the epigenomic information stored in our genome and use it for the benefit of human health,” he added. The new report spells out the needs, guidelines and expectations of a Human Epigenome Project (HEP), and describes the developing technologies that make the project currently feasible.

 “One of the most exciting points to emerge from the meeting is that the technology needed for doing epigenetics on a high-throughput basis has advanced so far that people are already engaged in epigenomic studies on a piecemeal basis,” said Peter A. Jones, Ph.D., D.Sc., president of the American Association for Cancer Research (AACR) and Director of the Norris Comprehensive Cancer Center at the University of Southern California. Jones and Robert Martienssen, Ph.D., a professor at Cold Spring Harbor Laboratory, New York, were co-organizers of the workshop.

“A coordinated, large-scale Human Epigenomic Project would pave the way for unforeseen breakthroughs in understanding normal and disease states,” Jones added.

 Epigenetic modifications to DNA exert profound influences on gene activity. For example, studies suggest that epigenetic variation may be responsible for subtle differences in appearance and behavior of identical twins, whose gene activity profiles at 3 years of age are nearly alike, but by age 50 diverge as much as unrelated individuals in the population at large.

 Epigenetic aberrations also can play a role in normal and pathological processes, such as aging, mental health, and cancer, among others. Several presenters at the workshop highlighted significant contributions that epigenetic phenomena make to a broad spectrum of human cancers. For example:

·      An analysis of 25 brain tumors showed that a putative tumor suppressor gene was silenced by epigenetic mechanisms much more frequently than by genetic means.

·     The bacterial species Helicobacter pylori, which has been widely linked to gastric cancer, was shown to induce epigenetic changes.

·     Epigenetic marks also demonstrate diagnostic and predictive value. Of 148 human breast tumors included in one study, specific epigenetic modifications within the    estrogen receptor gene correlated with greater chances of survival in response to tamoxifen.

·     Presence of a distinct epigenetic modification in 140 examined neuroblastoma cases correlated with a poor prognosis, and other marks were linked to colon cancer progression.

 Epigenetic modifications take several forms. The most intensively studied have been the addition of methyl groups, small “beads” of carbon and hydrogen, to DNA, which generally correlate with low gene activity. The histone proteins – molecular “clips” that hold the six feet of DNA tightly wound inside each cell - are modified by methylation, but also by the addition of chemical entities containing acetic acid, phosphorus, and a number of other species.

The complex nature of epigenetic modifications constitutes a challenge to the development of reliable, high-throughput methods of cataloging them. Several workshop participants, however, working in both industrial and academic settings, have developed techniques proving adept at tackling epigenetic complexity. These include the so-called ChIP/chip methodology, in which intact chromatin – the complex of DNA and histones – is immunoprecipitated (brought out of solution using antibodies that recognize specific histone modifications) and analyzed on microarray “chips.” Modifications of DNA are also tracked on chips, following treatment with enzymes that recognize sites of methylation. Impressive accounts of success with these methods were presented at the workshop.

These accounts included a report from the European Epigenome Project, headquartered at the Wellcome Trust Sanger Institute in Cambridge, England, which has completed a pilot phase and expects to analyze 10 percent of the genome by fall 2006.

 The proposed structure of a Human Epigenome Project takes into account that “there is not one epigenome,” according to the authors, “but rather many different epigenomes.” Epigenetic profiles differ among tissues, individuals and healthy vs. disease states. Workshop participants advocate choosing a small number of “reference” epigenomes to be analyzed at a high level of resolution. Tissues proposed for this analysis include peripheral blood cells and foreskin fibroblasts.

 Participants agreed that a much larger group of samples could be examined using a lower-resolution “scanning” approach that would help delineate basic principles of epigenetic effects on gene activity. The scanning approach would point out areas that should be “drilled down” with additional study.

 As stated by the authors: “The goal of the HEP (Human Epigenomic Project) is to identify all the chemical changes and relationships… that provide function to the DNA code, which will allow a fuller understanding of normal development, aging, abnormal gene control in cancer and other diseases, as well as the role of the environment in human health.” Jones, Martienssen and the other workshop participants call for any U.S. effort to coordinate closely with those in other countries, including additional European projects underway as well as efforts in Japan, where an active epigenetic research community exists.  The workshop, sponsored by AACR, was also attended by representatives of the National Cancer Institute, which sponsored a related workshop on epigenomics in December 2004 and another one last month defining the epigenome. 


A key that opens cells to the deadly malaria parasite

Hassan Belrhali (left) discusses with Amit Sharma (right) in the control

Hassan Belrhali (left) discusses with Amit Sharma (right) in the control cabin of the UK MRC-beamline BM14, at the ESRF

Press Release 21 December 2005 [PDF]

Researchers at the International Centre for Genetic Engineering and Biotechnology (ICGEB) in India and a unit of the European Molecular Biology Laboratory (EMBL) in France have made a key discovery about a molecule that helps the malaria parasite infect human cells. India is one of the countries most affected by this disease, which has infected 300 million people across the world and leads to over one million fatalities per year. The breakthrough, which was achieved at the European Synchrotron Radiation Facility (ESRF) in Grenoble, may represent an important step towards finding new therapies. The study appears in this week’s online edition of Nature (December 21).

Malaria is caused by a one-celled organism called Plasmodium, which is passed to humans through the bite of Anopheles mosquitoes. The parasite replicates inside red blood cells, which eventually burst. In order to enter these cells, it first has to bind to the cell through interactions of proteins on the surfaces of red blood cells and the parasite.

The new study reveals key features of a protein on the surface of Plasmodium that permits it to bind. The researchers obtained crystals of a module of this protein, called the Duffy-Binding Like (DBL) domain, which directly interacts with a "receptor" protein on red blood cells. Then they examined the crystals using very powerful X-rays of the UK-Medical Research Council Beamline BM14 at the European Synchrotron Radiation Facility (ESRF) in Grenoble. X-ray crystallography is one of the only methods available to create atom-by-atom maps of proteins, which are too small to be seen by microscopes.

"Until now we have not had a close-up view of the precise surface where the two proteins interact," explains Amit Sharma, the corresponding author of the paper. "That surface is absolutely crucial in permitting the parasite to enter the cell. If we can determine its features in atomic detail, we may be able to find weak points that could make good targets for drugs."

In addition to interfering with the binding process, such drugs would also have to be specific: in other words, they shouldn't interfere with normal processes in red blood cells. The receptor protein that allows Plasmodium to enter undoubtedly has other important functions. "What we've found is that the DBL has an absolutely unique architecture, which means that there should be a way to inhibit its activity without affecting healthy blood cells," says Hassan Belrhali, an EMBL researcher who participated in the project.

Evolution has produced many different species of Plasmodium. This work was carried out using a form of the parasite that doesn't normally infect humans, but DBL modules are similar in different forms of the organism. This makes it likely that the findings can be extended to other types of Plasmodium. “Our results provide a structural framework by which to understand the DBLs of most malaria parasites, and could have an impact in the design of drugs to fight against this illness,” explains Amit Sharma.

The researchers are also investigating molecules important at an earlier phase of malaria infections, when parasites invade the liver.

Source article
S.K. Singh, R. Hora, H. Belrhali, C.E. Chitnis & A. Sharma. Structural basis for Duffy recognition by malaria parasite Duffy-binding-like domain. Nature, online publication December 21, 2005.

 


The NASSL is run by a Council, the office bearers of which are presently as follows:

President

Prof. Arjuna Aluwihare

Vice President Prof. Sunethra Athukorale
Immediate Past President Dr. Wester Modder
General Secretary Prof. Kshanika Hirimburegama
Treasurer Prof. J.N.O. Fernando
Editor Dr. Kingsley  De Alwis
Secretary - Foreign Relations Prof. Ira Thabrew
Assistant Secretary Eng. Mervyn Gunasekera
Members: Prof. Arthur Bamunuarachchi
  Dr. Locana Gunaratne
  Prof. S. Karunaratne
  Dr. U. Pethiyagoda
  Dr. Ravi Perera
  Prof. L. Ratnayake
  Prof. D.A.Tantrigoda
  Mr. Leslie Wijesinghe
  Prof. M. J. S. Wijeyaratne

The Academy has no permanent employed staff at present. The scientific work as well as the correspondence is done by the Fellows of the Academy.  A permanent office room has, however, been rented from the Sri Lanka Association for the Advancement of Science at their Headquarters for use by the Academy.            


Contact Information

 

Telephone :(94)(11) 258-5038
Postal address :120/10 Vidya Mawatha, Colombo 7, Sri Lanka
 
Electronic mail
 
Secretary:         hirimk@pts.cmb.ac.lk
Editor:              kdealwis@sltnet.lk