Aturan Transgenik Abaikan Prinsip Kehati-hatian

JAKARTA, KOMPAS.com - Peraturan Menteri Pertanian Nomor 61/2011 tentang Pengujian, Penilaian, Pelepasan, dan Penarikan Varietas, mengabaikan prinsip kehati-hatian.

Demi kepentingan jangka pendek dan investor, Menteri Pertanian dinilai tidak memedulikan dampak serius produk rekayasa genetika pada lingkungan dan kesehatan warganya.

Hal ini mengemuka dalam diskusi yang menghadirkan Tejo Wahyu Jatmiko (koordinator Aliansi untuk Desa Sejahtera), Henri Subagiyo (Direktur Eksekutif Indonesian Center for Enviromental Law/ICEL), dan Huzna Zahir (Yayasan Lembaga Konsumen Indonesia), Kamis (20/10/2011) di Jakarta.

"Prinsip Kehati-hatian merupakan prinsip dasar dalam menangani produk hasil rekayasa genetik, dengan diakuinya potensi dampak lingkungan, sosial ekonomi, dan kesehatan. Sangat jelas, hal ini tidak menjadi roh dari permentan itu. Alasan demi menerapkan amanat MP3EI yang berpihak pada investor, membuat Menteri Pertanian berani mengabaikan kepentingan publik. Ini jelas salah," ucap Tejo.

Ia menunjukkan, pemerintah tidak mau belajar dari kesalahan 10 tahun lalu saat pelepasan kapas transgenik milik Monsanto yang merugikan petani dan gagal memenuhi janji.

"Perlu diingat saat itu keputusan juga dilakukan tergesa-gesa, dan sembunyi-sembunyi untuk memfasilitasi kepentingan perusahaan," katanya.

Sumber : http://sains.kompas.com/read/2011/10/20/17374561/Aturan.Transgenik.Abaikan.Prinsip.Kehati-hatian

New technique helps identify multiple DNA regulatory sites

Scientists at Lawrence Livermore National Laboratory (LLNL) and the Linnaeus Centre for Bioinformatics (LCB) at Uppsala University in Sweden have developed a new bioinformatics technique for systematically analyzing key regions in DNA that help control gene activity. The cooperative efforts were headed by Krzysztof Fidelis in the United States and by Jan Komorowski in Sweden.

Understanding the complex regulatory mechanisms that tell genes when to switch on and off is one of the toughest challenges facing researchers attempting to discover how life works. “Binding sites,” or areas of DNA that interact with the proteins that help control gene expression, can be a long distance on the DNA strand from the genes they influence. Recent research also has shown that gene expression can be controlled by several regulatory proteins working together at a combination of different binding sites.

(Regulatory proteins are known as “transcription factors”; transcription is the first step in the process by which the genetic information in DNA is decoded by the cell to manufacture proteins, the building blocks of life.)

It’s difficult to experimentally observe how transcription factors bind to DNA at a distance from a gene, or how regulation happens, said Fidelis, a computational biologist in Livermore’s Biosciences Directorate. But you can identify their binding sites in a promoter or regulatory region – there are usually a few of these for each gene. We wanted to see if we could somehow deduce how many transcription factors at a time, or combinations of factors, are coming together physically and how these combinations regulate genes.

“To accomplish this,” Komorowski said, “we used a machine learning technique called rough sets to mathematically model general rules that could associate known binding sites and gene expression in yeast, which is one of the most widely studied organisms.” From the analysis of gene activity under a variety of environmental conditions, the teams were able to develop a set of rules for predicting the location of binding site combinations based on limited binding site and gene expression data.

“We found that the same transcription factors, in slightly different combinations, could be responsible for the regulation of different genes,” said Torgeir R. Hvidsten of the LCB. “Thus we now know that binding sites can be combined to allow a large number of expression outcomes using relatively few transcription factors.”

Others collaborating in the project were Jerzy Tiuryn of the Faculty of Mathematics, Informatics, and Mechanics at Warsaw University in Poland; Bartosz Wilczynski of the Institute of Mathematics, Polish Academy of Sciences, and LLNL; and Andriy Kryshtafovych of LLNL. A report on the joint work appears in the June issue of the journal Genome Research.

The rough sets technique was developed by Zdzislaw Pawlak in Poland in the 1980s and is particularly suitable to build models from incomplete and uncertain data. It has been used in applications ranging from medical and financial data analysis to voice recognition and image processing. Applied to gene regulation, the approach was able to predict the location of regulatory sites for about one-third of the genes in the yeast genome – a success rate as good as or better than other current techniques.

“The next step is to test this approach on different organisms, including microbes and vertebrates,” Fidelis said. The growing number of organisms whose genomes have been sequenced has generated a wealth of DNA sequence information that could provide the raw material for analysis.

Primary funding for the research was provided by LLNL’s Laboratory Directed Research and Development Program, the Knut and Alice Wallenberg Foundation, and the Swedish Foundation for Strategic Research.

Founded in 1952, Lawrence Livermore National Laboratory has a mission to ensure national security and to apply science and technology to the important issues of our time. Lawrence Livermore National Laboratory is managed by the University of California for the U.S. Department of Energy’s National Nuclear Security Administration.

The Linnaeus Centre for Bionformatics is a joint initiative between Uppsala University and the Swedish University of Agricultural Sciences. The LCB researchers are involved in many interdisciplinary bioinformatics projects, including epigenetics, evolutionary studies, functional genomics, and computational tool integration for life sciences.

www.bioexchange.com