The organization set up by the Indian Government to take decisions regarding the validity of GM research and the safety of introducing GM organisms is:
(a) Genetic Engineering Approval Committee (GEAC)
Genetically Modified (GM) organisms are developed using genetic engineering techniques. While promising for various applications like agriculture and medicine, their research, development, and introduction require careful regulation to ensure safety for humans and the environment. The Indian government has established a specific organization to oversee these activities.
Let's examine the options provided to identify this regulatory body:
Based on the roles and responsibilities of these organizations, the body specifically set up by the Indian Government to take decisions regarding the validity of GM research and the safety of introducing GM organisms is the Genetic Engineering Approval Committee (GEAC).
Therefore, the correct option is (a).
| Organization | Primary Role | Relevance to GM Regulation (as per question) |
|---|---|---|
| Genetic Engineering Approval Committee (GEAC) | Apex regulatory body under MoEF&CC for environmental approval of activities involving genetically engineered organisms, including environmental release. | Directly responsible for decisions on validity of GM research and safety of introducing GM organisms. |
| Genetic Modification Approval Committee (GMAC) | Not the official name of the primary regulatory body in India. | Incorrect option. |
| Indian Council of Agricultural Research (ICAR) | Agricultural research and education. | Involved in research, but not the final regulatory approval body for environmental release/introduction. |
| All India Institute of Medical Sciences (AIIMS) | Medical education, research, and patient care. | Not involved in regulating environmental/broad safety aspects of GM organisms. |
| Key Term | Description |
|---|---|
| Genetic Engineering Approval Committee (GEAC) | India's apex body for regulating environmental release of genetically engineered organisms. |
| Role of GEAC | Decides on the validity of GM research and safety of introducing GM organisms. |
| Governing Ministry | Ministry of Environment, Forest and Climate Change (MoEF&CC). |
The regulatory framework for genetically engineered organisms and products in India is governed by the "Rules for the Manufacture, Use, Import, Export and Storage of Hazardous Microorganisms/Genetically Engineered Organisms or Cells, 1989" notified under the Environment (Protection) Act, 1986.
This framework involves multiple committees at different levels:
The GEAC's decision is crucial for allowing GM crops or other GM organisms to be grown or introduced commercially in India, ensuring potential environmental and health impacts are assessed.
Match List-I with List-II:
| List-I | List-II |
|---|---|
| (A) Produces crystals of toxic insecticidal proteins | (I) Meloidogyne incognita |
| (B) Nematode which infects the roots of tobacco plant | (II) Agrobacterium tumefaciens |
| (C) Vector used to transfer the nematode-specific gene into the host plant | (III) Bacillus thuringiensis |
| (D) Plasmids used to produce insulin chains | (IV) Escherichia coli |
Choose the correct answer from the options given below:
Identify the statements which hold true for transgenic animals.
(A) Transgenic animals can be used to study vaccine safety.
(B) Over 95% of transgenic animals are mice
(C) Transgenic animals cannot be used to study human diseases
(D) Transgenic animal possesses and express foreign gene
Choose the correct answer from the options given below:
Human protein α-1 antitrypsin is used to treat:
Match List-I with List-II:
| List-I | List-II |
|---|---|
| (A) Dodo | (I) Russia |
| (B) Quagga | (II) Australia |
| (C) Thylacine | (III) Mauritius |
| (D) Stellar’s Sea cow | (IV) Africa |
Choose the correct answer from the options given below:
Bacillus thuringiensis produces Bt toxin crystals, it does not kill the bacterium itself as the toxin is in the ______ in bacteria.