UPSC MainsZOOLOGY-PAPER-II201120 Marks
Q12.

Write the sequence of stages for production of clonal and non-clonal embryos by in vitro fertilisation (IVF) for transfer in recipient female(s)/ surrogate(s).

How to Approach

This question requires a detailed understanding of the IVF process, differentiating between clonal and non-clonal embryo production. The answer should outline the sequential steps involved in each process, highlighting the key differences. A clear, step-by-step explanation, potentially using a table to compare the two, is crucial. Focus on the gamete manipulation, fertilization, and early embryo development stages. Mentioning the role of surrogate mothers is also important.

Model Answer

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Introduction

In vitro fertilization (IVF) is a complex series of procedures used to help with fertility or to assist in the conception of a child. It involves retrieving eggs from the ovaries and fertilizing them with sperm in a laboratory setting. The resulting embryos are then transferred to the uterus. IVF can produce both clonal and non-clonal embryos, each with distinct implications for the offspring. Clonal embryos are derived from a single gamete, while non-clonal embryos result from the fusion of male and female gametes. Understanding the sequential stages involved in producing each type of embryo is vital for successful IVF outcomes and reproductive technologies.

Production of Non-Clonal Embryos via IVF

Non-clonal embryos are produced through the conventional IVF process, involving the fusion of sperm and egg. The sequence of stages is as follows:

  1. Ovarian Stimulation: The female recipient undergoes hormonal stimulation to induce the development of multiple follicles in the ovaries.
  2. Egg Retrieval: Eggs are retrieved from the mature follicles, typically using transvaginal ultrasound aspiration.
  3. Sperm Collection: Sperm is collected from the male partner or a donor.
  4. Fertilization: Eggs and sperm are combined in a laboratory dish (conventional insemination) or through Intracytoplasmic Sperm Injection (ICSI), where a single sperm is injected directly into each egg.
  5. Embryo Culture: Fertilized eggs (zygotes) are cultured in a controlled environment, allowing them to develop into embryos (cleavage-stage or blastocyst-stage).
  6. Embryo Selection: Embryos are assessed for quality and viability.
  7. Embryo Transfer: One or more selected embryos are transferred into the uterus of the recipient female.
  8. Pregnancy Test: A pregnancy test is performed approximately two weeks after embryo transfer.

Production of Clonal Embryos via IVF – Somatic Cell Nuclear Transfer (SCNT)

Clonal embryos, also known as parthenogenetically activated embryos or those produced via Somatic Cell Nuclear Transfer (SCNT), are created without fertilization. This process is more complex and is primarily used for research or potential therapeutic cloning. The sequence of stages is:

  1. Somatic Cell Collection: A somatic cell (any cell other than a sperm or egg cell) is collected from the individual to be cloned.
  2. Egg Retrieval & Enucleation: An egg is retrieved from a donor female, and its nucleus (containing the genetic material) is removed, creating an enucleated egg.
  3. Nuclear Transfer: The nucleus from the somatic cell is transferred into the enucleated egg.
  4. Activation: The reconstructed egg is stimulated (e.g., with electrical pulses or chemicals) to initiate cell division, mimicking fertilization.
  5. Embryo Culture: The activated egg develops into an embryo, genetically identical to the donor of the somatic cell.
  6. Embryo Transfer: The clonal embryo is transferred into the uterus of a recipient female or surrogate mother.
  7. Pregnancy Test: A pregnancy test is performed to determine if implantation has occurred.

Comparison of Clonal and Non-Clonal Embryo Production

Feature Non-Clonal Embryo Production (Conventional IVF) Clonal Embryo Production (SCNT)
Gamete Involvement Requires both sperm and egg Requires only an egg and a somatic cell nucleus
Fertilization Essential – fusion of gametes Absent – no sperm involved
Genetic Diversity High – offspring genetically unique Low – offspring genetically identical to somatic cell donor
Complexity Relatively simpler Technically more challenging
Ethical Considerations Fewer ethical concerns Significant ethical concerns (e.g., cloning)

Role of Recipient Female/Surrogate

In both scenarios, a recipient female or surrogate mother is crucial for carrying the pregnancy to term. The recipient female may be the intended mother who is unable to carry a pregnancy herself due to medical reasons. A surrogate mother is a woman who carries a pregnancy for another person or couple. Legal and ethical considerations surrounding surrogacy vary significantly across jurisdictions.

Conclusion

In conclusion, both clonal and non-clonal embryo production via IVF involve distinct sequential stages. Non-clonal embryos are produced through conventional fertilization, resulting in genetically diverse offspring, while clonal embryos are created via SCNT, yielding genetically identical copies. The choice between these methods depends on the specific reproductive goals and ethical considerations. The successful transfer and implantation of these embryos rely heavily on the health and receptivity of the recipient female or surrogate mother, highlighting the importance of comprehensive medical evaluation and support throughout the IVF process.

Answer Length

This is a comprehensive model answer for learning purposes and may exceed the word limit. In the exam, always adhere to the prescribed word count.

Additional Resources

Key Definitions

Intracytoplasmic Sperm Injection (ICSI)
A specialized form of IVF technique in which a single sperm is directly injected into an egg.
Parthenogenesis
A form of asexual reproduction where an egg can develop into an embryo without fertilization.

Key Statistics

According to the Society for Assisted Reproductive Technology (SART), in 2022, there were approximately 330,000 IVF cycles performed in the United States.

Source: SART, 2022

The global Assisted Reproductive Technology (ART) market size was valued at USD 28.6 billion in 2023 and is projected to reach USD 48.4 billion by 2032.

Source: Global Market Insights, 2024 (Knowledge Cutoff: Jan 2024)

Examples

Dolly the Sheep

Dolly the sheep, born in 1996, was the first mammal cloned from an adult somatic cell using SCNT, demonstrating the feasibility of clonal embryo production.

Frequently Asked Questions

What are the ethical concerns surrounding SCNT?

Ethical concerns include the potential for misuse of cloning technology, the moral status of cloned embryos, and the potential for exploitation of surrogate mothers.

Topics Covered

BiologyReproductive BiologyAssisted ReproductionEmbryologyIVF