Question map
Consider the following statements : 1. Genetic changes can be introduced in the cells that produce eggs or sperms of a prospective parent. 2. A person's genome can be edited before birth at the early embryonic stage. 3. Human induced pluripotent stem cells can be injected into the embryo of a pig. Which of the statements given above is/are correct ?
Explanation
The correct answer is Option 4 (1, 2 and 3) because all three statements describe scientifically established possibilities in modern biotechnology and genetic engineering.
- Statement 1 is correct: Germline gene editing allows for genetic modifications in gametes (eggs or sperm). Unlike somatic editing, these changes are heritable and passed to future generations. Tools like CRISPR-Cas9 have made such interventions technically feasible.
- Statement 2 is correct: A person’s genome can be edited at the early embryonic stage (zygote or blastocyst). This was notably demonstrated in 2018 (though controversially) to attempt resistance to certain diseases, proving the technical possibility of pre-birth genome editing.
- Statement 3 is correct: This refers to the creation of chimeras. Scientists have successfully injected human induced pluripotent stem cells (iPSCs) into pig embryos to grow human-compatible organs, aiming to solve the global organ shortage.
Since all three statements represent valid scientific applications or experimental realities, Option 4 is the most comprehensive and accurate choice.
PROVENANCE & STUDY PATTERN
Full viewThis is a classic 'Future Tech' question where the answer relies on the theoretical scope of technology rather than specific textbook facts. The key is recognizing that in Science & Tech, 'Can be' statements regarding emerging fields (CRISPR, Stem Cells) are almost always correct unless they violate basic laws of physics.
This question can be broken into the following sub-statements. Tap a statement sentence to jump into its detailed analysis.
- Statement 1: Can genetic changes be introduced in the human germline cells that produce eggs or sperm of a prospective parent (germline gene editing)?
- Statement 2: Can a human genome be edited before birth at the early embryonic stage (human embryo genome editing)?
- Statement 3: Can human induced pluripotent stem cells (iPSCs) be injected into pig embryos to create human–pig chimeras?
- Explicitly states that zygote or germline cells can transmit genetic changes to future generations, directly addressing the core idea of germline editing.
- Mentions policy responses (prohibitions for clinical use), indicating the passage treats germline editing as a real, actionable possibility.
- Describes specific laboratory methods for introducing foreign genes via sperm (incubating sperm with the gene and injecting into the oocyte by ICSI), showing technical routes to alter germline cells.
- Provides concrete procedural context that supports the feasibility of introducing genetic changes into reproductive cells or embryos.
- States there was broad agreement that germline editing of human cells for reproductive purposes was considered, indicating the scientific community regards such editing as a realistic application.
- Distinguishes germline from somatic applications, highlighting germline editing as a distinct, discussed practice.
Identifies where human germ cells (sperms) are produced (testes) and that spermatogenesis is a defined physiological process.
A student could use this to ask whether interventions (e.g., gene editing) targeted to the testes could alter sperm DNA prior to fertilisation.
Describes female germ cells (eggs) residing in ovaries and the site of fertilisation (fallopian tube) in humans.
One could extend this by considering whether gene-altering interventions to ovarian eggs or pre-fertilisation gametes might change the genetic material passed on.
Explains that gametes carry only half the parent's genetic material and combine at fertilisation to form a complete set.
A student can infer that changing the DNA in gametes would alter the genetic input to the zygote and thus be inherited.
States germ cells take one chromosome from each pair so that progeny restore the normal chromosome number—highlighting the mechanism by which parental DNA is transmitted.
This suggests that modifying chromosomes in germ cells could be propagated into the offspring's genome; a student could combine this with knowledge of editing tools to evaluate feasibility.
Defines genetic modification as altering hereditary material (DNA) in a way not occurring by normal mating or recombination.
A student could use this definition to frame germline editing as a form of genetic modification and then compare plant/animal examples to infer analogous possibilities in human germ cells.
- States that embryo editing is done as early as possible, typically at the single-cell stage.
- Explains rationale: editing at single-cell stage maximizes chance both parental genomes are edited before replication/division.
- Explicitly identifies zygote (early embryo) editing as the primary current approach for heritable human genome editing.
- Links the practice to the idea of undertaking heritable genome edits before development proceeds.
- Confirms current techniques involve treating zygotes at the single-cell stage.
- Notes practical constraint that genotype cannot be determined at this stage without destroying the cell, implying edits are done early pre-implantation.
Explains that a basic event in reproduction is creation and copying of DNA—cells build copies of DNA during reproduction.
A student could combine this with the basic fact that editing DNA at the single-cell or very early multi-cell stage might be propagated into later copies, so check whether interventions at DNA-copying stages can change the embryo's future cells.
Describes sexual reproduction involving special cell lineages and the problem of halving chromosomes, highlighting that early reproductive cells and stages have distinct DNA states.
Using external knowledge that the zygote/early embryo is the stage before cell lineages diverge, a student could infer that editing at that stage could affect germline vs somatic lineages and thus heritability.
Shows that a zygote develops into an embryo either inside the mother's body (mammals) or in an egg (birds), indicating where and when early development occurs.
A student could use a world/biological map of developmental environments to think about practical access to embryos for intervention (e.g., in vitro embryonic manipulation vs in utero), and then investigate whether human embryos are experimentally reachable at early stages.
Notes that the embryo implants in the uterine lining and then develops with maternal support, marking a timeline of developmental stages after fertilisation.
A student could combine this with basic timing facts (when implantation occurs) to ask whether there is a window before/after implantation when editing might be feasible and what barriers (access, maternal environment) exist.
States that humans give birth after internal development and that young gradually grow and develop over time, emphasising stages from embryo to birth.
A student could extend this by mapping embryonic stages to the possible timing of interventions, prompting a search for whether interventions at the 'early embryonic' stage would affect development up to birth.
Describes how embryos implant in the uterus and rely on maternal tissues (placenta) for nutrition and development — a general rule about in‑utero embryonic development and the host environment required for embryo growth.
A student could combine this with the fact that pig embryos develop in a pig maternal environment to ask whether human cells introduced to a pig embryo would be supported by pig placental/nutritional systems.
Explains basic cellular reproduction as DNA copying and cell division — a general rule about how new cells arise and integrate into developing tissues.
One could extend this to consider whether injected human iPSCs would divide and contribute genetically and structurally to a developing pig embryo.
Notes cells communicate chemically (not just electrically) and that communication is needed between cells in multicellular organisms.
This suggests examining whether human cells can chemically communicate with pig cells during development — a key factor for integration into host tissues.
Discusses rules of inheritance and that asexual organisms follow inheritance rules — a general point about genetic compatibility and transmission of traits in development.
A student could use this to raise the question of genetic compatibility between human and pig cells in a chimera and whether inherited cellular programs would be compatible.
Lists pigs among common domestic livestock — establishes that pigs are a species of animal commonly studied or managed.
One could combine this with outside knowledge (e.g., pigs are used in biomedical research) to justify focusing on pig embryos as a potential host for cross‑species experiments.
- [THE VERDICT]: Logical Sitter. While the specific news (Salk Institute, 2017) is niche, the 'Can be' phrasing makes it a pattern-based giveaway.
- [THE CONCEPTUAL TRIGGER]: Biotechnology > Genetic Engineering > Applications of CRISPR-Cas9 and Stem Cell Therapy (iPSCs).
- [THE HORIZONTAL EXPANSION]: 1. Germline vs. Somatic Editing (Germline is heritable). 2. iPSCs (Nobel 2012, Shinya Yamanaka) reprogram adult cells to embryonic state. 3. Mitochondrial Replacement Therapy (Three-Parent Baby). 4. Xenotransplantation (using animal organs for humans). 5. Cas9 vs. Cas12/13 (DNA vs RNA targeting).
- [THE STRATEGIC METACOGNITION]: Do not try to memorize every single experiment. Instead, understand the *capability* of the tool. If CRISPR cuts DNA, can it cut sperm DNA? Yes. If Stem Cells grow into tissue, can they grow in a pig? Theoretically, yes. Bet on the potential of the tech.
Gametes (sperm and egg) contain one set of chromosomes so that fertilisation restores a full genome in the offspring.
High-yield for heredity and reproduction questions: understanding haploid gametes is essential to reason about inheritance, effects of any genetic change in a gamete on the next generation, and to evaluate claims about germline transmission. Connects to Mendelian inheritance, chromosomal pairing and meiosis.
- Science ,Class VIII . NCERT(Revised ed 2025) > Chapter 13: Our Home: Earth, a Unique Life Sustaining Planet > Special cells for reproduction > p. 221
- Science , class X (NCERT 2025 ed.) > Chapter 8: Heredity > separate traits, shape and colour of seeds Figure 8.5 > p. 132
- Science , class X (NCERT 2025 ed.) > Chapter 8: Heredity > 8.2.3 How do these Traits get Expressed? > p. 131
Sperms are produced in testes and eggs in ovaries; gametogenesis is the biological process that generates germ cells.
Important for questions on reproductive biology, contraception, and any policy/ethical discussion about interventions in gametes (e.g., gene editing). Links physiology (testes/ovaries, temperature effects) with developmental biology and biomedical applications.
- Science , class X (NCERT 2025 ed.) > Chapter 7: How do Organisms Reproduce? > 7.3.3 (a) Male Reproductive System > p. 123
- Science ,Class VIII . NCERT(Revised ed 2025) > Chapter 13: Our Home: Earth, a Unique Life Sustaining Planet > Sexual reproduction in animals > p. 222
- Science , class X (NCERT 2025 ed.) > Chapter 7: How do Organisms Reproduce? > What you have learnt > p. 126
Genetic modification is defined as altering hereditary material in a way not achieved by normal mating or recombination.
Crucial for biotechnology and governance questions: differentiates conventional inheritance from deliberate gene alteration, framing debates on GMO regulation, biosafety, and ethical limits of interventions such as germline edits. Helps answer policy and ethical mains/GS questions on modern biotechnology.
- Indian Economy, Nitin Singhania .(ed 2nd 2021-22) > Chapter 9: Agriculture > GENETICALLY MODIFIED (GM) CROPS > p. 301
Knowing when a zygote becomes an embryo and when implantation and organ formation begin is central to any question about intervening before birth.
High-yield for UPSC because it links basic reproductive biology to policy debates on prenatal interventions and ethics; helps answer questions on timing of medical/biotechnological actions and their legal/ethical implications. Connects to topics on human reproduction, maternal health and biomedical regulation.
- Science , class X (NCERT 2025 ed.) > Chapter 7: How do Organisms Reproduce? > 7.3.3 (b) Female Reproductive System > p. 124
- Science ,Class VIII . NCERT(Revised ed 2025) > Chapter 13: Our Home: Earth, a Unique Life Sustaining Planet > Sexual reproduction in animals > p. 223
Genome editing interacts directly with cellular DNA-copying processes that underlie reproduction and inheritance.
Essential for understanding limits and consequences of genetic interventions; useful for biotechnology, genetics and public policy questions. Mastery enables critical evaluation of techniques that aim to alter heritable material and the biological constraints on such interventions.
- Science , class X (NCERT 2025 ed.) > Chapter 7: How do Organisms Reproduce? > 7.1 DO ORGANISMS CREATE EXACT COPIES OF THEMSEL THEMSELVES? > p. 113
- Science , class X (NCERT 2025 ed.) > Chapter 7: How do Organisms Reproduce? > 7.3.1 Why the Sexual Mode of Reproduction? > p. 120
Whether an embryo develops inside the mother or within an egg affects accessibility and timing for any early-stage intervention.
Relevant for comparative biology and for assessing practical feasibility of interventions across species; informs interdisciplinary questions linking life sciences, agriculture, and bioethics. Helps frame arguments on technical and logistical differences in reproductive technologies.
- Science-Class VII . NCERT(Revised ed 2025) > Chapter 6: Adolescence: A Stage of Growth and Change > Adolescence: A Stage of Growth and Change > p. 73
- Science ,Class VIII . NCERT(Revised ed 2025) > Chapter 13: Our Home: Earth, a Unique Life Sustaining Planet > Sexual reproduction in animals > p. 223
Mammalian embryos must implant in the uterine lining and receive nutrients via a placenta during development.
High-yield for questions on reproduction and developmental biology; helps evaluate feasibility and limits of experimental interventions in mammalian embryos and links to medical/biotech policy issues. Connects to human reproduction, animal husbandry and bioethics themes frequently tested in UPSC.
- Science , class X (NCERT 2025 ed.) > Chapter 7: How do Organisms Reproduce? > 7.3.3 (b) Female Reproductive System > p. 124
Mitochondrial Replacement Therapy (MRT). Since the exam touched on nuclear germline editing (Statement 1), the next logical sibling is MRT ('Three-parent baby'), which is the only form of germline modification currently legal in some countries (like the UK) to prevent mitochondrial disease.
The 'Science Possibility' Heuristic: In S&T questions, extreme caution is needed before marking a 'Can be' statement as incorrect. Proving something is scientifically *impossible* is very hard. Unless the statement violates a fundamental law (e.g., 'Energy can be created'), assume the technology exists in a lab somewhere. Mark All Correct (D).
GS-4 Ethics (Bioethics): The concept of 'Designer Babies' (Statement 2) and the moral status of Human-Animal Chimeras (Statement 3). Use these examples to discuss the 'playing God' argument vs. therapeutic benefits in Mains answers.