UPSC MainsANI-HUSB-VETER-SCIENCE-PAPER-I201315 Marks
Q19.

Explain the law of Independent Assortment given by Mendel with suitable examples taking dihybrid cross. Describe briefly the deviations from Mendelian Genetics.

How to Approach

This question requires a clear understanding of Mendelian genetics and the Law of Independent Assortment. The approach should involve first explaining Mendel's experiments and the Law itself with a dihybrid cross example. Subsequently, a discussion of deviations from Mendel's laws, like incomplete dominance, codominance, and linkage, is crucial. Structuring the answer with clear headings and subheadings will enhance readability and demonstrate a comprehensive understanding of the topic. Diagrams could be included if possible, even though not explicitly requested.

Model Answer

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Introduction

Gregor Mendel, the "father of genetics," laid the foundation for our understanding of heredity through his meticulous experiments with pea plants in the 19th century. His work, published in 1865, elucidated the principles of inheritance, initially overlooked until the rediscovery of his findings in the early 20th century. The Law of Independent Assortment is one of Mendel's foundational principles, explaining how traits are inherited independently of one another. This answer will explain this law using a dihybrid cross and then briefly explore deviations observed in inheritance patterns that contradict Mendel's original findings.

Mendel’s Law of Independent Assortment

Mendel’s Law of Independent Assortment states that the alleles of different genes assort independently of one another during gamete formation. This means that the inheritance of one trait does not influence the inheritance of another trait, provided the genes controlling those traits are located on different chromosomes or are far apart on the same chromosome.

Dihybrid Cross and Explanation

To illustrate this law, consider a dihybrid cross, which involves examining the inheritance of two traits simultaneously. Let's take the example of pea plants where seed color (yellow – Y, green – y) and seed shape (round – R, wrinkled – r) are the traits under consideration. Mendel proposed that these genes are located on different chromosomes.

A heterozygous plant for both traits (YyRr) will produce four types of gametes: YR, Yr, yR, and yr, each with equal probability. When two such heterozygous plants (YyRr x YyRr) are crossed, the resulting offspring (F1 generation) will exhibit a phenotypic ratio of 9:3:3:1. This ratio demonstrates the independent assortment of the genes for seed color and seed shape.

Gamete Possible Combinations
YR YYRR, YyRR, YYRr, YyRr
Yr YYRr, YyRr, YYrr, Yyrr
yR YYRr, YyRr, yyRR, yyRr
yr YYrr, Yyrr, yyRr, yyrr

The 9:3:3:1 ratio arises from the independent combination of alleles during fertilization. The ‘9’ represents the plants with both dominant traits (yellow, round), the ‘3’ represents plants with one dominant and one recessive trait (yellow, wrinkled or green, round), and the ‘1’ represents the plants with both recessive traits (green, wrinkled).

Deviations from Mendelian Genetics

While Mendel’s laws provide a robust framework for understanding inheritance, several deviations have been observed that challenge these original principles. These deviations often arise due to complexities in gene interaction and chromosomal behavior.

Incomplete Dominance

In incomplete dominance, the heterozygous phenotype is a blend of the two homozygous phenotypes. For example, in snapdragons, a cross between a red-flowered plant (RR) and a white-flowered plant (WW) results in pink-flowered offspring (RW). Neither red nor white is dominant.

Codominance

Codominance occurs when both alleles are equally expressed in the heterozygous phenotype. A classic example is the human ABO blood group system. Individuals with the IAIB genotype express both the A and B antigens on their red blood cells, resulting in AB blood type.

Linked Genes

Mendel’s law assumes independent assortment, but this is not always the case. Genes that are located close together on the same chromosome are called linked genes. They tend to be inherited together, violating the principle of independent assortment. The closer the genes are, the stronger the linkage. Crossing over during meiosis can sometimes separate linked genes, but this is less frequent.

Multiple Alleles

Some genes have more than two alleles within a population. The human ABO blood group system is an example, with three alleles: IA, IB, and i. This leads to a wider range of possible genotypes and phenotypes.

Polygenic Inheritance

Polygenic inheritance involves the simultaneous influence of multiple genes on a single trait, such as height or skin color in humans. The interaction of these genes results in a continuous range of phenotypes, rather than discrete categories.

Epistasis

Epistasis occurs when the expression of one gene masks or modifies the expression of another, independent gene. This can alter the expected phenotypic ratios in offspring.

The discovery of these deviations from Mendel’s original laws has expanded our understanding of genetics and highlighted the complexity of inheritance patterns. The work of Barbara McClintock on transposable elements (mobile genetic elements) provided a mechanism for explaining some of these deviations, earning her a Nobel Prize in 1983.

Conclusion

Mendel's Law of Independent Assortment remains a cornerstone of genetics, providing a fundamental understanding of how traits are inherited. While deviations from this law exist, they contribute to the complexity and diversity of life. Further research continues to refine our understanding of gene interaction and inheritance patterns, demonstrating the dynamic nature of genetic principles. The knowledge derived from these principles is crucial for advancements in areas like agriculture, medicine, and evolutionary biology.

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

Allele
One of two or more alternative forms of a gene at a particular locus.
Genotype
The genetic constitution of an individual organism.

Key Statistics

The Human Genome Project, completed in 2003, identified approximately 20,000-25,000 human genes, highlighting the complexity of genetic inheritance.

Source: National Human Genome Research Institute

Approximately 80% of genetic variation in human height is attributed to the combined effects of multiple genes (polygenic inheritance).

Source: University of Queensland, Australia - Research Study (Knowledge Cutoff)

Examples

Sickle Cell Anemia

Sickle cell anemia is an example of codominance, where individuals with one copy of the normal allele (A) and one copy of the sickle cell allele (S) (AS genotype) exhibit a milder form of the disease.

Flower Color in Camellias

Camellia flower color often displays incomplete dominance; a cross between a red-flowered camellia and a white-flowered camellia results in pink-flowered offspring.

Frequently Asked Questions

Why do linked genes sometimes get separated?

Linked genes can sometimes be separated during meiosis through a process called crossing over, where homologous chromosomes exchange genetic material.

How does environmental factors affect Mendelian inheritance?

While Mendel's laws describe the transmission of genes, environmental factors can influence the expression of those genes, leading to phenotypic variations.