UPSC MainsBOTANY-PAPER-II20175 Marks
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Q18.

Explain with suitable examples the importance and significance of the following : Sex-linked inheritance

How to Approach

This question requires a detailed explanation of sex-linked inheritance, its mechanisms, and its significance. The answer should begin with a clear definition of sex-linked inheritance and then delve into the chromosomal basis of sex determination. It should cover X-linked and Y-linked inheritance, providing specific examples of genetic disorders associated with each. The significance should be highlighted by discussing its implications for genetic counseling and understanding evolutionary processes. A structured approach using headings and examples will enhance clarity.

Model Answer

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Introduction

Sex-linked inheritance refers to the inheritance of traits determined by genes located on the sex chromosomes. These chromosomes, designated as X and Y in many species including humans, play a crucial role in sex determination. Unlike autosomal genes, which are present on non-sex chromosomes, sex-linked genes exhibit unique patterns of inheritance due to the differing number of X and Y chromosomes in males and females. Understanding sex-linked inheritance is vital for predicting the probability of offspring inheriting specific traits, particularly genetic disorders, and has significant implications for genetic counseling and evolutionary biology.

Chromosomal Basis of Sex Determination

In humans, sex is determined by the presence or absence of the Y chromosome. Females have two X chromosomes (XX), while males have one X and one Y chromosome (XY). The X chromosome is considerably larger and carries many more genes than the Y chromosome. Consequently, X-linked genes are more frequently involved in sex-linked inheritance patterns.

X-Linked Inheritance

X-linked inheritance refers to traits determined by genes located on the X chromosome. Because males have only one X chromosome, they are hemizygous for X-linked genes. This means that a single recessive allele on the X chromosome will express its phenotype in males, even if the corresponding allele on the Y chromosome is different. Females, having two X chromosomes, can be homozygous or heterozygous for X-linked genes.

Characteristics of X-Linked Inheritance:

  • Affected males inherit the allele from their mothers.
  • Affected females must inherit the allele from both parents.
  • X-linked recessive traits are more common in males than females.
  • Carrier females (heterozygotes) do not express the trait but can pass it on to their offspring.

Examples of X-Linked Disorders:

  • Hemophilia: A bleeding disorder caused by a deficiency in clotting factors. Historically prevalent in European royal families (e.g., Queen Victoria).
  • Color Blindness: A common genetic condition affecting the ability to distinguish between certain colors, particularly red and green. Approximately 8% of males of Northern European descent have some form of color blindness.
  • Duchenne Muscular Dystrophy (DMD): A progressive muscle-weakening disease caused by a mutation in the dystrophin gene.

Y-Linked Inheritance

Y-linked inheritance refers to traits determined by genes located on the Y chromosome. Since only males have a Y chromosome, Y-linked traits are exclusively inherited by males from their fathers. Y-linked traits are relatively rare, as the Y chromosome carries fewer genes than the X chromosome.

Characteristics of Y-Linked Inheritance:

  • Only males are affected.
  • Affected males transmit the trait to all their sons.
  • Affected males do not transmit the trait to their daughters.

Example of Y-Linked Trait:

  • Hairy Ears (Hypertrichosis): A rare trait characterized by excessive hair growth in the ears.

Significance of Sex-Linked Inheritance

The study of sex-linked inheritance has profound significance in several areas:

  • Genetic Counseling: Understanding sex-linked inheritance patterns allows genetic counselors to accurately assess the risk of inheriting genetic disorders and provide informed advice to families.
  • Evolutionary Biology: Sex-linked genes can provide insights into evolutionary processes, such as natural selection and genetic drift.
  • Animal Breeding: Sex-linked traits are important considerations in animal breeding programs, particularly for traits related to production or disease resistance.
  • Understanding Genetic Diversity: Studying sex-linked genes helps in understanding the overall genetic diversity within a population.

Pedigree Analysis: Pedigree charts are crucial tools in analyzing sex-linked inheritance patterns. By tracing the inheritance of traits through generations, geneticists can determine whether a trait is autosomal or sex-linked, and whether it is dominant or recessive.

Conclusion

Sex-linked inheritance is a fundamental concept in genetics with significant implications for understanding the transmission of traits, particularly genetic disorders. The unique inheritance patterns associated with genes located on the sex chromosomes necessitate specialized approaches to genetic counseling and analysis. Continued research into sex-linked genes will undoubtedly provide further insights into the complexities of inheritance and evolution, leading to improved diagnostic and therapeutic strategies for genetic diseases.

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

Hemizygosity
The condition of having only one copy of a gene, typically referring to X-linked genes in males, as they have only one X chromosome.
Sex Chromosomes
Chromosomes that determine an individual's sex. In humans, these are the X and Y chromosomes.

Key Statistics

Approximately 1 in 5,000 males are born with hemophilia A globally.

Source: World Federation of Hemophilia (2023)

Approximately 8% of males of Northern European descent have some form of red-green color blindness.

Source: National Eye Institute (as of knowledge cutoff 2023)

Examples

Queen Victoria and Hemophilia

Queen Victoria was a carrier of the hemophilia B allele. Through her descendants, she spread the gene throughout the European royal families, leading to a high incidence of the disorder in these lineages.

Frequently Asked Questions

Why are X-linked recessive traits more common in males?

Males have only one X chromosome, so a single recessive allele on that chromosome will be expressed. Females need two copies of the recessive allele to express the trait, making it less likely.

Topics Covered

GeneticsSex ChromosomesGenetic DisordersInheritance Patterns