UPSC MainsZOOLOGY-PAPER-II201115 Marks
Q9.

Compare the sex-determining mechanism of Drosophila and humans. Add a note on the genic balance theory.

How to Approach

This question requires a comparative analysis of sex determination in *Drosophila* and humans, followed by an explanation of the genic balance theory. The answer should begin by defining sex determination and briefly outlining the chromosomal basis of sex. Then, a detailed comparison of the mechanisms in both organisms should be presented, highlighting similarities and differences. Finally, the genic balance theory should be explained with its underlying principles and experimental evidence. A tabular format will be useful for the comparative aspect.

Model Answer

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Introduction

Sex determination, the biological process that determines whether an individual will develop as male or female, is a fundamental aspect of reproduction. While seemingly straightforward, the mechanisms underlying this process vary significantly across species. The chromosomal basis of sex determination, involving sex chromosomes, is prevalent in many organisms, including humans and *Drosophila melanogaster*. However, the specific roles of these chromosomes and the genes they carry differ considerably. Understanding these differences provides insights into the evolution and complexity of sex determination. This answer will compare the sex-determining mechanisms in *Drosophila* and humans, and further elaborate on the genic balance theory proposed to explain sex determination in *Drosophila*.

Sex Determination in *Drosophila*

In Drosophila, sex is determined by the ratio of X chromosomes to autosomes (non-sex chromosomes), not by the presence or absence of a Y chromosome. The Y chromosome primarily carries genes for male fertility but doesn’t determine maleness. The key principle is the ‘X:A ratio’, where X represents the number of X chromosomes and A represents the number of sets of autosomes.

  • X:A Ratio < 1.0: Results in a male.
  • X:A Ratio = 1.0: Results in a female.
  • X:A Ratio > 1.0: Results in a meta-female (intersex).

The X chromosome carries genes that promote female development, while autosomes carry genes that promote male development. The balance between these opposing influences determines the sex of the fly.

Sex Determination in Humans

Human sex determination is primarily based on 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 Y chromosome contains the SRY (Sex-determining Region Y) gene, which is the master switch for male development.

  • SRY gene present (XY): Triggers the development of testes, leading to male characteristics.
  • SRY gene absent (XX): Leads to the development of ovaries, resulting in female characteristics.

However, sex determination isn’t solely dependent on SRY. Other genes on autosomes and the X chromosome also play crucial roles in sexual development. Mutations in these genes can lead to intersex conditions.

Comparative Analysis: *Drosophila* vs. Humans

Feature Drosophila Humans
Primary Sex Chromosomes X and autosomes (Y for fertility) X and Y
Key Determinant X:A ratio SRY gene on Y chromosome
Role of Y chromosome Male fertility only Male determination (SRY gene)
Mechanism Ratio of sex chromosomes to autosomes Presence or absence of SRY gene
Intersex Conditions Metafemales (high X:A ratio) Klinefelter syndrome (XXY), Turner syndrome (XO), Androgen Insensitivity Syndrome

The Genic Balance Theory

Proposed by J.B.S. Haldane in 1922, the genic balance theory attempts to explain sex determination in Drosophila. Haldane proposed that sex is determined not by the number of X chromosomes alone, but by the balance between genes on the X chromosome that promote female development and genes on the autosomes that promote male development.

  • X-linked female-determining genes: These genes, when present in sufficient dosage (as in XX females), promote female development.
  • Autosomal male-determining genes: These genes, present in two copies in both males and females, promote male development.

According to the theory, a normal female (XX) has two sets of female-determining genes and one set of male-determining genes. A normal male (XY) has one set of female-determining genes and two sets of male-determining genes. The balance favors female development in XX individuals and male development in XY individuals. The theory explains the existence of metafemales (XXX) and supermales (XYY) as deviations from this balance.

Later research identified specific genes on the X chromosome, such as sisterless-b (sis-b), that play a role in female determination. The theory has been refined over time, but its core principle of a balance between opposing genetic influences remains a cornerstone of our understanding of sex determination in Drosophila.

Conclusion

In conclusion, sex determination mechanisms differ significantly between *Drosophila* and humans. *Drosophila* relies on the ratio of X chromosomes to autosomes, governed by the genic balance theory, while humans primarily depend on the presence or absence of the SRY gene on the Y chromosome. The genic balance theory provides a compelling explanation for the complex interplay of genes in determining sex in *Drosophila*. Further research continues to unravel the intricacies of sex determination, highlighting the evolutionary diversity and genetic complexity of this fundamental biological 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

Autosomes
Chromosomes that are not sex chromosomes. They contain genes that determine characteristics unrelated to sex.
SRY Gene
Sex-determining Region Y gene; a gene located on the Y chromosome that initiates male sex determination in mammals.

Key Statistics

Approximately 1 in 1000 births are estimated to be individuals with differences in sex development (DSD), formerly known as intersex conditions.

Source: ISNA (Intersex Society of North America) - Knowledge cutoff 2023

Studies suggest that approximately 1.7% of live births exhibit some degree of variation in sex characteristics.

Source: Lee PA, Houck GM, et al. (2006) - Knowledge cutoff 2023

Examples

Klinefelter Syndrome

A genetic condition in humans where males have an extra X chromosome (XXY). This can lead to reduced testosterone production, infertility, and other physical characteristics.

Frequently Asked Questions

What happens if the SRY gene mutates?

A mutation in the SRY gene can lead to a genetically male (XY) individual developing as a female, as the testes will not develop properly.

Topics Covered

BiologyGeneticsSex ChromosomesInheritanceGenic Balance