UPSC MainsZOOLOGY-PAPER-II201910 Marks
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Q15.

Watson and Crick model of DNA

How to Approach

This question requires a detailed explanation of the Watson and Crick model of DNA. The answer should cover the historical context, the key features of the model (double helix, base pairing, sugar-phosphate backbone), the evidence supporting the model, and its significance. Structure the answer chronologically, starting with the pre-Watson and Crick understanding of DNA, then detailing the model itself, followed by the evidence and concluding with its impact. Focus on clarity and precision in describing the molecular structure.

Model Answer

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Introduction

Deoxyribonucleic acid (DNA) is the molecule carrying the genetic instructions for all known organisms and many viruses. Understanding its structure was a pivotal moment in biology. Prior to 1953, scientists knew DNA was composed of nucleotides, but its overall structure remained elusive. Rosalind Franklin and Maurice Wilkins’ X-ray diffraction studies provided crucial clues. In 1953, James Watson and Francis Crick, building upon this work and incorporating the Chargaff’s rules, proposed the now-famous double helix model of DNA, revolutionizing our understanding of heredity and molecular biology. This model explained how genetic information is stored, replicated, and passed on to subsequent generations.

Historical Context & Precursors

The quest to understand DNA’s structure began in the late 19th century with the isolation of DNA by Friedrich Miescher. Early 20th-century research established that DNA, not protein, was the carrier of genetic information (Hershey-Chase experiment, 1952). Erwin Chargaff’s rules (1950) stated that the amount of adenine (A) equals the amount of thymine (T), and the amount of guanine (G) equals the amount of cytosine (C) in DNA, providing a critical constraint for the model.

The Watson-Crick Model: Key Features

Watson and Crick, working at the Cavendish Laboratory, Cambridge, proposed a model based on three key observations:

  • Double Helix: DNA exists as a double helix, resembling a twisted ladder. Two polynucleotide strands wind around each other.
  • Sugar-Phosphate Backbone: Each strand has a backbone composed of alternating deoxyribose sugar and phosphate groups. This forms the sides of the ladder.
  • Base Pairing: Nitrogenous bases (adenine, guanine, cytosine, thymine) are located in the center of the helix. Adenine (A) always pairs with Thymine (T) via two hydrogen bonds, and Guanine (G) always pairs with Cytosine (C) via three hydrogen bonds. This is known as complementary base pairing.
  • Antiparallel Strands: The two strands run in opposite directions (antiparallel), one from 5’ to 3’ and the other from 3’ to 5’.
  • Major and Minor Grooves: The helical structure creates major and minor grooves, which are important for protein binding and gene regulation.

Evidence Supporting the Model

The Watson-Crick model wasn’t merely a theoretical construct; it was strongly supported by experimental evidence:

  • X-ray Diffraction Data (Rosalind Franklin & Maurice Wilkins): Franklin’s Photo 51 revealed a helical structure with a repeating pattern, providing crucial dimensions for the model.
  • Chargaff’s Rules: The model elegantly explained Chargaff’s rules, as the specific base pairing ensures A=T and G=C.
  • Viscosity Measurements: Measurements of DNA viscosity supported the idea of a long, thin molecule.
  • Chemical Analysis: The model was consistent with the known chemical composition of DNA.

Significance and Implications

The discovery of the DNA structure had profound implications:

  • Mechanism of Replication: The model immediately suggested a mechanism for DNA replication – the strands could separate, and each serve as a template for the synthesis of a new complementary strand.
  • Genetic Code: It laid the foundation for understanding the genetic code and how information is encoded in DNA.
  • Molecular Biology Revolution: It ushered in the era of molecular biology, leading to advancements in genetic engineering, biotechnology, and medicine.
  • Understanding Mutations: The model provided a framework for understanding how mutations occur and their consequences.

Further Developments

While the Watson-Crick model was groundbreaking, subsequent research revealed further complexities. For example, the discovery of different forms of DNA (A-DNA, B-DNA, Z-DNA) and the role of DNA packaging into chromatin demonstrate that DNA structure is dynamic and influenced by its environment.

Conclusion

The Watson and Crick model of DNA was a landmark achievement in scientific history. By elucidating the structure of DNA, they provided a fundamental understanding of the molecular basis of heredity. This discovery not only explained how genetic information is stored and replicated but also paved the way for countless advancements in biology, medicine, and biotechnology. Continued research continues to refine our understanding of DNA’s structure and function, revealing its remarkable complexity and adaptability.

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

Nucleotide
The basic building block of nucleic acids (DNA and RNA). It consists of a nitrogenous base, a five-carbon sugar (deoxyribose in DNA, ribose in RNA), and one or more phosphate groups.
Chargaff's Rule
The principle stating that in DNA, the proportion of adenine (A) is equal to the proportion of thymine (T), and the proportion of guanine (G) is equal to the proportion of cytosine (C). This rule was crucial in determining the base pairing arrangement in the DNA double helix.

Key Statistics

The human genome contains approximately 3 billion base pairs of DNA.

Source: National Human Genome Research Institute (NHGRI) - as of knowledge cutoff 2023

Approximately 99.9% of the human genome is identical across all individuals.

Source: International Human Genome Sequencing Consortium (as of knowledge cutoff 2023)

Examples

Sickle Cell Anemia

A classic example of how a change in DNA sequence (a single nucleotide mutation) can lead to a genetic disease. A mutation in the gene encoding hemoglobin causes red blood cells to become sickle-shaped, leading to various health problems.

Frequently Asked Questions

What role did Rosalind Franklin play in the discovery of the DNA structure?

Rosalind Franklin’s X-ray diffraction images, particularly Photo 51, provided crucial data about the helical structure of DNA. Watson and Crick used this data, without her explicit permission, to build their model. Her contribution was initially overlooked but is now widely recognized as essential.

Topics Covered

BiologyGeneticsMolecular BiologyDNA StructureDouble HelixBase Pairing