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Chapter 10: Problem 25

What did the Watson-Crick model suggest about the replication of DNA?

Short Answer

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Question: Summarize the key features of the Watson-Crick model and explain the DNA replication process as suggested by this model. Answer: The Watson-Crick model proposes DNA as a double helix structure with two complementary strands that run in opposite directions. It is characterized by specific base pairing, where A pairs with T and C pairs with G. The model suggests semi-conservative replication, where each original strand serves as a template to create a new strand. The DNA replication process involves unwinding the DNA, primer binding, complementary base pairing, joining of nucleotides, and continuation until two complete double-stranded DNA molecules are formed, each containing one parent strand and one newly synthesized daughter strand.

Step by step solution

01

Introduction to the Watson-Crick Model

The Watson-Crick model is a proposition made by James Watson and Francis Crick in 1953 which presents the structure of DNA as a double helix, with two complementary strands running in opposite directions. The model also explains how the genetic material is capable of replicating itself, which is a crucial aspect of growth, development, and inheritance.
02

Key Features of the Watson-Crick Model

The model is based on four key features: 1. Double helix structure: DNA is made up of two strands, with each strand having a backbone made of sugar and phosphate groups. These backbones are linked together by specific pairing of nitrogenous bases. 2. Complementary base pairing: The nitrogenous bases in each strand pair up according to specific rules, where Adenine (A) always pairs with Thymine (T), and Cytosine (C) pairs with Guanine (G). 3. Antiparallel arrangement: The two strands of the DNA double helix run in opposite directions, with one strand oriented in the 5' to 3' direction and the other in the 3' to 5' direction. This configuration is essential for the replication process. 4. Semi-conservative replication: The process by which each original strand of the DNA serves as a template to create a new daughter strand, ensuring that both daughter molecules of DNA retain one of the original strands.
03

DNA Replication Process as Suggested by the Watson-Crick Model

The Watson-Crick model suggests the following steps for DNA replication: 1. DNA unwinding: The DNA double helix is unwound by the action of helicase, breaking the hydrogen bonds between the complementary base pairs. 2. Primer binding: A short RNA primer binds to each of the separated DNA strands, providing a starting point for the addition of new nucleotides. 3. Complementary base pairing: DNA polymerase facilitates the addition of free nucleotides to the growing daughter strand, with each nucleotide pairing according to the Watson-Crick base pairing rules (A with T, and C with G). 4. Joining of nucleotides: The newly added nucleotides are joined together by phosphodiester bonds, forming the sugar-phosphate backbone of the new strand. 5. Continuation and completion: DNA replication continues along the entire length of the parent strands until two complete double-stranded DNA molecules are formed, each consisting of one original parent strand and one newly synthesized daughter strand. This explanation of DNA replication, as provided by the Watson-Crick model, has become the foundation for understanding how genetic information is copied and passed on to new cells.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

DNA Structure
The mesmerizing architecture of DNA is fundamental to its function. Picture a twisted ladder, known as a double helix, where each 'rung' consists of two nitrogenous bases bound together. These bases are adenine (A), thymine (T), cytosine (C), and guanine (G). Each 'side' of the ladder is a sugar-phosphate backbone, which acts as a sturdy frame holding the structure together. Imagine each sugar molecule attaching to a base, and a phosphate group linking one sugar to the next, creating a continuous chain. This elegant structure not only stores genetic information but also allows it to be copied and transferred reliably during cell division.

Significance of the Double Helix

The helical shape provides a compact form for storing immense amounts of information. The twisted form also aids in the unwinding and replication processes, which are pivotal for cell function and propagation.
Semi-conservative Replication
Semi-conservative replication is a graceful ballet of molecular precision, where each original DNA strand serves as a template for a new, complementary strand. During replication, the two strands of the double helix separate. Then, new nucleotides come into play, pairing with the exposed bases on the original strands. This ensures that each new DNA molecule consists of one strand from the 'parent' and one freshly synthesized 'daughter' strand, effectively conserving half of the original genetic material. It's like a parent passing down a family recipe, with each child adding their own touch while retaining the essence of the original.

Ensuring Accurate Genetic Transmission

By preserving one of the original strands, semi-conservative replication ensures that the genetic information is passed down with high fidelity, which is vital for maintaining the integrity of the genetic code across generations.
Complementary Base Pairing
Complementary base pairing is the heart of DNA's replicating mechanism, akin to finding the perfect jigsaw puzzle piece. In DNA, adenine always pairs with thymine (A-T), and cytosine pairs with guanine (C-G). This pairing is due to the shapes and chemical structures of the bases, which allow them to form hydrogen bonds with their respective partners. The rules of base pairing are strict, ensuring that each new DNA strand is an exact complement of the template strand.

The Power of Precision

This precise pairing is crucial for accurate replication and transcription of DNA. Any mistake in this process could result in mutations, which might lead to various genetic anomalies or diseases. Thus, the fidelity of complementary base pairing forms the very thread of life, weaving through the fabric of genetic continuity.
Antiparallel DNA Strands
In a DNA molecule, the two strands run in opposite directions; they are antiparallel. This means while one strand runs in a 5' to 3' direction, the other runs 3' to 5'. The numbers here refer to the carbon atoms of the deoxyribose sugar in the backbone. Enzymes that replicate DNA, such as DNA polymerase, can only add nucleotides to the 3' end of a growing strand. This antiparallel nature is essential--it ensures that the replication machinery can operate smoothly, like traffic rules that guide vehicles along a roadway, preventing collisions and ensuring orderly movement.

Importance of Directionality

This orientation impacts how replication occurs, with one strand being synthesized continuously as the leading strand, and the other, the lagging strand, being replicated in short bursts. The interplay between the antiparallel strands and enzyme action underscores nature's ingenuity in preserving life's blueprint.

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Most popular questions from this chapter

During gel electrophoresis, DNA molecules can easily be separated according to size because all DNA molecules have the same charge-to-mass ratio and the same shape (long rod). Would you expect RNA molecules to behave in the same manner as DNA during gel electrophoresis? Why or why not?

What is the physical state of DNA after it is heated and denatured?

Does the design of the Hershey-Chase experiment distinguish between DNA and RNA as the molecule serving as the genetic material? Why or why not?

Adenine may also be named 6 -amino purine. How would you name the other four nitrogenous bases, using this alternative system? (O is indicated by "oxy-," and \(\mathrm{CH}_{3}\) by "methyl.")

One of the most common spontaneous lesions that occurs in DNA under physiological conditions is the hydrolysis of the amino group of cytosine, converting the cytosine to uracil. What would be the effect on DNA structure of a uracil group replacing cytosine?
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