Chapter 16: Problem 25
What are the four bases found in DNA? List the complement of each one.
Short Answer
Expert verified
The four bases of DNA are Adenine (A), Thymine (T), Guanine (G), Cytosine (C). The complements are A-T, T-A, G-C, and C-G respectively.
Step by step solution
01
Identifying the Four Bases in DNA
The first step is to identify the four nitrogenous bases found in DNA. These bases are Adenine (A), Thymine (T), Guanine (G), and Cytosine (C).
02
Understanding Base Pairing
DNA structure is based on the principle of complementary base pairing. Adenine (A) always pairs with Thymine (T), and Guanine (G) pairs with Cytosine (C). This means that the complement of A is T, and the complement of G is C.
03
Listing the Complements
The complements of each of the four DNA bases are: Adenine (A) pairs with Thymine (T), and Guanine (G) pairs with Cytosine (C). Therefore, the complement of A is T, the complement of T is A, the complement of G is C, and the complement of C is G.
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Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Nucleotide Bases
The building blocks of DNA are known as nucleotide bases, which are critical to the formation of DNA's double helix structure. Within each nucleotide, there is a combination of three components: a sugar molecule (deoxyribose), a phosphate group, and one of four nitrogenous bases. These bases fall into two categories: purines and pyrimidines.
The purines consist of Adenine (A) and Guanine (G), which are larger, double-ring structures. On the flip side, the pyrimidines, which are smaller and have a single-ring structure, include Cytosine (C) and Thymine (T). The order of these bases along the DNA strand encodes genetic information, much like how letters arrange to form words and sentences.
Understanding the unique structure of each of these bases helps explain their specificity in pairing, which is fundamental to the accurate replication and transcription of genetic information.
The purines consist of Adenine (A) and Guanine (G), which are larger, double-ring structures. On the flip side, the pyrimidines, which are smaller and have a single-ring structure, include Cytosine (C) and Thymine (T). The order of these bases along the DNA strand encodes genetic information, much like how letters arrange to form words and sentences.
Understanding the unique structure of each of these bases helps explain their specificity in pairing, which is fundamental to the accurate replication and transcription of genetic information.
Complementary Base Pairs
The concept of complementary base pairing is analogous to the idea of puzzle pieces fitting together perfectly. In DNA, this precise fit is achieved through hydrogen bonds that form between specific pairs of nucleotide bases. Adenine (A) pairs with Thymine (T), forming two hydrogen bonds, while Guanine (G) pairs with Cytosine (C), forming three hydrogen bonds.
This specificity is due to the size, shape, and chemical composition of the bases. The pairing is such that a purine (a larger molecule) always pairs with a pyrimidine (a smaller molecule), maintaining a uniform width of the DNA double helix. This complementary pairing ensures the DNA strand can be copied accurately during cell division and is essential for the integrity of genetic information.
This specificity is due to the size, shape, and chemical composition of the bases. The pairing is such that a purine (a larger molecule) always pairs with a pyrimidine (a smaller molecule), maintaining a uniform width of the DNA double helix. This complementary pairing ensures the DNA strand can be copied accurately during cell division and is essential for the integrity of genetic information.
Why Does Complementary Base Pairing Matter?
- Replication Accuracy: Enzymes can ‘read’ the sequence of one DNA strand and create a complementary strand, resulting in identical DNA copies.
- Genetic Stability: Complementary pairs maximize the efficiency of DNA repair mechanisms, contributing to genetic stability.
DNA Structure
The magnificent structure of DNA is that of a double helix, a twisted ladder-like arrangement discovered by scientists James Watson, Francis Crick, along with contributions from Rosalind Franklin and Maurice Wilkins. The sides of the 'ladder' consist of alternating sugar and phosphate groups, forming the DNA's backbone, while the 'rungs' are the complementary base pairs connected by hydrogen bonds.
The double helix structure is not only visually striking but functionally significant. It allows DNA to be incredibly compact, fitting vast amounts of genetic information into a tiny space within the cell's nucleus. Moreover, the structure is designed to easily unzip along the base pairs, enabling the DNA to replicate and to be read by the cell to make proteins.
The double helix structure is not only visually striking but functionally significant. It allows DNA to be incredibly compact, fitting vast amounts of genetic information into a tiny space within the cell's nucleus. Moreover, the structure is designed to easily unzip along the base pairs, enabling the DNA to replicate and to be read by the cell to make proteins.
Key Features of the DNA Double Helix:
- Antiparallel Strands: The two strands of DNA run in opposite directions, which is critical for the replication and function of DNA.
- Major and Minor Grooves: These grooves are indentations in the double helix that allow proteins to bind to DNA, controlling gene expression and DNA replication.