/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 34 Suppose that each of the bases i... [FREE SOLUTION] | 91Ó°ÊÓ

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Suppose that each of the bases in DNA were capable of pairing with any other base. What effect would this capability have on DNA's capacity to serve as the source of genetic information?

Short Answer

Expert verified
Random base pairings would disrupt accurate DNA replication, leading to genetic instability and unreliable transmission of genetic information.

Step by step solution

01

Review DNA Structure

DNA is composed of four nucleotide bases: adenine (A), thymine (T), cytosine (C), and guanine (G). In normal DNA, A pairs with T and C pairs with G, which maintains a stable and predictable structure.
02

Understand Base Pairing Rules

The specific pairing (A-T and C-G) is crucial for replication and transcription as it ensures that the genetic code is copied accurately and consistently passed on during cell division.
03

Consider Hypothetical Scenario

If each base could pair with any other base, it would result in random base pairings.
04

Analyze Impact on Genetic Information

Random base pairings would disrupt the precise replication process of DNA, as the sequence of bases that forms the genetic code would not be copied accurately. This lack of specificity would lead to genetic instability.
05

Evaluate Consequences

The precise genetic information, crucial for developing and functioning organisms, would become unreliable, leading to increased mutations and potentially harmful variations.

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Key Concepts

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

Genetic Information
Genetic information is the blueprint of life, containing all the instructions that an organism needs to develop, function, and reproduce. It is encoded within the DNA molecule, consisting of sequences of nucleotide bases. These sequences form genes, which act as the instructions for building proteins that perform a vast array of functions in the body.
Each specific sequence of nucleotide bases in a gene corresponds to a specific protein or function. This means that even slight changes in the sequence can have significant effects on an organism. Accurate replication and maintenance of genetic information are crucial for the continuity of these instructions across generations. The integrity of genetic information ensures that offspring have the same functional capacities as their parents, allowing life to continue and evolve over time.
Nucleotide Bases
Nucleotide bases are the building blocks of DNA and play a vital role in storing genetic information. There are four types of nucleotide bases in DNA: adenine (A), thymine (T), cytosine (C), and guanine (G).
Each nucleotide consists of three components: a sugar group, a phosphate group, and a nitrogenous base (acytosine, guanine, adenine, or thymine). These bases pair in specific ways to form the double-stranded structure of DNA.
  • A pairs with T
  • C pairs with G
These pairings are held together by hydrogen bonds, forming the characteristic ladder-like structure of the DNA double helix. This specificity in base pairing is vital for DNA replication and maintaining the integrity of genetic information. If nucleotide bases could pair randomly, it would disrupt the DNA structure and genetic code.
Genetic Stability
Genetic stability refers to the accurate maintenance and transmission of genetic information across generations. This stability is essential for ensuring that genetic disorders are minimized and that functional traits are passed on accurately. Stable and precise base pairing is a key factor in maintaining genetic stability. It ensures that during the process of DNA replication, the genetic information is copied correctly.
Without this stability, organisms would experience an increase in mutations, leading to variations that could be harmful. Additionally, genetic stability supports the proper functioning of biological processes and allows for the organisms to survive environmental changes and evolutionary pressures over time.
DNA Replication
DNA replication is a crucial biological process that ensures genetic information is accurately copied for new cells. It occurs before a cell divides, allowing each daughter cell to receive a complete set of genetic information.
The process begins with the separation of the two strands of DNA, with each serving as a template for the creation of a new complementary strand. The specific base pairing (A-T and C-G) is vital for this replication process, guaranteeing that the sequence of bases is preserved from one generation to the next.
Enzymes such as DNA polymerase play critical roles in adding nucleotides to the growing DNA strand by following the complementary base pairing rules. If the base pairs were not specific, the replication process could become error-prone, leading to incorrect genetic information being transferred, and potentially resulting in malfunctioning proteins or cellular structures.

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Most popular questions from this chapter

Each nucleotide pair of a DNA double helix weighs about \(1 \times\) \(10^{-21} \mathrm{~g}\). The human body contains approximately \(0.5 \mathrm{~g}\) of DNA. How many nucleotide pairs of DNA are in the human body? If you assume that all the DNA in human cells is in the B-DNA form, how far would the DNA reach if stretched end to end?

¿Imagine that you are a student in Alfred Hershey and Martha Chase's lab in the late 1940 s. You are given five test tubes containing \(E .\) coli bacteria infected with \(\mathrm{T} 2\) bacteriophages that have been labeled with either \({ }^{32} \mathrm{P}\) or \({ }^{35} \mathrm{~S}\). Unfortunately, you forget to mark the tubes and are now uncertain about which were labelec with \({ }^{32} \mathrm{P}\) and which with \({ }^{35} \mathrm{~S}\). You place the contents of each tube in a blender and turn it on for a few seconds to shear off the phageprotein coats. You then centrifuge the contents to separate the protein coats from the cells. You check for the presence of radioactivity and obtain the following results. Which tubes contained \(E\). coli infected with \({ }^{32}\) P-labeled phage? Explain your answer. $$ \begin{array}{cc} \text { Tube number } & \text { Radioactivity present in } \\ \hline 1 & \text { Cells } \\ \hline 2 & \text { Protein coats } \\\ \hline 3 & \text { Protein coats } \\ \hline 4 & \text { Cells } \\ \hline 5 & \text { Cells } \end{array} $$

DNA molecules of different sizes are often separated with the use of a technique called electrophoresis (see Chapter 19 ). With this technique, DNA molecules are placed in a gel, an electrical current is applied to the gel, and the DNA molecules migrate toward the positive (+) pole of the current. What aspect of its structure causes a DNA molecule to migrate toward the positive pole?

Briefly outline the history of our knowledge of the structure of DNA until the time of Watson and Crick. Which do you think were the principal contributions and developments?

If a double-stranded DNA molecule is \(15 \%\) thymine, what are the percentages of all the other bases?

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