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91Ó°ÊÓ

The DNA double helix does not have which of the following? a. anti parallel configuration b. complementary base pairing c. major and minor grooves d. uracil

Short Answer

Expert verified
d. uracil

Step by step solution

01

Identify the components of DNA

Review the key structural features of DNA: anti-parallel strands, complementary base pairs (adenine pairs with thymine, and cytosine pairs with guanine), and the presence of major and minor grooves.
02

Understand the role of uracil

Note that uracil is a nitrogenous base found in RNA, not DNA. In DNA, thymine is used instead of uracil.
03

Evaluate the options

Compare each option to the known characteristics of DNA. Options 'a', 'b', and 'c' are accurate descriptions of DNA structure. Option 'd', uracil, does not apply to DNA as it is part of RNA.
04

Conclusion

Therefore, the DNA double helix does not contain uracil.

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Key Concepts

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

anti-parallel configuration
The strands of DNA run in opposite directions, which is known as anti-parallel configuration. This means that one strand runs from the 5' to 3' direction, while the complementary strand runs from 3' to 5'. This configuration is crucial for the correct pairing of bases and the replication process.
The enzyme DNA polymerase, which is responsible for replicating DNA, can only add nucleotides to the 3' end of the newly forming strand. Hence, the anti-parallel nature ensures that the enzyme works efficiently on both strands.
This concept helps to maintain stability and integrity in the DNA molecule, letting it store genetic information accurately. Understanding this is key to appreciating how genetic information is passed down through generations.
complementary base pairing
Complementary base pairing is essential for the structure and function of DNA. In this pairing, adenine (A) pairs with thymine (T), and cytosine (C) pairs with guanine (G). These pairs are held together by hydrogen bonds: two between A and T, and three between C and G.
This specificity in pairing allows for the accurate copying of DNA during cell division. If the complementary base pairs did not match up correctly, replication errors would occur, leading to mutations.
The idea of complementary base pairing also extends to how RNA pairs with DNA. Although RNA uses uracil (U) in place of thymine, it still follows the rule where adenine pairs with uracil during transcription.
major and minor grooves
The DNA double helix creates two types of grooves, major and minor, as it twists. These grooves are areas where proteins and other molecules can interact with the DNA.

The major groove is wider and more exposed, making it an essential site for binding of proteins like transcription factors, which regulate gene expression. Proteins that bind to the major groove often recognize specific sequences of bases.

In contrast, the minor groove is narrower and less accessible but still plays a role in interactions with smaller molecules and some specific proteins.
The existence of these grooves allows the DNA to be more versatile in interactions, playing a key role in the complex regulation of cellular activities.
uracil in RNA
Uracil is one of the four nitrogenous bases found in RNA. It replaces thymine, which is used in DNA. Uracil pairs with adenine during the process of RNA formation.
The presence of uracil instead of thymine allows RNA to be more versatile and less stable than DNA. This instability makes RNA suitable for temporary tasks like transmitting genetic information for protein synthesis.
Messenger RNA (mRNA) is a key example where uracil's presence is crucial. During transcription, DNA is copied into mRNA, where A pairs with U instead of T. This mRNA then carries the genetic code from the nucleus to the ribosomes, where proteins are made.
The switch from thymine to uracil is beneficial for RNA's roles and helps distinguish RNA from DNA in cells.

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Most popular questions from this chapter

Explain how forensic scientists are able to use DNA analysis to identify individuals. a. Comparison of DNA from a known source or individual with analysis of the sequence of an unknown sample of DNA allows scientists to find out if both of them are similar or not. b. DNA from the unknown sample is sequenced and analyzed. The result of the analysis is then matched with any random population. The matching individual then helps in forensics. c. Comparison of DNA from a known source or individual with analysis of the sequence of bases in strands of an unknown sample of RNA allows scientists to find out if both of them are similar or not. d. Comparison of DNA from a known source or individual with analysis of the sugars and phosphates in strands of an unknown sample of DNA allows scientists to find out if both of them are similar or not.

How do the linear chromosomes in eukaryotes ensure that their ends are replicated completely? a. The ends of the linear chromosomes are maintained by the activity of the telomerase enzyme. b. The ends of the linear chromosomes are maintained by the formation of a replication fork. c. The ends of the linear chromosomes are maintained by the continuous joining of Okazaki fragments. d. The ends of the linear chromosomes are maintained by the action of the polymerase enzyme.

Who was the first person to isolate the material that came to be known as nucleic acids? a. Frederick Griffith b. Friedrich Miescher c. James Watson d. Oswald Avery

Describe how the model of DNA replication illustrates the function of topoisomerase. a. Topoisomerase relieves the pressure that results from supercoiling by breaking and reforming DNA’s phosphate backbone ahead of the replication fork. b. Topoisomerase increases the pressure to increase supercoiling by breaking and reforming DNA’s phosphate backbone ahead of the replication fork. c. Topoisomerase relieves the pressure that results from supercoiling by breaking and reforming DNA’s nucleotide base pairs ahead of the replication fork. d. Topoisomerase relieves the pressure that results from separation of DNA strands by breaking and reforming DNA’s phosphate backbone ahead of the replication fork.

What is the difference in the rate of replication of nucleotides between prokaryotes and eukaryotes? a. Eukaryotes are 50 times slower. b. Eukaryotes are 20 times faster. c. Prokaryotes are 100 times slower. d. Prokaryotes are 10 times faster

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