/*! 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 22 Which of the following does the ... [FREE SOLUTION] | 91影视

91影视

Which of the following does the enzyme primase synthesize? a. DNA primer b. Okazaki fragments c. phosphodiester linkage d. RNA primer

Short Answer

Expert verified
RNA primer

Step by step solution

01

Identify the Function of Primase

Primase is an enzyme involved in the process of DNA replication. Its main function is to synthesize a short segment of nucleic acid known as a primer.
02

Determine the Type of Primer

DNA replication requires an initial nucleotide strand to which DNA polymerase can attach and start adding nucleotides. This initial strand, or primer, is not composed of DNA but of RNA.
03

Synthesize the Primer

Primase synthesizes this RNA primer, providing a starting point for DNA polymerase to begin forming the new DNA strand during replication.
04

Choose the Correct Option

Among the given options, RNA primer is the correct product synthesized by primase.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91影视!

Key Concepts

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

primase enzyme function
Primase plays a crucial role in DNA replication. It synthesizes a short segment of nucleic acid called a primer. This primer is essential for initiating DNA synthesis.
Primase works by laying down an RNA primer on the template DNA strand.
Without this primer, DNA polymerase cannot start forming the new DNA strand.
Primase is, therefore, vital for the beginning steps of DNA replication as it sets up the stage for subsequent DNA synthesis.
RNA primer synthesis
RNA primer synthesis is a key step in DNA replication. Once primase is bound to the DNA template strand, it starts synthesizing a short RNA primer.
This primer is usually about 10 nucleotides long.
The primer serves as the starting point for DNA polymerase.
The significance of RNA primer lies in its ability to provide a free 3'-OH group.
This 3'-OH group is necessary for DNA polymerase to begin adding DNA nucleotides to form a new strand.
Thus, RNA primers are indispensable for the synthesis of the DNA strand.
DNA polymerase
DNA polymerase is the enzyme responsible for synthesizing new DNA strands. It adds nucleotides to the free 3'-OH group provided by the RNA primer.
This allows for continuous DNA strand formation.
DNA polymerase travels along the template strand, reading the DNA sequence and incorporating complementary nucleotides.
It ensures that the new DNA strand is an accurate copy of the template strand.
Additionally, DNA polymerase possesses proofreading abilities.
It can remove and correct mismatched nucleotides to prevent errors during DNA replication.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Describe the structure and complementary base pairing of DNA. a. DNA is made up of two strands that are twisted around each other to form a helix. Adenine pairs up with thymine and cytosine pairs with guanine. The two strands are anti-parallel in nature; that is, the 3鈥 end of one strand faces the 5鈥 end of other strand. Sugar, phosphate and nitrogenous bases contribute to the DNA structure. b. DNA is made up of two strands that are twisted around each other to form a helix. Adenine pairs up with cytosine and thymine pairs with guanine. The two strands are anti-parallel in nature; that is, the 3鈥 end of one strand faces the 5鈥 end of other strand. Sugar, phosphate and nitrogenous bases contribute to the DNA structure. c. DNA is made up of two strands that are twisted around each other to form a helix. Adenine pairs up with thymine and cytosine pairs with guanine. The two strands are parallel in nature; that is, the 3鈥 end of one strand faces the 3鈥 end of other strand. Sugar, phosphate and nitrogenous bases contribute to the DNA structure. d. DNA is made up of two strands that are twisted around each other to form a helix. Adenine pairs up with thymine and cytosine pairs with guanine. The two strands are anti-parallel in nature; that is, the 3鈥 end of one strand faces the 5鈥 end of other strand. Only sugar contributes to the DNA structure.

What is bacterial transformation? a. The transformation of a bacterium occurs during replication. b. It is the transformation of a bacterium into a pathogenic form. c. Transformation of bacteria involves changes in its chromosome. d. Transformation is a process in which external DNA is taken up by a cell, thereby changing morphology and physiology.

Which portion of a chromosome contains Okazaki fragments? a. helicase b. lagging strand c. leading strand d. primer

Explain why half of DNA is replicated in a discontinuous fashion. a. Replication of the lagging strand occurs in the direction away from the replication fork in short stretches of DNA, since access to the DNA is always from the 5鈥 end. This results in pieces of DNA being replicated in a discontinuous fashion. b. Replication of the leading strand occurs in the direction away from the replication fork in short stretches of DNA, since access to the DNA is always from the 5鈥 end. This results in pieces of DNA being replicated in a discontinuous fashion. c. Replication of the lagging strand occurs in the direction of the replication fork in short stretches of DNA, since access to the DNA is always from the 5鈥 end. This results in pieces of DNA being replicated in a discontinuous fashion. d. Replication of the lagging strand occurs in the direction away from the replication fork in short stretches of DNA, since access to the DNA is always from the 3鈥 end. This results in pieces of DNA being replicated in a discontinuous fashion.

The mitochondria of eukaryote cells contain their own circular DNA (mtDNA), consistent with their origin according to the theory of endosymbiosis. The mitochondrial genome is highly conserved in Eukarya. In humans, the 50 to 100 mitochondria in each of the cells in most tissues have 5 to 10 copies of the genome. Each has 37 genes that primarily encode proteins of the electron transport chain. Point mutations in which a single nucleotide is incorrectly placed is not repaired because the error-checking provided by DNA polymerase is not present in the mitochondria. The mutation rate for mtDNA is approximately 100 times higher than the mutation rate for nuclear DNA. The simultaneous existence of multiple alleles in each cell is likely, a condition called heteroplasmy. In mammals, sperm mitochondria are destroyed prior to fertilization. A. Explain how point mutations in mtDNA can result in a loss of function in critical cellular components such as cytochrome c yet not be lethal to the cell. B. Oocyte mitochondria are randomly segregated during meiosis, resulting in variation in the frequency of mtDNA mutations in offspring relative to the parent. Explain how a loss of function does not accumulate, lowering the metabolic performance from generation to generation. As described in the Evolution Connection in this chapter of the text, a fossil fingertip found in a Siberian cave revealed an evolutionary link between Neanderthals and Denisovans. Fossils from 28 individuals were located in the 鈥減it of bones,鈥 Sima de los Huesos, in Spain, thousands of miles from the Siberian cave. In 2013, mtDNA from a femur of one of these individuals was compared with mtDNA of Denisovans, Neanderthals, and modern humans. It was found that the Sima fossil shared many more alleles with Denisovans than with either Neanderthals or modern humans. In 2016, the same group of scientists who sequenced the mtDNA from the femur of one of the Sima fossils partially sequenced the DNA from that fossil, showing a clear connection to Neanderthals. C. Analyze these data to draw alternative conclusions regarding the relatedness of the three fossils and support each with evidence. D. Design a plan to differentiate or resolve these alternative conclusions.

See all solutions

Recommended explanations on Biology Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.