Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Topic Video
Question
What is difference between the leading and lagging strands in
Which?
-Okazaki fragments are connected together with DNA polymerase.
-The lagging strand has continuous DNA replication.
-The leading strand produces short DNA fragments that get combined later.
-The leading strand makes one, long piece of DNA.
-The DNA polymerase on the lagging strand moves in the same direction as the replication fork.
Expert Solution
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
This is a popular solution
Trending nowThis is a popular solution!
Step by stepSolved in 3 steps with 1 images
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- Below is a study of a colony of cells, determine that some of these cells have a mutated DNA polymerase I that results in loss of function of this enzyme. - What will the effect of the mutation in DNA polymerase I be on DNA replication? Include leading and lagging strand - Will this mutation in DNA polymerase I have an impact on another step in DNA replication? Will DNA be replicatation be impacted? Are any enzymes involved?arrow_forwardIn DNA replication, the fundamental reason that Okasaki fragments are produced is that Group of answer choices DNA replication can proceed only in the 5’ to 3’ direction replication on the leading strand is slower than replication on the lagging strand DNA polymerase tends to slip while replicating the lagging strand DNA polymerase has to alternate between the leading and lagging strands during replication none of these are true.arrow_forwardWhich of the following DNA repair processes is known to be "error-prone" (i.e. resulting in incorporation of incorrect nucleotides as part of the repair process)? Mark all the answers that are correct. Base Excision Repair (BER) non-homologous end-joining of double-stranded DNA breaks. O Nucleotide Excision Repair (NER) post-replication repair SO-responsearrow_forward
- Which of the following statements about DNA replication is INCORRECT? Select one: O a. DNA polymerase is the enzyme that adds nucleotides to the growing DNA strand. O b. DNA polymerase can only synthesize the new DNA strand in the 5' to 3' direction. O c. helicase is the enzyme which connects Okazaki fragments on the lagging strand. O d. the lagging strand has many primers. O e. the leading strand has only one primer.arrow_forwardWhat is the function of DNA helicase in DNA replication? to create an RNA primer to initiate DNA replication O to insert new bases during elongation, using the parent strand as a template O to anneal (splice) smaller fragments of DNA to create one continuous strand to create replication bubbles by unravelling the parental strands of DNA O all of the abovearrow_forwardMedgie is creating his science fair project on DNA replication. His final display board shows the following. Human DNA Replication Steps Step 1 DNA unwinds in the nucleus Step 2 Complementary base pairs are deleted Step 3 DNA rewinds back together Step 4 The newly made DNA helix is placed in a cell formed in Mitosis According to Medgie's project, which of the following identifies and explains which of the steps is incorrect? O Step 4 is incorrect because not all human cells require DNA. O Step 3 is incorrect because the DNA remains unwound to be transcribed into RNA. Step 2 is incorrect because the complementary base pairs are used as a template, not deleted. Step 1 is incorrect because DNA doesn't unwind in the nucleus, instead it unwinds in the cytoplasm Previousarrow_forward
- DNA polymerase occasionally incorporates the wrong nucleotide during DNA replication. If left unrepaired, the base-pair mismatch that results will lead to mutation in the next replication. As part of a template strand, the incorporated wrong base will direct the incorporation of a base complementary to itself, so the bases on both strands of the DNA at that position will now be different from what they were before the mismatch event. The MER-minus strain of yeast does not have a functional mismatch excision repair system, but it has normal base excision repair and nucleotide excision repair systems. Which of the following statements is correct about differences in the mutation spectrum between MER-minus and wildtype yeast? More than one answer is correct. Options: More point mutations will arise in MER-minus yeast. Fewer point mutations will arise in MER-minus yeast as compared with wildtype. Of the total point mutations that…arrow_forwardA drug that inhibits the DNAa protein is added to a culture of E. coli cells. What is the first step of DNA replication that will be impaired by this drug? Group of answer choices Keeping parent DNA strands separated Releasing tension generated by supercoiling Activating the origin of replication Making primers Forming phosphodiester bondsarrow_forwardWhich of the following statements is/are TRUE for DNA Replication? Two daughter DNAs are formed, each one contains an old and new strands. When the (parent) DNA strands unwind, the 3'→ 5' strand is the leading strand while the 5'→3' strand is the lagging strand. Requires dATP, dTTP, dGTP, dCTP and Mg2+ The replisome is the biological machine responsible in replicating DNA.arrow_forward
arrow_back_ios
arrow_forward_ios
Recommended textbooks for you
- Human Anatomy & Physiology (11th Edition)BiologyISBN:9780134580999Author:Elaine N. Marieb, Katja N. HoehnPublisher:PEARSONBiology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStaxAnatomy & PhysiologyBiologyISBN:9781259398629Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa StouterPublisher:Mcgraw Hill Education,
- Molecular Biology of the Cell (Sixth Edition)BiologyISBN:9780815344322Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter WalterPublisher:W. W. Norton & CompanyLaboratory Manual For Human Anatomy & PhysiologyBiologyISBN:9781260159363Author:Martin, Terry R., Prentice-craver, CynthiaPublisher:McGraw-Hill Publishing Co.Inquiry Into Life (16th Edition)BiologyISBN:9781260231700Author:Sylvia S. Mader, Michael WindelspechtPublisher:McGraw Hill Education
Human Anatomy & Physiology (11th Edition)
Biology
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:PEARSON
Biology 2e
Biology
ISBN:9781947172517
Author:Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:OpenStax
Anatomy & Physiology
Biology
ISBN:9781259398629
Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter
Publisher:Mcgraw Hill Education,
Molecular Biology of the Cell (Sixth Edition)
Biology
ISBN:9780815344322
Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter
Publisher:W. W. Norton & Company
Laboratory Manual For Human Anatomy & Physiology
Biology
ISBN:9781260159363
Author:Martin, Terry R., Prentice-craver, Cynthia
Publisher:McGraw-Hill Publishing Co.
Inquiry Into Life (16th Edition)
Biology
ISBN:9781260231700
Author:Sylvia S. Mader, Michael Windelspecht
Publisher:McGraw Hill Education