Answer-
Mutation is hereditary change in the genetic make up of an individual other than that which may be caused by simple recombination of genes. These include changes in gene structure or composition and the changes in the chromosomes either in structure or number. So, mutation is the process by which the sequence of base pairs in DNA is altered. The mutation caused by the addition (insertion) or deletion (losing) of nitrogenous bases in the DNA or mRNA are known as Frame-shift mutations, because these shift the reading frame of codons from the site of change onward. Frame-shift mutations are of 2 types:
1) Deletion mutation- These mutations are caused due to the loss or deletion of one or more nucleotides. 2) Insertion mutation- These mutations are caused by the addition of one or more extra nucleotides in a DNA molecule at one or more places.
If mutation produced, codes for one of the terminator or nonsense codon (UAA, UAG, UGA), the reading of RNA would stop at that point. This would end up with inactivation of that particular gene i.e. this would prevent a complete polypeptide chain from being formed. This usually results in the formation of non-functional proteins. Several intercalating agents such as acridine, proflavin, Ethidium bromide cause the frame-shift mutation which sometimes, results in inactivation of genes,
Picture of nonsense mutation is given below:
DNA repair errors include losing or inserting random nucleotides at the cut site. Explain how these...
Funcions of the After Cas9 cleaves the DNA, cellular enzymes will attempt to repair the break. Most of the time, these enzymes repair the DNA without errors. However, Cas9 will keep cutting the DNA at the same location until an error is made. 7. DNA repair errors include losing or inserting random nucleotides at the cut site. Explain how these changes might inactivate a gene. PART 2: Inactivating Genes in Butterflies Robert Reed, a biologist at Cornell University, wanted to...
Suppose the restriction enzyme GsuII binds a site that is 2 nucleotides in length. How often (how many base pairs) does this enzyme cut DNA? Your answer must be numeric.
Suppose the restriction enzyme Gsull binds a site that is 3 nucleotides in length. How often (how many base pairs) does this enzyme cut DNA? Your answer must be numeric.
Explain how a molecular biologist could determine whether a cut-site was in the middle of an antibiotic-resistance gene. Explain how restriction enzyme digestion results would change if a foreign gene were inserted into a plasmid.
Help with these two would be appreciated JUVIJVVEL In a large unbiased random DNA sequence, how often would you expect a 6 base targeting site specific restriction enzyme to cut? O On average every 4096 base pairs (446) O Never O On average every 1.296 base pairs (6^4) O Every 6 base pairs QUESTION 5 2 points Save Answer How do bacteria possessing restriction systems avoid targeting and cutting their own DNA? By methylating their chromosomal DNA O By methylating...
Explain how the lethal gene in the plasmid's multiple cloning site(MCS) will function with and without a DNA insert.
Cloning / Subcloning When subcloning engineering new plasmids, by inserting new DNA fragments (inserts) me plasmids (now called a vector because it will carry your gene of interest) it is important to considering existing genes / DNA elements. If a site is in the middle of a gene, you could lose or destroy that gene. If there are multiple sites for an enzyme, when you paste them together, multiple possible outcomes can arise. This is undesirable, because it confounds verification...
Which of the following statements could explain how a cell with a defect in DNA repair could become cancerous? The cell could accumulate mutations that lead to additional defects in normal cell behavior. Transcription in the cell may be halted. Apoptosis may be triggered. The cell cycle will arrest at the G1 to S phase cell cycle checkpoint.
What are the three functional groups that comprise a nucleotide? What do nucleotides have in common with amino acids or simple sugars? When the structure of DNA was first elucidated, many biologists quickly saw how this structure explained the passage of information from one generation to another. How does the structure of DNA explain generation-to-generation flow of information? In other words, give a brief description of the structure of DNA and tell how this structure allows for replication. Which of...
4. The CRISPR-Cas9 system is an important new technique in molecular biology. What is the natural function of this system? Describe how you would use this system to generate a null mutation in another organism (i.e. explain Figure 6-43). How does it work? What is the modification of the method that allows for correction of a mutation (e.g. the mouse crystalline gene)? And lastly, what are the problems with the CRISPR system? FIGURE 6-43 Single-nucleotide mutations can be introduced into...