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Level 1: Knowledge/Comprehension In DNA technology, the term vector can refer to (A) the enzyme that cuts DNA into restriction fragments. (B) the sticky end of a DNA fragment. (C) a SNP marker. (D) a plasmid used to transfer DNA into a living cell.

Short Answer

Expert verified
Option (D) is correct: a plasmid used to transfer DNA into a living cell.

Step by step solution

01

Understand the Question

The question is asking about the definition of the term 'vector' in the context of DNA technology.
02

Analyze Option (A)

Option (A) mentions an enzyme that cuts DNA into restriction fragments. This enzyme is known as a restriction enzyme, not a vector.
03

Analyze Option (B)

Option (B) refers to the sticky end of a DNA fragment. Sticky ends are short, single-stranded sequences at the ends of DNA fragments that allow for base-pairing with complementary sequences, but they are not vectors.
04

Analyze Option (C)

Option (C) involves a SNP marker, which stands for Single Nucleotide Polymorphism. SNP markers are variations in a single nucleotide that occur at a specific position in the genome, not vectors.
05

Analyze Option (D)

Option (D) mentions a plasmid used to transfer DNA into a living cell. Plasmids can carry foreign DNA into host cells and are commonly used as vectors in DNA technology.
06

Choose the Best Answer

Review the options and determine that the best choice is (D), as it correctly defines a vector in DNA technology.

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Key Concepts

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

DNA plasmid
In the realm of DNA technology, plasmids serve as vital tools. These small, circular DNA molecules are distinct from the chromosomal DNA found in the nucleus of cells. Plasmids naturally occur in bacterial cells. Scientists often use plasmids to transfer genetic material into a host cell, making them essential in genetic engineering.
When a plasmid is introduced into a bacterial cell, it can replicate independently of the chromosomal DNA. This unique ability allows plasmids to be used as vectors. They carry foreign DNA and introduce it into another cell. Scientists can add genes of interest to plasmids. Then, these modified plasmids can be used to produce proteins, enzymes, or other substances of value. This process is a cornerstone of biotechnology.
  • Plasmids are circular molecules.
  • They replicate independently of chromosomal DNA.
  • Used to transfer genetic material into host cells.
restriction enzyme
Restriction enzymes, also known as restriction endonucleases, are proteins that cut DNA at specific sequences. They were first discovered in bacteria, where they serve as a defense mechanism against viral DNA infection.
These enzymes scan the DNA sequence and make cuts at specific sites known as restriction sites. The cuts can result in fragments with 'blunt' or 'sticky ends,' depending on the enzyme used. Scientists harness this cutting ability to manipulate DNA in the lab. For example, they can cut out a gene from one organism and insert it into a plasmid for cloning.
  • Restriction enzymes cut DNA at specific sequences.
  • They create fragments with 'blunt' or 'sticky ends.'
  • They are crucial for DNA cloning and genetic engineering.
SNP marker
Single Nucleotide Polymorphisms, or SNPs, are differences in a single nucleotide that occur at specific positions in the genome. These markers are highly useful in genetic studies because they can help identify variations in the DNA sequence between different individuals.
Scientists use SNP markers to study genetic diversity, trace inheritance patterns, and even locate genes associated with diseases. By analyzing these markers, experts can understand how genes contribute to individual traits and susceptibilities.
  • SNPs are single nucleotide variations in the genome.
  • Useful for studying genetic diversity and inheritance patterns.
  • Help locate genes linked to diseases.
sticky end
When restriction enzymes cut DNA, they can leave behind 'sticky ends.' These are short, single-stranded sequences of DNA that hang off the cut ends of a DNA fragment. These sequences can easily pair with complementary 'sticky ends' from another DNA fragment. This property makes sticky ends very useful in DNA cloning.
When scientists insert a gene into a plasmid, they often use restriction enzymes to create sticky ends on both the gene and the plasmid. The complementary sticky ends can then pair up, making it easier for the gene to be inserted precisely into the plasmid. This technique ensures that genetic constructs are made accurately and efficiently.
  • Sticky ends result from the action of restriction enzymes.
  • They are single-stranded sequences that facilitate base-pairing.
  • Useful for inserting genes into plasmids accurately.

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Most popular questions from this chapter

Level 1: Knowledge/Comprehension Plants are more readily manipulated by genetic engineering than are animals because (A) plant genes do not contain introns. (B) more vectors are available for transferring recombinant DNA into plant cells. (C) a somatic plant cell can often give rise to a complete plant. (D) plant cells have larger nuclei.

Level 3: Synthesis/Evaluation MAKE CONNECTIONS Imagine you want to study one of the human crystallins, proteins present in the lens of the eye (see Figure 1.8). To obtain a sufficient amount of the protein of interest, you decide to clone the gene that codes for it. Assume you know the sequence of this gene. Explain how you would go about this.

Level 3: SynthesislEvaluation SYNTHESIZE YOUR KNOWLEDGE The water in the Yellowstone National Park hot springs shown here is around \(160^{\circ} \mathrm{F}\) \(\left(70^{\circ} \mathrm{C}\right) .\) Biologists assumed that no species of organisms could live in water above about \(130^{\circ} \mathrm{F}\left(55^{\circ} \mathrm{C}\right),\) so they were surprised to find several species of bacteria there, now called thermophiles ("heat-lovers"). You've learned in this chapter how an enzyme from one species, Thermus aquaticus, made feasible one of the most important DNA-based techniques used in labs today. Identify the enzyme, and indicate the value of its being isolated from a thermophile. Suggest other reasons why enzymes from this bacterium (ot other thermophiles) might also be valuable.

Level 3: SynthesislEvaluation Evoution connection Ethical considerations aside, if DNA-based technologies became widely used, discuss how they might change the way evolution proceeds, as compared with the natural evolutionary mechanisms that have operated for the past 4 billion years.

Which of the following sequences in double-stranded DNA is most likely to be recognized as a cutting site for a restriction enzyme? (A) AAGG TTCC (B) GGCC CCGG (C) ACCA TGGT (D) AAAA TTTT

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