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Can a DNA strand bind to a complementary RNA strand? Explain.

Short Answer

Expert verified
Yes, a DNA strand can bind to a complementary RNA strand, as they share similar base pairing rules. Adenine (A) in DNA pairs with uracil (U) in RNA, while guanine (G) in DNA pairs with cytosine (C) in RNA. These interactions are crucial for transcription, which transfers genetic information from DNA to RNA for protein synthesis.

Step by step solution

01

Understanding DNA and RNA structure

DNA (deoxyribonucleic acid) and RNA (ribonucleic acid) are both nucleic acids, composed of nucleotide units. The structure of a nucleotide consists of a nitrogenous base, a five-carbon sugar (deoxyribose in DNA and ribose in RNA), and a phosphate group. The nitrogenous bases found in DNA are adenine (A), guanine (G), cytosine (C), and thymine (T), while the bases found in RNA are adenine (A), guanine (G), cytosine (C), and uracil (U), with uracil replacing thymine.
02

Base pairing rules

In DNA, strands bind together due to complementary base pairing, where adenine (A) binds with thymine (T) and cytosine (C) binds with guanine (G). These specific base pairings are due to hydrogen bonding, which can be formed between specific pairs of bases. In RNA, similar base pairings occur, with adenine (A) binding to uracil (U) and cytosine (C) binding to guanine (G).
03

DNA and RNA binding

A single DNA strand can potentially bind to a complementary RNA strand through similar base pairing rules. The adenine (A) in the DNA strand can pair with uracil (U) in the RNA strand, and guanine (G) in the DNA strand can pair with cytosine (C) in the RNA strand. This type of interaction between a DNA strand and its complementary RNA strand is the basis for the transcription process, where the information encoded in the DNA is transferred to RNA, which in turn is used to synthesize proteins.
04

Conclusion

Yes, a DNA strand can bind to a complementary RNA strand through specific base pairings, such as adenine (A) with uracil (U) and guanine (G) with cytosine (C). This binding is essential for biological processes like transcription, where genetic information is transferred from the DNA to RNA for protein synthesis.

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Most popular questions from this chapter

Which statement best explains the chemical differences between DNA and RNA? (a) DNA has two different sugars in its sugar-phosphate backbone, but RNA only has one. (b) Thymine is one of the DNA bases, whereas RNA's corresponding base is thymine minus a methyl group. (c) The RNA sugar-phosphate backbone contains fewer oxygen atoms than DNA's backbone. (d) DNA forms double helices but RNA cannot.

(a) One test for the presence of an alkene is to add a small amount of bromine, which is a red-brown liquid, and look for the disappearance of the red-brown color. This test does not work for detecting the presence of an aromatic hydrocarbon. Explain. (b) Write a series of reactions leading to para-bromoethylbenzene, beginning with benzene and using other reagents as needed. What isomeric side products might also be formed?

Write the condensed structural formulas for two alkenes and one alkyne that all have the molecular formula \(\mathrm{C}_{6} \mathrm{H}_{10}\) .

A typical amino acid with one amino group and one carboxylic acid group, such as serine, can exist in water in several ionic forms. (a) Suggest the forms of the amino acid at low pH and at high pH. (b) Amino acids generally have two pK\(_{a}\) values, one in the range of 2 to 3 and the other in the range of 9 to \(10 .\) Serine, for example, has pK\(_{a}\) values of 2.19 and \(9.21 .\) Using species such as acetic acid and ammonia as models, suggest the origin of the two pK\(_{a}\) values. (c) Glutamic acid is an amino acid that has three \(\mathrm{p} K_{a}^{\prime} \mathrm{s} : 2.10,4.07,\) and \(9.47 .\) Draw the structure of glutamic acid, and assign each \(\mathrm{pK}_{a}\) to the appropriate part of the molecule. (d) An unknown amino acid is titrated with strong base, producing the following titration curve. Which amino acids are likely candidates for the unknown?

(a) When cyclopropane is treated with HI, 1 -i-iodopropane is formed. A similar type of reaction does not occur with cyclopentane or cyclohexane. Suggest an explanation for cyclopropane's reactivity. (b) Suggest a method of preparing ethylbenzene, starting with benzene and ethylene as the only organic reagents.

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