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The two purine nucleotides found in RNA A. are formed in a branched pathway from a common intermediate. B. are formed in a sequential pathway, C must come from exogenous sources. D. are formed by oxidation of the deoxy forms. E. are synthesized from nonpurine precursors by totally separate pathways.

Short Answer

Expert verified
Answer: The two purine nucleotides found in RNA are formed in a branched pathway from a common intermediate.

Step by step solution

01

Identify the purine nucleotides found in RNA

The two purine nucleotides found in RNA are Adenine (A) and Guanine (G).
02

Analyze the options.

Let's go through each option and assess its validity based on the biosynthesis of purine nucleotides: A. "are formed in a branched pathway from a common intermediate." B. "are formed in a sequential pathway." C. "must come from exogenous sources." D. "are formed by oxidation of the deoxy forms." E. "are synthesized from nonpurine precursors by totally separate pathways."
03

Evaluate Option A

Purine nucleotides are, in fact, synthesized through a branched pathway originating from a common intermediate, inosine monophosphate (IMP). IMP is the first purine nucleotide synthesized and can be converted into either AMP (adenosine monophosphate) or GMP (guanosine monophosphate). This option seems to be correct.
04

Evaluate Option B

Purine nucleotides are not synthesized in a sequential pathway because IMP serves as a common intermediate for both AMP and GMP. Developing separately would make it a branched pathway, not a sequential one. Option B is incorrect.
05

Evaluate Option C

Purine nucleotides can be synthesized in cells by the de novo biosynthesis pathway, meaning they are not solely dependent on exogenous sources. Option C is incorrect.
06

Evaluate Option D

Purine nucleotides in RNA are not formed by the oxidation of their deoxy forms. Deoxy forms are found in DNA, and their formation involves the reduction of ribonucleotides, not their oxidation. Option D is incorrect.
07

Evaluate Option E

AMP and GMP are synthesized from IMP, a common precursor, and not from totally separate nonpurine precursors. Therefore, option E is incorrect.
08

Conclusion

After evaluating each option, option A, "are formed in a branched pathway from a common intermediate," is the correct statement describing the formation of the purine nucleotides found in RNA.

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Key Concepts

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

RNA Biosynthesis
Understanding RNA biosynthesis is crucial for grasping cellular functions. RNA, or ribonucleic acid, plays an essential role in the coding, decoding, regulation, and expression of genes. During biosynthesis, RNA is assembled from nucleotides, which are the basic building blocks of RNA.

Inclusive of four different nucleotides in its structure—one of them being uracil (U), which replaces thymine (T) found in DNA—the other three are cytosine (C), adenine (A), and guanine (G). The latter two, A and G, are known as purine nucleotides and have a distinct synthesis pathway in cells. RNA polymerase, the enzyme responsible for catalyzing the formation of RNA, binds to DNA and helps in the transcription of DNA into RNA by following the sequence of the template DNA strand.

Purine synthesis in RNA is a fascinating process where a single precursor, inosine monophosphate (IMP), can give rise to both adenine and guanine nucleotides. It demonstrates the efficiency of the cellular machinery in utilizing common pathways to create different end products.
Inosine Monophosphate (IMP)
Inosine monophosphate (IMP) is the pivotal molecule in purine nucleotide biosynthesis. It is the first nucleotide formed in the de novo synthesis pathway and serves as a branching point for the formation of the other two purine nucleotides, AMP and GMP.

To envision IMP’s importance, picture it as a central hub in a railway network with trains (enzymes) departing towards two distinct cities (nucleotides). The versatile structure of IMP allows it to be readily converted into either AMP or GMP through specific biochemical reactions involving energy and certain enzymes. These reactions include the transfer of an amine group from aspartate to IMP to form adenylosuccinate, which then converts to AMP, and the oxidation of IMP followed by the addition of an amine group to form GMP.
Adenosine Monophosphate (AMP)
Adenosine monophosphate (AMP), a critical molecule in multiple cellular processes, is derived from IMP through a series of enzyme-catalyzed reactions. AMP carries the adenine base, a purine derivative, bonded to a ribose sugar and a single phosphate group.

In energy transfer, AMP can be phosphorylated to ADP or ATP, molecules essential for cellular energetics. It also plays a role in signaling pathways as a component of cyclic AMP (cAMP), which acts as a messenger for intracellular signals. The particular structure of AMP allows it to integrate into RNA during transcription processes, where it pairs with the pyrimidine nucleotide uracil.
Guanosine Monophosphate (GMP)
Guanosine monophosphate (GMP) is another outcome of the branched de novo pathway starting from IMP. GMP contains the guanine base and, like AMP, is made up of the base attached to a ribose sugar and a single phosphate group.

Just as AMP is necessary for several cellular functions, GMP too participates in similar processes. It can be further phosphorylated to become GDP or GTP, actively participating in protein synthesis and other energy-dependent cellular activities. GMP also plays a role in the formation of RNA, pairing up with the pyrimidine nucleotide cytosine when RNA is synthesized from a DNA template.
De Novo Biosynthesis Pathway
The de novo biosynthesis pathway refers to the 'from scratch' creation of nucleotides inside a cell. Starting with basic molecules like amino acids, carbon dioxide, and ammonia, this pathway elaborately pieces together the purine ring, eventually forming IMP—a common starting point for both AMP and GMP synthesis.

This process of de novo biosynthesis is regulated by the cellular needs and availability of substrates. It is energy-intensive, yet vital, as nucleotides are not just the building blocks of RNA and DNA, but also involved in energy transfer, metabolism, and cell signaling. The efficiency of this pathway allows the cell to respond dynamically to changes in metabolic demands, ensuring the availability of nucleotides for various critical cellular processes.

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Most popular questions from this chapter

If a cell capable of de noto synthesis of purine nucleotides has adequate AMP but is deficient in GMP, how would the cell regulate synthesis to increase [GMP]? If both AMP and GMP were present in appropriate concentrations, what would happen?

Gout is a disease characterized by hyperuricemia from an overproduction of purine nucleotides via the de novo pathway. The specific cause of Lesch-Nyhan syndrome is a severe deficiency of HGPRTase. Allopurinol is used in the treatment of gout to reduce the production of uric acid. In Lesch-Nyhan syndrome, the decrease in uric acid is balanced by an increase in xanthine plus hypoxanthine in blood. In the other forms of gout, the decrease in uric acid is greater than the increase in xanthine plus hypoxanthine. The explanation for this difference in the two forms of gout is A. it is an experimental artifact and the decrease in uric acid and increase in xanthine plus hypoxanthine in non-Lesch-Nyhan gout is the same. B. allopurinol is less effective in non-Lesch-Nyhan gout. C. there is an increased excretion of xanthine and hypoxanthine in non-Lesch- Nyhan gout. D. PRPP levels are reduced in Lesch-Nyhan. E. in non-Lesch-Nyhan gout hypoxanthine and xanthine are salvaged to IMP and XMP and inhibit PRPP amidotransferase.

There are two distinct immunodeficiency diseases that lead to the formation of uric acid as the end product. Mutation in genes for adenosine deaminase (ADA) leads to severe combined immunodeficiency (SCID) in which both T-cells and B-cells are affected. Defects in purine nucleoside phosphorylase (PNP) affect only T-cells. These two enzymes are in the pathways for degradation of nucleic acids. Gene therapy has had some success in treating ADA deficiency. In nucleic acid degradation, all of the following are correct except A there are nucleases that are specific for either DNA or RNA. B. nucleotidases convert nucleotides to nucleosides. C. the conversion of a nucleoside to a free base is an example of a hydrolysis. D. because of the presence of deaminases, hypoxanthine rather than adenine is formed. E. both DNA and RNA degradation lead to uric acid.

The synthesis of the coenzymes NAD, FAD, and coenzyme A have in common A. the same vitamin. B. PRPP. \(\mathrm{C} . \mathrm{AMP}\) D. ATP. E. a nucleotidase.

There are two distinct immunodeficiency diseases that lead to the formation of uric acid as the end product. Mutation in genes for adenosine deaminase (ADA) leads to severe combined immunodeficiency (SCID) in which both T-cells and B-cells are affected. Defects in purine nucleoside phosphorylase (PNP) affect only T-cells. These two enzymes are in the pathways for degradation of nucleic acids. Gene therapy has had some success in treating ADA deficiency. The best estimate of the turnover of DNA comes from a measurement in urine of A. uric acid. B. \(\mathrm{NH}_{4}^{+}\) and \(\mathrm{CO}_{2}\) C. \(\beta\) -alanine. D. \(\beta\) -aminoisobutyrate. E. cytidine.

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