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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?

Short Answer

Expert verified
Answer: In a cell with adequate AMP and deficient GMP, AMP inhibits the enzyme adenylosuccinate synthetase, preventing further synthesis of AMP. The deficiency of GMP activates IMP dehydrogenase and GMP synthetase, leading to an increased production of GMP. When both AMP and GMP are present in the appropriate concentrations, they provide a balanced feedback inhibition on their respective synthesis pathways, maintaining an optimal balance of purine nucleotides needed for various cellular processes.

Step by step solution

01

Understand purine nucleotide synthesis

Purine nucleotides, such as AMP and GMP, are synthesized in a pathway called de novo purine nucleotide synthesis. This pathway involves a series of enzyme-catalyzed reactions that lead to the formation of Inosine monophosphate (IMP), which is a common precursor for both AMP and GMP. IMP can be then converted into AMP or GMP via specific enzymatic reactions.
02

Explain the regulation of purine nucleotide synthesis in the presence of adequate AMP and deficient GMP

The cell regulates purine nucleotide synthesis through feedback inhibition by the end products of the pathway. When a cell has adequate AMP but deficient GMP, AMP will inhibit the enzyme adenylosuccinate synthetase, which is responsible for the conversion of IMP to AMP. This prevents further production of AMP. On the other hand, the deficiency of GMP leads to the activation of IMP dehydrogenase, which converts IMP to xanthosine monophosphate (XMP), and GMP synthetase, which further converts XMP to GMP. As a result, the cell increases the production of GMP to maintain a balance between AMP and GMP concentrations.
03

Describe the regulation of synthesis when both AMP and GMP are present in appropriate concentrations

When both AMP and GMP are present in appropriate concentrations, they will provide a balanced feedback inhibition on their respective synthesis pathways. AMP will inhibit adenylosuccinate synthetase, and GMP will inhibit IMP dehydrogenase and GMP synthetase. This ensures that the cell maintains an appropriate balance of both purine nucleotides, essential for various cellular processes like DNA and RNA synthesis, energy production, and signaling.

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Most popular questions from this chapter

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.

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.

Elements involved in the effectiveness of the dietary treatment include A. conversion of exogenous uridine to UMP by uridine phosphotransferase. B. UTP from exogenous uridine providing substrate for synthesis of CTP. C. inhibition of carbamoyl phosphate synthetase II by UTP. D. all of the above. E. none of the above. In the de novo synthesis of pyrimidine nucleotides A. reactions take place exclusively in the cytosol. B. a free base is formed as an intermediate. C. PRPP is required in the rate-limiting step. D. UMP and CMP are formed from a common intermediate. E. UMP inhibition of OMP-decarboxylase is the major control of the process.

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.

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.

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