UPSC MainsZOOLOGY-PAPER-II201310 Marks
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Q16.

What is cyclic AMP? How is it derived ? Mention the role of cyclic AMP in eukaryotic cells.

How to Approach

This question requires a detailed understanding of cyclic AMP (cAMP), its synthesis, and its multifaceted roles within eukaryotic cells. The answer should begin with a clear definition of cAMP, followed by an explanation of its derivation from ATP. The core of the answer should focus on the diverse functions of cAMP in eukaryotic cells, covering signal transduction, gene regulation, and metabolic processes. A structured approach, utilizing subheadings, will enhance clarity and comprehensiveness.

Model Answer

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Introduction

Cyclic adenosine monophosphate (cAMP) is a crucial second messenger involved in numerous cellular signaling pathways in eukaryotic organisms. Discovered in the 1960s, cAMP plays a pivotal role in mediating the effects of various hormones and neurotransmitters. It acts as an intracellular signal, translating extracellular signals into intracellular responses. Understanding cAMP is fundamental to comprehending cellular communication and regulation, impacting processes from metabolism to gene expression. Its discovery revolutionized our understanding of how cells respond to external stimuli.

What is Cyclic AMP?

Cyclic AMP (cAMP) is a nucleotide derived from adenosine triphosphate (ATP). It is a cyclic molecule, meaning its phosphate groups are linked in a ring structure. Chemically, it’s adenosine 3′,5′-cyclic monophosphate. cAMP is not a building block for DNA or RNA, but rather a signaling molecule that relays signals within cells.

How is cAMP Derived?

cAMP is synthesized from ATP by the enzyme adenylyl cyclase. This enzyme is located in the plasma membrane and is activated by various extracellular signals, such as hormones (e.g., epinephrine, glucagon) that bind to G protein-coupled receptors (GPCRs). The process involves:

  • Hormone Binding: An extracellular signal binds to a GPCR.
  • G Protein Activation: The activated receptor activates a G protein.
  • Adenylyl Cyclase Activation: The activated G protein stimulates adenylyl cyclase.
  • ATP Conversion: Adenylyl cyclase catalyzes the conversion of ATP to cAMP, releasing pyrophosphate (PPi) in the process.

The enzyme phosphodiesterase (PDE) degrades cAMP into 5′-AMP, effectively terminating the signal. Different isoforms of PDE exist, providing a level of regulation over cAMP levels in different tissues and cellular compartments.

Role of Cyclic AMP in Eukaryotic Cells

1. Signal Transduction

cAMP is a key component of many signal transduction pathways. Upon its production, cAMP activates protein kinase A (PKA). PKA is a serine/threonine kinase that phosphorylates a variety of target proteins, altering their activity. This phosphorylation cascade amplifies the initial signal, leading to a significant cellular response.

2. Gene Regulation

cAMP can also influence gene expression. Activated PKA can phosphorylate transcription factors, such as CREB (cAMP response element-binding protein). Phosphorylated CREB binds to specific DNA sequences called cAMP response elements (CREs) in the promoter regions of target genes, increasing or decreasing their transcription. This mechanism allows cAMP to regulate the synthesis of specific proteins in response to external signals.

3. Metabolic Regulation

cAMP plays a crucial role in regulating metabolic pathways. For example:

  • Glycogen Metabolism: In liver and muscle cells, cAMP activates PKA, which phosphorylates and activates glycogen phosphorylase, promoting glycogen breakdown and glucose release.
  • Lipolysis: In adipose tissue, cAMP activates PKA, which phosphorylates hormone-sensitive lipase, promoting the breakdown of triglycerides into fatty acids and glycerol.

4. Other Cellular Processes

Beyond these core functions, cAMP is involved in a wide range of cellular processes, including:

  • Muscle Contraction: Regulating smooth muscle contraction.
  • Neuronal Function: Modulating neuronal excitability and synaptic plasticity.
  • Immune Response: Influencing immune cell activation and function.
  • Cell Growth and Differentiation: Participating in signaling pathways that control cell proliferation and specialization.
Process cAMP’s Role Enzyme Involved
Glycogen Breakdown Activates glycogen phosphorylase Protein Kinase A (PKA)
Lipid Breakdown Activates hormone-sensitive lipase Protein Kinase A (PKA)
Gene Transcription Phosphorylates CREB Protein Kinase A (PKA)

Conclusion

Cyclic AMP is a versatile second messenger that plays a central role in eukaryotic cell signaling. Its synthesis from ATP, mediated by adenylyl cyclase, and its degradation by phosphodiesterases, provide a dynamic system for regulating cellular responses to external stimuli. From metabolic control to gene expression and neuronal function, cAMP’s influence is widespread and essential for maintaining cellular homeostasis and coordinating complex physiological processes. Further research continues to reveal the intricate details of cAMP signaling and its implications for human health and disease.

Answer Length

This is a comprehensive model answer for learning purposes and may exceed the word limit. In the exam, always adhere to the prescribed word count.

Additional Resources

Key Definitions

Second Messenger
A second messenger is an intracellular signaling molecule released by cells in response to the binding of a first messenger (e.g., a hormone) to a cell surface receptor. They amplify the initial signal and trigger downstream cellular responses.
G Protein-Coupled Receptors (GPCRs)
GPCRs are a large family of transmembrane receptors that mediate cellular responses to a wide range of extracellular signals, including hormones, neurotransmitters, and sensory stimuli. They are characterized by their association with intracellular G proteins.

Key Statistics

Approximately 80% of human genes are regulated by cAMP signaling pathways.

Source: Lodish et al., Molecular Cell Biology, 7th Edition (2016)

GPCRs are the target of approximately 34% of all approved drugs.

Source: Lundstrom, M. (2009). G protein-coupled receptors as drug targets. *Journal of Medicinal Chemistry*, *52*(18), 5859-5882.

Examples

Epinephrine and Liver Glycogenolysis

During the “fight or flight” response, epinephrine binds to GPCRs in liver cells, leading to increased cAMP levels. This activates PKA, which phosphorylates and activates glycogen phosphorylase, resulting in the rapid release of glucose from glycogen stores to provide energy for the body.

Frequently Asked Questions

What happens if cAMP levels are abnormally high?

Abnormally high cAMP levels can lead to various disorders, depending on the affected tissues. For example, in some endocrine tumors, constitutive activation of adenylyl cyclase results in excessive cAMP production, leading to hormone hypersecretion.

Topics Covered

BiologyBiochemistryCell SignalingHormonesMetabolism