Cell Biology and Organelles — MCQs
Which of the following statements regarding collagen synthesis is incorrect?
Which of the following helps in cell-to-cell adhesion?
What is the main component of a bilayer cell membrane?
Major mechanism of transport of drugs across biological membranes is:
Identify the gene commonly involved in the condition shown in the image?
Which of these is not a part of extracellular matrix:
Most radio-resistant phase in the cell cycle:
Which of the following statements regarding mitochondrial DNA is FALSE?
Which organelle produces and destroys H2O2?
All the following features are seen in neurons from dorsal root ganglia, EXCEPT:
Cell Biology and Organelles Indian Medical PG Practice Questions and MCQs
Question 1: Which of the following statements regarding collagen synthesis is incorrect?
- A. Hydroxylation of lysine occurs in ER
- B. Synthesized in ribosomes as preprocollagen
- C. Triple helix assembly occurs in ER
- D. Hydroxylation of proline occurs in Golgi apparatus (Correct Answer)
Explanation: ***Hydroxylation of proline occurs in Golgi apparatus*** - This statement is incorrect because the **hydroxylation of proline** residues occurs in the **endoplasmic reticulum** (ER), not the Golgi apparatus. - This step is critical for forming stable **triple helix** structures of collagen and requires **vitamin C**. *Synthesized in ribosomes as preprocollagen* - This statement is correct. Collagen synthesis begins in the cytoplasm, where mRNA is translated by **ribosomes** into **preprocollagen**, which contains a signal peptide. - The signal peptide directs the nascent polypeptide chain into the lumen of the **endoplasmic reticulum**. *Hydroxylation of lysine occurs in ER* - This statement is correct. Following entry into the ER, specific **lysine** residues are hydroxylated by **lysyl hydroxylase** to form hydroxylysine. - This hydroxylation, along with that of proline, is crucial for **cross-linking** and stability of the collagen molecule. *Triple helix assembly occurs in ER* - This statement is correct. After hydroxylation and glycosylation of some residues, three procollagen alpha chains self-assemble to form a **triple helix** within the **endoplasmic reticulum**. - This assembly is stabilized by **disulfide bonds** at the C-terminal ends and molecular chaperones.
Question 2: Which of the following helps in cell-to-cell adhesion?
- A. Interleukins
- B. Interferons
- C. E-Cadherin (Correct Answer)
- D. Matrix metalloproteinases
Explanation: ***E-Cadherin*** - E-Cadherin is a **cell adhesion molecule** that plays a crucial role in maintaining the structure of tissues by promoting **cell-to-cell adhesion** [1]. - It is mainly involved in the **adherens junctions**, helping cells stick together, especially in epithelial tissues. *Matrix metallo proteinase* - Matrix metallo proteinases (MMPs) are enzymes that degrade **extracellular matrix** components, rather than promoting adhesion between cells. - They are involved in **tissue remodeling** and **wound healing**, not in direct cell-to-cell interactions. *Interleukins* - Interleukins are a group of **cytokines** that mediate **immune responses**, but they do not facilitate direct cell adhesion. - Their primary function involves **cell signaling** and communication, rather than adhesion processes. *Interferons* - Interferons are signaling proteins involved in the **immune defense against viral infections** and do not have a role in cell-to-cell adhesion. - They primarily act to induce an **antiviral state** in neighboring cells and modulate the immune response. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Neoplasia, pp. 314-315.
Question 3: What is the main component of a bilayer cell membrane?
- A. Cholesterol ester
- B. Triacyl glycerol
- C. Cholesterol
- D. Phospholipids (Correct Answer)
Explanation: ***Correct: Phospholipids*** - **Phospholipids** are the primary structural components of cell membranes, forming a **bilayer** due to their amphipathic nature. - The **hydrophilic heads** face the aqueous environment, while the **hydrophobic tails** form the core of the membrane. *Incorrect: Cholesterol* - **Cholesterol** is an important component of animal cell membranes, contributing to fluidity and stability, but it is not the **main structural component**. - It inserts between phospholipids, modulating membrane fluidity by preventing the tight packing of fatty acid tails at lower temperatures and hindering excessive movement at higher temperatures. *Incorrect: Cholesterol ester* - **Cholesterol esters** are storage forms of cholesterol and are primarily found in intracellular lipid droplets or associated with lipoproteins in the bloodstream. - They are generally too **hydrophobic** to be significant structural components within the phospholipid bilayer itself. *Incorrect: Triacyl glycerol* - **Triacylglycerols** (triglycerides) are the primary form of **energy storage** in cells, found in lipid droplets within the cytoplasm. - They are highly **hydrophobic** and do not form a structural part of the cell membrane bilayer.
Question 4: Major mechanism of transport of drugs across biological membranes is:
- A. Passive diffusion (Correct Answer)
- B. Facilitated diffusion
- C. Active transport
- D. Endocytosis
Explanation: ***Passive diffusion*** - This is the **most common mechanism** for drug transport across biological membranes, especially for **lipid-soluble** drugs. - It occurs down a **concentration gradient** and does not require energy or carrier proteins. *Facilitated diffusion* - This process requires **carrier proteins** to move drugs across membranes, but it still occurs down a **concentration gradient** and does not consume energy directly. - It handles substances that are **too large or too polar** to cross by passive diffusion, but it is not the primary mechanism for most drugs. *Active transport* - This mechanism uses **carrier proteins** and **expends energy (ATP)** to move drugs against their **concentration gradient**. - It is important for the transport of specific drugs, but it is not the predominant mode for the majority of drug molecules. *Endocytosis* - This involves the **engulfment of large molecules** or particles by the cell membrane, forming vesicles. - It is a less common mechanism for drug absorption, primarily used for **very large molecules** like proteins or nanoparticles.
Question 5: Identify the gene commonly involved in the condition shown in the image?
- A. RAS
- B. RET
- C. BRAF V600E (Correct Answer)
- D. P53
Explanation: ***BRAF V600E*** - The image displays cells with **Langerhans cell morphology**, including folded nuclei and abundant pale cytoplasm, which are characteristic of **Langerhans cell histiocytosis (LCH)** [1]. - The **BRAF V600E mutation** is the most common genetic alteration found in LCH, present in about 50-60% of cases and activating the MAPK pathway [1]. *RAS* - **RAS mutations** are frequently seen in various cancers, including colorectal adenocarcinoma, pancreatic adenocarcinoma, and non-small cell lung cancer. - While RAS pathway activation can occur in LCH, a direct RAS mutation is not the most common genetic driver; rather, downstream effectors like BRAF V600E are more prominent [1]. *RET* - **RET mutations** are primarily associated with **medullary thyroid carcinoma** (in both sporadic and inherited forms like MEN 2A and MEN 2B) and can also be found in certain types of lung cancer. - They are not a characteristic genetic alteration for Langerhans cell histiocytosis. *P53* - The **TP53 gene** encodes the tumor suppressor protein p53, and mutations in this gene are among the most frequent genetic alterations across a wide spectrum of human cancers. - Although p53 plays a critical role in cell cycle regulation and apoptosis, it is not a primary or common driver mutation specifically associated with Langerhans cell histiocytosis [1]. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Diseases of White Blood Cells, Lymph Nodes, Spleen, and Thymus, pp. 629-630.
Question 6: Which of these is not a part of extracellular matrix:
- A. Collagen
- B. Laminin
- C. Fibronectin
- D. Integrins (Correct Answer)
Explanation: ***Integrins*** - Integrins are **transmembrane receptors** on the cell surface that facilitate cell-extracellular matrix (ECM) adhesion and cell-cell adhesion. - They are part of the cell membrane, **not** an extracellular component. *Laminin* - **Laminin** is a major protein component of the **basal lamina**, a specialized extracellular matrix that underlies epithelial cells. - It plays a crucial role in cell adhesion, differentiation, and migration within the ECM. *Fibronectin* - **Fibronectin** is a large glycoprotein present in the **extracellular matrix** and in soluble form in blood plasma. - It mediates cell adhesion to the ECM by binding to integrins and various ECM components like collagen and proteoglycans. *Collagen* - **Collagen** is the most abundant protein in the human body and a primary structural component of the **extracellular matrix**. - It provides tensile strength and structural integrity to tissues like skin, bone, tendons, and cartilage.
Question 7: Most radio-resistant phase in the cell cycle:
- A. G2
- B. Late S (Correct Answer)
- C. Early S
- D. G1
Explanation: ***Late S*** - The **late S phase** is the **most radio-resistant phase** of the cell cycle due to high levels of DNA repair enzymes and mechanisms active during this period. - During late S phase, chromatin is **tightly packed** and DNA synthesis is accompanied by robust **homologous recombination repair** capacity, making cells less vulnerable to radiation-induced damage. - This is a well-established principle in radiobiology, with cells in late S showing **2-3 times more resistance** compared to G2/M phases. *Early S* - While S phase overall is relatively radio-resistant, **early S is less resistant than late S** because repair mechanisms are not yet fully upregulated. - DNA replication has just begun, and the cell has moderate levels of repair enzymes compared to late S phase. *G1* - Cells in G1 phase have **moderate radio-sensitivity**, more sensitive than S phase but less sensitive than G2/M phases. - While cells have time for repair in G1, they lack the enhanced repair enzyme levels present during S phase. - G1 cells are in an **active metabolic state** preparing for DNA synthesis. *G2* - G2 phase is one of the **most radio-sensitive phases** along with mitosis (M phase). - Cells have **duplicated DNA** (4n content) and are preparing for division, making them highly vulnerable to radiation damage. - Any unrepaired DNA damage will be transmitted to both daughter cells during the upcoming mitosis.
Question 8: Which of the following statements regarding mitochondrial DNA is FALSE?
- A. Double stranded
- B. Inherited from mother
- C. High mutation rate
- D. All respiratory proteins are synthesized within the mitochondria (Correct Answer)
Explanation: ***All respiratory proteins are synthesized within the mitochondria.*** - While mitochondrial DNA (mtDNA) encodes some proteins essential for the **electron transport chain** (respiratory proteins), not all respiratory proteins are synthesized within the mitochondria. - Many crucial respiratory proteins are encoded by **nuclear DNA** and imported into the mitochondria from the cytoplasm. *Double stranded* - **Mitochondrial DNA (mtDNA)** is a **double-stranded**, circular molecule, similar to bacterial chromosomes. - This structure provides stability and allows for efficient replication within the organelle. *Inherited from mother* - Mitochondria and their DNA are exclusively inherited from the **mother** during fertilization, as sperm primarily contributes nuclear DNA. - This **maternal inheritance pattern** is a key feature of mtDNA and is used in tracing ancestry. *High mutation rate* - mtDNA has a significantly **higher mutation rate** compared to nuclear DNA due to several factors, including lack of robust repair mechanisms and exposure to reactive oxygen species. - This contributes to the rapid evolution of mtDNA and its use in **population genetics** studies.
Question 9: Which organelle produces and destroys H2O2?
- A. Peroxisome (Correct Answer)
- B. Lysosome
- C. Ribosome
- D. Golgi body
Explanation: ***Peroxisome*** - **Peroxisomes** are involved in metabolic processes, including **fatty acid oxidation**, which produces **hydrogen peroxide (H2O2)** as a byproduct. - They also contain the enzyme **catalase**, which breaks down the toxic H2O2 into water and oxygen, thus both producing and destroying it. *Lysosome* - **Lysosomes** are responsible for waste breakdown and cellular garbage disposal using **hydrolytic enzymes** in an acidic environment. - They are not primarily involved in the production or destruction of **H2O2**. *Ribosome* - **Ribosomes** are responsible for **protein synthesis** and are composed of ribosomal RNA and protein. - They do not play a role in the metabolism of **H2O2**. *Golgi body* - The **Golgi apparatus** modifies, sorts, and packages **proteins and lipids** for secretion or delivery to other organelles. - It is not associated with the production or breakdown of **H2O2**.
Question 10: All the following features are seen in neurons from dorsal root ganglia, EXCEPT:
- A. They are multipolar (Correct Answer)
- B. They are derived from neural crest cells
- C. They have eccentrically located nuclei
- D. They contain lipofuscin granules
Explanation: ***They are multipolar*** - Dorsal root ganglia (DRG) neurons are typically **pseudounipolar**, meaning they have a single process that branches into two (peripheral and central) rather than multiple dendrites and an axon [1]. - **Multipolar neurons** are characteristic of motor neurons and interneurons in the central nervous system, not DRG sensory neurons [1]. *They contain lipofuscin granules* - **Lipofuscin granules** are common in long-lived, post-mitotic cells like neurons and are considered "wear and tear" pigments, accumulating with age. - Their presence in DRG neurons is a normal finding and reflects the neuron's metabolic activity over time. *They have eccentrically located nuclei* - While not universally present in all DRG neurons, an **eccentrically located nucleus** is a common histological feature of certain types of DRG neurons, particularly larger ones. - This feature helps distinguish them from other neuron types and can be accentuated by the large amount of cytoplasm in these cells. *They are derived from neural crest cells* - All sensory neurons of the DRG, along with other components like Schwann cells and sympathetic ganglia, originate from **neural crest cells**. - This developmental origin is a fundamental characteristic of DRG neurons, distinguishing them from CNS neurons derived from the neural tube.
Want unlimited practice?
Get full access to all questions, explanations, and performance tracking.
Start For Free