Biochemistry
7 questionsWhich enzyme polymerises Okazaki fragments?
Which type of DNA polymerase is responsible for the replication of mitochondrial DNA?
Which type of RNA contains codons for specific amino acids?
Which type of RNA is most commonly associated with pseudouridine?
In eukaryotic cells, where does the majority of functional RNA activity occur?
Which of the following is NOT a characteristic of the genetic code?
A frameshift mutation does not affect the complete amino acid sequence if it occurs in multiples of what number?
NEET-PG 2013 - Biochemistry NEET-PG Practice Questions and MCQs
Question 191: Which enzyme polymerises Okazaki fragments?
- A. DNA polymerase I
- B. DNA polymerase II
- C. DNA polymerase III (Correct Answer)
- D. RNA polymerase
Explanation: ***DNA polymerase III*** - **DNA polymerase III** is the primary replicative enzyme in **prokaryotes (bacteria)** responsible for synthesizing new DNA strands, including the **polymerization of Okazaki fragments** on the lagging strand. - It possesses high processivity (can add ~500 nucleotides without dissociating), essential for rapid and efficient DNA synthesis during replication, adding nucleotides in a **5' to 3' direction**. - In **eukaryotes**, DNA polymerase δ (delta) performs the analogous function of polymerizing Okazaki fragments. *DNA polymerase I* - **DNA polymerase I** in prokaryotes primarily functions in **removing RNA primers** left by primase and **filling the resulting gaps** with DNA nucleotides. - It has 5' to 3' exonuclease activity for primer removal and polymerase activity for gap filling, but is **not the main enzyme for elongating Okazaki fragments**. - Its role is in **DNA repair and finishing replication**, not the extensive synthesis of Okazaki fragments. *DNA polymerase II* - **DNA polymerase II** in prokaryotes is primarily involved in **DNA repair mechanisms**, particularly in **restarting stalled replication forks** and responding to DNA damage. - It is not the main enzyme responsible for the polymerization of **Okazaki fragments** during normal DNA replication. *RNA polymerase* - **RNA polymerase** (specifically **primase**, a specialized RNA polymerase) synthesizes short **RNA primers** (8-12 nucleotides) during DNA replication, which provide the 3'-OH group necessary to initiate DNA synthesis. - It does not synthesize DNA or polymerize **Okazaki fragments**; its function is to create RNA primers, not extend DNA strands.
Question 192: Which type of DNA polymerase is responsible for the replication of mitochondrial DNA?
- A. DNA polymerase delta
- B. DNA polymerase alpha
- C. DNA polymerase gamma (Correct Answer)
- D. DNA polymerase beta
Explanation: ***DNA polymerase gamma*** - **DNA polymerase gamma** is the sole DNA polymerase responsible for replicating and repairing the mitochondrial DNA in eukaryotic cells. - It consists of a large catalytic subunit and two smaller accessory subunits that provide **proofreading** and processivity functions. *DNA polymerase alpha* - **DNA polymerase alpha** is primarily involved in initiating DNA replication on both the leading and lagging strands of nuclear DNA. - It forms a complex with **primase** to synthesize short RNA primers followed by a short stretch of DNA. *DNA polymerase delta* - **DNA polymerase delta** is a key enzyme in nuclear DNA replication, primarily responsible for the **elongation of the lagging strand**. - It also plays a significant role in various DNA repair pathways, including **nucleotide excision repair**. *DNA polymerase beta* - **DNA polymerase beta** is mainly involved in **DNA repair processes**, specifically **base excision repair (BER)** in the nucleus. - It has a low processivity and lacks **proofreading activity**, making it unsuitable for bulk DNA replication.
Question 193: Which type of RNA contains codons for specific amino acids?
- A. Transfer RNA (tRNA)
- B. Messenger RNA (mRNA) (Correct Answer)
- C. Small nuclear RNA (snRNA)
- D. Ribosomal RNA (rRNA)
Explanation: ***Messenger RNA (mRNA)*** - **mRNA** carries the genetic information from **DNA** in the nucleus to the **ribosomes** in the cytoplasm. - This information is encoded in sequences of three nucleotides called **codons**, each specifying a particular amino acid. *Transfer RNA (tRNA)* - **tRNA** molecules are responsible for **carrying specific amino acids** to the ribosome during protein synthesis. - Each **tRNA** has an **anticodon** that base-pairs with a complementary **codon** on the **mRNA** strand. *Small nuclear RNA (snRNA)* - **snRNA** is primarily involved in **RNA splicing**, a process that removes introns from pre-mRNA. - It forms part of the **spliceosome** complex, which is crucial for mature mRNA formation but does not contain codons itself. *Ribosomal RNA (rRNA)* - **rRNA** is a major component of **ribosomes**, the cellular machinery responsible for protein synthesis. - While it plays a critical structural and catalytic role in translation, it does not carry genetic code in the form of codons.
Question 194: Which type of RNA is most commonly associated with pseudouridine?
- A. messenger RNA (mRNA)
- B. ribosomal RNA (rRNA)
- C. transfer RNA (tRNA) (Correct Answer)
- D. DNA
Explanation: ***Transfer RNA (tRNA)*** - **Pseudouridine (ψ)** is one of the most abundant modified nucleosides in RNA, and **tRNA contains the highest proportion** of pseudouridine modifications among all RNA types. - **tRNA molecules can contain up to 10-15% modified bases**, with pseudouridine being particularly abundant in the **TψC arm** (thymine-pseudouridine-cytosine loop). - These modifications are critical for **tRNA stability, proper folding, and accurate codon-anticodon recognition** during translation. - Pseudouridine enhances base stacking and stabilizes RNA structure through additional hydrogen bonding capability. *Ribosomal RNA (rRNA)* - While rRNA does contain pseudouridine modifications, they are present in **lower proportions compared to tRNA**. - rRNA pseudouridine modifications do play important roles in **ribosomal assembly and function**, but tRNA remains the RNA type most commonly associated with this modification. *Messenger RNA (mRNA)* - **mRNA is generally much less modified** than tRNA or rRNA. - Pseudouridine modifications in mRNA are relatively rare in prokaryotes and were only recently discovered to be more common in eukaryotic mRNA. - When present, they may affect **mRNA stability and translation efficiency**. *DNA* - **DNA does not contain pseudouridine** as this is an RNA-specific modification. - Pseudouridine is formed by **post-transcriptional isomerization** of uridine residues in RNA.
Question 195: In eukaryotic cells, where does the majority of functional RNA activity occur?
- A. Nucleus
- B. Ribosome
- C. Cytoplasm (Correct Answer)
- D. None of the options
Explanation: ***Cytoplasm*** - The **cytoplasm** is the cellular compartment where the **majority of functional RNA activity** occurs, including **translation** (protein synthesis) involving mRNA, tRNA, and rRNA. - **Ribosomes** (the sites of translation) are located in the cytoplasm, either free-floating or bound to the endoplasmic reticulum. - Many types of **regulatory RNAs** such as microRNAs (miRNAs) and small interfering RNAs (siRNAs) exert their functions in the cytoplasm by targeting mRNAs for degradation or translational repression. - **mRNA degradation** and **RNA interference pathways** primarily operate in the cytoplasm. - The question asks for the broader location rather than the specific molecular machinery, making cytoplasm the most comprehensive answer. *Nucleus* - While RNA is **transcribed** from DNA and **processed** (capping, polyadenylation, splicing) in the nucleus, these are preparatory steps. - The nucleus is primarily the site of **RNA synthesis**, not where most RNA performs its functional roles. - Only a small fraction of functional RNA activity (like rRNA processing in the nucleolus) occurs here compared to the cytoplasm. *Ribosome* - While **ribosomes are the specific sites of translation** and are composed of rRNA and proteins, they represent molecular machinery rather than a cellular location. - Ribosomes themselves are located **within the cytoplasm**, making cytoplasm the more inclusive answer for where RNA activity occurs. - The question asks "where" in terms of cellular compartment, not which molecular complex. *None of the options* - This is incorrect as the cytoplasm is indeed the primary site where the majority of functional RNA activities occur in eukaryotic cells.
Question 196: Which of the following is NOT a characteristic of the genetic code?
- A. Overlapping (Correct Answer)
- B. Universal
- C. Degeneracy
- D. Nonambiguous
Explanation: ***Overlapping*** - The genetic code is generally **non-overlapping**, meaning each nucleotide is part of only one codon, and codons are read sequentially. - An overlapping code would mean that a single nucleotide could be part of multiple codons, which is not how protein synthesis typically occurs. *Nonambiguous* - This statement IS a characteristic; each codon specifies **only one amino acid**, meaning there is no ambiguity about which amino acid will be added. - While multiple codons can specify the same amino acid, a single codon never specifies more than one different amino acid. *Universal* - This statement IS a characteristic; the genetic code is largely **universal** across almost all organisms, from bacteria to humans. - The same codons typically specify the same amino acids in different species, which supports the idea of common ancestry. *Degeneracy* - This statement IS a characteristic; the genetic code is **degenerate**, meaning that most amino acids are specified by more than one codon. - This redundancy helps protect against the effects of single-nucleotide mutations.
Question 197: A frameshift mutation does not affect the complete amino acid sequence if it occurs in multiples of what number?
- A. 1
- B. 2
- C. 3 (Correct Answer)
- D. None of the options
Explanation: ***3*** - A **frameshift mutation** occurs when nucleotides are inserted or deleted in a number not divisible by three, altering the **reading frame** of the codons. - If insertions or deletions occur in multiples of **three**, the reading frame is restored after the mutation, largely preserving the downstream amino acid sequence. *1* - An insertion or deletion of a single nucleotide (1) definitively causes a **frameshift mutation**. - This alters all subsequent **codons**, leading to a completely different amino acid sequence downstream from the mutation. *2* - An insertion or deletion of two nucleotides (2) also results in a **frameshift mutation**. - This change shifts the **reading frame**, leading to the production of an altered protein or a premature stop codon. *None of the options* - This option is incorrect because a specific number, **three**, can allow for a frameshift mutation to not affect the complete amino acid sequence. - Multiples of three maintain the original **reading frame** (although potentially adding or removing a specific amino acid), whereas other numbers guarantee a frameshift.
Pathology
1 questionsWhich of the following are examples of trinucleotide repeat mutations?
NEET-PG 2013 - Pathology NEET-PG Practice Questions and MCQs
Question 191: Which of the following are examples of trinucleotide repeat mutations?
- A. Friedreich ataxia
- B. Fragile X syndrome
- C. Huntington's chorea
- D. All of the options (Correct Answer)
Explanation: ***All of the options*** - **Fragile X syndrome**, **Friedreich ataxia**, and **Huntington's chorea** are all well-known examples of genetic disorders caused by trinucleotide repeat expansions [1]. - The mutations involve an abnormal increase in the number of repetitions of a specific three-nucleotide sequence in the DNA [1]. *Fragile X syndrome* - This condition is caused by an expansion of the **CGG repeat** in the **FMR1 gene** on the X chromosome [1]. - The expansion leads to hypermethylation and silencing of the gene, impairing the production of fragile X mental retardation protein [1]. *Friedreich ataxia* - This is an autosomal recessive neurodegenerative disorder caused by an expansion of the **GAA repeat** in an intron of the **frataxin gene (FXN)**. - The repeat expansion interferes with transcription, leading to reduced frataxin protein levels. *Huntington's chorea* - This is an autosomal dominant neurodegenerative disorder caused by an expansion of the **CAG repeat** in the **huntingtin gene (HTT)**. - The expanded polyglutamine tract in the huntingtin protein leads to protein misfolding and neuronal damage, particularly in the striatum [1]. **References:** [1] Kumar V, Abbas AK, et al.. Robbins and Cotran Pathologic Basis of Disease. 9th ed. Genetic Disorders, pp. 177-181.
Physiology
2 questionsAfter injecting testosterone in a hypoandrogenic male, which of the following occurs ?
In the breast, lactiferous ducts are formed under the influence of which hormone?
NEET-PG 2013 - Physiology NEET-PG Practice Questions and MCQs
Question 191: After injecting testosterone in a hypoandrogenic male, which of the following occurs ?
- A. Decreased LH secretion
- B. Decreased FSH secretion (Correct Answer)
- C. Increased spermatogenesis
- D. None of the options
Explanation: ***Decreased FSH secretion*** - Exogenous testosterone administration leads to **negative feedback** on the hypothalamic-pituitary-gonadal axis, suppressing **GnRH** release, which in turn decreases both **LH** and **FSH** secretion. - FSH suppression is particularly clinically significant because it results in **inhibition of spermatogenesis**, which is a key consideration when using testosterone replacement therapy. - The decrease in FSH, combined with reduced **intratesticular testosterone** (due to LH suppression), impairs Sertoli cell function and sperm production. *Decreased LH secretion* - **This also occurs** with exogenous testosterone administration due to negative feedback on the hypothalamus and pituitary. - Testosterone primarily suppresses **LH** through direct negative feedback at the hypothalamic-pituitary level. - However, in the context of this question focusing on the consequences in a hypoandrogenic male receiving testosterone, the **FSH suppression** and its impact on spermatogenesis is the more clinically emphasized outcome. - **Note:** Both LH and FSH decrease; this question likely emphasizes FSH due to its role in fertility concerns with testosterone therapy. *Increased spermatogenesis* - This is **incorrect**. Exogenous testosterone actually **suppresses spermatogenesis** through multiple mechanisms: - Decreased **FSH** (essential for Sertoli cell function) - Decreased **intratesticular testosterone** concentration (despite high systemic levels) - The high local testosterone concentration within the seminiferous tubules (30-100x serum levels) cannot be achieved by systemic testosterone alone. *None of the options* - This is incorrect because exogenous testosterone administration clearly causes **suppression of gonadotropins** (both LH and FSH) through well-established negative feedback mechanisms.
Question 192: In the breast, lactiferous ducts are formed under the influence of which hormone?
- A. Progesterone
- B. LH
- C. FSH
- D. Estrogen (Correct Answer)
Explanation: ***Estrogen*** - **Estrogen** plays a primary role in the development and branching of the **lactiferous ducts** in the breast. - It stimulates the proliferation of ductal epithelial cells, contributing to the growth of the duct system. *Progesterone* - **Progesterone** is primarily responsible for the development of the **lobuloalveolar system** and secretory differentiation within the breast. - While essential for lactation, its main function is not duct formation but rather the maturation of secretory units. *LH* - **Luteinizing hormone (LH)** is crucial for ovulation and the formation of the **corpus luteum** in the ovaries. - It has no direct role in the structural development of the lactiferous ducts in the breast. *FSH* - **Follicle-stimulating hormone (FSH)** is essential for the growth and maturation of **ovarian follicles**. - It does not directly influence the formation or development of lactiferous ducts in the breast.