Nursing Elites

1. How are sister chromatids distinguished from homologous chromosomes in meiosis I?

• A. Sister chromatids share the same centromere, while homologous chromosomes have different centromeres.
• B. Sister chromatids have identical DNA sequences, while homologous chromosomes have slightly different sequences due to crossing over.
• C. Sister chromatids repel each other, while homologous chromosomes attract each other during synapsis.
• D. Sister chromatids separate during anaphase I, while homologous chromosomes separate during anaphase II.

Correct answer: B

Rationale: In meiosis I, sister chromatids are exact copies of each other, containing identical DNA sequences. On the other hand, homologous chromosomes are pairs of chromosomes, with one inherited from each parent, and they can have different versions of genes due to genetic recombination during crossing over in prophase I. Choice A is incorrect because homologous chromosomes naturally have different centromeres. Choice C is incorrect as sister chromatids and homologous chromosomes do not exhibit repulsion or attraction during synapsis. Choice D is incorrect as sister chromatids separate during anaphase II, not anaphase I, while homologous chromosomes separate during anaphase I.

2. Which of the following is an example of a salt?

• A. Sodium hydroxide (NaOH)
• B. Hydrochloric acid (HCl)
• C. Sodium chloride (NaCl)
• D. Sulfuric acid (Hâ‚‚SOâ‚„)

Correct answer: C

Rationale: Sodium chloride (NaCl) is an example of a salt. Salts are ionic compounds formed by the reaction of an acid with a base. In this case, sodium chloride is formed by the reaction of sodium hydroxide (a base) with hydrochloric acid (an acid). Sodium hydroxide (NaOH), hydrochloric acid (HCl), and sulfuric acid (Hâ‚‚SOâ‚„) are not salts because they are not formed by the neutralization reaction of an acid and a base, which is a characteristic of salts.

3. What is an alteration in the normal gene sequence called?

• A. DNA mutation
• B. Gene migration
• C. Polygenic inheritance
• D. Incomplete dominance

Correct answer: A

Rationale: A DNA mutation is the correct term used to describe an alteration in the normal gene sequence. It refers to changes in the DNA sequence that can result in different traits or characteristics. Gene migration involves the movement of genes between populations, polygenic inheritance refers to the inheritance of traits controlled by multiple genes, and incomplete dominance is a pattern of inheritance where neither allele is dominant.

4. What is the function of arrector pili muscles?

• A. To control sweat production
• B. To contract and cause goosebumps
• C. To produce sebum
• D. To sense touch

Correct answer: B

Rationale: The correct function of arrector pili muscles is to contract and cause goosebumps. These small muscles are attached to hair follicles in mammals. When they contract, they cause the hair to stand on end, resulting in goosebumps. This physiological response is often triggered by cold temperatures or emotional states like fear, helping mammals conserve heat or appear larger in threatening situations. Choices A, C, and D are incorrect. Arrector pili muscles are not involved in controlling sweat production (Choice A), producing sebum (Choice C), or sensing touch (Choice D).

5. Which of the following is directly transcribed from DNA and represents the first step in protein synthesis?

• A. siRNA
• B. rRNA
• C. mRNA
• D. tRNA

Correct answer: C

Rationale: mRNA (messenger RNA) is directly transcribed from DNA in the nucleus during the process of transcription. It serves as a template for protein synthesis during translation in the cytoplasm. mRNA carries genetic information from the DNA to the ribosomes, where it determines the sequence of amino acids in a protein. Thus, mRNA represents the first step in protein synthesis as it carries the code from the DNA to be translated into a protein. Choice A, siRNA (small interfering RNA), is involved in post-transcriptional gene silencing and does not play a role in protein synthesis. Choice B, rRNA (ribosomal RNA), is a component of the ribosome and plays a structural and functional role in protein synthesis but is not directly transcribed from DNA. Choice D, tRNA (transfer RNA), is responsible for bringing amino acids to the ribosome during protein synthesis but is not directly transcribed from DNA.

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