Which hormone is responsible for the development of female secondary sexual characteristics such as breast development, menstrual cycle, and widening of hips?
A. Progesterone
B. Testosterone
C. Estrogen
D. FSH
The correct answer is choice C. Estrogen.
Estrogen is a steroid hormone responsible for the development of female secondary sexual characteristics such as breast development, menstrual cycle, and widening of hips.
Choice A, Progesterone, is not the correct answer because it is required to maintain pregnancy and delivery.
Choice B, Testosterone, is not the correct answer because it is a hormone produced by the testes which controls the development of male secondary sexual characteristics.
Choice D, FSH (Follicle Stimulating Hormone), is not the correct answer because it stimulates the growth of ovarian follicles in females and regulates spermatogenesis in males.
Therefore, the Correct Answer is C.
More Questions on TEAS 7 Science
-
Q #1: Which cytotoxic lymphocyte granules contain serine proteases that induce apoptosis in target cells?.
A. Perforins.
B. Cytokines.
C. Granzymes.
D. Interferons.
Answer Explanation
Granzymes.
Granzymes are a family of serine proteases that are stored in and secreted from the cytotoxic granules of cytotoxic T lymphocytes (CTL) and natural killer (NK) cells.
They work in synergy with perforin, a pore-forming toxin, to induce apoptosis in target cells.
Perforin is necessary for the delivery of granzyme B to the target cell cytosol where caspase-dependent and -independent pathways to apoptosis are activated.
Perforins (choice A) are pore-forming toxins that work in synergy with granzymes to induce apoptosis in target cells.
Cytokines (choice B) are signaling molecules that regulate immune responses but do not directly induce apoptosis in target cells.
Interferons (choice D) are a type of cytokine that play a role in immune responses but do not directly induce apoptosis in target cells.
-
Q #2: What is a primer in DNA sequencing?
A. A short piece of double-stranded DNA that binds to the template DNA and acts as a "starter" for the polymerase.
B. A short piece of double-stranded DNA that binds to the primer and acts as a "starter" for the template.
C. A short piece of single-stranded DNA that binds to the template DNA and acts as a "starter" for the polymerase.
D. A short piece of single-stranded DNA that binds to the polymerase and acts as a "starter" for the template.
Answer Explanation
A primer is a short single-stranded DNA fragment used in certain laboratory techniques, such as the polymerase chain reaction (PCR).
In the PCR method, a pair of primers hybridizes with the sample DNA and defines the region that will be amplified.
Choice A) A short piece of double-stranded DNA that binds to the template DNA and acts as a “starter” for the polymerase is incorrect because primers are single-stranded, not double-stranded.
Choice B) A short piece of double-stranded DNA that binds to the primer and acts as a “starter” for the template is incorrect because it does not make sense for a primer to bind to itself.
Choice D) A short piece of single-stranded DNA that binds to the polymerase and acts as a “starter” for the template is incorrect because primers bind to the template DNA, not to the polymerase.
Note: DNA primers are used instead of RNA primers in DNA sequencing and PCR because DNA is more stable, specific, and compatible with the enzymes and processes involved in these techniques.
-
Q #3: What is the purpose of using PCR (polymerase chain reaction) in the laboratory?
A. To separate DNA fragments by size.
B. To amplify specific regions of DNA.
C. To sequence DNA fragments.
D. To analyze protein expression levels.
Answer Explanation
The correct answer is choice B.
To amplify specific regions of DNA.
PCR (polymerase chain reaction) is a laboratory technique used to make many copies of a specific region of DNA.
The goal of PCR is to make enough of the target DNA region that it can be analyzed or used in some other way.
PCR has many research and practical applications, including DNA cloning, medical diagnostics, and forensic analysis of DNA.
Choice A is incorrect because PCR does not separate DNA fragments by size. Choice C is incorrect because PCR does not sequence DNA fragments.
Choice D is incorrect because PCR does not analyze protein expression levels.
