ATI TEAS 7
TEAS Test 7 science quizlet
1. What is the difference between mitosis and meiosis?
- A. Mitosis produces haploid cells, while meiosis produces diploid cells
- B. Mitosis involves crossing over, while meiosis does not.
- C. Mitosis results in four daughter cells, while meiosis results in two
- D. Mitosis is responsible for sexual reproduction, while meiosis is responsible for asexual reproduction.
Correct answer: C
Rationale: - Mitosis is a type of cell division that results in two identical daughter cells with the same number of chromosomes as the parent cell. Therefore, mitosis results in two daughter cells. - Meiosis is a type of cell division that results in four daughter cells, each with half the number of chromosomes as the parent cell. This reduction in chromosome number is essential for sexual reproduction. - Option A is incorrect because mitosis produces diploid cells (cells with the same number of chromosomes as the parent cell), while meiosis produces haploid cells (cells with half the number of chromosomes as the parent cell). - Option B is incorrect because crossing over, the exchange of genetic material between homologous chromosomes, occurs during meiosis and not during mitosis. - Option D is incorrect because mitosis is not responsible for sexual reproduction; it is a process of asexual reproduction and
2. What element is responsible for the red color of blood?
- A. Magnesium
- B. Iron
- C. Copper
- D. Zinc
Correct answer: B
Rationale: The correct answer is B: Iron. Hemoglobin, the protein responsible for carrying oxygen in red blood cells, contains iron in its heme group, contributing to the blood's characteristic red color. Magnesium (choice A), copper (choice C), and zinc (choice D) are not responsible for the red color of blood. Magnesium is an essential mineral involved in various physiological processes, copper is a trace element important for enzyme function, and zinc is a micronutrient essential for multiple cellular functions but not related to the red color of blood.
3. The Human Genome Project is a worldwide research project launched in 1990 to map the entire human genome. Although the Project was faced with the monumental challenge of analyzing tons of data, its objective was completed in 2003, two years ahead of its deadline. Which of the following inventions likely had the greatest impact on this project?
- A. The sonogram
- B. X-ray diffraction
- C. The microprocessor
- D. Magnetic Resonance Imaging (MRI)
Correct answer: C
Rationale: The microprocessor, a key component of modern computers, played a crucial role in the success of the Human Genome Project. The ability of microprocessors to process vast amounts of data quickly and efficiently allowed scientists to analyze the massive amounts of genetic information generated by the project. This technological advancement significantly accelerated the pace of genome sequencing and data analysis, ultimately leading to the completion of the project ahead of schedule. Choices A, B, and D are incorrect. The sonogram is used for imaging in medical diagnostics, X-ray diffraction is a technique for studying the structure of materials at the atomic level, and Magnetic Resonance Imaging (MRI) is a medical imaging technique that uses magnetic fields and radio waves to produce detailed images of the body. While these inventions have their own importance in various fields, they did not have the same impact on the Human Genome Project as the microprocessor did.
4. What is the term for a genetic disorder caused by a mutation on the X chromosome?
- A. Autosomal dominant disorder
- B. Autosomal recessive disorder
- C. Sex-linked recessive disorder
- D. Sex-linked dominant disorder
Correct answer: C
Rationale: A genetic disorder caused by a mutation on the X chromosome is termed a sex-linked recessive disorder (Option C). This type of disorder is more commonly seen in males due to their single X chromosome, making them more vulnerable to X-linked mutations. Females have two X chromosomes, providing a protective effect against X-linked disorders.\n- Autosomal dominant disorders (Option A) result from a mutation in one copy of a gene on non-sex chromosomes (autosomes) and are not specifically related to the X chromosome.\n- Autosomal recessive disorders (Option B) occur due to mutations in both copies of a gene on autosomes, not on the X chromosome.\n- Sex-linked dominant disorders (Option D) are rare and lead to more severe symptoms in males as they only require one copy of the mutated gene on the X chromosome to express the disorder. However, this is not the term for a genetic disorder caused by an X chromosome mutation.
5. Which of the following statements is NOT true about DNA?
- A. DNA contains the nucleotides A, T, C, G and is read 5' to 3'.
- B. DNA contains genetic information and is tightly coiled with proteins to form chromosomes.
- C. DNA contains the nucleotides A, T, C, G and is read 3' to 5'.
- D. DNA is a double-stranded molecule connected by hydrogen bonds.
Correct answer: C
Rationale: The correct answer is C because DNA is typically read from the 5' end to the 3' end, not from 3' to 5'. Choices A, B, and D are all true statements about DNA. DNA contains the nucleotides A, T, C, G and is read in a 5' to 3' direction. DNA also contains genetic information and is tightly coiled with proteins to form chromosomes. Additionally, DNA is a double-stranded molecule connected by hydrogen bonds.
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