Unit 2 of 5
Study guide for CLEP CLEP Biology — Unit 2: Genetics and Molecular Biology. Practice questions, key concepts, and exam tips.
88
Practice Questions
39
Flashcards
9
Key Topics
Try these 5 questions from this unit. Sign up for full access to all 88.
What type of inheritance pattern is observed in ABO blood type?
Codominance
Sex-linked
Dominant-recessive
Polygenic
Incomplete dominance
Answer: A — Codominance is correct because both A and B alleles have equal effect, and the individual expresses both.
What is the term for the process by which a single gene can have multiple different effects on an organism's phenotype?
Polygenic inheritance
Pleiotropy
Mutation
Genetic drift
Epigenetics
Answer: B — Pleiotropy occurs when one gene influences two or more seemingly unrelated phenotypic traits. This is a key concept in understanding the complex relationships between genotype and phenotype.
What type of inheritance pattern does the ABO blood type exhibit?
Incomplete dominance
Dominant-recessive
Codominance
Sex-linked inheritance
Polygenic inheritance
Answer: C — The ABO blood type exhibits Codominance, where two alleles have an equal effect on the phenotype, resulting in a combination of both. This occurs because both the A and B alleles are expressed fully, producing both A and B antigens on red blood cells. In contrast to incomplete dominance, where one allele is partially expressed, Codominance allows both alleles to be fully expressed, making it distinct. This is why dominant-recessive inheritance, where one allele masks the other, does not apply to ABO blood types.
What type of cells are produced by meiosis in humans?
Somatic cells
Diploid gametes
Haploid gametes
Triploid zygotes
Tetraploid embryos
Answer: C — Haploid gametes is correct because meiosis produces haploid gametes.
What is the term for the movement of a chromosome segment to a non-homologous chromosome?
Gene conversion
Crossing over
Translocation
Independent assortment
Mutation
Answer: C — Translocation is correct because translocation involves the transfer of a segment to a non-homologous chromosome.
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