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BIOD 210 Genetics Final Exam | 2025/2026 | Complete Questions and Verified Answers

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This document contains the full collection of final exam questions and verified answers for the BIOD 210 Genetics course. It covers essential genetic principles, inheritance patterns, DNA structure and function, gene expression, and related molecular biology concepts. The material is organized to support targeted exam preparation and reflects the most recent 2025/2026 updates.

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BIOD 210 Genetics Final Exam Questions
and Answers () (Verified Answers)
In a monohybrid cross between two heterozygous pea plants (Tt × Tt), what proportion
of the F1 generation is expected to be homozygous recessive?

A. 1/4

B. 1/2

C. 3/4

D. 1/8

Correct Answer: A

Rationale: A standard Punnett square of Tt × Tt yields 1 TT : 2 Tt : 1 tt; thus 1/4 of
offspring are homozygous recessive (tt).

In snapdragons, red (CRCR) crossed with white (CWCW) produces pink (CRCW) F1
progeny. This is an example of:

A. complete dominance

B. incomplete dominance

C. codominance

D. epistasis

Correct Answer: B

Rationale: Incomplete dominance produces an intermediate heterozygous phenotype
(pink) between the two parental extremes.

A man with type A blood (genotype IAi) marries a woman with type B blood (IBi). What
is the probability their first child has type O blood?

A. 0%

B. 25%

C. 50%

D. 75%

Correct Answer: B

,Rationale: Both parents are heterozygous (IAi × IBi); 1/4 of offspring inherit ii (type O).

In humans, red-green color blindness is X-linked recessive. A color-blind man and a
carrier woman produce a son. The probability the son is color-blind is:

A. 0%

B. 25%

C. 50%

D. 100%

Correct Answer: C

Rationale: Sons inherit the X chromosome from the mother; a carrier female (XCXc)
passes Xc to half her sons, who are therefore color-blind.

A pedigree shows affected males in every generation with no affected females. The
most likely mode of inheritance is:

A. autosomal dominant

B. autosomal recessive

C. X-linked recessive

D. mitochondrial

Correct Answer: C

Rationale: X-linked recessive traits appear predominantly in males and are transmitted
through carrier females; absence of affected females supports this.

DNA replication in eukaryotes begins at specific sites called:

A. telomeres

B. origins of replication

C. promoters

D. centromeres

Correct Answer: B

Rationale: Origins of replication are short DNA sequences recognized by initiation
proteins where bidirectional replication starts.

, The 5’ → 3’ exonuclease activity of DNA polymerase I in prokaryotes is primarily
involved in:

A. adding nucleotides to the 3’ end

B. proofreading newly synthesized DNA

C. removing RNA primers

D. joining Okazaki fragments

Correct Answer: C

Rationale: DNA polymerase I uses its 5’ → 3’ exonuclease activity to excise RNA
primers and replace them with DNA during lagging-strand synthesis.

Which enzyme is responsible for joining Okazaki fragments on the lagging strand?

A. DNA polymerase III

B. primase

C. DNA ligase

D. helicase

Correct Answer: C

Rationale: DNA ligase seals nicks between adjacent DNA fragments by forming
phosphodiester bonds, completing lagging-strand synthesis.

Telomerase maintains chromosome ends by:

A. adding histone proteins

B. synthesizing RNA primers

C. extending the 3’ overhang of telomeres

D. sealing telomere loops

Correct Answer: C

Rationale: Telomerase is a reverse transcriptase that uses its RNA template to add
repetitive DNA sequences to the 3’ overhang, counteracting shortening.

The Meselson-Stahl experiment demonstrated that DNA replication is:

A. conservative

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