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BCHM 4360 FINAL PAPER 2026 FULL QUESTIONS AND CORRECT ANSWERS

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BCHM 4360 FINAL PAPER 2026 FULL QUESTIONS AND CORRECT ANSWERS

Institution
BCHM 4360
Course
BCHM 4360

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BCHM 4360 FINAL PAPER 2026 FULL
QUESTIONS AND CORRECT ANSWERS



◉Biochemical pathway epistasis rule. Answer: Upstream mutation is
epistatic to downstream mutation.


◉Synthetic phenotype. Answer: Double mutant produces new
phenotype not seen in single mutants.


◉Synthetic lethality. Answer: Two viable mutations become lethal
when combined.


◉Pathway ordering using epistasis. Answer: Phenotype reveals gene
order in biological pathway.


◉Genetic screen. Answer: Experimental method used to identify
genes responsible for a phenotype by analyzing mutants.


◉Forward genetic screen. Answer: Starts with phenotype and
identifies the gene responsible.

,◉Reverse genetic screen. Answer: Starts with a known gene and
determines its phenotype after mutation.


◉Mutagenesis. Answer: Process of introducing mutations to
generate genetic variation for screening.


◉Phenotype-based selection. Answer: Identifying mutants based on
observable traits


◉Selection. Answer: Screen where only desired mutants surviveS


◉Screen (vs selection). Answer: Requires examining individuals to
find mutants rather than survival filtering.


◉Reporter gene. Answer: Gene producing measurable signal used to
monitor gene activity.


◉CRISPR screen. Answer: High-throughput gene disruption using
CRISPR to identify gene function.


◉Enhancer mutation. Answer: Mutation that increases severity of
another mutation's phenotype

, ◉Suppressor mutation. Answer: Mutation occurs within same gene
restoring function


◉Extragenic suppressor. Answer: Mutation in different gene
compensates for defect.


◉Bypass supressor. Answer: Mutation activates alternative pathway
to restore phenotype.


◉Mutation. Answer: Change in DNA sequence


◉Loss-of-function mutation. Answer: Mutation that reduces or
eliminates gene activity.


◉Typical inheritance of loss-of-function. Answer: Usually recessive
because one functional allele is sufficient.


◉Haploinsufficiency. Answer: One functional copy is not enough for
normal phenotype


◉Dominant negative mutation. Answer: Mutant protein interferes
with function of normal protein

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