AP®︎ Biology: Topic 6.7 Flashcards

Master key terms and definitions for Topic 6.7 of AP Biology – Mutations to help you prep for quizzes and the AP exam.


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Term

Mutation

Definition

A heritable change in DNA sequence that can alter gene product or phenotype.

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Mutation
Not Started

A heritable change in DNA sequence that can alter gene product or phenotype.

6.7.A6.7.A.1
Point Mutation
Not Started

A change in one nucleotide pair, usually by substitution of one base for another.

6.7.A6.7.A.1
Insertion, Deletion, and Frameshift Mutations
Not Started

Insertion adds bases, deletion removes bases, and frameshift shifts codon reading when bases are not in threes.

6.7.A6.7.A.1
Nonsense Mutation
Not Started

A base substitution that creates a premature stop codon, producing a shortened polypeptide.

6.7.A6.7.A.1
Silent Mutation
Not Started

A DNA change that does not alter the amino acid sequence of the protein.

6.7.A6.7.A.1
Genotype Change and Phenotype Change
Not Started

Altered DNA can change RNA or protein type or amount, producing different observable traits.

6.7.B6.7.B.1
Coding vs Regulatory Region Mutations
Not Started

Coding changes can alter protein sequence, while regulatory changes can alter when or how much is made.

6.7.B6.7.B.1
Replication and DNA Repair Errors
Not Started

Mistakes during copying or correction of DNA can introduce random sequence changes.

6.7.B6.7.B.1
Mutagens
Not Started

External agents such as radiation and reactive chemicals that increase the rate of DNA mutations.

6.7.B6.7.B.1
Nondisjunction
Not Started

Failure of homologous chromosomes or sister chromatids to separate properly during cell division.

6.7.B6.7.B.2
Aneuploidy and Triploidy
Not Started

Aneuploidy is an abnormal chromosome number; triploidy is three complete chromosome sets.

6.7.B6.7.B.2
Polyploidy
Not Started

Having more than two complete sets of chromosomes, often affecting vigor or fertility.

6.7.B
Chromosomal Structural Alterations
Not Started

Deletions remove segments, duplications repeat them, inversions reverse them, and translocations move them elsewhere.

6.7.B6.7.B.2
Transformation, Transduction, Conjugation, and Transposition
Not Started

DNA uptake, viral DNA transfer, direct cell-to-cell DNA transfer, and movement of DNA segments.

6.7.C6.7.C.1
Viral Recombination
Not Started

Mixing of genetic material between related viruses that infect the same host cell.

6.7.C6.7.C.1
Variation-Increasing Reproductive Processes
Not Started

Conserved mechanisms like mutation, meiosis, crossing over, and gene transfer that generate heritable diversity.

6.7.C6.7.C.1
Cystic Fibrosis and CFTR
Not Started

A disorder caused by CFTR mutations that disrupt ion transport across cell membranes.

6.7.A6.7.A.1
Adaptive Melanism in Pocket Mice
Not Started

A dark-fur phenotype caused by mutation that improves camouflage in dark environments.

6.7.C6.7.C.1
Sickle Cell Anemia
Not Started

A beta-globin mutation causing sickled red blood cells, harmful overall but advantageous against malaria when heterozygous.

6.7.C6.7.C.1
Mutation Effects and Environmental Context
Not Started

A DNA change may be beneficial, harmful, or neutral depending on environmental conditions.

6.7.B6.7.B.1
Mutations, Genetic Variation, and Natural Selection
Not Started

Heritable DNA changes create variation that natural selection can increase or decrease.

6.7.C6.7.C.1
Missense Mutation
Not Started

A base substitution that changes one amino acid in a polypeptide sequence.

6.7.A