Mutation

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46 Terms

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Mutation

A change or variation in a gene that can be neutral, harmful, or beneficial.

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Somatic mutation

A mutation that occurs in body cells and can lead to diseases like cancer.

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Germ-line mutation

A mutation in germ cells (egg and sperm) that can be passed on to offspring.

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Large-scale mutations

Mutations involving deletions or chromosomal rearrangements that affect important species traits.

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Small-scale mutations

Point mutations involving changes to one or a few nucleotides, often neutral or non-functional.

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Silent mutation

A nucleotide-pair substitution that changes the DNA sequence without altering the protein.

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Missense mutation

A mutation that changes the DNA sequence and results in a change in the amino acid sequence.

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Nonsense mutation

A mutation that introduces a new stop codon, leading to an incomplete and usually nonfunctional protein.

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Frameshift mutation

A mutation caused by insertions or deletions that change the reading frame of the DNA sequence.

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Point mutation

A small mutation that typically affects one or two nucleotides in the DNA sequence.

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Mutagen

An environmental agent, such as radiation or chemicals, that can cause mutations.

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Carcinogen

A substance capable of causing cancer by inducing mutations.

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DNA Polymerase

An enzyme responsible for synthesizing DNA during cell division, which can introduce errors.

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Failed transposition

A failure in the process where 'jumping genes' move within or between genomes, potentially causing mutations.

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Environmental causes of mutations

External factors like radiation or chemicals that can induce genetic changes.

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Nucleotide-pair insertion

The addition of one or two nucleotides, which can lead to frameshift mutations.

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Nucleotide-pair deletion

The removal of one or two nucleotides that results in a frameshift mutation.

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Genetic code wobble

The phenomenon where the 3rd nucleotide in a codon can vary without affecting the amino acid produced.

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Early stop codon

A premature termination signal in the protein synthesis caused by nonsense mutations.

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Cellular causes of mutations

Intrinsic factors within a cell, such as failed DNA repair mechanisms that lead to mutations.

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Radiation

Energy emitted in the form of waves or particles that can cause mutations, such as UV light or X-rays.

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Hazardous chemicals

Toxic substances that can induce mutations, including certain carcinogens.

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Viruses

Infectious agents that can integrate their DNA into host genomes and potentially cause mutations.

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Change to a gene

The alteration in the genetic material that can result from mutations.

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Protein coding

The process by which genes are transcribed and translated to produce proteins.

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Chromosomal rearrangements

Structural changes in chromosomes that can lead to large scale mutations.

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Gene variation

Differences in genes among individuals, often caused by mutations.

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Cancer

A disease caused by mutations that lead to uncontrolled cell growth.

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Evolutionary effects of mutations

Changes in genetic variations that can be acted upon by natural selection over time.

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Synonymous mutation

A term synonymous with silent mutation, where the amino acid remains unchanged.

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Amino acid sequence

The order of amino acids in a protein, which determines its structure and function.

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Change in mRNA

The alteration of messenger RNA as a result of mutation, which can affect protein synthesis.

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Protein function

The biological activity of proteins which can be altered by base pair changes.

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Genetic variability

The diversity in gene frequencies that can be caused by mutations.

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Uracil

A nitrogenous base found in RNA, replacing thymine as in DNA.

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Transcription

The process of copying a segment of DNA into RNA.

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Translation

The process by which ribosomes synthesize proteins using mRNA.

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Nucleotide

The basic building block of nucleic acids, consisting of a phosphate group, a sugar, and a nitrogenous base.

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Codon

A sequence of three nucleotides in mRNA that encodes a specific amino acid.

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Base pair substitution

A mutation where one nucleotide is replaced by another.

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Repeat expansion

A type of mutation that occurs when a small segment of DNA is repeated multiple times.

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Phenotype

The physical and physiological traits of an organism, influenced by its genotype and environment.

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Genotype

The genetic constitution of an individual organism.

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DNA repair enzymes

Proteins that correct DNA mistakes during replication and damage repair.

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Genetic diversity

The total number of genetic characteristics in the genetic makeup of a species.

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Selection pressure

Environmental factors that cause differential survival and reproduction of individuals.