23 Study Guide-Genetics

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51 Terms

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Genetics

The study of how characteristics are transmitted from parents to offspring.

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Gregor Mendel

Known as the father of genetics, he conducted extensive work with garden peas and discovered the principles of heredity.

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Heredity

The passing on of traits from parents to offspring.

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Probability

The likelihood of a particular outcome occurring, used by Mendel to interpret his results in genetics.

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True-breeding strains

Plants that are pure or true breeding for a trait and always produce offspring with that trait.

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P1 strain

The parental generation, consisting of pure-breeding strains used by Mendel in his experiments.

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F1 generation

The first generation of offspring produced by crossing the P1 strains.

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F2 generation

The second generation of offspring produced by allowing the F1 generation to breed.

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Hybrid

Offspring produced by crossing two different pure-breeding parents, showing only the dominant trait.

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Law of Segregation

Mendel's conclusion that paired factors separate during the formation of reproductive cells, resulting in each gamete receiving only one factor of each pair.

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Principle of Dominance

The idea that in a hybrid, one factor may completely hide the presence of the partner factor.

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Law of Independent Assortment

Mendel's observation that traits produced by dominant factors do not necessarily appear together, indicating that the factors for different characteristics are not connected.

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Genotype

A description of the specific alleles carried by an organism with respect to the particular genes being considered.

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Phenotype

The actual description of the characteristics observed in an organism.

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Pure Breeding

A term referring to individuals that, when paired with an appropriate partner, always produce offspring with the same characteristics.

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Hybrid

An individual produced by crossing two different pure-breeding parents.

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Wild Type

The version of a trait that is overwhelmingly most common in nature.

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Homozygous

An individual whose two alleles for a specific trait are identical.

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Heterozygous

An individual who has two different alleles for a specific trait.

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Homogametic Gender

The gender with two identical sex chromosomes.

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Heterogametic Gender

The gender with two different sex chromosomes.

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Dominance

The relationship between two alleles where the phenotype of the heterozygote is indistinguishable from the phenotype of one of the homozygotes.

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Complete Dominance

A type of dominance where the phenotype of the heterozygote is indistinguishable from the phenotype of one of the homozygotes.

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Recessive

The allele that is hidden in the heterozygote and is not expressed in the phenotype.

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Incomplete Dominance

A type of dominance where the phenotype of the heterozygote is intermediate between the phenotypes of the two homozygotes.

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Co-dominance

A type of dominance where the heterozygote expresses both allelic traits simultaneously.

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Pseudo Dominance

A situation where a particular combination of alleles produces a lethal effect, initially resembling complete dominance.

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Locus

The location of a gene on the chromosomes of a species.

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Pedigree

A charted family history used in genetics to determine the inheritance patterns of genetic factors.

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Linked Genes

Genes that have their loci on the same chromosome and are inherited together unless separated by crossing over.

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Chromosomes

Structures in the nucleus of a cell that contain genes and are made up of protein and DNA.

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Nucleus

The part of a cell that contains the genetic material, including genes.

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DNA

Deoxyribonucleic acid, a molecule that carries genetic information and is found in chromosomes.

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Protein

A macromolecule made up of long chains of amino acids, used by biochemists as a candidate for carrying genetic information.

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DNA

Deoxyribonucleic acid, a molecule made up of nucleotides that carries genetic information and determines the characteristics of living organisms.

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Nucleotides

Smaller molecules that make up DNA, consisting of a sugar, a phosphate group, and a nitrogenous base.

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Protein

A large biomolecule made up of amino acids that plays a crucial role in the structure and function of cells.

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Chromosome

A thread-like structure made up of DNA that carries genetic information in the form of genes.

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X-ray crystallography

A technique used to determine the three-dimensional structure of molecules by analyzing the pattern of X-ray diffraction.

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Double-stranded helix

The structure of DNA, consisting of two strands that are twisted around each other in a spiral shape.

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Rosalind Franklin

A scientist who made significant contributions to the discovery of the structure of DNA through her work on X-ray crystallography.

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Maurice H

A scientist who worked with Rosalind Franklin and shared her X-ray photographs of DNA with James Watson, contributing to the discovery of its structure.

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James Watson and Francis Crick

Scientists who, along with Maurice Wilkins, were awarded the Nobel Prize for their discovery of the structure of DNA as a double-stranded helix.

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RNA

Ribonucleic acid, a molecule similar to DNA that plays a role in protein synthesis.

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Base pairing

The specific pairing of nucleotides in DNA, where adenine (A) pairs with thymine (T) and guanine (G) pairs with cytosine (C).

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Complementary base pairing

The strict pairing of nucleotides in DNA, where the bases on one strand pair with their complementary bases on the other strand.

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Self-replication

The ability of DNA to make copies of itself by separating the two strands and assembling new partner strands based on complementary base pairing.

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Transfer RNA

Small RNA molecules that act as adapters between the nucleotide language of DNA and RNA and the amino acid language of proteins.

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Transcription

The process of creating messenger RNA (mRNA) from a segment of DNA, using complementary base pairing between ribonucleotides and one side of the DNA.

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Translation

The process of converting the information coded in mRNA into a string of amino acids by ribosomes, according to the genetic code.

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