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Chapter 10 Vocab

Gene

Sequence of DNA that encodes a specific protein or RNA molecule

Allele

one of two or more alternative forms of a gene

Chromosome

A continuous molecule of DNA wrapped around protein in the nucleus of a eukaryotic cell; also, the genetic material of a prokaryotic cell

Diploid Cell

A cell containing two full sets of chromosomes, one from each parent; also called 2n

Autosomes

A nonsex chromosome

Sex Chromosomes

A chromosome that carries genes that determine sex

Homologous Pair

Two chromosomes that look alike and have the same sequence of genes

Meiosis

Division of genetic material that halves the chromosome number and yields genetically variable nuclei

Haploid Cell

A cell containing one set of chromosomes; also called n

Gamete

A sex cell; sperm or egg cell

Fertilization

The union of two gametes

True-Breeding

Always producing offspring identical to the parent for one or more traits; homozygous

Hybrid (genetics)

Producing a mix of offspring for one or more traits; heterozygous

Dominant Allele

Allele that is expressed whenever it is present

Recessive Allele

Allele whose expression is masked if a dominant allele is present

Genotype

An individual’s combination of alleles for a particular gene

Homozygous

Possessing two identical alleles for a particular gene

Heterozygous

Possessing two different alleles for a particular gene

Phenotype

Observable characteristic of an organism

Wild-Type Allele

The most common allele, genotype, or phenotype

Mutant Allele

An allele, genotype, or phenotype that is not the most common in a population or that has been altered from the “typical” (wild-type) condition

P (parental) Generation

The first generation (true-breeding) in a genetic cross

F1 Generation

The offspring of the P generation in a genetic cross

F2 Generation

The offspring of the F1 generation in a genetic cross

Locus

The physical location of a gene on a chromosome

Monohybrid Cross

Mating between two individuals that are heterozygous for the same gene

Punnett Square

Diagram that uses the genotypes of the parents to reveal the possible results of a genetic cross

Test Cross

A mating of an individual of unknown genotype to a homozygous recessive individual to reveal the unknown genotype

Law of Segregation

Mendel’s law stating that the two alleles of each gene are packaged into separate gametes

Dihybrid Cross

Mating between two individuals that are both heterozygous for one gene

Law of independent assortment

Mendel’s law stating that during gamete formation, the segregation of the alleles for one gene does not influence the segregation of the alleles for another gene

Product Rule

The chance of two independent events occurring equals the product of the individual chances of each event

Linked Genes

Genes on the same chromosome

Linkage Group

Group of genes that tend to be inherited together because they are on the same chromosome

Crossing Over

Exchange of genetic material between homologous chromosomes during prophase I of meiosis

Parental Chromatid

Chromatid containing genetic information from only one parent

Recombinant Chromatid

Chromatid containing genetic information from both parents as a result of crossing over

Linkage Map

Diagram of gene order and spacing on a chromosome, based on crossover frequencies

Recombinant Offspring

An individual that inherits a recombinant chromatid

Incomplete Dominance

Mode of inheritance in which a heterozygote’s phenotype is intermediate between the phenotypes of the two homozygotes

Codominance

Mode of inheritance in which two alleles are fully expressed in a heterozygote

Pleiotropy

Multiple, seemingly unrelated phenotypic effects of one genotype

Epistasis

One gene masks the phenotype associated with another gene

Complete Dominance

One allele masks the expression of another in a heterozygote

Sex-Linked

Describes genes or traits on the X or Y chromosome

Y-Linked

Describes traits controlled by genes on the Y chromosome

X-Linked

Describes traits controlled by genes on the X chromosome

X Inactivation

Turning off all but one X chromosome in each cell of a mammal (usually female) early in development

Autosomal Dominant

Inheritance pattern of a dominant allele on an autosome

Autosomal Recessive

Inheritance pattern of a recessive allele on an autosome

Pedigree

Chart showing family relationships and phenotypes

Epigenetics

The study of changes in gene expression that do not involve changes in the DNA sequence

Polygenic

Caused by more than one gene; polygenic traits are typically expressed as a continuum of possible phenotypes

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