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44 Cards in this Set

  • Front
  • Back

Principle of Dominance

One of the factors for a pair of inherited traits will be dominant and the other recessive

Principle of Inheritance

Term that refers to the three principles that have to do with heredity for acquired characteristics

Codon

A sequence of three nucleotides that together form a unit of genetic code in DNA or RNA molecule

Locus

The specific location of a gene, DNA sequence or position on a chromosome

Recessive

Gene that is not dominant but only manifests when a gene of both parents is the same


(receiving blue eyes from a mom and dad with blue eyes)

Chromosome

Protein found in the nucleus of most living cells carrying genetic information in the form of genes

Autosome

Any chromosome that is not a sex chromosome

Natural Selection

Process where organisms better adapt to their environment tend to survive an produce more offspring

Gene Flow

The transfer of alleles or genes from one population to another.


-Results of interbreeding with different organisms

Centromere

The point on a chromosome by which it is attached to a spindle fiber during cell division

Incomplete Dominance

A genetic situation in which one allele does not completely dominate other allele, and therefore results in a new phenotype

X- linked Recessive

A mode of inheritance in which a mutation in a gene on the X chromosome causes the phenotype to be expressed


-In males who are necessarily homozygous for the gene mutation because they only have one x chromosome


- In females who are homozygous for the gene mutation

Homozygous

An organism that has two copies of the same allele/trait


-AA or aa.


Homozygous Dominant

Two or more of the same allele in diploid organisms

Messenger RNA

Form of RNA in which genetic information transcribed from DNA as a sequence of bases is transferred to a ribosome

Transfer RNA

RNA consisting of folded molecules that transport amino acids from the cytoplasm of a cell to a ribosome

Translation

Process in which cellular ribosomes create proteins.

Chromosomal Mutation

Changes in the number of chromosomes in a cell or changes in the structure of a chromosome.

F-1 Generation

first filial generation produced by crossing two parental lines


First generation produced by a cross and consisting of individuals heterozygous for characters in which the parents differ and are homozygous


P Generation

First set of parents crossed in which their genotype is the basis of predicting the genotype of their offspring


P generation is the generation you start with, then breed to get F1

Genotype

Combination of alleles situated on corresponding chromosomes hat determines a specific trait

Principle Of Segregation

When sperm and egg unite at fertilization each contributes its allele, restoring the paired condition in the offspring.

Principle of Independent Assortment

Different genes independently separate from one another when reproductive cells develop.

Gene

DNA molecule that serves as the basic unit of heredity

Dominant

A trait that will appear in the offspring if one of the parents contribute to it


- Brown eyes(mom) Blue eyes(dad)


baby will have brown eyes

Allele

pairs of series of genes on a chromosome that determine the hereditary characteristics

Homologous

set of one maternal chromosome and one paternal chromosome that pair up with each other during meiosis.

Gametes

Cell containing only one set of dissimilar chromosomes or half the genetic material necessary to form a complete organization

Founder Effect

Reduced genetic diversity that results when a population is descended from a small number of colonizing ancesters

Bottle Neck

When a population of a species is drastically reduced to the point where the species is still able to carry on, but the genetic diversity of the species is severely limited.

Autosomal Dominant

A way that a trait or disorder can be passed down through families. If a disease is autosomal dominant it means you only need to get the abnormal gene from one parent in order for you to inherit the disease

Autosomal Recessive

Two copies of an abnormal gene must be present in order for the disease or trait to develop

Codominance

Relationship between two versions of a gene.


Individuals receive one version of a gene, called an allele, from each parent. If the alleles are different, the dominant allele usually will be expressed, while the effect of the other allele, called recessive is masked

Transcription

Process by which the information in a strand of DNA is copied into a new molecule of messenger RNA(mRNA)

Heterozygous

Pair of genes where one is dominant and one is recessive--theyre different


Hetero= different

Homozygous Recessive

The trait only shows if two copies of the allele are present. If the individual has two copies of the same allele it is Homozygous Recessive

Ribonucleic acid

single stranded composed of repeating nucleotide units of ribose, sugar, phosphate group and nitrogenous base


RNA

Genetic Code

Set of DNA and RNA molecules that carry genetic information in living cells

Anticodon

Sequence of three nucleotides forming a unit of genetic code in a transfer RNA molecule, corresponding to a complementary codon in a messenger RNA

Genetic mutation

Permanent alteration in the DNA sequence that makes up a gene, such that the sequence differs from what is found in most people.

F-2 Generation

Second filial generation consists of the offspring from allowing two of F-1 individuals to interbreed


P, F1, F2

After you breed two members of the P generation (parent)--their offspring is the F1 Generation. When you breed two members of the F1 generation (parents kids) their offspring is the F2 generation (grandchildren)

Phenotype

constellation of observable traits. phenotype= genotype+development.

Deoxyribonucleic acid

long macromolecule that is the main component of chromosomes and is the material that transfers genetic information...DNA