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59 Cards in this Set
- Front
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The study of genes and heredity, the branch of biology dealing with the principle of variation and inheritance in organisms. |
Genetics |
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The processes of passing genetic information and traits from one generation to the next. |
Heredity |
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This is a specific characteristics of an individual, or phenotypic feature of an individual. |
Traits |
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Traits can be determined by what? |
Environment factors, genes or both |
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This refers to an individuals observable traits |
Phenotype |
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This can be defined as the forms of traits, or significant deviations from the normal biological form, function, or structure. |
Biological variation or variations |
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This is the parent generation, which is the original pair of parents at the start of a genetic cross experiment. |
P generation |
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The first filla generation of the off spring of the parents |
F1 Generation |
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The second filial generation of the offspring, generated through inbreeding of the F individuals |
F2 generation |
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This is an offspring of the parent that differs genetically in traits. It is an organism that is heterozygous for a trait. |
Hybrid |
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Having descended from ancestors of a distinct type of breed. |
Purebred |
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This is when one allele is fully dominant over the other. The type of inheritance in which both heterozygotes & dominant homozygous have the same phenotype. |
Complete dominance |
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This is one of two or more DNA sequence occuring at a particular gene. |
Allele |
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This is the presence of two different alleles at one locus in an individual. |
Heterozygous |
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This is the genetic make-up of an organism; remains constant throughout an individuals life. Usually indicated by the combinations of letters in a punnet square. |
Genotype |
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This is the specific sequence of DNA that governs the expression of a particular trait and can be passed to an offspring. |
Gene |
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The type of trait in which the characteristics is always expressed, or appears in an individual. |
Dominant |
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A type of trait that isn't always expressed, having an allele that is present but inactive and therefore is not expressed. |
Recessive |
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This describes an individual with two alleles at one locus that are identical. |
Homozygous |
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This is a cross of two heterozygous individuals that differ in one trait (ex. Aa×Aa) |
Monohybrid |
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The square diagram that is used to predict the genotypes of a particular cross or breeding experiment. |
Punnet square |
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This is when the hereditary traits are determined by pairs of alleles from each parent. These alleles seperate during gamete formation, giving each offspring only one allele from each parent. |
Mendel's Law of Segregation |
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This is when individuals of contrasting traits are crossed, the offspring will express only the dominant trait. |
Mendels Principle of Dominance |
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This is a cross between two heterozygous individuals that differ in two traits (ex. AaBb×AaBb) |
Dihybrid Cross |
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This states that different pairs of alleles are passed to the offsprings independently of each other. Meaning that the offspring may have new combinations of alleles that are not present in either parent. |
The Law of Independent Assortment |
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This is the blending of traits of two different alleles at one locus that occurs when neither allele is dominant. |
Incomplete Dominance |
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This describes a situation where two alleles may be expressed equally. The situation occurs when two different alleles for a trait are both dominant. |
Co-dominance |
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This is patterns of inheritance when a gene may have more than two alleles for any given trait. |
Multiple alleles |
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This states that genes are found at specific locations on a chromosome, and that chromosomes provide basis for the process of Segregation and independent Assortment of the gene. |
The Chromosome Theory of Inheritance |
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This states that genes exist at specific sites arranged in a linear line fashion along chromosomes. |
The Gene-Chromosome Theory of Inheritance |
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This is the process in which non-sister chromatids exchange genes during prophase 1 of meiosis allowing for recombination of genes. |
Crossing Over |
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This is the transfer of genes on the X or Y chromosome from one generation to the next. |
Sex-Linked Inheritance |
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This is the result of many traits being controlled by more than one gene (ex. Eye colour, hair or fur colour, body shape, etc) |
Polygenic inheritance |
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These are the monomers of nucleic acids |
Nucleotides |
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The four nitrogenous bases that are found in DNA: |
Adenine (A), Guanine (G), Cytosine (C), and Thymine (T) |
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The four nitrogenous bases that are found in RNA: |
Adenine (A), Guanine (G), Cytosine (C), and Uracil (U) |
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This consists of two double helical strands twisted around each other in a double helix. Each strand containing a sugar, a phosphate group, and a base. |
Watson and Crick's Model of DNA |
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DNA model & how it is like a ladder: |
The handrails of the molecule are made up of alternating sugar and phophaste groups, with the phosphate groups serving as bridges between nucleotides. Rungs of the ladder are the nitrogenous bases. |
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The two strands of DNA double helix are complementary with each other so each purine base pairs with a pyrimidine base on the opposite side: |
A pairs with T or U. C pairs with G |
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The three main structural differences between RNA and DNA: |
1. RNA contains Uracil - DNA contains Thymine. 2. RNA has sugar ribose - DNA has the sugar deoxyribose. 3. RNA is a single strand - DNA is double stranded. |
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This means that when a molecule of DNA is copied, each new molecule contains one strand of parental DNA and one strand of new DNA. |
Semi-conservative |
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The three main stages of DNA replication: |
Initiation, Elongation and Termination. |
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This is when a portion of the double helix is unwound. |
Initiation |
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This is when two new strands of DNA are assembled. |
Elongation |
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This is when the new DNA molecules re-form into helices. |
Termination |
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This is the transfer of genetic information from DNA to protein. |
Gene expression |
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The two stages of gene expression: |
Transcription and translation |
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This is when a strand of mRNA is produced that is complementary to a segment of DNA. This process takes place in the cell nucleus of an eukaryotic cell and in the cytoplasm of a prokaryotic cell. |
Transcription |
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This is the second stage of gene expression in which a ribosome produces a polypeptide, using the coded mRNA instructions. |
Translation |
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This is a linear strand of RNA that carries information from DNA in the nucleus to the protein synthesis machinery of the cell. |
Messenger RNA or mRNA |
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They have a characteristic cloverleaf shape and at the end of one lobe is the anticodon. |
Transfer RNA or tRNA |
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This is a linear strand of RNA that always stays bound to proteins within ribosomes. Function is to supply the site on the ribosome where the polypeptide is assembled during polypeptide synthesis. |
Ribosomal RNA or rRNA |
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This is a permanent change in the genetic material of an organism and it can change the genetic information of a gene, causing the gene to function improperly or not at all. |
Mutation |
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This is a pattern of inheritance in which a trait is controlled by more than one gene. |
Polygenic inheritance |
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This is the range of variation in one trait resulting from the protein products produced by many genes. |
Continuous variation |
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These work along other genes to control the expression of a trait. |
Modifier genes |
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This is the change in physical structure of a chromosome in which portion of the chromosome is lost. |
Deletion |
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This is the change in physical structure of a chromosome in which a gene sequence is repeated one or more times within one or several chromosomes. |
Duplication |
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This is the physical change of a chromosome where a part of one chromosome changes places with part of the same or different chromosome. |
Translocation |