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Chapter 11 – Genetics Vocabulary Overview
Mr. Davis Biology
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Genetic Vocabulary Allele: one of two or more different versions of the same gene. Dominant Allele: allele that masks the presence of another allele for the same gene when they occur together in a heterozygote. Genetics: the science of heredity.. Genotype: alleles an individual inherits at a particular genetic locus Heterozygote: organism that inherits two different alleles for a given gene. Homozygote: organism that inherits two alleles of the same type for a given gene. Hybrid: offspring that results from a cross between two different types of parents . Biology
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Genetic Vocabulary Law of Independent Assortment: Mendel’s second law stating that factors controlling different characteristics are inherited independently of each other. Law of Segregation: Mendel’s first law stating that the two factors controlling a characteristics separate and go to different gametes. Locus: position of a gene on a chromosome. Phenotype: characteristics of an organism that depend on how the organism’s genotype is expressed. Pollen: tiny grains that bear the male gametes of seed plants and transfer sperm to female reproductive structures. Pollination: fertilization in plants in which pollen is transferred to female gametes in an ovary. Recessive Allele: allele that is masked by the presence of another allele for the same gene when they occur together in a heterozygote. Biology
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Genetic Vocabulary Codominance: relationship between two alleles for the same gene in which both alleles are expressed equally in the phenotype of the heterozygote. Incomplete Dominance: relationship between the alleles for a gene in which one allele is only partly dominant to the other allele so an intermediate phenotype results. Polygenic Characteristic: characteristic, or trait, controlled by more than one gene, each of which may have two or more alleles. Probability: the likelihood, or chance, than a certain event will occur. Punnett Square: chart for determining the expected percentages of different genotypes in the off spring of two parents. Biology
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Biology
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Meiosis
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Mr. Davis Genetic Mutations Biology
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Mutations Mutations are mistakes that occur in copying their own DNA. Mutations are changes in the genetic material. Gene mutations result from changes in a single gene. Genetic mutations affect the amino acid sequences of the proteins for which they code. Biology
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Biology
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Mutation A mutation is a permanent change in the DNA sequence of a gene. Sometimes mutations can be useful but mostly they are harmful as changes in DNA can change the way a cell behaves. As genes are a set of hereditary materials that contain instructions necessary for a cell to work so if some of these instructions go wrong the cell may not know how to function. Biology
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Biology
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Kinds of Mutations 2 Gene Mutations Point Mutation Frameshift Mutation
4 Chromosomal Mutations Deletion Duplication Inversion Translocation Biology
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Point Mutation Gene mutations involving changes in one or a few nucleotides because they occur at a single point in the DNA sequence. Biology
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Sickle Cell Anemia Sickle cell anemia is the result of a point mutation in codon 6 of the -globin gene resulting in the substitution of amino acid Glutamic acid by Valine. Biology
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Sickle Cell Anemia Under conditions of low oxygen atmospheres containing a low oxygen level, the following changes occur: (1) The hemoglobin agglutinates to form insoluble rod-shaped polymers; (2)Red blood cells become distorted and sickle-shaped (3) The sickle-shaped cells rupture easily causing hemolytic anemia; (4)The sickle shaped cells tend to block capillaries interfering with the blood flow to various organs. Biology
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Sickle Cell Anemia Biology
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Frameshift Mutation A frameshift mutation is a genetic mutation caused by a deletion or insertion in a DNA sequence that shifts the way the sequence is read. A DNA sequence is a chain of many smaller molecules called nucleotides. Biology
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Frameshift Mutation Biology
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Frameshift Mutations Frameshift mutations can alter a protein so much that it is unable to perform its normal functions. Biology
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Biology
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Chromosomal Mutations
Chromosomal Mutations involve changes in the number or structure of chromosomes. Chromosomal mutations change the number of copies of genes. Biology
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4 Types of Chromosomal Mutations
Deletions Duplication Inversions Translocations Biology
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1. Chromosomal Mutation - Deletion
Original Chromosome: ABCDEF Deletion: ACDEF: deletions involve the loss of all or part of a chromosome. Biology
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2. Chromosomal Mutation - Duplication
Duplication: ABBCDEF: duplications produce extra copies of parts of a chromosome. Biology
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Biology
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3. Chromosomal Mutation - Inversion
Original Chromosome: ABCDEF Inversion: AEDCBF: inversions reverse the direction of parts of a chromosome. Biology
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Inversion Biology
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4. Chromosomal Mutation - Translation
Translocation: ABCJKL: translations occur when part of one chromosome breaks off GHIDEF and attaches to another Biology
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4 Types of Chromosomal Mutations
Biology
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Genetic Mutagens Mutagens are substances or conditions that cause mutations. Mutations are changes in the genetic code. Biology
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Mutagen Examples Radiation (UV-light) Extreme High Temp. Chemicals
Tar & Nicotine Biology
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Examples of Mutagens Biology
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Genetic Mutagens Biology
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Chemical Mutagens Biology
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Biology
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