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Human Genetic Mutations 2 Main Types of Mutations 1. __________________________________ 2. __________________________________ • What are chromosomes? Humans have ______________ pairs of chromosomes, with one chromosome from each parent. The chromosomes are coiled up ______________. Under normal conditions all of the chromosomes are inherited in tact. Chromosomal Mutations • Any change in the ____________________ or ______________________of chromosomes • Large scale: Affect ____________________ genes • 5 Types 1. _____________________________ 2. _____________________________ 3. _____________________________ 4. _____________________________ 5. _____________________________ • Chromosomal Deletion What is it? __________________________________________________________________ What does it cause? _______________________________________________________ • Chromosomal Duplication What is it? __________________________________________________________________ What does it cause? _______________________________________________________ • Chromosomal Inversion What is it? _______________________________________________________________ What does it cause? _____________________________________________________ • • Chromosomal Translocation What is it? _________________________________________________________________ What does it cause? _____________________________________________________ Nondisjunction-Chromosomes _____________ TO SEPARATE during ________________ • Nondisjunction Produces gametes (and therefore a baby) with one missing chromosome or one extra chromosome Nondisjunction (in Meiosis II) Fertilization Nondisjunction • Every cell in that baby’s body will have ______ copies of this chromosome instead of________. • This condition is called ________________________. • Trisomy 21 = Individual has _____ copies of chromosome # ________ Chromosomal Mutations • Most chromosomal mutations are ______________________ • If the fetus survives: Tend to cause wide-spread abnormalities • Example: Down Syndrome • Down Syndrome Cause: _______________________________________________ __________ copies of chromosome 21 = ______________________________________ • Genetic Screening - __________________________________________ • Karyotypes A pictorial display of ________________________ chromosomes from a mitotic cell Homologous chromosomes- pairs Chromosomes pairs 1-22 are called ___________________________ Chromosome pair 23 are called the _______________chromosomes • • • • • • • • • Klinefelter’s Syndrome Due to _______________________________ Chromosome makeup is __________________ Creates a sterile male Turner’s Syndrome Due to nondisjunction __________________________- the condition in which there is a missing chromosome. Sex chromosome make up is ___________ only Females that will not undergo puberty. Edward’s Syndrome Due to nondisjunction Extra number ____________ chromosome (trisomy 18) Traits: Low ears, kidney and heart defects Patau’s Syndrome Extra number __________ chromosome (trisomy 13) Traits: Deformed eyes, ears and lips KEY POINT #1 Too much or too little DNA is bad! Gene Mutations Small scale: one ____________ is affected Any change to the DNA sequence of a gene: Nucleotides/Bases may be __________________, __________________or ______________________ Gene Mutations: 2 Types • • • • • • • • • • • 1. __________________________ 2. __________________________ Point Mutation One base (A, T, C, or G) is substituted for another Can Cause: Sickle-cell anemia 3 Possible Consequences: 1. ___________________mutations: code for a stop, which can translate the protein 2. ___________________mutations: code for a different amino acid 3. ___________________ mutations: code for the same amino acid Frameshift Mutation One or more bases (A, T, C, or G) are added or deleted Can Cause: Cystic Fibrosis Caused by: _______________________: adding a base _______________________: removing a base Causes of Mutations 1. spontaneous 2. occur during DNA replication 3. Caused by _____________________________ i. ________________________ ex: radiation from UV rays, X-rays or extreme heat ii. _________________________(molecules that misplace base pairs or disrupt the helical shape of DNA). Gene Mutations KEY IDEA: A mutated gene will make a mutated _______________________ Example: Sickle Cell Anemia Normal Red Blood Cell – Red blood cells shaped like a disc – ____________________________ (protein) carries oxygen to all parts of the body Sickle Red Blood Cell – Red blood cells form an abnormal ________________________ shape – Hemoglobin (protein) is abnormally shaped – don't move easily through your blood vessels – form ______________________ and get stuck in the blood vessels Mutation located on Chromosome _______________ Effects mostly African Americans Example: Cystic Fibrosis (CF) What is it?____________________________________________ Where is it found? ______________________________ Symptoms – Thick ___________________________in the lungs and digestive track – Constant lung infections and impaired digestion Who gets it? – Most common in Caucasians Prevalence – 1 in ~3,000 Americans has CF – 1 in 23 white Americans carries the mutant allele! Cause of Cystic Fibrosis (CF) The “CFTR” gene is mutated 3 base pairs are _____________________________ Mutant protein is missing an __________________________ and cannot fold correctly • • • • • • • Albinism Due to the lack of the pigment ____________________ (a protein) in the skin, eyes, and hair. Hemophilia Disorder that is linked to the sex chromosomes Missing a protein needed for the blood to ________________ Tay-Sachs Disease Inability to synthesize an enzyme that prevents _________________buildup in brain cells. Causes the breakdown of nervous system Phenylketonuria (PKU) Inability to code for an enzyme needed for changing the amino acid ____________________________ to tyrosine. Damages brain cells and causes mental retardation. Duchenne Muscular Dystrophy Linked to the sex chromosomes Results in the progressive ___________________________ and loss of skeletal muscle. Colorblindness Carried on the ____________ of the sex chromosomes. Occurs more frequently in ____________________ than females. KEY POINT #2 Mutation of a gene = Mutant protein ____________________________ proteins cause the symptoms of the disorder