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Medical Genetics-Biochemical Genetics Robert F. Waters, PhD

Medical Genetics-Biochemical Genetics Robert F. Waters, PhD. One gene-One enzyme Many proteins are different but do not cause clinical problems Polymorphism (multiple structures) Multiple “normal” forms Caused by mutations Different types of proteins..not just enzymes. Main Categories.

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Medical Genetics-Biochemical Genetics Robert F. Waters, PhD

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  1. Medical Genetics-Biochemical GeneticsRobert F. Waters, PhD • One gene-One enzyme • Many proteins are different but do not cause clinical problems • Polymorphism (multiple structures) • Multiple “normal” forms • Caused by mutations • Different types of proteins..not just enzymes

  2. Main Categories • The Hemoglobins • Inborn Errors of Metabolism • Genetic response to drugs • Pharmacogenetics

  3. The Hemoglobins • Defects in hemoglobin synthesis • Hemoglobinopathies • One of the first was Sickle Cell Anemia • Neel (1949) • Pauling, et. al. (1949) • Sickle Cell Anemia is essentially a “molecular disease”

  4. Structure of Hemoglobin • Two main parts • Globin (Polypeptide Chains) • Two alpha and two beta • Heme (Porphyrin) • Iron containing portion • Oxygen binding

  5. Normal Hemoglobin • Adult hemoglobin (HbA) • MW. Approx. 68000 • Structural formula • 22 • Alpha chains have 141 AAs • Beta chains 146 AAs • Alpha and beta chains are very similar in primary and tertiary structure

  6. Myoglobin is Different • Oxygen carrying molecule of muscles • Single polypeptide chain

  7. Different Gene Loci for Globin Part of Hb •      • Alpha, beta, gamma, delta, epsilon • Five different structural gene loci • HbF (Fetal Hemoglobin) • Formed in uterus • Disappears after birth • 2 2 • Two different types of HbF differing by only one amino acid…glycine • HbA2 • 2% of adult variant • 2 2 • Two types of embryonic hemoglobin • First 90 days • Gower I (4) and Gower II (22)

  8. Abnormal Hemoglobin • HbS (Sickle Cell - 6:glu val) • HbC (-6:glulys) • Hb Hopkins-2 (- 112:hisasp) • HbC Georgetown (- 6:glu val+) • + means another substitution as well • Hb Freiburg (-23 deletion)

  9. Sickle Cell Disease • Severe hemolytic anemia • Anemia • Jaundice • Vascular obstruction (Sickle cells) • Painful infarcts • High incidence in equatorial Africa • Separated originally by electrophoresis • Pauling, Sanger, Wells (1949) • Mixture of normal and abnormal (heterozygous)

  10. Hereditary Persistence of HbF • Rare • Sub-clinical • Gene to turn on HbA formation is blocked

  11. Thalassemias • Beta gene turned on just before birth • Alpha gene throughout gestation • Derived from Greek word for sea—thalassa • Due to low production of alpha or beta chains NOT amino acid substitution

  12. Alpha Thalassemia • Usually high expressivity • Lethal • Associated with operator gene malfunction

  13. Beta Thalassemia • Mediterranean Anemia • Wide expressivity • May be expressed neonatally • Differential diagnosis • Different from iron-deficiency anemia

  14. Inborn Errors of Metabolism • Enzymatic defect (structure) • Enzyme substrate problem • Enzyme co-enzyme malfunction • Enzyme co-factor (metal) malfunction • Build up before—feed after • Usually autosomal recessive • Otherwise would probably be lethal • Some are hemizygous (XY)

  15. Consequences-Overview • Accumulation of a precursor • Accumulated precursor may be toxic • E.g., pyruvate • Alternate minor pathways may start producing other toxic metabolites • E.g., PKU • Deficiency of product • Product may be precursor to other substance. • E.g., tyrosine and thyronines • Feedback inhibition may be impaired due to lack of product • Causes lack of feedback inhibition

  16. Partial Listing of Lesions • Glycolytic Pathway • PDH Complex • Albinism (Two Types) • Cystinuria • Increased secretion of cystine, lysine, arginine, ornithine • Aminoaciduria • AR (variable expressivity) • Renal failure

  17. Partial Listing of Lesions:Cont • Galactosemia • Galactose-1-phosphate uridyltransferase • AR • Hepatosplenomegaly • Mental retardation • Note: Galactokinase deficiency

  18. Partial Listing of Lesions:Cont • G6PD Deficiency • Many Variants • Hemolytic anemia • XR • Oxidative stress • Sickle Cell Anemia

  19. Partial Listing of Lesions:Cont • Glycogen storage diseases • Type I (von Gierke’s) • Hepatomegaly, mental retardation, hypoglycemia • Glucose-6-phosphatase • Type VIII (Glycogen Storage Disease) • Hepatomegaly,mild acidosis, hypoglycemia • XR • Phorphorylase kinase

  20. Partial Listing of Lesions:Cont • Tay-Sachs Disease • Onset at 4 to 6 months • Death 2 to 4 years • AR • Degenerative neurological changes • Gangliosidosis • Reduced hexosaminidase

  21. Partial Listing of Lesions:Cont • Hartnup Disease • Tryptophan transport • Neurological change • AR • Hemoglobinopathies (See Earlier) • Thalassemias

  22. Partial Listing of Lesions:Cont • Homocystinuria • Dislocated lenses • AR • Accumulation of methionine and homocystine

  23. Partial Listing of Lesions:Cont • Lesch-Nyhan Syndrome • Uric Aciduria • Self-mutilation • Mental retardation • Cerebral palsy • Hypoxanthine-guanine phosphoribosyl transferase (HGPRT) • XR

  24. Partial Listing of Lesions:Cont • Mucopolysaccharidoses I • Hurler’s Syndrome • “Gargoyle” Appearance • Mental retardation • Corneal clouding • Cardiovascular degeneration • Dwarfism • Mucopolysaccharide accumulation

  25. Partial Listing of Lesions:Cont • Mucopolysaccharidoses II • Hunter’s Syndrome • Less severe than Hurler’s • No evidence of corneal clouding • Orotic aciduria • Urinary excretion of orotic acid • Precursor to pyrimidine nucleotides • Pentosuria • AR • “False Diabetes”

  26. Partial Listing of Lesions:Cont • PKU • Porphyria (Acute Intermittent) • Abdominal pain • Neurological problems • Excessive excretion of -amino levulinic acid (ALA) • Excessive hepatic ALA synthetase • AR

  27. Partial Listing of Lesions:Cont • Congenital Spherocytosis • Episodes of hemolytic anemia • Defect in RBC membrane • AD • Patients are heterozygous

  28. Partial Listing of Lesions:Cont • Tyrosinemia • Acute liver disease • AR • Tyrosine transaminase • Wilson’s Disease • Cirrhosis of liver • Neurological damage • Improper copper metabolism • AR • Build up of stored copper • Decreased serum levels of ceruloplasmin • Treatment by Penicillamine removes stored Cu

  29. Partial Listing of Lesions:Cont • Maple Syrup Urine Disease • BCAA dehydrogenase • Alcaptonuria • Dark Urine Disease • Other Metabolic Pathways • Vitamin Pathways • E.g., holoenzyme carboxylase • Pyruvate carboxylase and biotin

  30. Pharmacogenetics • Drug reactions and interactions associated with genetics • Genetic Profiling • Genetic Probes

  31. Genetic Polymorphisms • Different phenotypes • G6PD Variants (Example) • BA • A- • BA- • B- • B • A

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