medical genetics - shandong university...medical genetics: hybrid clinical genetics is a hybrid of...
TRANSCRIPT
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Medical GeneticsMedical Genetics
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Public Health and Medical GeneticsPublic Health and Medical Genetics
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Outline
Definition of Medical GeneticsDefinition of Medical Genetics
A Short History of Medical Genetics A Short History of Medical Genetics
Classification of Genetics DisordersClassification of Genetics Disorders
Future of Medical GeneticsFuture of Medical Genetics
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Medical Genetics Medical Genetics is the application is the application of genetics to medical practiceof genetics to medical practice..
Medical GeneticsMedical Genetics
Genetic diseases Genetic diseases are the diseases are the diseases which are due to altered genetic which are due to altered genetic materials (genes or chromosomes).materials (genes or chromosomes).
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Medical Genetics: Medical Genetics: HybridHybrid
Clinical genetics is a hybrid of clinical medicine with genetics.
Biochemical genetics is a hybrid of biochemistry, mainly of amino acids and proteins, with genetics.
Molecular genetics is a hybrid of the biochemistry of DNA and RNA with genetics.
Cytogenetics is a hybrid of cytology and genetics; it involves the study of chromosomes under the microscope.
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1865, Mendel G1865, Mendel G
A Brief History of GeneticsA Brief History of Genetics
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———— Experiments in Plant HybridizationExperiments in Plant Hybridization1865, Mendel G1865, Mendel G
A Brief History of GeneticsA Brief History of Genetics
———— hereditary factor, hereditary factor, A aA a
1909, Johannson 1909, Johannson ———— genegene
1957, Benzer 1957, Benzer ———— cistroncistron
1977, Sanger 1977, Sanger ———— overlapping geneoverlapping gene
1978, Gilbert 1978, Gilbert ———— split genesplit gene
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———— Experiments in Plant HybridizationExperiments in Plant Hybridization1865, Mendel G1865, Mendel G
A Brief History of GeneticsA Brief History of Genetics
1900, Landsteiner K 1900, Landsteiner K ———— ABOABO1924, Bernstein F 1924, Bernstein F ———— multiple allelesmultiple alleles
1908, Hardy1908, Hardy--Weinberg lawWeinberg law1909, Nilsson1909, Nilsson--EhleEhle H H ———— multifactorial inheritancemultifactorial inheritance
1902, Garrod AE 1902, Garrod AE ———— inborn errors of metabolisminborn errors of metabolism
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1941, Beadle GW & Tatum EL 1941, Beadle GW & Tatum EL
Biochemical GeneticsBiochemical Genetics
1949, Pauling L 1949, Pauling L
1956, Ingram VM 1956, Ingram VM ———— 6Glu6GluValVal
———— the One Gene the One Gene -- One Enzyme TheoryOne Enzyme Theory
———— sickle cell disease; sickle cell disease; molecular diseasemolecular disease
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1910, Morgan TH 1910, Morgan TH ———— Theory of GeneTheory of Gene (1926)(1926)
CytogeneticsCytogenetics
1923, Painter TS 1923, Painter TS ———— 2n = 48; XX, XY2n = 48; XX, XY
1956, Tjio JH 1956, Tjio JH ———— 2n = 462n = 46
1959, Lejune J 1959, Lejune J ———— DownDown’’s (s (++21)21)
Ford CE Ford CE ———— Turner (XO)Turner (XO)Jacob PA Jacob PA ———— Klinefelter (XXY)Klinefelter (XXY)
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1969, Pardue ML —— in site hybridization, ISH
CytogeneticsCytogenetics
1971, Seabright M —— G band1975, Yunis JJ —— Microcytogenetics
1986, Penkel D —— FISH
1960, 1960, Denver systemDenver system
1961, Lyon M 1961, Lyon M ———— Lyon hypothesisLyon hypothesis
1970, Caspersson T —— banding pattern
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MitosisMitosis
A single division of a cell, which results in two A single division of a cell, which results in two daughter cells that are genetically daughter cells that are genetically identicalidentical to to one another one another andand to their mother cell. Regardless to their mother cell. Regardless of their chromosome number, all kinds of of their chromosome number, all kinds of eukaryotic cells can undergo mitosis. eukaryotic cells can undergo mitosis.
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Somatic Cells Divide by MitosisSomatic Cells Divide by Mitosis
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MeiosisMeiosis
Two consecutive divisions of a particular cell type, which results in four daughter cells that have half of the chromosome number of their mother cell. The daughter cells are thus genetically different from the mother cell, and due to independent, random assortment of chromosomes and crossing over, they are genetically different from one another as well.
The first division is called the reduction division, since this is the one during which chromosome number in the cells is reduced.
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Germ Cells Are Formed by MeiosisGerm Cells Are Formed by Meiosis
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ChromosomeChromosome
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KaryogramKaryogram of the human chromosomesof the human chromosomes
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Chromosomal Theory of InheritanceChromosomal Theory of Inheritance
Sex Chromosomes and Sex Chromosomes and AutosomesAutosomes
Genes Direct Protein ExpressionGenes Direct Protein Expression
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1961, Jacob F & Monod J —— lactose operon
Molecular GeneticsMolecular Genetics
1953, Watson JD & Crick FHC —— DNA double helix structure
1944, Avery OT, et al 1944, Avery OT, et al ———— DNADNA
1967 ,Holley RW, et al 1967 ,Holley RW, et al ———— genetic codegenetic code
1968, Arber W, et al —— restriction endonucleases
1970, Baltimore D, et al —— reverse transcriptase
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1977, Sanger F 1977, Sanger F ———— dideoxy sequencingdideoxy sequencing
1985, Mullis K 1985, Mullis K ———— polymerase chain reactionpolymerase chain reaction
Molecular GeneticsMolecular Genetics
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Molecular GeneticsMolecular Genetics
1953, Watson JD & Crick FHC —— DNA double helix structure
1944, Avery OT, et al 1944, Avery OT, et al ———— DNADNA
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XX--ray diffraction photograph of the ray diffraction photograph of the DNA double helixDNA double helix
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Solving the Structure of DNASolving the Structure of DNA
Photo AnalysisPhoto Analysis ““XX”” pattern characteristic pattern characteristic
of helixof helix Diamond shapes indicate Diamond shapes indicate
long, extended moleculeslong, extended molecules Smear spacing reveals Smear spacing reveals
distance between repeating distance between repeating structuresstructures
Missing smears indicate Missing smears indicate interference from second interference from second helixhelix
The x-ray diffraction image that allowed Watson and Crick to solve the structure of DNAwww.pbs.org/wgbh/nova/photo51
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Solving the Structure of DNASolving the Structure of DNA
The x-ray diffraction image that allowed Watson and Crick to solve the structure of DNA
Photo AnalysisPhoto Analysis ““XX”” pattern characteristic pattern characteristic
of helixof helix Diamond shapes indicate Diamond shapes indicate
long, extended moleculeslong, extended molecules Smear spacing reveals Smear spacing reveals
distance between repeating distance between repeating structuresstructures
Missing smears indicate Missing smears indicate interference from second interference from second helixhelix
www.pbs.org/wgbh/nova/photo51
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Solving the Structure of DNASolving the Structure of DNA
The x-ray diffraction image that allowed Watson and Crick to solve the structure of DNA
Photo AnalysisPhoto Analysis ““XX”” pattern characteristic pattern characteristic
of helixof helix Diamond shapes indicate Diamond shapes indicate
long, extended moleculeslong, extended molecules Smear spacing reveals Smear spacing reveals
distance between repeating distance between repeating structuresstructures
Missing smears indicate Missing smears indicate interference from second interference from second helixhelix
www.pbs.org/wgbh/nova/photo51
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Solving the Structure of DNASolving the Structure of DNA
The x-ray diffraction image that allowed Watson and Crick to solve the structure of DNA
Photo AnalysisPhoto Analysis ““XX”” pattern characteristic pattern characteristic
of helixof helix Diamond shapes indicate Diamond shapes indicate
long, extended moleculeslong, extended molecules Smear spacing reveals Smear spacing reveals
distance between repeating distance between repeating structuresstructures
Missing smears indicate Missing smears indicate interference from second interference from second helixhelix
www.pbs.org/wgbh/nova/photo51
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Solving the Structure of DNASolving the Structure of DNA
The x-ray diffraction image that allowed Watson and Crick to solve the structure of DNA
Photo AnalysisPhoto Analysis ““XX”” pattern characteristic pattern characteristic
of helixof helix Diamond shapes indicate Diamond shapes indicate
long, extended moleculeslong, extended molecules Smear spacing reveals Smear spacing reveals
distance between repeating distance between repeating structuresstructures
Missing smears indicate Missing smears indicate interference from second interference from second helixhelix
www.pbs.org/wgbh/nova/photo51
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Molecular GeneticsMolecular Genetics
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The Nobel Prize in Physiology or Medicine 1965The Nobel Prize in Physiology or Medicine 1965
"for their discoveries concerning genetic control of "for their discoveries concerning genetic control of enzyme and virus synthesisenzyme and virus synthesis““--Lactose Lactose operonoperon
Jacob F Monod J
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The Nobel Prize in Physiology or Medicine 1968The Nobel Prize in Physiology or Medicine 1968
"for their interpretation of the genetic code and "for their interpretation of the genetic code and its function in protein synthesis"its function in protein synthesis"
Holley RWHolley RW KhoranaKhorana HGHG NirenbergNirenberg MWMW
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The Nobel Prize in Physiology or Medicine 1978The Nobel Prize in Physiology or Medicine 1978
Arber WArber W Nathans DNathans D Smith HSmith H
"for the discovery of restriction enzymes and their "for the discovery of restriction enzymes and their application to problems of molecular genetics"application to problems of molecular genetics"
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The Nobel Prize in Physiology or Medicine 1975The Nobel Prize in Physiology or Medicine 1975
Baltimore DBaltimore D Temin HM Temin HM
"for their discoveries concerning the interaction between "for their discoveries concerning the interaction between tumour viruses and the genetic material of the cell"tumour viruses and the genetic material of the cell"
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The Nobel Prize in Chemistry 1980The Nobel Prize in Chemistry 1980
Sanger FSanger F
"for their contributions concerning the deter"for their contributions concerning the deter--mination of base sequences in nucleic acids"mination of base sequences in nucleic acids"
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The Nobel Prize in Chemistry 1993The Nobel Prize in Chemistry 1993
Mullis FMullis F
"for his invention of the polymerase chain "for his invention of the polymerase chain reaction (PCR) method"reaction (PCR) method"
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1977, Sanger F 1977, Sanger F ———— dideoxy sequencingdideoxy sequencing
1985, Mullis K 1985, Mullis K ———— polymerase chain reactionpolymerase chain reaction
Molecular GeneticsMolecular Genetics
1979, Kan YW 1979, Kan YW ———— gene diagnosis (RFLP)gene diagnosis (RFLP)1986, Woo LC 1986, Woo LC ———— gene diagnosis (ASO)gene diagnosis (ASO)
1991, Anderson WF 1991, Anderson WF ———— gene therapy (ADA)gene therapy (ADA)1990, human genome project (HGP)1990, human genome project (HGP)
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1908, Hardy-Weinberg law
Population GeneticsPopulation Genetics
1954, Neel JV, et al —— epidemiologic genetics
Human Genome Diversity
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Major Types of Genetic Diseases Major Types of Genetic Diseases
Monogenic DiseaseMonogenic Disease--single gene disordersingle gene disorder
Polygenic DiseasePolygenic Disease
Chromosome DiseaseChromosome Disease
Somatic Cell Somatic Cell Genetic Diseases Genetic Diseases
Mitochondrial DisordersMitochondrial Disorders
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These disorders are due to single These disorders are due to single mutant genes mutant genes (major gene)(major gene) with a large with a large effect on the patient's health and effect on the patient's health and inherited in inherited in Mendelian fashionMendelian fashion..
Single Gene DisorderSingle Gene Disorder
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Single Gene DisorderSingle Gene Disorder Autosomal dominant diseases (AD)Autosomal dominant diseases (AD)
Autosomal recessive diseases (AR) Autosomal recessive diseases (AR)
XX--linked dominant diseases (XD)linked dominant diseases (XD)
XX--linked recessive diseases (XR)linked recessive diseases (XR)
YY--linked diseaseslinked diseases
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MendelianMendelian Disorders Disorders
Dominant Disorders Dominant Disorders MarfanMarfan DiseaseDisease
Recessive Disorders Recessive Disorders sickle cell anemia sickle cell anemia
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Polygenic DiseasePolygenic DiseaseMultifactorial disease, MFResult from a combination of multiple
genetic and environmental factors. Each of these genes may have a relatively minor effect (minor gene) and their effects are additive.
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MultifactorialMultifactorial Disorders Disorders
Neural Tube DefectsNeural Tube Defects
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Chromosome DiseaseChromosome DiseaseThese diseases are due to the
chromosomal aberration, chromosome numerical abnormality and chromosome structural aberration.
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Chromosome DisordersChromosome Disorders
Down Syndrome TurnerDown Syndrome Turner’’s Syndromes Syndrome
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Other DisordersOther Disorders
Somatic genetic disorders: not inherited but occur after Somatic genetic disorders: not inherited but occur after conception. They often involve environmental and conception. They often involve environmental and genetic influences. genetic influences.
Mitochondrial disorders arise from mutations in the Mitochondrial disorders arise from mutations in the genetic material in mitochondria. Mitochondrial DNA genetic material in mitochondria. Mitochondrial DNA is transmitted only through the maternal line. is transmitted only through the maternal line.
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In the crowd, monogenic disease 3%~5%polygenic disease polygenic disease 15%~20%chromosome disease chromosome disease 1%
2.2%2.2% mental retardationmental retardation
mmore than 1/3ore than 1/3 relate to genetic factorrelate to genetic factor
the Hazard of Genetic Diseasethe Hazard of Genetic Disease
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Prenatal TestingPrenatal Testing
All patients have the right to receive information All patients have the right to receive information about the genetic risk associated with a about the genetic risk associated with a pregnancy. This allows parents to make an pregnancy. This allows parents to make an informed choice about having a child with an informed choice about having a child with an abnormality.abnormality.
Genetic screening is not expected to detect all Genetic screening is not expected to detect all genetic disorders in a given population.genetic disorders in a given population.
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Cancer and Genetics Cancer and Genetics
Certain families have an increased risk for Certain families have an increased risk for specific cancers. specific cancers.
Many of these families have an identifiable gene Many of these families have an identifiable gene associated with the disorder. associated with the disorder.
Possession of the gene does not automatically Possession of the gene does not automatically mean that cancer will develop in the patient. mean that cancer will develop in the patient.
The expression of most genes can be altered by The expression of most genes can be altered by environmental factors and by other genes. environmental factors and by other genes.
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Breast Cancer GenesBreast Cancer Genes
BRCA1, a tumorBRCA1, a tumor--suppressor gene, accounts for 5 to 10 suppressor gene, accounts for 5 to 10 percent of all cases of breast cancer. percent of all cases of breast cancer.
It is It is autosomalautosomal dominant. A woman from a family dominant. A woman from a family prone to breast or ovarian cancer who carries certain prone to breast or ovarian cancer who carries certain mutations of BRCA1 has about an 80 percent chance mutations of BRCA1 has about an 80 percent chance that breast cancer will develop and a 40 to 60 percent that breast cancer will develop and a 40 to 60 percent chance of getting ovarian cancer. chance of getting ovarian cancer.
Members of a family with multiple cases of breast or Members of a family with multiple cases of breast or ovarian cancer can be tested to determine whether they ovarian cancer can be tested to determine whether they have a genetic alteration in BRCA1. have a genetic alteration in BRCA1.
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The Future of Medical GeneticsThe Future of Medical Genetics
Sequencing of the human genome was completedSequencing of the human genome was completedin 2000. The completion of this task will speed thein 2000. The completion of this task will speed thedevelopment of molecular recognition anddevelopment of molecular recognition andtreatment in medical genetics. treatment in medical genetics.