Dr. Triwani, M.

Kes

Mendel did not know what the physical properties of his particles were when he proposed his laws of inheritance. August Weismann suggested that chromosomes (discovered in 1882) were the location of hereditary material. Genes are located on chromosomes The idea that genes are located on chromosomes is known as the chromosome theory of inheritance.

The physical location of a gene on a chromosome is called a locus. Chromosomes that pair during meiosis and contain the same gene loci and structure are called homologous chromosomes. See Figure below for a diagram of homologous chromosomes.

Chromosomes that determine gender are called sex chromosomes; all other chromosomes are called autosomes. Autosomes are homologous pairs. Sex chromosomes can be homologous or nonhomologous pairs (see Figure 13.2). Sex determination in humans Human females have two X chromosomes, and all their gametes contain one X chromosome. Human males have one X and one Y chromosome; half their gametes contain an X chromosome, and the other half contain a Y chromosome. The chromosome carried by the sperm determines sex in humans. Genetic anomalies such as XY females and XX males can occur because of chromosomal mutations.

Crossing-over disrupts genetic linkage If the linkage between two genes on a chromosome were complete, all offspring would be of a parental type. Morgans experiments showed that complete linkage was not occurring as a result of the presence of nonparental genotypes (see Figure 13.3). To explain the appearance of nonparental genotypes in linked genes, Morgan proposed that genes are physically exchanged between homologous chromosomes during meiosis.

The exchange of genes between homologous chromosomes is called crossing-over (see Figure 13.4). Genes that are far from each other on a chromosome are more likely to be separated by crossing-over than are genes that are close to each other. Genes that are very distant from one another on a chromosome will assort independently.

1) Single gene disorders autosomal dominan autosomal ressif X-linked 2) Chromosomal abnormalities 3) Common disorders with appreciable genetic component/multifactorial 4) Congenital malformations

Autosomal traits the genetic information for the trait is found on chromosome 1-22, not on one of the sex chromosomes Autosomal disorders may be:
Recessive Co-dominant blood type Dominant

Several thousand human genetic disorders are inherited as recessive characters, most of which are caused by recessive mutations of genes on autosomes (Figure 13.6). For genetic disorders caused by a recessive allele (a), only homozygous (aa) individuals get the disease.

Heterozygous individuals (Aa) are called carriers because they have one copy of the disease-causing allele but do not get the disease. If two carriers of a recessive genetic disorder (Aa) mate, there is a 25 percent chance that their offspring will get the disease (see Figure 13.7). If a genetic disorder is dominant (A), then AA and Aa individuals are symptomatic for the disease.

Either parent can carry the recessive allele on an autosomal chromosome. Heterozygotes are symptom-free; homozygotes have the disorder. Two heterozygous parents have a 25 percent chance of producing a child with the disorder. When both parents are homozygous, all children can be affected.

More than 2 alleles for a given trait Some versions of the gene are dominant over others But they are not dominant over all of the alleles Both dominant alleles are expressed in heterozygotes

There are 3 alleles for blood type A (IA ) and B (IB ) are co-dominant Both A and B are dominant over type O blood Writing alleles for blood type A = IA B = IB O = i

X-linked: genetic information for the trait is located on the X chromosome no genetic info about the trait on the Y chromo Examples: Hemophilia, color blindness, Duschenne muscular dystrophy Y-linked (not many known) Allele for hairy ears is Y-linked

 Genes

located on the X or Y chromosome are called sexlinked. Genes on the X chromosome are called X-linked.

 Males

are more likely than females to have recessive Xlinked genetic disorders, because they need to inherit only one copy of the disease-causing allele to be affected.

hereditary = derived from parents familial = transmitted in the gametes through generations congenital = present at birth (not always genetically determined - e.g. congenital syphilis, toxoplasmosis) ! not all genetical diseases are congenital - e.g. Huntington disease 3rd to 4th decade of life

3 groups of genetic diseases 1. Disorders with multifactorial inheritance (polygenic) 2. Monogenic (mendelian) disorders 3. Chromosomal aberrations

 influence

of multiple genes + environmental factors relatively frequent Diabetes mellitus Hypertension Gout (discussed here + see Crystals) Schizophrenia (Psychiatry)

 Congenital

heart disease - certain forms (see Heart) Some types of cancer (ovarian, breast, colon) (see Neoplasms) often familial occurrence - probability of disease is in 1st degree relatives about 5-10%; 2nd degree relatives 0,5-1%

 mutation

of 1 gene, mendelian type of inheritance today about 5000 diseases Autosomal dominant Autosomal recessive X-linked

 both

homozygotes and heterozygotes are affected usually heterozygotes (inherited from one parent) both males and females are affected transmission from one generation to the other 50% of children are affected

 (=

subgroup of hyperlipoproteinemia) most frequent mendelian disorder 1:500 mutation of gene encoding LDLreceptor (70% of plasma cholesterol) heterozygotes 2-3 elev. of plasma cholesterol levels

 homozygotes

5 elevation of plasma cholesterol levels

heterozygotes

asymptomatic until adulthood - xanthomas along tendon sheets, coronary AS homozygotes - xanthomas in childhood, death due to MI by the age of 15Y

French pediatrician Marfan - 1896 - young girl with typical habitus abnormal protein fibrillin - secreted by fibroblasts, part of ECM impairment of collagenous and elastic tissue - decreased firmness of connective tissue principal clinical manifestations - 3 systems

 slender,

elongated habitus long legs, arms and fingers (arachnodactyly) - El Greco! high, arched (Gothic) palate hyperextensibility of joints spinal deformities, pectus excavatum, pigeon breast - pres. Lincoln???

 dislocation

or subluxation of the lens (weakness of suspensory ligaments)

3. cardiovascular system
fragmentation of elastic fibers in tunica media - aorta aneurysmal dilatation - aortic dissection - rupture (35-45% of pts.) incompetence (dilatation) - aortic valve tricuspidal and/or mitral valve floppy valve

 similar

to Marfan syndrome genetic defect of collagen fibrils several types - both autosomal dominant and recessive hyperextensibility of skin, hypermobility of joints - contortionist! joint dislocations, vulnerability rupture of large vessels, colon, cornea

majority of mendelian disorders only homozygotes are affected, heterozygotes (parents) are only carriers 25% of descendants are affected if the mutant gene occurs with low frequency - high probability in consanguineous marriages onset of symptoms often in childhood frequently enzymatic defect testing of parents and amnial cells

1:2000 live births - most common lethal genetic disease in white population defect in the transport of chloride ions across epithelia - increased absorption of Na+ and water to the blood widespread defect in the exocrine glands - abnormally viscid mucous secretions blockage of airways, pancreatic ducts, biliary ducts

Pancreatic abnormalities (85%) - dilatation of ducts, atrophy of exocrine part, fibrosis Pulmonary lesions - dilatation of bronchioles, mucus retention, repeated inflammation, bronchiectasis, lung abscesses, emphysema and atelectasis (100%), cor pulmonale chronicum GIT - meconium ileus (newborns) (25%), biliary cirrhosis (2%) Male genital tract - sterility (obstruction of vas deferens, epididymis, seminal vesicles) (95%)

recurrent pulmonary infections pancreatic insufficiency, malabsorption syndrome (large, foul stool), hypovitaminosis A, D, E, K, poor weight gain high level of sodium in the sweat - "salty" children - mother's diagnosis death usually in 3. decade due to respiratory failure

absence of enzyme phenylalanine-hydroxylase (PAH) Phe ->Tyr increase of plasmatic Phe since birth - rising levels - impairs brain development after 6M - severe mental retardation - IQ under 50 decreased pigmentation of hair and skin - absence of Tyr EARLY SCREENING TEST!!! DIET!!! mothers with PKU - increased levels of Phe transplacental transport - child with severe mental defect (although heterozygous!) - maternal PKU DIET!!!

defect of galactose metabolism lactose -> Gal+Glc Gal -> Glc - defect - accumulation of Gal in blood liver, eyes, brain are affected hepatomegaly (fatty change - fibrosis cirrhosis) lens - opacification - cataracts brain - loss of neurons, gliosis, edema Symptomatology - from birth vomiting, diarrhea, jaundice, hepatomegaly later - cataracts, mental retardation DIET!

deficiency of any one of the enzymes involved in degradation or synthesis depending on the type of defect - tissue distribution, type of accumulated product 12 forms - most important: type I. - von Gierke disease - hepatorenal type type II. - Pompe disease - generalized type (liver, heart, skeletal muscle) type V. - McArdle syndrome - skeletal muscle only biopsy: PAS, Best's carmine

defect of lysosomal enzymes, hydrolyzing various substances (a.o. sphingolipids, mucopolysacharides) - storage of insoluble metabolites in lysosomes extremely rare

Sphingolipidoses more frequent in Ashkenazi Jews

 defect

of glucocerebrosidase - 3 types (type 1 - survival, type 2 lethal, type 3 - intermediate) accumulation of glucocerebroside (Glc-ceramide) - kerasin Gaucher cells - spleen (red pulp), liver (sinuses), bone marrow

 defect

of sphingomyelinase accumulation of cholesterol and sphingomyelin in spleen, liver, BM, LN, lungs - massive visceromegaly CNS (foamy cells) - severe neurological deterioration death during first 4-5 years

 neurons

and glial cells of CNS - mental retardation, blindness

MP synthesized in the connective tissue by fibroblasts - part of the ground substance several clinical variants (I-VII) involvement of liver, spleen, heart (valves, coronary arteries), blood vessels Symptoms: coarse facial features (gargoylism), clouding of the cornea, joint stiffness, mental retardation usually death in childhood (cardiac complications) most frequent Hurler syndrome and Hunter syndrome (X-linked!)

transmitted by heterozygous mother to sons daughters - 50% carriers, 50% healthy sons - 50% diseased, 50% healthy Children of diseased father - sons are healthy, all daughters are carriers Hemophilia A (defect of Factor VIII) Hemophilia B (defect of Factor IX) Muscle dystrophy (Duchen disease)

Inversion

Translocation

Deletion

Duplication

alternations in the number or structure of chromosomes autosomes or sex chromosomes studied by cytogenetics cell cycle arrested in metaphase (colchicin) - staining by Giemsa method (G-bands) - photographing - karyotype

sets of 23 chromosomes 22 pairs of autosomes, 2 sex chromosomes (XX or XY) cytogenetic disorders are relatively frequent! (1:160 newborns; 50% of spontaneous abortions)

Aneuploidy - One extra or one less chromosome

Nondisjunction: Aneuploidy: Monosomy Trisomy Polyploidy

euploidy - normal 46 (2n) polyploidy (3n or 4n) - spontaneous abortion Aneuploidy trisomy (2n+1)- 47- compatible with life monosomy (2n-1) - autosomal - incompatible with life - sex chromosomal - compatible with life

Down Syndrome - Trisomy 21

Age of Mother 30 35 36 37 38 39 40 45

Frequency of Down Syndrome 1 in 800 1 in 384 1 in 307 1 in 242 1 in 189 1 in 146 1 in 112 1 in 32

 Turner

Syndrome X0 Syndrome XXY

Klinefelters XYY

Condition

 Categories

of chromosome

aberration

Deletion
Duplication

Inversion
Translocation

breakage followed by loss or rearrangement deletion, translocation Generally: loss of chromosomal material is more dangerous than gain abnormalities of sex chromosomes are better tolerated than autosomal abnormalities of sex chromosomes sometimes symptomatic in adult age (e.g. infertility) usually origin de novo (both parents and siblings are normal)

Trisomy 21 (Down syndrome) most frequent - 1:700 births; parents have normal karyotype maternal age has a strong influence: <20 y. 1:1550 live births, >45 y. 1:25 live births most frequently is abnormality in ovum (ovum is under long-time influence of enviroment)

mental retardation (IQ 25-50) flat face + epicanthus congenital heart defects neck skin folds skeletal muscle hypotonia hypermobility of joints increased risk of acute leukemias mortality 40% until 10Y (cardiac complications)

Trisomy 18 (Edwards syndrome) 1:8000 Trisomy 13 (Patau syndrome) 1:15000

a number of karyotypes from 45(X0) to 49 (XXXXY) - compatible with survival normally - in females 1 of X is inactivated (all somatic cells contain Barr body) ! male phenotype is encoded by Y

1:1000 males additional X is either of paternal or maternal origin advanced maternal age, history of irradiation of either of parents wide range of clinical manifestations distinctive body habitus - increase length between soles and pubic bone reduced body and facial hair gynecomastia testicular atrophy - impaired spermatogenesis - sterility (rarely fertility! - mosaics)

 1:3000

females primary hypogonadism in phenotypic female growth retardation (short stature, webbing of the neck, low posterior hairline, broad chest, cubitus valgus) streak ovaries - infertility, amenorrhea, infantile genitalia, little pubic hair

amniocentesis - analysis of amniotic fluid cytogenetic analysis (karyotype - e.g. Down) biochemical activity of various enzymes (e.g. Tay-Sachs) analysis of various specific genes (CF gene - PCR) sex of the fetus (X-linked disorders hemophilia)

 infants

and children first year of life - high mortality highest mortality - neonatal period (first 4W; perinatal first 1W) between 1Y and 15Y of age - the leading cause of death = injuries from accidents

structural defects present at birth - some may become apparent later! etiology is either genetic or environmental viral infections (rubella, CMV) - during first 3M other infectious (toxoplasmosis, syphilis, HIV) drugs (thalidomide, alcohol, cytostatics) irradiation in 40-60% is the cause unknown!

 ascending

(transcervical) - in utero or during birth (HSV, HIV) transplacental - syphilis, toxoplasmosis, rubella, CMV

The earlier the abortion the more likely to be chromosomal 50% of spontanous abortion are chromosomal abnormal Mostly triploidy. 45 XO, trisomy 16 98% of fetus with turner abort Generally 6/1000 the incidence of chromosomal abnormalities

 Unexplained

infertility/ balanced translocation Multiple abortion >2 Prior case of defective baby

 Presence

of congenital anomalies 45% have minor single anomalies 9% 3 minor anomalies 1.5% HAVE major anomaly 2 or more major anomalies may represent genetic syndrome or chromosomal abnormalities(10%).

Incidence 1/700 2/3 of down fetus spontaneously abort Clinical diagnosis depend on gestalt Trisomy 21 in 94% of cases with extra chromosome from mother mostly(95%) Risk correlate with maternal age <25 y/o 1/1600 >40 y/0 1/80 2% are mosaic

 Hypotonia

without weakness Clinodactaly protruded tongue,small ears,brachycephaly,small up turned nose, depressed nasal bridge. Mental retardation, socially do better with good environment (Happy children)

 Cardiac

and GI Hypothyriodism Transient leukemoid reaction Alzheimers disease up to 25% over 40 y/o Early death relate to cardiac dysfunction

 Incidence

1/8000 Overlaps with trisomy 13 Sever Mental retardation >90% dead in 1st year

 Small

face with prominant occiput Small sternum and pelvis Flexion deformity of the finger VSD and horseshoe kidney

 Complete

extra set of chromosomes Mostly miscarriages Fetal wastage skeleton more than cephalic, 2% survive to be recognized Large hydatidiform placenta VSD, ASD, Syndactaly Genital and CNS abnormalities

Severe developmetal retardation Incidence 1/20000 90% dead in the 1st year

 Midline

brain defect Malformed ear Microophalmos and coloboma Scalp defect

Congenital abnormalities include severe mental retardation, seizures, microcephaly, scalp defects (absent skin), microphthalmia, cleft lip and/or palate, hypotelorism, simian crease, extra digits

Characterized by short stature and the lack of sexual development at puberty

 Most

common abnormality in early abortion Female, short stature, primary amenorrhea, sterility, spares hair and underdeveloped breast Neonatal: wide spaced nipple, lymphedema , shield chest, Coarctation of the aorta

 Normal

IQ scale with difficulty in spatial orientation such as map Present with short stature or delay sex maturation Hormonal therapy

 Mosaisim

(15%), remove gonads Recurrent risk is 1-2% Noonan syndrom AD, fresh mutation Pulmonary stenosis, nl stature, microceph, mental retardation

 20%

of aspermic adult male (blocked spermatogenesis 47 XXY in 80% and mosaic in 20% IQ is 98 (normal) with mild decrease in verbal IQ Scoliosis, decrease libido may improve with testesterone, gynecomastia

 Moderate

to severe mental retardation Speech delay, short attention, hyperactivity Poor motor coordination and mouthing objects Poor socialization, temper tantrum Mood disorder (bipolar), schizophrenia

 Long

protruding ears Long face and prominent jaw Flattened nasal bridge High arch palate Macroorchidism Genetic is complex, 80% penetration in male and 30% penetration in female

 Means:

as genomes pass through meiosis it is normal for part of it to change. During meiosis inactive X chromosome become active and changes on fragile X gene (imprinting) make it malignant

Severe mental retardation Inappropriate laughter Decrease pigmentation of choroid or iris (pale blue eyes) Ataxia and jerky eye movement Sever speech proplem Deletion of 15q11q13, maternal in origin Paternal uniparental disomy

(A fat red faced boy in state of somnolency) Charles Diickens Early hypotonia Obesity Short stature as adult Almond shaped blue eyes Mental retardation (mild to moderate) Narrow hands