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Beyond Mendel’s Laws of Inheritance
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Extending Mendelian genetics
Mendel worked with a simple system peas are genetically simple most traits are controlled by a single gene each gene has only 2 alleles, 1 of which is completely dominant to the other The relationship between genotype & phenotype is rarely that simple
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Incomplete dominance Heterozygote shows an intermediate, blended phenotype example: RR = red flowers rr = white flowers Rr = pink flowers make 50% less color RR WW RW RR RW WW
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It’s like flipping 2 pennies!
Incomplete dominance X P true-breeding red flowers true-breeding white flowers 100% 100% pink flowers F1 generation (hybrids) It’s like flipping 2 pennies! self-pollinate 25% white F2 generation 25% red 1:2:1 50% pink
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Co-dominance 2 alleles affect the phenotype equally & separately
not blended phenotype human ABO blood groups 3 alleles IA, IB, i IA & IB alleles are co-dominant glycoprotein antigens on RBC IAIB = both antigens are produced i allele recessive to both
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Genetics of Blood type A IA IA or IA i B IB IB or IB i AB IA IB O i i
pheno-type genotype antigen on RBC antibodies in blood donation status A IA IA or IA i type A antigens on surface of RBC anti-B antibodies __ B IB IB or IB i type B antigens on surface of RBC anti-A antibodies AB IA IB both type A & type B antigens on surface of RBC no antibodies universal recipient O i i no antigens on surface of RBC anti-A & anti-B antibodies universal donor
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Pleiotropy Most genes are pleiotropic
one gene affects more than one phenotypic character 1 gene affects more than 1 trait dwarfism (achondroplasia) gigantism (acromegaly) The genes that we have covered so far affect only one phenotypic character, but most genes are pleiotropic
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Achondroplasia is the most common.(3/4)
occurs in 1 of every 15,000 to 40,000 births. People with achondroplasia have an average-size torso (the upper body) but noticeably shorter arms and legs. Their heads are usually larger than average, with a prominent forehead. Their fingers are typically short. Adults with achondroplasia can develop a sway of the lower back, and some have bowed legs. The average height for an adult with achondroplasia is a little over 4 feet.
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Diastrophic dysplasia
Diastrophic dysplasia occurs in about 1 of every 100,000 births. People with diastrophic dwarfism have short calves and forearms and progressive curvature of the spine. They can have an inward- or downward-pointing foot (club foot) and differently positioned thumbs (sometimes called "hitchhiker thumbs"). Most diastrophic dwarfs have joint differences, severe curvature of the spine, can make it difficult for people with diastrophic dwarfism to walk, especially when they get older. Some people may need to use crutches, a scooter, or a wheelchair to get around.
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Acromegaly: André the Giant
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Acromegaly Acromegaly occurs in about 6 of every 100,000 adults. It is caused by abnormal production of growth hormone after the skeleton and other organs finish growing Body odor, Carpal tunnel syndrome, Decreased muscle strength (weakness) Easy fatigue, Excessive height (when excess growth hormone production begins in childhood) Excessive sweating, Headache, Joint pain Large bones of the face, Large feet, Large hands, Large glands in the skin (sebaceous glands) Large jaw (prognathism) and tongue, Limited joint movement Sleep apnea, Thickening of the skin, skin tags Widely spaced teeth, Widened fingers or toes due to too much skin growth, with swelling, redness, and pain
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Inheritance pattern of Achondroplasia
Aa x aa Aa x Aa dominant inheritance a a A a Aa Aa AA Aa A A dwarf dwarf lethal a aa aa a Aa aa 50% dwarf:50% normal or 1:1 67% dwarf:33% normal or 2:1
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How would you know that difference wasn’t random chance?
Epistasis One gene completely masks another gene coat color in mice = 2 separate genes C,c: pigment (C) or no pigment (c) B,b: more pigment (black=B) or less (brown=b) cc = albino, no matter B allele 9:3:3:1 becomes 9:3:4 B_C_ B_C_ bbC_ bbC_ _ _cc _ _cc How would you know that difference wasn’t random chance? Chi-square test!
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Epistasis in Labrador retrievers
2 genes: (E,e) & (B,b) pigment (E) or no pigment (e) pigment concentration: black (B) to brown (b) eebb eeB– E–bb E–B–
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Polygenic inheritance
Some phenotypes determined by additive effects of 2 or more genes on a single character phenotypes on a continuum human traits skin color height weight intelligence behaviors
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Johnny & Edgar Winter Skin color: Albinism However albinism can be inherited as a single gene trait aa = albino albino Africans melanin = universal brown color enzyme tyrosine albinism melanin
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OCA1 albino Bianca Knowlton
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Sex linked traits 1910 | 1933 Genes are on sex chromosomes
as opposed to autosomal chromosomes first discovered by T.H. Morgan at Columbia U. Drosophila breeding good genetic subject prolific 2 week generations 4 pairs of chromosomes XX=female, XY=male
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Classes of chromosomes
autosomal chromosomes sex chromosomes
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Discovery of sex linkage
true-breeding red-eye female true-breeding white-eye male X P Huh! Sex matters?! 100% red eye offspring F1 generation (hybrids) 100% red-eye female 50% red-eye male 50% white eye male F2 generation
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What’s up with Morgan’s flies?
x x RR rr Rr Rr r r R r R Rr Rr R RR Rr Doesn’t work that way! R Rr Rr r Rr rr 100% red eyes 3 red : 1 white
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Genetics of Sex X Y X XX XY X XX XY
In humans & other mammals, there are 2 sex chromosomes: X & Y 2 X chromosomes develop as a female: XX gene redundancy, like autosomal chromosomes an X & Y chromosome develop as a male: XY no redundancy X Y X XX XY X XX XY 50% female : 50% male
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Let’s reconsider Morgan’s flies…
x x XRXR XrY XRXr XRY Xr Y XR Y XR XR XRXr XRY XRXR XRY BINGO! XR Xr XRXr XRY XRXr XrY 100% red females 50% red males; 50% white males 100% red eyes
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Genes on sex chromosomes
Y chromosome few genes other than SRY sex-determining region master regulator for maleness turns on genes for production of male hormones many effects = pleiotropy! X chromosome other genes/traits beyond sex determination Mutations: Hemophelia , Duchenne muscular dystrophy, color-blindness Duchenne muscular dystrophy affects one in 3,500 males born in the United States. Affected individuals rarely live past their early 20s. This disorder is due to the absence of an X-linked gene for a key muscle protein, called dystrophin. The disease is characterized by a progressive weakening of the muscles and loss of coordination.
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Human X chromosome Sex-linked usually means “X-linked”
Duchenne muscular dystrophy Becker muscular dystrophy Ichthyosis, X-linked Placental steroid sulfatase deficiency Kallmann syndrome Chondrodysplasia punctata, X-linked recessive Hypophosphatemia Aicardi syndrome Hypomagnesemia, X-linked Ocular albinism Retinoschisis Adrenal hypoplasia Glycerol kinase deficiency Incontinentia pigmenti Wiskott-Aldrich syndrome Menkes syndrome Charcot-Marie-Tooth neuropathy Choroideremia Cleft palate, X-linked Spastic paraplegia, X-linked, uncomplicated Deafness with stapes fixation PRPS-related gout Lowe syndrome Lesch-Nyhan syndrome HPRT-related gout Hunter syndrome Hemophilia B Hemophilia A G6PD deficiency: favism Drug-sensitive anemia Chronic hemolytic anemia Manic-depressive illness, X-linked Colorblindness, (several forms) Dyskeratosis congenita TKCR syndrome Adrenoleukodystrophy Adrenomyeloneuropathy Emery-Dreifuss muscular dystrophy Diabetes insipidus, renal Myotubular myopathy, X-linked Androgen insensitivity Chronic granulomatous disease Retinitis pigmentosa-3 Norrie disease Retinitis pigmentosa-2 Sideroblastic anemia Aarskog-Scott syndrome PGK deficiency hemolytic anemia Anhidrotic ectodermal dysplasia Agammaglobulinemia Kennedy disease Pelizaeus-Merzbacher disease Alport syndrome Fabry disease Albinism-deafness syndrome Fragile-X syndrome Immunodeficiency, X-linked, with hyper IgM Lymphoproliferative syndrome Ornithine transcarbamylase deficiency Human X chromosome Sex-linked usually means “X-linked” more than 60 diseases traced to genes on X chromosome
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Map of Human Y chromosome?
< 30 genes on Y chromosome Sex-determining Region Y (SRY) linked Channel Flipping (FLP) Catching & Throwing (BLZ-1) Self confidence (BLZ-2) note: not linked to ability gene Devotion to sports (BUD-E) Addiction to death & destruction movies (SAW-2) Scratching (ITCH-E) Spitting (P2E) Inability to express affection over phone (ME-2) Selective hearing loss (HUH) Total lack of recall for dates (OOPS) Air guitar (RIF)
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Hemophilia is a sex-linked recessive trait defined by the absence of one or more clotting factors.
These proteins normally slow and then stop bleeding. Individuals with hemophilia have prolonged bleeding because a firm clot forms slowly. Bleeding in muscles and joints can be painful and lead to serious damage. Individuals can be treated with intravenous injections of the missing protein.
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Hemophilia XHXh XHY Hh x HH XH XHXh XH Y Xh XHXH XHXH XHY XHY XH Xh XH
sex-linked recessive Hemophilia XHXh XHY Hh x HH XH XHXh XH Y male / sperm Xh XHXH XHXH XHY XHY XH Xh female / eggs XH XHY XHXh XHXh XhY XhY Y carrier disease
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X-inactivation Female mammals inherit 2 X chromosomes XH XHXh Xh
one X becomes inactivated during embryonic development condenses into compact object = Barr body which X becomes Barr body is random patchwork trait = “mosaic” patches of black XH XHXh Xh tricolor cats can only be female patches of orange
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Male pattern baldness Sex influenced trait
autosomal trait influenced by sex hormones age effect as well = onset after 30 years old dominant in males & recessive in females B_ = bald in males; bb = bald in females
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Environmental effects
Phenotype is controlled by both environment & genes Human skin color is influenced by both genetics & environmental conditions Coat color in arctic fox influenced by heat sensitive alleles The relative importance of genes & the environment in influencing human characteristics is a very old & hotly contested debate a single tree has leaves that vary in size, shape & color, depending on exposure to wind & sun for humans, nutrition influences height, exercise alters build, sun-tanning darkens the skin, and experience improves performance on intelligence tests even identical twins — genetic equals — accumulate phenotypic differences as a result of their unique experiences Color of Hydrangea flowers is influenced by soil pH
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