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Download EXTENSIONS AND DEVIATIONS OF MENDELIAN INHERITANCE
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EXTENSIONS AND DEVIATIONS OF MENDELIAN INHERITANCE INTRODUCTION   In this lecture we will examine traits that deviate from the simple dominant/recessive relationship The inheritance patterns of these traits still obey Mendelian laws  However, they are more complex and interesting than Mendel had realized   Mendelian inheritance describes inheritance patterns that obey two laws  Law of segregation  Law of independent assortment Simple Mendelian inheritance involves  A single gene with two different alleles  Alleles display a simple dominant/recessive relationship Reminder Mendel’s First Law: Law of Segregation   Each individual has a pair of factors (alleles) for each trait The factors (alleles) segregate (separate) during gamete (sperm & egg) formation  Each gamete contains only one factor (allele) from each pair  Fertilization gives the offspring two factors for each trait Reminder Mendel’s Second Law: Law of Independent Assortment    The pair of factors for one trait segregate independently of the factors for other traits All possible combinations of factors can occur in the gametes But not all traits follow simple Mendelian inheritance Simple Mendelian: Alleles that obey Mendel’s laws, and follow a discrete dominant/recessive relationship X Linked: Inheritance of genes that are located on the X chromosome. In mammals and fruit flies, males are hemizygous for x-linked genes, while females have two copies Lethal alleles: An allele that has the potential for causing the death of an organism Incomplete dominance: Inheritance where heterozygotes have intermediate phenotypes e.g. production of pink flowers in crosses of plants with red and white flowers Codominance: Inheritance where heterozygotes express both alleles e.g. inheritance of ABO blood group in humans Overdominance: Inheritance where heterozygotes have traits that are more beneficial than homozygotes. e.g. sickle-cell trait Incomplete penetrance: Inheritance where dominant phenotype is not expressed even though an individual carries the dominant allele e.g. individuals that carry polydactyly allele but have normal number of fingers/toes Sex-influenced inheritance: Some alleles are dominant in one sex and recessive in the other e.g. baldness in humans Sex-limited inheritance: Traits that occur in only one of the sexes e.g. breast development in mammals   Prevalent alleles in a population are termed wild-type alleles  These typically encode proteins that  Function normally  Are made in the right amounts Reminder Alleles that have been altered by mutation are termed mutant alleles  These tend to be rare in natural populations  They are likely to cause a reduction in the amount or function of the encoded protein  Such mutant alleles are often inherited in a recessive fashion   Consider, for example, the traits that Mendel studied Wild-type (dominant) allele Mutant (recessive) allele Purple flowers White flowers Axial flowers Terminal flowers Yellow seeds Green seeds Round seeds Wrinkled seeds Smooth pods Constricted pods Green pods Yellow pods Tall plants plants Another example is from Drosophila Wild-type (dominant) allele Mutant (recessive) allele Red eyes White eyes Normal wings Miniature wings   Genetic diseases are caused by mutant alleles In many human genetic diseases , the recessive allele contains a mutation  This prevents the allele from producing a fully functional protein  e.g. Niemann-Pick Type C (NPC1)    Neurodegenerative lysosomal storage disorder Characterized by accumulation of cholesterol and other fatty acids in endosomes and lysosomes Defect in NPC1 gene  In a simple dominant/recessive relationship, the recessive allele does not affect the phenotype of the heterozygote   So how can the wild-type phenotype of the heterozygote be explained? There are two possible explanations   1. 50% of the normal protein is enough to accomplish the protein’s cellular function 2. The heterozygote may actually produce more than 50% of the functional protein  The normal gene is “up-regulated” to compensate for the lack of function of the defective allele 1. Lethal Alleles    Essential genes are those that are absolutely required for survival  The absence of their protein product leads to a lethal phenotype  It is estimated that about 1/3 of all genes are essential for survival Nonessential genes are those not absolutely required for survival A lethal allele is one that has the potential to cause the death of an organism  These alleles are typically the result of mutations in essential genes  They are usually inherited in a recessive manner    Many lethal alleles prevent cell division  These will kill an organism at an early age Some lethal allele exert their effect later in life  Huntington disease  Characterized by progressive degeneration of the nervous system, dementia and early death  The age of onset of the disease is usually between 30 to 50 Conditional lethal alleles may kill an organism only when certain environmental conditions prevail  Temperature-sensitive (ts) lethals  A developing Drosophila larva may be killed at 30 C  But it will survive if grown at 22 C    Semilethal alleles  Kill some individuals in a population, not all of them  Environmental factors and other genes may help prevent the detrimental effects of semilethal genes A lethal allele may produce ratios that seemingly deviate from Mendelian ratios An example is the “creeper” allele in chicken  Creepers have shortened legs and must creep along  Such birds also have shortened wings  Creeper chicken are heterozygous Creeper X Normal Creeper X Creeper 1 creeper : 1 normal 1 normal : 2 creeper Creeper is a dominant allele Creeper is lethal in the homozygous state 2. Incomplete Dominance   In incomplete dominance the heterozygote exhibits a phenotype that is intermediate between the corresponding homozygotes Example:  Flower color in the four o’clock plant  Two alleles R  C = wild-type allele for red flower color W = allele for white flower color  C 1:2:1 phenotypic ratio NOT the 3:1 ratio observed in simple Mendelian inheritance In this case, 50% of the CR protein is not sufficient to produce the red phenotype Incomplete Dominance   Whether a trait is dominant or incompletely dominant may depend on how closely the trait is examined Take, for example, the characteristic of pea shape  Mendel visually concluded that  RR and Rr genotypes produced round peas  rr genotypes produced wrinkled peas  However, a microscopic examination of round peas reveals that not all round peas are “created equal” 3. Multiple Alleles and Codominance   Many genes have multiple alleles  Three or more different alleles An interesting example is coat color in rabbits  Four different alleles  C (full coat color) ch (chinchilla pattern of coat color)  c  Partial defect in pigmentation h  c (himalayan pattern of coat color)  Pigmentation in only certain parts of the body  c (albino)  Lack of pigmentation  The dominance hierarchy is as follows: ch > ch > c  C > c    The ABO blood group provides another example of multiple alleles It is determined by the type of antigen present on the surface of red blood cells  Antigens are substances that are recognized by antibodies produced by the immune system there are three different types of antigens found on red blood A  Antigen A, which is controlled by allele I B  Antigen B, which is controlled by allele I  Antigen O, which is controlled by allele i   Allele i is recessive to both IA and IB Alleles IA and IB are codominant  They are both expressed in a heterozygous individual N-acetylgalactosamine B    The carbohydrate tree on the surface of RBCs is composed of three sugars A fourth can be added by the enzyme glycosyl transferase  The i allele encodes a defective enzyme  The carbohydrate tree is unchanged A  I encodes a form of the enzyme that can add the sugar Nacetylgalactosamine to the carbohydrate tree B  I encodes a form of the enzyme that can add the sugar galactose to the carbohydrate tree Thus, the A and B antigens are different enough to be recognized by different antibodies   For safe blood transfusions to occur, the donor’s blood must be an appropriate match with the recipient’s blood For example, if a type O individual received blood from a type A, type B or type AB blood  Antibodies in the recipient blood will react with antigens in the donated blood cells  This causes the donated blood to agglutinate  A life-threatening situation may result because of clogging of blood vessels 4. Overdominance   Overdominance is the phenomenon in which a heterozygote is more vigorous than both of the corresponding homozygotes  It is also called heterozygote advantage Example = Sickle-cell anemia  Autosomal recessive disorder  Affected individuals produce abnormal form of hemoglobin  Two alleles A Æ Encodes the normal hemoglobin, hemoglobin A  Hb S Æ Encodes the abnormal hemoglobin, hemoglobin S  Hb  HbSHbS individuals have red blood cells that deform into a sickle shape under conditions of low oxygen tension  This has two major ramifications  1. Sickling phenomenon greatly shortens the life span of the red blood cells  Anemia results  2. Odd-shaped cells clump  Partial or complete blocks in capillary circulation  Thus, affected individuals tend to have a shorter life span than unaffected ones    The sickle cell allele has been found at a fairly high frequency in parts of Africa where malaria is found  How come? Malaria is caused by a protozoan, Plasmodium  This parasite undergoes its life cycle in two main parts  One inside the Anopheles mosquito  The other inside red blood cells  Red blood cells of heterozygotes, are likely to rupture when infected by Pasmodium sp.  This prevents the propagation of the parasite Therefore, HbAHbS individuals are “better” than S S  Hb Hb , because they do not suffer from sickle cell anemia A A  Hb Hb , because they are more resistant to malaria    At the molecular level, overdominance is due to two alleles that produce slightly different proteins But how can these two protein variants produce a favorable phenotype in the heterozygote Well, there are three possible explanations for overdominance at the molecular/cellular level  1. Disease resistance  2. Homodimer formation  3. Variation in functional activity     Overdominance is related to a common mating strategy used by animal and plant breeders Two different highly inbred strains are crossed  The hybrids may display traits superior to both parents  This phenomenon is termed hybrid vigor or heterosis Heterosis is used to improve quantitative traits such as size, weight and growth rate Heterosis is different from overdominance, because it typically involves many genes  Nevertheless, its beneficial effects may be attributed to overdominance in one or more heterozygous genes 5. Incomplete Penetrance   In some instances, a dominant allele is not expressed in a heterozygote individual Example = Polydactyly  Autosomal dominant trait  Affected individuals have additional fingers and/or toes   A single copy of the polydactyly allele is usually sufficient to cause this condition In some cases, however, individuals carry the dominant allele but do not exhibit the trait Inherited the polydactyly allele from his mother and passed it on to a daughter and son Does not exhibit the trait himself even though he is a heterozygote Incomplete Penetrance    The term indicates that a dominant allele does not always “penetrate” into the phenotype of the individual The measure of penetrance is described at the population level  If 60% of heterozygotes carrying a dominant allele exhibit the trait allele, the trait is 60% penetrant Note:  In any particular individual, the trait is either penetrant or not Expressivity   Expressivity is the degree to which a trait is expressed In the case of polydactyly, the number of digits can vary  A person with several extra digits has high expressivity of this trait  A person with a single extra digit has low expressivity   The molecular explanation of expressivity and incomplete penetrance may not always be understood In most cases, the range of phenotypes is thought to be due to influences of the  Environment and/or  Other genes Environment   Environmental conditions may have a great impact on the phenotype of the individual Example 1  Snapdragon flower color vs. Temperature and degree of sunlight Environment  Example 2 = Phenylketonuria  Autosomal recessive disorder in humans  Caused by a defect in the gene that encodes the enzyme phenylalanine hydroxylase  Converts phenylalanine to tyrosine  Affected individuals cannot metabolize phenylalanine  Phenylalanine will thus accumulate  It ultimately causes a number of detrimental effects  Mental retardation, for example Environment  Example 2 = Phenylketonuria     Newborns are now routinely screened for PKU Individuals with the disease are put on a strict dietary regimen  Their diet is essentially phenylalanine-free These individuals tend to develop normally Thus the PKU test prevents a great deal of human suffering  Furthermore, it is cost-effective Sex and Traits   The inheritance pattern of certain traits is governed by the sex of the individual These traits are of two main types  Sex-influenced  Sex-limited 7. Sex-influenced Traits  Traits where an allele is dominant in one sex but recessive in the opposite sex  Thus, sex influence is a phenomenon of heterozygotes Sex-influenced Traits  Example: Pattern baldness in humans  Caused by an autosomal gene  Allele B behaves as dominant in males, but recessive in females Genotype Phenotype in Females Phenotype in Males BB bald bald Bb nonbald bald bb nonbald nonbald Sex-influenced Traits   Pattern baldness appears to be related to the level of male sex hormones In females, a rare tumor of the adrenal gland can cause the secretion of large amounts of male sex hormones  If this case a heterozygous Bb female will become bald  When the tumor is removed surgically, her hair returns to its normal condition  The autosomal nature of pattern baldness has been revealed by analysis of human pedigrees Bald fathers can pass the trait to their sons 8. Sex-limited Traits   Traits that occur in only one of the two sexes For example in humans  Breast development is normally limited to females  Beard growth is normally limited to males  Another example: Feather plumage in chicken  Caused by an autosomal gene  Hen-feathering is controlled by a dominant allele expressed in both sexes  Cock-feathering is controlled by a recessive allele only expressed in males Genotype Phenotype in Females Phenotype in Males hh hen-feathered cock-feathered Hh hen-feathered hen-feathered HH hen-feathered hen-feathered Sex-limited Traits   The pattern of hen-feathering depends on the production of sex hormones If the single ovary is surgically removed from a newly hatched hh female  She will develop cock-feathering and look indistinguishable from a male GENE INTERACTIONS   Gene interactions occur when two or more different genes influence the outcome of a single trait Indeed, morphological traits such as height weight and pigmentation are affected by many different genes in combination with environmental factors
 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
                                             
                                             
                                             
                                             
                                             
                                             
                                             
                                             
                                             
                                             
                                            