Name:_______________________________Date:__________Period:_____________ NonMendelian Genetics Review – Smith 2015 Inc/ Co Dominant, Sex Determination, Sex Linkage, Nondisjunction, Pedigree, Karyotyping Some Punnett Squares are not completed due to the complexity of typing them. Sorry for any inconvenience. Write your answer in the numbered blanks. Word bank is for questions 1-14 Multiple Alleles Sex-linked (X) Somatic Beard Down’s Syndrome Autosomes 23 Colorblindness Hemophilia Mutation Blood 23 Drosophila (Trisomy 21) 1. somatic They are considered the “body cells”; any cells excluding sex cells. 2.46 or 23 Human cells have _____ or _____pair of chromosomes. 3.23 Human gametes have _______ chromosomes. 4.autosomes They are considered the “body chromosomes”; any pair of chromosomes excluding sex chromosomes. 5.sex-linked (X) A recessive trait carried on the X type of chromosome. 6.Drosophilia Scientific name of the fruit fly; see practice problems 7.mutation is a sudden genetic change. 8.non-disjunction is the abnormal segregation of chromosomes. 9.Down’s Syndrome (Trisomy 21) results in 3 X’s in 21st pair 10.multiple alleles having many alleles for one trait 11.Blood Type give an example for #10. 12.Colorblindness and Hemophilia 2 sex-linked diseases 13. Sex-Limited a characteristic where genes are present in both sexes but traits show up only in one sex. 14.beard, breast give 2 examples for #13. 46 Non-disjunction Sex limited Breasts Word bank for questions 15-25 Mother i (O) IA 100% Hemophilia Karyotype Y 50% IAIB IB 15._________ 100%_________ What % of offspring get a X chromosome? 16.____ Hemophilia ________ A sex-linked disease when blood does not clot properly. 17.___ IA ___, ___ IB _____ Name 2 dominant genes in blood. 18.______ IAIB ________ Name the blood type that shows codominance. 19._______ i (O) _________ Name the recessive blood allele. 20._____ Mother ______ A male inherits a sex-linked trait from which parent? 21.________ 50%_________ What % offspring get a Y chromosome from their father? 22._____________________ Symbol for male 23._________________ Symbol for female 24. _________ Y _________ The male sex chromosome is ____. 25.____ Karyotype ____ - an array of chromosomes found in an individual’s cells at metaphase of mitosis and arranged in homologous pairs and in order of diminishing size. -------------------------------------------------------------------------------------------------------(no word bank) 26. Name the 4 blood types and their respective genotypes. Phenotype/Genotype A – AA, AO B – BB, BO O - OO AB - AB Word Bank for questions 27-42. Hormones Polygenic Estrogen Banding pattern Smallest Pedigree Trisomy Non-disjunction gender carrier Monosomy environment roman largest testosterone chromosomes arabic size 27. polygenic traits develop from the interaction of multiple pairs of genes. Ex. skin color, eye color, height. Human skin color is thought to be controlled by 12 genes! 28. The environment influences many traits. Factors such as sunlight, temperature, and water can affect an organism’s phenotype. Ex. Siamese catcooler parts of the cat’s body , such as the ears, nose, feet and tail are darker. Heart disease can be inherited, but diet and exercise also strongly influence the disease. Sex-limited/Sex-influenced – Genes are present in both male and females, but show up only in one sex due to the presence of 29. hormones. The examples of this are a man’s beard, development of breasts and the plumage in birds. These occur because of the hormone 30.testosterone in males and 31. estrogen in females. Explain why the trait for hemophilia and colorblindness is rare in females? The traits for colorblindness and hemophilia are “X-linked” traits. The traits are only carried on the X chromosome. Males have only one X chromosome so their options are to either have the trait or not. Females have 2 X chromosomes so females have a second chance to mask the recessive trait. Nondisjunction During cell division, the chromosomes separate, with one of each of the sister chromatids going to opposite poles of the cell. Therefore, each new cell has the correct number of chromosomes. If sister chromatids fail to separate properly in cell division 32. Non-disjunction occurs If nondisjunction occurs during meiosis I or meiosis II, the resulting gametes will not have the correct number of33. chromosomes. When one of these gametes fertilizes another gamete, the resulting offspring will not have the correct number of chromosomes O Notice that nondisjunction can result in extra copies of a certain chromosome or only one copy of a particular chromosome in the offspring. O 34.Trisomy set of three chromosomes of one kind O 35.Monosomy only one of a particular type of chromosome Complete the punnett square by showing an example of non-disjunction in sex cells. This is one way genetic disorders can be passed to the offspring Nondisjunction in the female Nondisjunction in the male X Y x X X In the female, the X’s could stay together leaving some eggs with 2 X’s and some eggs with no sex chromosome (O) X Y x X X In the male, the X’s and Y’s could stay together leaving some sperm with XY and some sperm with no sex chromosome (O) XX O X XXX XO XY XXY XXY Y XXY OY O XO XO X X XO – Turner’s Syndrome (female), XXY – Klienfelter’s Syndrome (male), XXX – Super Female, OY – will not survive --------------------------------------------------------------------------------------------------------36. Scientists use a diagram called a pedigree to trace inheritance of trait through several generations. 37. An individual who has the gene but not the disease is called a carrier. Draw Symbols used in a pedigree. Refer to your pedigree worksheet/notes. _____- Normal female _____- Normal male _____- Female who expresses trait _____- Male who expresses trait _____- Female who is a carrier _____- Male who is a carrier _____- Marriage _____- Siblings 38. Roman numbers are used to represent generations 39. Arabic numbers are used to represent individuals in a certain generation I II III How many generations are represented in the pedigree?3 How many children do II5 and II6 have?3 What is the relationship between III5 and I2? Grandson and grandmother What is a Karyotype? (refer to notes, computer packet or cinch packet) A micrograph of whole chromosomes that allow scientists to view all 23 pair in a human cell 40. Scientists use size, banding pattern and centromere position as a guide in making a karyotype. 41. In a karyotype, chromosome are arranged and numbered from largest to smallest. 42. In a karyotype, the last pair of chromosomes determine gender (male or female.) Is this karyotype normal or abnormal?abnormal because there are 3 chromosome #21 and there should only be 2 of each chromosome. Why?This is Trisomy 21 or Down Syndrome Word Bank for questions 43-48 Identical Fraternal Multiple Alleles Klinefelter’s Blood Turners 43.Name the form of inheritance that is determined by more than two alleles. Multiple alleles 44.An example of such a trait is Blood Type. 45. Fraternal twins-these individuals arise from and develop from separate eggs fertilized by separate sperm. Can they be different genders?Yes 46. Identical twins- these individuals started as a single egg fertilized by one sperm. 47.Klinefelter’s – XXY syndrome- male with 47 chromosomes. An extra “X” is present 48.Turner’s – XO syndrome- female with 45 chromosomes Only one “X” chromosome is present 49.Who determines the sex (gender) of a child? MALE Show your work Sex-linked Problems 50.A father with hemophilia and a mother who is normal but is a carrier for hemophilia have children. The correct gene(s) for the father would be:Xh Y The correct genes for the mother would be: XHXh Out of four children, the expected number of girls with hemophilia would be: 1 out of 4 chance Out of the four children, the expected number of boys with hemophilia would be: 1 of 4 chance Out of the four children, how many boys and girls would be normal? 2 of 4 chance normal 51.A color-blind male and a normal non-carrier female have a child. Complete a punnett square. Write all results. Multiple allele problem: 52. The possible blood types of the offspring resulting when a heterozygous type A person is crossed with type 0. Complete a punnett square and write all results. 53. What is meant by incomplete dominance? Neither trait is dominant, incomplete dominance is seen as a “blend” or mixture and creates a third genotype that looks nothing like the parents 54. Red (r) is incompletely dominant to white (w) producing pink (rw) offspring. Show a cross between a red snapdragon flower and a pink snapdragon flower. Show all steps. 55. Define Codominance-Both traits are dominant, codominance is shown as spots or stripes typically, both dominant traits will be visible in the codominant organism 56. In chicken, black feather color(B) is codominant to white feather color (W). The heterozygous individual is a combination of black and white feathers that results in a checkered pattern (BW) called erminette. Cross a checkered chicken with a checkered chicken. Show all steps. What percentage of the offspring will be Black? 1 of 4 or 25% White? 1 of 4 or 25%