Exam 5: Sex Determination and Sex Chromosomes
Exam 1: Introduction to Genetics54 Questions
Exam 2: Mitosis and Meiosis45 Questions
Exam 3: Mendelian Genetics58 Questions
Exam 4: Modification of Mendelian Ratios60 Questions
Exam 5: Sex Determination and Sex Chromosomes50 Questions
Exam 6: Chromosome Mutations: Variation in Number and Arrangement48 Questions
Exam 7: Linkage and Chromosome Mapping in Eukaryotes39 Questions
Exam 8: Genetic Analysis and Mapping in Bacteria and Bacteriophages47 Questions
Exam 9: DNA structure and Analysis51 Questions
Exam 10: DNA Replication and Recombination50 Questions
Exam 11: Chromosome Structure and DNA Sequence Organization34 Questions
Exam 12: The Genetic Code and Transcription51 Questions
Exam 13: Translation and Proteins46 Questions
Exam 14: Gene Mutation,DNA Repair,and Transposition53 Questions
Exam 15: Regulation of Gene Expression69 Questions
Exam 16: The Genetics of Cancer48 Questions
Exam 17: Recombinant DNA Technology50 Questions
Exam 18: Genomics,Bioinformatics,and Proteomics44 Questions
Exam 19: Applications and Ethics of Genetic Engineering and Biotechnology37 Questions
Exam 20: Developmental Genetics39 Questions
Exam 21: Quantitative Genetics and Multifactorial Traits52 Questions
Exam 22: Population and Evolutionary Genetics58 Questions
Exam 23: Conservation Genetics35 Questions
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Give the sex of the following organisms assuming that the autosomes are present in the normal number.
Sex Chromosome Organism Complement Humans Drosophila XX --- --- XY --- --- XO --- --- XXX --- --- XXY --- ---
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Correct Answer:
Below is a pedigree of a fairly common human hereditary trait; the boxes represent males and the circles represent females.Filled-in symbols indicate the abnormal phenotype.Given that one gene pair is involved,
(a)Is the inheritance pattern X-linked or autosomal?
(b)Give the genotype of each individual in the pedigree.If more than one genotypic possibility exists,present all possible alternatives.

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Correct Answer:
(a)autosomal recessive
(b)
How many Barr bodies would one expect to see in cells of Turner syndrome females and Klinefelter syndrome males?
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(Short Answer)
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Correct Answer:
zero and one,respectively
One form of hemophilia is caused by a sex-linked recessive gene.Assume that a man with hemophilia marries a phenotypically normal woman whose father had hemophilia.What is the probability that they will have a daughter with hemophilia? (Note: In this problem,you must include the probability of having a daughter in your computation of the final probability.)
(Multiple Choice)
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What particular karyotype was once considered to be related to criminal predisposition?
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Give the sex-chromosome constitution (X and Y chromosomes)and possible genotypes of offspring resulting from a cross between a white-eyed female (Xw XwY)and a wild-type male (normal chromosome complement)in Drosophila melanogaster.Include all zygotic combinations whether viable or unviable.
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Studies done in the 1960s suggested that individuals with the XYY condition were prone to criminal behavior.What conclusions currently seem appropriate concerning this chromosomal condition?
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Normally in humans,all the sons of a male showing a sex-linked phenotype will inherit the trait.
(True/False)
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A cross is made between a female calico cat and a male cat having the gene for black fur on his X chromosome.What fraction of the offspring would one expect to be calico?
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In humans,the genetic basis for determining the sex "male" is accomplished by the presence of ________.
(Multiple Choice)
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Data produced by C.Bridges in the early part of this century indicate that sex in Drosophila is determined by ________.
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Describe an experiment in which transgenic mice were used to identify the male-determining region of the Y chromosome.
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A color-blind woman with Turner syndrome (XO)has a father who is color-blind.Given that the gene for the color-blind condition is recessive and X-linked,provide a likely explanation for the origin of the color-blind and cytogenetic conditions in the woman.
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How many chromosomes do Klinefelter and Turner syndromes have,respectively?
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An individual with Klinefelter syndrome generally has one Barr body.
(True/False)
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Klinefelter syndrome in humans,which leads to underdeveloped testes and sterility,is caused by which chromosomal condition?
(Multiple Choice)
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Glucose-6-phosphate dehydrogenase (G6PD)deficiency is inherited as an X-linked recessive gene in humans.A woman whose father suffered from G6PD marries a normal man.
(a)What proportion of their sons is expected to be G6PD?
(b)If the husband were not normal but were G6PD deficient,would you change your answer in part (a)?
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