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Test your basic knowledge |
GRE Chromosomal And Molecular Basis Of Inheritance
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Subjects
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gre
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science
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biology
Instructions:
Answer 50 questions in 15 minutes.
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study here
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Match each statement with the correct term.
Don't refresh. All questions and answers are randomly picked and ordered every time you load a test.
This is a study tool. The 3 wrong answers for each question are randomly chosen from answers to other questions. So, you might find at times the answers obvious, but you will see it re-enforces your understanding as you take the test each time.
1. Offspring that inherit a phenotype that matches one of the parental phenotypes.
DNA Ligase
Cytogenetic Maps
Parental Types
4 Type of Changes in Chromosome Structure as a Result of Chromosome Breakage
2. A gene located on either sex chromosome. In humans - the term has historically referred specifically to a gene on the X chromosome so fathers pass sex-linked alleles to all of their daughters and none of their sons while mothers can pass sex-linked a
Sex-Linked Gene
Chronic Myelogenous Leukemia (CML)
Law of Segregation
Nondisjunction
3. An enzyme that joins the sugar-phosphate backbones of the Okazaki fragments - forming a single new DNA strand.
Sex-Linked Gene
Wild Type
DNA Ligase
Replication Fork
4. Helps relieve strain from the DNA double helix when helicase untwists it at the replication forks - causing tighter twisting ahead of the forks.
Signal-strand Binding Protein
Helicase
Topoisomerase
Leading Strand
5. A result of nondisjuction of sex chromosomes. Do not exhibit any well-defined syndrome but tend to be somewhat taller than average.
Trisomic
Males with XYY
Monosomic
Aneuploidy
6. The process that accounts for the recombination of linked genes. Occurs while replicated homologous chromosomes are pair during prophase of meiosis I - one maternal chromatid and one paternal chromatid break at corresponding points and then are rejoi
Crossing Over
Helicase
Leading Strand
Farther apart
7. A change in genotype and phenotype due to the assimilation of external DNA by a cell.
Transformation
Chromosome Theory of Inheritance
Extranuclear Genes
Process of DNA Polymerase Adding a Nucleotide
8. A method that maps chromosomes and locates genes with respect to chromosomal features - such as stained bands - that can be seen in the microscope. Ultimately show the physical distances between gene loci in DNA nucleotides.
Origins of Replication
Conservative Model of DNA Replication
Cytogenetic Maps
Insulin-like Growth Factor 2 (Igf2)
9. Special site on a DNA molecule which replication begins. Indicated by a specific sequence of nucleotides.
Origins of Replication
4 Type of Changes in Chromosome Structure as a Result of Chromosome Breakage
Telomerase
Topoisomerase
10. Each nucleotide added to a growing DNA strand is a nucleoside triphosphate - which is a sugar and a base with three phosphate groups. The triphosphate monomers used are chemically reactive - partly because their triphosphate tails have an unstable cl
Wild Type
Law of Segregation
Process of DNA Polymerase Adding a Nucleotide
'The DNA Replication Machine'
11. An aneuploid condition. Usually the result of an extra chromosome 21 so that each body cell has a total of 47 chromosomes. Also termed trisomy 21. Includes characteristic facial feature - short stature - heart defects - susceptibility to respiratory
The Z-W System
Topoisomerase
DNA Structure
Down Syndrome
12. An enzyme that can start an RNA chain from scratch. Joins RNA nucleotides together one at a time - making a primer complimentary to the template strand at the location where initiation of the new DNA strand will occur.
'The DNA Replication Machine'
Aneuploidy
Dispersive Model of DNA Replication
Primase
13. A type of change in chromosome structure as a result of some sort of chromosomal breakage. Occurs when a segment within a chromosome reverses.
Inversion
Down Syndrome
Chronic Myelogenous Leukemia (CML)
The Haplo-diploid System
14. A chromosome is present in triplicate in an aneuploid cell.
Trisomic
Lagging Strand
Males with XYY
Polyploidy
15. Phenotypically female but are sterile because their sex organs do not mature. When provided with estrogen replacement therapy - girls with Turners develop secondary sex characteristics.
Bacteriophages
Mutant Phenotypes
Law of Independent Assortment
Monosomy X (XO)
16. A occasional mishap that may occur during meiosis in which the members of a pair of chromosomes do not move apart properly during meiosis I or sister chromatids fail to separate during meiosis II.
'The DNA Replication Machine'
The X-O System
Nondisjunction
The Haplo-diploid System
17. A type of change in chromosome structure as a result of some sort of chromosomal breakage. Occurs when a chromosomal fragment breaks and joins a nonhomologous chromosome.
Translocation
DNA Structure
Hemophilia
Bacteriophages
18. The short initial nucleotide chain put in place before DNA polymerase begins synthesizing in the 5' to 3' direction. May consist of either DNA or RNA. In initiating the replication of cellular DNA - the primer is a short stretch of RNA with an availa
Lagging Strand
Nuclease
Sex-Linked Gene
Primer
19. 1. deletion 2. duplication 3. inversion 4. translocation
The Z-W System
4 Type of Changes in Chromosome Structure as a Result of Chromosome Breakage
Klinefelter Syndrome
Deletion
20. A result of nondisjuction of sex chromosomes. In this case - it is the result of an extra X chromosome in a male - producting XXY. People have male sex organs - but the testes are abnormally small and the man is sterile. Some breast enlargement and o
Nitrogenous Bases of DNA
Klinefelter Syndrome
Turner Syndrome
Monosomy X (XO)
21. According to this theory - Mendelian genes have specific loci (positions) on chromosomes - and it is the chromosomes that undergo segregation and independent assortment.
Farther apart
Klinefelter Syndrome
SRY
Chromosome Theory of Inheritance
22. A cancer implicated by chromosomal translocations. The exchange of a larger portion of chromosome 22 with a small fragment from a tip of chromosome 9 produces a much shorted - easily recognized chromosome 22 - called the Philadelphia chromosome. Affe
SRY
Process of DNA Polymerase Adding a Nucleotide
Genetic Map
Chronic Myelogenous Leukemia (CML)
23. The system for determining sex in most species of bees and ants. There are no sex chromosomes in these species - Females develop from fertilized ova and are thus diploid. Males - however - develop from unfertilized ova and are haploid; they have no f
Cytogenetic Maps
Monosomic
The Haplo-diploid System
Nuclease
24. A genetic map based on recombination frequencies.
Okazaki Fragments
Linkage Map
Nitrogenous Bases of DNA
Cri du Chat
25. The system for determining sex in birds - some fishes - and some insects. The sex chromosome present in the ovum determines the sex of offspring. The sex chromosomes are designated Z and W. Females are ZW and males are ZZ.
Leading Strand
DNA Ligase
The Z-W System
Wild Type
26. The segments of the lagging strand that get added to the template strand. The segments get joined together by DNA ligase.
Okazaki Fragments
Translocation
The X-Y System
Sex-Linked Gene
27. A human sex-linked disorder. A disease characterized by progressive weakening of the muscles and loss of coordination. Affected individuals rarely live past their early 20s. A result of the absence of a key muscle protein called dystrophin.
DNA Structure
Law of Segregation
Nitrogenous Bases of DNA
Duchenne Muscular Dystrophy
28. Traits that depend on which parent passed along the alleles for those traits. An exception to the display of Mendelian inheritance.
Klinefelter Syndrome
DNA Excision Repair
Translocation
Genomic Imprinting
29. Nucleotide sequences found in eukaryotic chromosomal DNA that make up for the fact that DNA polymerases cannot replicate the ends of DNA strands since there is no 3' end there. Do not contain genes but rather the DNA has multiple repetitions of one s
Chromosome Theory of Inheritance
Wild Type
Down Syndrome
Telomeres
30. Or phages. Viruses that infect bacteria.
Helicase
Bacteriophages
Aneuploidy
Farther apart
31. Traits that are alternatives to the wild type because they are due to alleles assumed to have arisen as changes - or mutations - in the wild-type allele.
Mutant Phenotypes
Genetic Map
The X-Y System
Duchenne Muscular Dystrophy
32. Y-shaped region at the end of a replication bubble where the new strands of DNA are elongating.
Parental Types
Primer
Females with XXX
Replication Fork
33. Disorder caused by structurally altered chromosomes - specifically a deletion in chromosome 5. A child born with this deletion is mentally retarded - has a small head with unusual facial features - and has a cry that sounds like the mewing of a cat.
Polyploidy
Parental Types
Cri du Chat
Helicase
34. A result of nondisjuction of sex chromosomes. Females are healthy and cannot be distinguished phenotypically from other females.
Law of Segregation
Females with XXX
Wild Type
Mutant Phenotypes
35. The system for determining sex in grasshoppers - cockroaches - and some other insects. In these insects - there is only one type of chromosome - the X. Females are XX and males are XO. Sex of the offspring is determined by whether the sperm cell cont
The X-O System
Duplication
Chromosome Theory of Inheritance
Recombinant Types (or Recombinants)
36. The ___________ two genes are - the higher the probability that a crossover will occur between them and therefore the higher the recombination frequency. This process can occasionally break the physical connection between genes on the same chromosome
Nuclease
Farther apart
Helicase
Down Syndrome
37. Helps in repairing and proofreading DNA. An enzyme that cuts out a segment of the strand of DNA containing damage - creating a gap which is filled in with nucleotides properly paired with the nucleotides in the undamaged strand by DNA polymerase and
DNA Excision Repair
Farther apart
Nuclease
Process of DNA Polymerase Adding a Nucleotide
38. A type of change in chromosome structure as a result of some sort of chromosomal breakage. Occurs when a chromosomal fragment lacking a centromere is lost. The affected chromosome is then missing certain genes.
Linked Genes
Law of Independent Assortment
The X-Y System
Deletion
39. Occurs when a mismatched nucleotide evades proofreading by DNA polymerase or arise after DNA synthesis is completed.
Topoisomerase
Deletion
Turner Syndrome
Mismatch Repair
40. An enzyme that catalyzes the lengthening of telomeres in eukaryotic germ cells - thus restoring their original length and compensating for the shortening that occurs during DNA replication. Made possible by the presence in the telomerase of a short
Recombinant Types (or Recombinants)
Semiconservative Model of DNA Replication
Telomeres
Telomerase
41. A chromosome is missing in a aneuploid cell.
Topoisomerase
Nitrogenous Bases of DNA
Telomerase
Monosomic
42. A type of change in chromosome structure as a result of some sort of chromosomal breakage. Occurs when a chromosomal fragment repeats a segment. In some cases - if meiosis is in progress - a deleted fragment may become as an extra segment to a sister
The Haplo-diploid System
Duplication
Monosomy X (XO)
Conservative Model of DNA Replication
43. The two alleles for each gene separate during gamete formation.
Primase
Turner Syndrome
Females with XXX
Law of Segregation
44. Each nucleotide (monomer) consists of a hydrophobic nitrogenous base (T - A - C - or G) - the sugar dioxyribose - and a phosphate group. The phosphate of one nucleotide is attached to the sugar of the next - making up the 'backbone' of alternating ph
Farther apart
DNA Structure
Mismatch Repair
Mutant Phenotypes
45. A sex-linked recessive disorder. Defined by the absence of one or more of the proteins required for blood clotting. When injured - people with this disease have prolonged bleeding because a firm clot is slow to form. Patients receive intravenous inje
Linked Genes
Hemophilia
Nitrogenous Bases of DNA
Genetic Map
46. A molecule that binds unpaired DNA strands - after its been separated by helicase - and stabilizes them until they serve as templates for the synthesis of new complementary strands.
Turner Syndrome
Signal-strand Binding Protein
Law of Independent Assortment
Primase
47. The sex-determining region of Y. The gene on the Y chromosome required for the development of testes. In the absence of SRY - the gonads develop into ovaries. SRY is simply the trigger and other genes on the Y chromosome are required for normal testi
Conservative Model of DNA Replication
The X-Y System
Replication Fork
SRY
48. Offspring that have new combinations of their parent'S phenotypes. When 50% of offspring are recombinants - geneticists say that there is a 50% frequency of recombination and is observed for any two genes that are located on different chromosomes.
Genomic Imprinting
Extranuclear Genes
Parental Types
Recombinant Types (or Recombinants)
49. The various proteins that participate in DNA replication actually form a single large complex since many of the protein-protein interactions actually facilitate the efficiency of the machine as a whole.
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50. Can be distinguished from Watson and Crick'S semiconservative model in which the parent molecule somehow re-forms after the process of replication. Proved incorrect and support came out for the semiconservative model.
Semiconservative Model of DNA Replication
Telomerase
The X-O System
Conservative Model of DNA Replication