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Test your basic knowledge |
PCAT Biology Genetics
Start Test
Study First
Subjects
:
pcat
,
biology
Instructions:
Answer 50 questions in 15 minutes.
If you are not ready to take this test, you can
study here
.
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. Either the failure of homologous chromosomes to separate properly during meiosis I or the failure of sister chromatids to separate properly during meiosis II -zygote might either have 3 copies of that chromosome (trisomy) or just a single copy (monos
Backcross
Nondisjunction
Anticodon
Bacterial Genome
2. Structural component of ribsomes and is the most abundant of all RNA types -synthesized in the nucleolus
Binary fission
Ribosomes
Mendelian Genetics
Ribosomal RNA (rRNA)
3. Diagnostic tool to determine the genotype of an organism -Only with a recessive phenotype can genotype be predicted with 100% accuracy -if dominant phenotype is expressed - the genotype can be either homozygous dominant or heterozygous -used to deter
Mutations
Codons
Aminoacyl-tRNA synthetase
Testcross
4. Language of DNA consists of four letters: A -T -C -G -language of proteins consists of 20 'words': 20 amino acids -universal for almost all organism
Genetic Code
Mutagenic Agents
Plasmids
Phenotype
5. May occur spontaneously or be induced by environmental factors
Lyse
Chromosomal Breakage
Nucleotide
Mendelian Genetics
6. Double stranded DNA molecule unwinds and separates into two single strands
DNA Replication
Virulent
Inducible Systems
Chromosomal Breakage
7. Each strand of DNA that is a template in the synthesis of two new daughter helices
Plasmid
Aminoacyl-tRNA synthetase
Complementary Base-Pairing
Heterozygous
8. Sugar-phosphate chains on the outside of the helix and the bases on the inside -C-G - T-A -AKA Watson Crick DNA model
Double-Stranded Helix
Nondisjunction
Lysogenic Cycle
Translocation
9. New codon may code for a different amino acid
Triplet Code
Nonsense Mutation
Peptide Bond
Missense Mutation
10. Plasmids that are capable of integration into the bacterial genome
Episomes
Heterozygous
Anticodon
Okazaki fragments
11. Consists of a single circular chromosome located in the nucleoid region of the cell
Regulator Gene
Codons
Monohybrid Cross
Bacterial Genome
12. Daughter strand that is continuously synthesized by DNA polymerase in the 5'->3' direction
Peptide Bond
Translation
Leading Strand
Heterozygous
13. Organisms that carry two different alleles
Heterozygous
Messenger mRNA
Mendel's Second Law: Law of Independent Assortment
Non-Mendelian Inheritance Patterns
14. Genes on the same chromosome will stay together unless crossing over occurs -crossing over exchanges information between chromosomes and may break the linkage of certain patterns
15. Location of genes on DNA
Heredity
Mendelian Genetics
Chromosomes
Pyrimidines
16. Codes for the synthesis of a repressor molecule that binds to the operator and blocks RNA polymerase form transcribing the structural genes
Drosophila Melanogaster
Bacterial Replication
Nucleotide
Regulator Gene
17. Composed of two subunits (consisting of proteins and rRNA) - one large and one small - that bind together only during protein synthesis -have 3 binding sites (for mRNA and two tRNA)
Virulent
DNA Replication
Ribosomes
Peptide Bond
18. Occurs when linked genes are separated
Recombination
DNA
Lagging Strand
Codominance
19. Degeneracy/redundancy of the genetic code since there are 64 different codons and only 20 amino acids
Recombination
Transfer RNA (tRNA)
Synonyms
Gene
20. Genetic makeup of an individual
Codominance
Codons
Operon
Genotype
21. Cell burst
Lyse
Genetic Code
Lysogenic Cycle
Autosomes
22. Progeny phenotypes are apparently blends of the parental phenotypes
Genotype
Testcross
Incomplete Dominance
Phenotype
23. Each new daughter helix contains an intact strand from the parent helix and a newly synthesized strand
Semiconservative
P-site
Mutable
Dihybrid Cross
24. The process by which a foreign plasmid is incorporated into the bacterial chromosome via recombination - creating new inheritable genetic combinations
Transformation
Mendel's First Law: Law of Segregation (Four Principles)
Plasmids
tRNA Job
25. System where the repressor binds to the operator - forming a barrier that prevents RNA polymerase from transcribing the structural genes
Silent Mutation
Filial (F generations)
Mendel's First Law: Law of Segregation (Four Principles)
Inducible Systems
26. Small circular rings of DNA which contain accessory genes
Pyrimidines
Genetics
Termination Codons
Plasmids
27. Silent allele -usually assigned capital letters
Mendel's Law of Dominance
Recessive Allele
Missense Mutation
Peptide Bond
28. Adenine and guanine
Episomes
Purines
Mutable
Virulent
29. Recessive genes that are carried on the X chromosome will produce the recessive phenotypes whenever they occur in men because no dominant allele is present to mask them -ex: hemophilia and color blindness
Testcross
Dihybrid Cross
Lyse
Sex Linked Recessives
30. (UAA - UAG - or UGA) terminates polypeptide synthesis
Translocation
Operator Gene
Sex Linked
Termination Codons
31. System where the repressor is inactive until it combines with the corepressor
Repressible Systems
Elongation
Ribosomes
Sex Linked Recessives
32. Nucleic acid is replaced by another nucleic acid
Point Mutation
Monocistronic
DNA Replication
Lysogenic Cycle
33. Progeny generations
Filial (F generations)
Phenotype
Lyse
Leading Strand
34. True-breeding individuals (which - if self-crossed - produce progeny only with the parental phenotype) with different traits - mated them - and statistically analyzed the inheritance of the traits in the progeny
Crosses
Chromosomal Breakage
Episomes
RNA
35. Process whereby mRNA codons are translated intoa sequence of amino acids -occurs in cytoplasm and involves tRNA - ribosomes - mRNA - amino acids - enzymes - and other proteins
Crosses
Translation
Purines
Peptide Bond
36. The parents differ in two traits - as long as the genes are on separate chromosomes and assort independently during meiosis
Dihybrid Cross
Bacterial Replication
Polypeptide Synthesis
Recessive Allele
37. On amino acid which has an active site that binds to both the amino acid and its corresponding tRNA - ctalyzing their attachment to form an aminoacyl-tRNA complex
Translocation
Lysogenic Cycle
Aminoacyl-tRNA synthetase
Mutagenic Agents
38. Basic unit of heredity
Inducible Systems
Ribosomes
Silent Mutation
Gene
39. Virus that infcts its host bacterium by attaching to it - boring a hole through the bacterial cell wall - and injecting its DNA while its protein coat remains attached to the cell wall and enters the host in either a lytic cycle or a lysogenic cycle
Bacteriophage
Operon
Mendelian Genetics
Regulator Gene
40. May infect other bacteria and introduce new genetic arrangements through recombination with the new host cell's DNA
Varions
Nonsense Mutation
Antibody resistance
Ribosomes
41. Dominant allele is expressed in the phenotype
42. Changes in the genetic information of a cell coded in the DNA -if occured in the somatic cells - it can lead to tumors in an individual
Transcription
Sex Linked Recessives
Mutations
Parental (P Generation)
43. Self replication ensures that its coded sequence will be passed on to successive generations
Chromosomal Breakage
Heredity
Recessive Allele
Parental (P Generation)
44. Genes that are located on the X or Y chromosome -in humans - most are located on the X
Mendel's Law of Dominance
Sex Linked
Peptide Bond
Triplet Code
45. One way of predicting the genotypes expected form a cross -genotypes are determined by looking at the intersections of the grid -indicates all potential progeny genotypes and the relative frequencies of the different genotypes and phenotypes can be e
Incomplete Dominance
Lytic Cycle
Recombination
Punnet Square Diagram
46. Nitrogen bases are added - deleted - or substituted - thus crating different genes; inappropriate amino acids may be inserted into polypeptide chains - and a mutated protein may be produced
Ribosomes
Mendelian Genetics
Gene Mutation
Inducer-Repressor Complex
47. Where protein synthesis occurs
Regulator Gene
Ribosomes
Anticodon
Chromosomes
48. Ribonucleic acid -polynucleotide structurally similar to DNA except that its sugar is ribose -contains uracil instead of thymine -usually single stranded -found in both nucleus and cytoplasm -several types are involved with mRNA - tRNA - and rRNA
Incomplete Dominance
Monohybrid Cross
RNA
Chromosomes
49. Deoxyribonucleic acid -contains information coded in the sequence of its base pairs - provding the cell with a blueprint for protein synthesis -regulate all life functions -has the ability to self replicate -basis of heredity -mutable
Regulator Gene
DNA
Semiconservative
Frameshift Mutation
50. (AUG) ribosome scans the mRNA until it bonds to this (methionine) and UAC on anticodon of tRNA
Triplet Code
Translation
Start Codon
Semiconservative