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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. Bacteriophages that replicate by the lytic cycle - killing their host cells
Genetics
Ribosomes
Virulent
Transcription
2. Binds to the incoming aminoacyl-tRNA complex (Arriving site)
Missense Mutation
A-site
Antibody resistance
Binary fission
3. Pairs of homologues in sexually differentiated species
Messenger mRNA
Mendelian Genetics
Heterozygous
Autosomes
4. New codon may code for a different amino acid
Monocistronic
Ribosomes
Missense Mutation
Autosomes
5. 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
Polypeptide Synthesis
Double-Stranded Helix
Mutations
Nucleotide
6. Dominant allele is expressed in the phenotype
7. Formed between the amino acid attached to the tRNA in the A site and the fmet attached to the tRNA in the P site
Peptide Bond
Operon
DNA Replication
Codons
8. 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)
Monohybrid Cross
Silent Mutation
Monocistronic
Ribosomes
9. Basic unit of DNA - which is composed of deoxyribose (a sugar) bonded to both a phosphate group and a nitrogenous base -bases: purines and pyrimidines
Dihybrid Cross
Double-Stranded Helix
Inducible Systems
Nucleotide
10. Include incomplete dominance - and codominance
Triplet Code
Plasmid
Dihybrid Cross
Non-Mendelian Inheritance Patterns
11. New codon may be a stop codon
Environmental Factors
Nonsense Mutation
Mendel's Law of Dominance
Lyse
12. Base sequence of mRNA is translated as a series of triplets
Mutagenic Agents
Backcross
Homozygous
Codons
13. Consists of a single circular chromosome located in the nucleoid region of the cell
Bacterial Genome
Codons
Lysogenic Cycle
Inducer-Repressor Complex
14. 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
DNA Replication
Gene
Sex Linked Recessives
Promoter gene
15. One mRNA strand codes for one polypeptide
Start Codon
Monocistronic
Genetic Code
Inducible Systems
16. Small circular rings of DNA which contain accessory genes
Plasmids
Gene Mutation
Autosomes
Transcription
17. 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
Binary fission
Heterozygous
Aminoacyl-tRNA synthetase
Dominant Allele
18. 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
19. Transfer of genetic material between two bacteria that re temporarily joined
Antibody resistance
P-site
Conjugation
Synonyms
20. Short segments from lagging strand
P-site
Translocation
Incomplete Dominance
Okazaki fragments
21. Self replication ensures that its coded sequence will be passed on to successive generations
Double-Stranded Helix
Non-Mendelian Inheritance Patterns
Heredity
Peptide Bond
22. The sequence of nontranscribable DNA that is the repressor binding site
Heredity
Operator Gene
Antibody resistance
Lyse
23. Double stranded DNA molecule unwinds and separates into two single strands
Mendel's Law of Dominance
Nonsense Mutation
Semiconservative
DNA Replication
24. Small RNA found in the ctyoplasm that aids in the translation of mRNA's nucleotide code into a sequence of amino acids -brings amino acids to the ribosomes during protein synthesis
Pyrimidines
Transfer RNA (tRNA)
Chromosomal Breakage
Nonsense Mutation
25. 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
Transcription
Translation
Filial (F generations)
Dominant Allele
26. Consists of structural genes
Operon
Translocation
DNA Replication
Lytic Cycle
27. Progeny phenotypes are apparently blends of the parental phenotypes
Conjugation
Incomplete Dominance
Silent Mutation
Anticodon
28. Genes that are located on the X or Y chromosome -in humans - most are located on the X
Nucleotide
Virulent
Sex Linked
Non-Mendelian Inheritance Patterns
29. The noncoding sequence of DNA that serves as the initial binding site for RNA polymerase
Dihybrid Cross
Polypeptide Synthesis
Translocation
Promoter gene
30. Brings amino acids to the ribosomes in the correct sequence for polypeptide synthesis -recognizes both the amino acid and the mRNA codon
Operon
tRNA Job
Gene Mutation
Episomes
31. Induce mutations -include cosmic rays - X rays - UV rays - and radioactivity
Mutagenic Agents
Termination Codons
Mendel's Second Law: Law of Independent Assortment
Genetics
32. May occur spontaneously or be induced by environmental factors
Transformation
Non-Mendelian Inheritance Patterns
Chromosomal Breakage
Triplet Code
33. Can be altered under certain conditions - altering the corresponding characteristics in the organism
Mutable
Transduction
Messenger mRNA
Leading Strand
34. New codon may code for the same amino acid
Crosses
Start Codon
Homozygous
Silent Mutation
35. Expressed allele -usually assigned capital letters
Sex Linked Recessives
Double-Stranded Helix
Dominant Allele
Recombination
36. 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
Non-Mendelian Inheritance Patterns
Gene Mutation
Synonyms
Mutagenic Agents
37. Complex that can't bind to the operator - thus permitting transcription
Chromosomes
Inducer-Repressor Complex
Nondisjunction
Transcription
38. Adenine and guanine
Start Codon
tRNA Job
Phenotype
Purines
39. DNA language must be translated by mRNA in such a way as to produce the 20 words in the amino acid language
Point Mutation
Episomes
Regulator Gene
Triplet Code
40. Genetic makeup of an individual
DNA Replication
Sex Linked
Genotype
Gene Mutation
41. Alternative forms of genes when it exists in more than one form
Okazaki fragments
Alleles
Double-Stranded Helix
Elongation
42. Cell burst
Leading Strand
Bacteriophage
Lyse
Monocistronic
43. System where the repressor is inactive until it combines with the corepressor
Transcription
Repressible Systems
Polypeptide Synthesis
Bacterial Replication
44. Plasmids that are capable of integration into the bacterial genome
Bacteriophage
Peptide Bond
Episomes
Testcross
45. Developed the basic principles of genetics through his experiments with the garden pea
Mendelian Genetics
Heredity
Okazaki fragments
Ribosomal RNA (rRNA)
46. System where the repressor binds to the operator - forming a barrier that prevents RNA polymerase from transcribing the structural genes
Sex Linked
Inducible Systems
Translation
Mendelian Genetics
47. 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
Testcross
Mutable
Antibody resistance
Parental (P Generation)
48. Degeneracy/redundancy of the genetic code since there are 64 different codons and only 20 amino acids
Monocistronic
Synonyms
Polypeptide Synthesis
Ribosomal RNA (rRNA)
49. (AUG) ribosome scans the mRNA until it bonds to this (methionine) and UAC on anticodon of tRNA
Start Codon
Sex Linked
Nucleotide
Testcross
50. 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
Lyse
Leading Strand
Nondisjunction
Transfer RNA (tRNA)