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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. Silent allele -usually assigned capital letters
Punnet Square Diagram
Plasmids
Homozygous
Recessive Allele
2. Basic unit of heredity
Gene
Mendelian Genetics
Monocistronic
Frameshift Mutation
3. Genetic makeup of an individual
Sex Linked
Genotype
Repressible Systems
Conjugation
4. TRNA binding site for ribosomes to attach to the growing polypeptide chain (peace out site)
Monohybrid Cross
Mutagenic Agents
Anticodon
P-site
5. 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
Dominant Allele
Chromosomal Breakage
Sex Linked Recessives
Transfer RNA (tRNA)
6. 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
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7. 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
Plasmid
Peptide Bond
Operon
Bacteriophage
8. May infect other bacteria and introduce new genetic arrangements through recombination with the new host cell's DNA
Lysogenic Cycle
Varions
Lagging Strand
Transduction
9. Location of genes on DNA
Nucleotide
Antibody resistance
Start Codon
Chromosomes
10. Regulation of gene expression and enables prokaryotes to control their metabolism
Peptide Bond
Transcription
Regulator Gene
Lysogenic Cycle
11. Structural component of ribsomes and is the most abundant of all RNA types -synthesized in the nucleolus
Dihybrid Cross
Ribosomal RNA (rRNA)
Anticodon
Recombination
12. Degeneracy/redundancy of the genetic code since there are 64 different codons and only 20 amino acids
RNA
Synonyms
Environmental Factors
Regulator Gene
13. Include incomplete dominance - and codominance
Okazaki fragments
Start Codon
Backcross
Non-Mendelian Inheritance Patterns
14. New codon may be a stop codon
Bacterial Genome
Nonsense Mutation
Mendel's First Law: Law of Segregation (Four Principles)
Promoter gene
15. Complex that can't bind to the operator - thus permitting transcription
Crosses
Triplet Code
Genetics
Inducer-Repressor Complex
16. The sequence of nontranscribable DNA that is the repressor binding site
Operator Gene
Homozygous
Lytic Cycle
Plasmid
17. Daughter strand that is continuously synthesized by DNA polymerase in the 5'->3' direction
Leading Strand
Plasmid
Environmental Factors
Mendel's Second Law: Law of Independent Assortment
18. Cell burst
Ribosomal RNA (rRNA)
Non-Mendelian Inheritance Patterns
Lyse
Anticodon
19. Each new daughter helix contains an intact strand from the parent helix and a newly synthesized strand
Gene Mutation
Repressible Systems
Semiconservative
Heterozygous
20. Complementary to one of the mRNA codons
DNA
Anticodon
Purines
Promoter gene
21. The process whereby information coded in the base sequence of DNA is transcribed into a strand of mRNA that leaves the nucleus through nuclear pores. the remaining events of protein synthesis occur in the cytoplasm
Codons
Termination Codons
Plasmids
Transcription
22. 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)
Frameshift Mutation
Ribosomes
RNA
Purines
23. 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
Peptide Bond
Gene Mutation
Mendel's Second Law: Law of Independent Assortment
Leading Strand
24. Hydrogen bonds form between the mRNA codon in the A site and its complementary anticodon on the incoming aminoacyl-tRNA complex
Elongation
Double-Stranded Helix
Heterozygous
Plasmids
25. 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
Inducible Systems
Punnet Square Diagram
Gene Mutation
Chromosomes
26. Chromosome fragment
Heterozygous
Dihybrid Cross
Plasmid
Pyrimidines
27. Each strand of DNA that is a template in the synthesis of two new daughter helices
Frameshift Mutation
Heterozygous
Inducible Systems
Complementary Base-Pairing
28. (AUG) ribosome scans the mRNA until it bonds to this (methionine) and UAC on anticodon of tRNA
Homozygous
Triplet Code
Conjugation
Start Codon
29. Progeny phenotypes are apparently blends of the parental phenotypes
DNA Replication
Okazaki fragments
Incomplete Dominance
RNA
30. 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
Elongation
Lytic Cycle
Synonyms
Crosses
31. Synthesized discontinuously in the 5'->3' direction (since DNA polymerase synthesizes only in that direction) as a series Okazaki fragments
Mendelian Genetics
Bacteriophage
Lagging Strand
Sex Linked
32. May occur spontaneously or be induced by environmental factors
Chromosomal Breakage
Ribosomes
Sex Linked Recessives
Heredity
33. Occurs when linked genes are separated
Codominance
Recombination
Non-Mendelian Inheritance Patterns
Sex Linked Recessives
34. An organism with a dominant phenotype of unknown genotype (Ax) is crossed with a phenotypically recessive organism
Backcross
Codons
Regulator Gene
Inducer-Repressor Complex
35. Genes that are located on the X or Y chromosome -in humans - most are located on the X
Double-Stranded Helix
Sex Linked
Translation
Binary fission
36. System where the repressor is inactive until it combines with the corepressor
Heredity
Incomplete Dominance
Repressible Systems
Missense Mutation
37. Small circular rings of DNA which contain accessory genes
Plasmid
DNA Replication
Mendel's Law of Dominance
Plasmids
38. The study of how traits are inherited from one generation to the next
Frameshift Mutation
Leading Strand
Polyribosome
Genetics
39. Fruit fly -produces often (short life cycle) -reproduces in large numbers (large sample size) -chromosomes (especially in the salivary gland) are large and easily recognizable in size and shape -its chromosomes are few (4 pairs - 2n=8) -Mutations occ
Drosophila Melanogaster
Punnet Square Diagram
Nonsense Mutation
Codominance
40. Can be altered under certain conditions - altering the corresponding characteristics in the organism
Mutable
Gene Mutation
Transfer RNA (tRNA)
Heterozygous
41. Initiation - elongation - and termination
RNA
Okazaki fragments
Polypeptide Synthesis
Virulent
42. The ribosome advances three nucleotides along the mRNA in the 5' to 3' direction and the uncharged tRNA from the P site is expelled - and the peptidyl-tRNA from the A site moves into the P site and completes the cycle
Pyrimidines
Autosomes
Translocation
Varions
43. 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
Aminoacyl-tRNA synthetase
Bacterial Genome
Messenger mRNA
Lysogenic Cycle
44. Only one trait is being studied in this particular mating
Mutable
Recombination
Monohybrid Cross
Purines
45. 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
Recessive Allele
RNA
Non-Mendelian Inheritance Patterns
Nucleotide
46. 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
Purines
Phenotype
RNA
Operator Gene
47. Sugar-phosphate chains on the outside of the helix and the bases on the inside -C-G - T-A -AKA Watson Crick DNA model
Purines
Mutations
Double-Stranded Helix
Phenotype
48. Formed between the amino acid attached to the tRNA in the A site and the fmet attached to the tRNA in the P site
Incomplete Dominance
Peptide Bond
Start Codon
Transfer RNA (tRNA)
49. Bacteriophages that replicate by the lytic cycle - killing their host cells
Recombination
Chromosomal Breakage
Virulent
Plasmids
50. Self replication ensures that its coded sequence will be passed on to successive generations
tRNA Job
Operon
Incomplete Dominance
Heredity