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PCAT Biology Genetics
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Subjects
:
pcat
,
biology
Instructions:
Answer 50 questions in 15 minutes.
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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. 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
Transcription
Mendelian Genetics
Dihybrid Cross
Testcross
2. Structure formed when many ribosomes simultaneously translate a single mRNA molecule
Polyribosome
Sex Linked
Crosses
Pyrimidines
3. 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
Translation
Lysogenic Cycle
Semiconservative
Operon
4. 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
Repressible Systems
Dihybrid Cross
P-site
Punnet Square Diagram
5. Self replication ensures that its coded sequence will be passed on to successive generations
Bacterial Genome
Transfer RNA (tRNA)
Heredity
Mutations
6. Progeny generations
Filial (F generations)
Messenger mRNA
Triplet Code
Mendel's First Law: Law of Segregation (Four Principles)
7. Carries the complement of a DNA sequence and transports it from the nucleus to the ribosomes -assembled from ribonucleotides that are complementary to the 'sense' strand of the DNA -monocistronic
Ribosomal RNA (rRNA)
Transfer RNA (tRNA)
Heredity
Messenger mRNA
8. 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
Crosses
DNA
Nucleotide
Start Codon
9. Bacteriophages that replicate by the lytic cycle - killing their host cells
Lysogenic Cycle
Conjugation
RNA
Virulent
10. 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
Mutations
Mutable
Testcross
Crosses
11. Plasmids that are capable of integration into the bacterial genome
Plasmids
Translation
Transcription
Episomes
12. Can often affect the expression of a gene -interaction betwen the enironment and the genotype produces the phenotype
Bacterial Replication
Environmental Factors
DNA
Messenger mRNA
13. Genetic makeup of an individual
Heterozygous
Backcross
Genotype
Bacterial Replication
14. (AUG) ribosome scans the mRNA until it bonds to this (methionine) and UAC on anticodon of tRNA
Repressible Systems
Start Codon
Antibody resistance
Crosses
15. One mRNA strand codes for one polypeptide
Transformation
Lagging Strand
Mendel's Law of Dominance
Monocistronic
16. 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
Heredity
Gene Mutation
Nucleotide
17. Basic unit of heredity
Point Mutation
Gene
Bacteriophage
Complementary Base-Pairing
18. Genes that are located on the X or Y chromosome -in humans - most are located on the X
Ribosomal RNA (rRNA)
Sex Linked
Monocistronic
Plasmid
19. Codes for the synthesis of a repressor molecule that binds to the operator and blocks RNA polymerase form transcribing the structural genes
Regulator Gene
Transfer RNA (tRNA)
Transformation
Point Mutation
20. Nucleic acids are deleted or inserted into the genome sequence (lethal)
Frameshift Mutation
Bacterial Replication
Lyse
Lysogenic Cycle
21. The parents differ in two traits - as long as the genes are on separate chromosomes and assort independently during meiosis
Okazaki fragments
Dihybrid Cross
Mutations
Frameshift Mutation
22. Alternative forms of genes when it exists in more than one form
Binary fission
Backcross
Dominant Allele
Alleles
23. Small circular rings of DNA which contain accessory genes
Triplet Code
Incomplete Dominance
Autosomes
Plasmids
24. Binds to the incoming aminoacyl-tRNA complex (Arriving site)
A-site
Recessive Allele
Polyribosome
Backcross
25. 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
Recombination
Genotype
Promoter gene
RNA
26. Occurs while multiple alleles exist for a given gene and more than one of them is dominant -expression of both dominant alleles are simultaneous -ex: ABO blood group
Monohybrid Cross
Codominance
Nucleotide
Complementary Base-Pairing
27. 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
Double-Stranded Helix
Ribosomes
Plasmid
28. Short segments from lagging strand
Non-Mendelian Inheritance Patterns
Nondisjunction
Okazaki fragments
Aminoacyl-tRNA synthetase
29. Initiation - elongation - and termination
Antibody resistance
Polypeptide Synthesis
Backcross
Ribosomes
30. Degeneracy/redundancy of the genetic code since there are 64 different codons and only 20 amino acids
Chromosomes
Monohybrid Cross
Synonyms
Bacterial Genome
31. Transfer of genetic material between two bacteria that re temporarily joined
Binary fission
Conjugation
Mutagenic Agents
Repressible Systems
32. Include incomplete dominance - and codominance
Okazaki fragments
Dominant Allele
Non-Mendelian Inheritance Patterns
Translation
33. Individuals being crossed
Recessive Allele
Translocation
Anticodon
Parental (P Generation)
34. May occur spontaneously or be induced by environmental factors
Chromosomal Breakage
Episomes
Gene Mutation
Genotype
35. The process by which a foreign plasmid is incorporated into the bacterial chromosome via recombination - creating new inheritable genetic combinations
Gene Mutation
Pyrimidines
Transformation
DNA Replication
36. 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
Regulator Gene
Sex Linked Recessives
Genotype
Operon
37. Occurs when linked genes are separated
Filial (F generations)
Recombination
Plasmid
Polypeptide Synthesis
38. Reproduction of bacterial cells and proliferate very rapidly under favorable conditions -asexual prcoess -3 kinds (transformation - conjugation and transduction)
Chromosomes
Start Codon
Binary fission
Chromosomal Breakage
39. 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
DNA
Dihybrid Cross
Plasmids
Translation
40. Progeny phenotypes are apparently blends of the parental phenotypes
Polyribosome
Incomplete Dominance
Lysogenic Cycle
Chromosomes
41. 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
Promoter gene
Nondisjunction
Lagging Strand
Recombination
42. Daughter strand that is continuously synthesized by DNA polymerase in the 5'->3' direction
Recombination
Ribosomal RNA (rRNA)
Heterozygous
Leading Strand
43. Each new daughter helix contains an intact strand from the parent helix and a newly synthesized strand
Autosomes
Monohybrid Cross
Semiconservative
RNA
44. Hydrogen bonds form between the mRNA codon in the A site and its complementary anticodon on the incoming aminoacyl-tRNA complex
DNA
Sex Linked
Elongation
Lyse
45. (UAA - UAG - or UGA) terminates polypeptide synthesis
Termination Codons
Lyse
Dominant Allele
Complementary Base-Pairing
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
Heterozygous
Gene Mutation
Transduction
Ribosomes
47. TRNA binding site for ribosomes to attach to the growing polypeptide chain (peace out site)
DNA
Translocation
P-site
Repressible Systems
48. New codon may code for a different amino acid
Missense Mutation
Environmental Factors
Plasmids
Regulator Gene
49. Silent allele -usually assigned capital letters
Transcription
Homozygous
Lysogenic Cycle
Recessive Allele
50. 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
Mutations
Varions
Transduction
Inducer-Repressor Complex
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