| a. 25% | ||
| b. 50% | ||
| c. 75% | ||
| d. 100% |
| a. Semiconservative | ||
| b. Conservative | ||
| c. Dispersive | ||
| d. Random |
| a. This is because the purple flower phenotype is recessive, the white flower phenotype is dominant, and both parent plants were heterozygous. | ||
| b. This is because the purple flower phenotype is recessive, the white flower phenotype is dominant, and both parent plants were homozygous. | ||
| c. This is because the purple flower phenotype is dominant, the white flower phenotype is recessive, and both parent plants were heterozygous. | ||
| d. This is because the purple flower phenotype is dominant, the white flower phenotype is recessive, and both parent plants were homozygous. |
| a. This is because the round seed phenotype is recessive, the wrinkled seed phenotype is dominant, and both parent plants were heterozygous. | ||
| b. This is because the round seed phenotype is recessive, the wrinkled seed phenotype is dominant, and both parent plants were homozygous. | ||
| c. This is because the round seed phenotype is dominant, the wrinkled seed phenotype is recessive, and both parent plants were heterozygous. | ||
| d. This is because the round seed phenotype is dominant, the wrinkled seed phenotype is recessive, and both parent plants were homozygous. |
| a. Further away from; more frequently; close to | ||
| b. Further away from; less frequently; close to | ||
| c. Close to; more frequently; further away from | ||
| d. Close to; same frequency; further away from |
| a. one gene-one enzyme hypothesis | ||
| b. one gene-one RNA hypothesis | ||
| c. one gene-one protein hypothesis | ||
| d. one protein-one RNA hypothesis |
| a. 32P; DNA; protein; transforming principle | ||
| b. 35S; DNA; protein; transforming principle | ||
| c. 32P; DNA; protein; hereditary material | ||
| d. 35S; DNA; protein; hereditary material |
| a. The genetic code | ||
| b. DNA is composed of bases, sugar, and phosphate | ||
| c. The Chargaff's rules | ||
| d. DNA is the hereditary material |
| a. Double stranded helix; single stranded. | ||
| b. Single stranded helix; double stranded. | ||
| c. Triple helix; single stranded. | ||
| d. Double stranded helix; triple helix |
| a. Proteins and ribosomes, respectively; stabilizing | ||
| b. Proteins and ribosomes, respectively; diminishing | ||
| c. Biological catalysts; increasing | ||
| d. Biological catalysts; lowering |
| a. 40% | ||
| b. 20% | ||
| c. 10% | ||
| d. 30% |
| a. Minor; hidden; interact | ||
| b. Major; hidden; not interact | ||
| c. Minor; exposed; interact | ||
| d. Major; exposed; interact |
| a. Amino acids; ribosome | ||
| b. Amino acids; tRNA | ||
| c. Amino acids; DNA | ||
| d. Amino acids; mRNA |
| a. ATCCGTAACGT | ||
| b. TAGGCATTGCA | ||
| c. UAGGCAUUGCA | ||
| d. ACGUUACGGAU |
| a. Products; active site; substrate | ||
| b. Substrates; allosteric site; product | ||
| c. Products; allosteric site; substrate | ||
| d. Substrates; active site; product |
| a. 3'-ATCCGTAACGT-5' | ||
| b. 5'-ATCCGTAACGT-3' | ||
| c. 5'-TGCAATGCCTA-3' | ||
| d. 5'-TAGGCATTGCA-3' |
| a. uses the energy of ATP; histones; transcription | ||
| b. makes ATP; DNA; transcription | ||
| c. dephosphorylates; lamin; translation | ||
| d. removes histone tail modifications; histone heads; translation |
| a. looser; translation | ||
| b. tighter; translation | ||
| c. looser; transcription | ||
| d. tighter; transcription |
| a. histone; acetyl transferase | ||
| b. scaffold; topoisomerase | ||
| c. lamine; phosphatase | ||
| d. nucleolus; RNA |
| a. Nuclear lamina should reassemble, which requires the dephosporylation of lamins | ||
| b. Nuclear lamina should disassemble, which requires the phosphorylation of lamins | ||
| c. Nuclear lamina should disassemble, which requires phosphatase activity. | ||
| d. Nuclear lamina should reassemble, which requires kinase activity. |
| a. Positively; basic histone | ||
| b. Negatively; basic histone | ||
| c. Negatively; acidic histone | ||
| d. Positively; acidic histone |
| a. Heterochromatin; very condensed; few if any. | ||
| b. Euchromatin; very condensed; few if any. | ||
| c. Heterochromatin; hardly condensed; few if any. | ||
| d. Euchromatin; very condensed; few if any. |
| a. Chemical; reversible | ||
| b. Physical; reversible | ||
| c. Chemical; irreversible | ||
| d. Physical; irreversible |
| a. Condensation; translated | ||
| b. Condensation; transcribed | ||
| c. De-condensation; translated | ||
| d. De-condensation; transcribed |
| a. Topoisomerases; cleave | ||
| b. Helicases; separate | ||
| c. Polymerases; elongate | ||
| d. Replication complexes; bind to |
| a. Topoisomerases; cleave; reseal | ||
| b. Helicases; separate; supercoil | ||
| c. Polymerases; copy; elongate | ||
| d. Replication complexes; bind to; copy |
| a. Multiple copies; multiple copies; multiple copies | ||
| b. One copy; one copy; one copy | ||
| c. One copy; multiple copies; multiple copies | ||
| d. One copy; one copy; multiple copies |
| a. DNA polymerase is frequently released from the template strand, thus it has to start the synthesis of a new piece | ||
| b. DNA polymerase cannot start DNA synthesis; it can only add nucleotides to an existing strand | ||
| c. DNA polymerase can add nucleotides only to the 3' end of the growing strand | ||
| d. DNA polymerase can add nucleotides only to the 5' end of the growing strand |
| a. DNA polymerase, which does not require priming | ||
| b. Ligase, which can link telomere regions to the end of linear chromosomes | ||
| c. DNA polymerase, which can add nucleotides to 5'-ends | ||
| d. Reverse transcriptase associated with an RNA primer |
| a. Hayflick's limit; shortening | ||
| b. Priming; elongation | ||
| c. Ligation; conjugation | ||
| d. Okazaki fragment; primer |
| a. Clamp-loading | ||
| b. Helicase | ||
| c. Sliding clamp | ||
| d. Replication origin |
| a. Okazaki fragment; template | ||
| b. Lagging; leading | ||
| c. Leading strand; lagging | ||
| d. Template; leading |
| a. Without releasing the substrate; release the polymer substrate | ||
| b. Utilizing the work of many enzymes at the same time on one polymer; work without releasing the substrate | ||
| c. Resulting in the growth of the substrate; shorten the polymer by one monomer unit | ||
| d. With a high reaction rate; progress very slowly |
| a. Before the first 30 nucleotides are transcribed | ||
| b. When the mRNA transcription is finished | ||
| c. After the RNA enters the cytoplasm | ||
| d. When the first two nucleotides are linked with a phosphodiester bond |
| a. Follow the exact same mechanism | ||
| b. Are somewhat different: in prokaryotes transcription and translation take place simultaneously, while they are separated in eukaryotes | ||
| c. Are somewhat different: in eukaryotes transcription and translation take place simultaneously, while they are separated in prokaryotes | ||
| d. Are indistinguishable with an exception of translation at the rough ER, which is slower in prokaryotes |
| a. Is not processed; nucleus | ||
| b. Is processed; cytoplasm | ||
| c. Is capped, polyadenylated, and spliced; nucleus | ||
| d. Is not processed; cytoplasm |
| a. Splisosome; introns; exons | ||
| b. Splisosome; exons; introns | ||
| c. Ribosome; introns; exons | ||
| d. Ribosome; exons; introns |
| a. Is not processed; nucleus | ||
| b. Is processed; cytoplasm | ||
| c. Is capped, polyadenylated, and spliced; nucleus | ||
| d. Is not processed; cytoplasm |
| a. Rare; protein | ||
| b. Common; protein | ||
| c. Rare; RNA turnover | ||
| d. Common; RNA turnover |
| a. Ribozymes; RNase; freshly synthesized mRNA | ||
| b. Enzymes; subunits; pre-mRNA | ||
| c. Scaffolding centers; miRNA; translationally repressed | ||
| d. Splicing centers; ribozymes; alternatively spliced mRNA |
| a. 5' mRNA regions; certain metabolite | ||
| b. Transcription factors; second messenger | ||
| c. Ribosome components; translation elongation factor | ||
| d. 3' mRNA regions; certain nutrient |
| a. Links different exons of one pre-mRNA to produce several mature mRNA | ||
| b. Links different exons of two pre-mRNAs to produce several mature mRNA | ||
| c. Is modifying gene structure by splicing out regions of a chromosome. | ||
| d. Is a chromosomal inversion, which is responsible for making new genes |
| a. genomic DNA | ||
| b. mRNA | ||
| c. cDNA | ||
| d. introns |
| a. 1070 | ||
| b. 1069 | ||
| c. 1071 | ||
| d. 3210 |
| a. UGA | ||
| b. UCA | ||
| c. TCA | ||
| d. TGA |
| a. 5' to 3'; carboxy to amino terminus | ||
| b. 5' to 3'; amino to carboxy terminus | ||
| c. 3' to 5'; carboxy to amino terminus | ||
| d. 3' to 5'; amino to carboxy terminus |
| a. Open reading source | ||
| b. Mature mRNA | ||
| c. Open reading frame | ||
| d. Spliced mRNA |
| a. The protein release factor binds to a stop codon at the A site of the ribosome | ||
| b. An uncharged tRNA is bound to a stop codon at the A site of the ribosome | ||
| c. A termination factor cleaves off the growing polypeptide chain | ||
| d. The mRNA ends at the stop codon and runs off the ribosome |
| a. 3'-CCA-5' | ||
| b. 5'-CCA-3' | ||
| c. 3'-UGG-3' | ||
| d. 5'-UGG-3' |
| a. Kozak sequence; also by the Kozak; | ||
| b. Shine-Delgarno sequence; by the Kozak sequence | ||
| c. Kozak sequence; by the Shine-Delgarno sequence | ||
| d. Shine-Delgarno sequence; also by the Shine-Delgarno sequence |
| a. ATGCGAGGCTATGCUCGGTGA | ||
| b. AUGCGAGGCUAUGCUCGGUGA | ||
| c. AGUGGCUCGUAUGGGAGCGUA | ||
| d. AGTGGCTCGTATGGGAGCGTA |
| a. The template of the RNA can be ssDNA-2; ssDNA-1 is unrelated | ||
| b. The template of the RNA can be ssDNA-1; ssDNA-2 is unrelated | ||
| c. ssDNA-1 and ssDNA-2 can be complement strands, but they are unrelated to the RNA | ||
| d. All three nucleic acids are unrelated |
| a. DNA sequences can be read in six open reading frames: three forward and three reverse | ||
| b. DNA sequences can be read in three open reading frames: three forward | ||
| c. DNA sequences can be read in one open reading frame: one forward | ||
| d. DNA sequences can be read in two open reading frames: one forward and one reverse |
| a. Aminoacyl-transfer RNA synthetase has no proofreading activity. | ||
| b. tRNA spontaneously reacts with an amino acid, since this reaction is thermodynamically favorable. | ||
| c. Aminoacyl-transfer RNA synthetase links the carboxyl group of an amino acid to a tRNA ribose hydroxyl group through an ester bond. | ||
| d. Only one enzyme is needed to charge all tRNAs with the appropriate amino acid. |
| a. Inosine; A, C, U | ||
| b. Nicotinamide; G, U | ||
| c. Flavin; A, G, U | ||
| d. Niacin; A, U |
| a. 112 | ||
| b. 150 | ||
| c. 173 | ||
| d. 211 |
| a. There would be no lac operon repression, thus lacA, lacZ and lacY genes would be constitutively expressed regardless of the presence of lactose. | ||
| b. There would be no lac operon repression, thus lacA, lacZ and lacY genes would be expressed in the presence of lactose. | ||
| c. There would be no lac operon repression, thus lacA, lacZ and lacY genes would be constitutively expressed regardless of the presence of glucose. | ||
| d. There would be no lac operon repression, thus lacA, lacZ and lacY genes would be expressed in the presence of allolactose. |
| a. DNA and histones | ||
| b. DNA | ||
| c. Histone | ||
| d. RNA |
| a. Catabolic pathways; lac operon; anabolic pathways; trp operon | ||
| b. Catabolic pathways; trp operon; anabolic pathways; lac operon | ||
| c. Anabolic pathways; lac operon; catabolic pathways; trp operon | ||
| d. Anabolic pathways; trp operon; catabolic pathways; lac operon |
| a. Denomic imprinting; de novo methylation; none of them | ||
| b. De novo methylation; genomic imprinting; none of them | ||
| c. Genomic imprinting; de novo methylation; both of them | ||
| d. Genomic imprinting; de novo methylation; none of them |
| a. Absent; inactive; repressor is | ||
| b. Present; inactive; repressor is not | ||
| c. Absent; active; repressor is not | ||
| d. Present; active; repressor is |
| a. Turned off; tryptophan-activated repressor | ||
| b. Turned on; tryptophan-activated repressor | ||
| c. Turned off; tryptophan-inhibited repressor | ||
| d. Turned on; tryptophan-inhibited repressor |
| a. Tissue specific gene expression; combination | ||
| b. Genomic imprinting; absence | ||
| c. X inactivation; absence | ||
| d. Development; abundance |
| a. Catabolite activator protein (CAP); lactose | ||
| b. Allolactose; cAMP | ||
| c. The catabolite activator protein (CAP); glucose | ||
| d. cAMP; lactose |
| a. Either altered bases or nucleotides | ||
| b. Only altered bases by cleaving the base-sugar bonds | ||
| c. Only nucleotides by cleaving phosphodiester bonds | ||
| d. Only apurinic sites |
| a. Mismatch repair; daughter; parent | ||
| b. Mutagen activity; daughter; parent | ||
| c. Mismatch repair; parent; daughter | ||
| d. Mutagen activity; parent; daughter |
| a. Slower protein turnover | ||
| b. No gene product | ||
| c. Lower metabolic rate | ||
| d. Loss of inhibition |
| a. New; adenine methylation | ||
| b. Old; adenine methylation | ||
| c. New; Okazaki fragment ligation | ||
| d. New; Okazaki fragment ligation |
| a. More rapidly than | ||
| b. At the same rate as | ||
| c. Less rapidly than | ||
| d. Less efficiently than |
| a. SOS; inaccurate | ||
| b. Recombinational; error-prone | ||
| c. Postreplicational; always high fidelity | ||
| d. SOS; high fidelity |
| a. Cystic fibrosis | ||
| b. Fragile X syndrome | ||
| c. Philadelphia syndrome | ||
| d. Huntington's disease |
| a. Early nonsense | ||
| b. Early silent | ||
| c. Late missense | ||
| d. Late frameshift |
| a. SOS repair mechanism | ||
| b. Initiating DNA replication | ||
| c. Homologous recombination of chromosomes | ||
| d. Terminating RNA transcription |
| a. Crossing over of nonsister; variability | ||
| b. Crossing over of sister; variability | ||
| c. Crossing over of nonsister; stability | ||
| d. Crossing over of sister; stability |
| a. RNA intermadiate; retrotransposase | ||
| b. DNA intermediate; retrotransposase | ||
| c. RNA intermediate; reverse transcriptase | ||
| d. DNA intermediate; reverse transcriptase |
| a. Can; can | ||
| b. Can; cannot | ||
| c. Cannot; cannot | ||
| d. Cannot; can |
| a. DNA crossover | ||
| b. DNA ligation | ||
| c. SOS gap repair | ||
| d. PCR amplification |
| a. Retrotransposase | ||
| b. The cut-and-paste mechanism | ||
| c. The involvement of a reverse transcriptase | ||
| d. The copy-and-paste mechanism |
| a. Exon shuffling; combination | ||
| b. Alternative splicing; combination | ||
| c. Exon shuffling; conformation | ||
| d. Alternative splicing; conformation |
| a. Mismatch | ||
| b. Strand separation | ||
| c. Backbone break | ||
| d. Crosslink between bases |
| a. Antibiotic resistance gene; cloning site; reporter gene | ||
| b. Restriction enzyme gene; ligase gene; repair gene | ||
| c. PCR amplified segment; GC-rich region; reporter gene | ||
| d. Antibiotic resistance gene; ligation site; repair gene |
| a. GCTAA and TAGCG | ||
| b. GCTAA and CGCTA | ||
| c. CGATT and TAGCG | ||
| d. CGATT and CGCTA |
| a. Multiple-cloning site; foreign | ||
| b. Ligation site; foreign | ||
| c. PCR site; antibiotic resistance gene | ||
| d. Insertion site; reporter gene |
| a. Sticky; ligase | ||
| b. Blunt; ligase | ||
| c. Sticky; DNA polymerase | ||
| d. Blunt; DNA polymerase |
| a. Link; phosphodiester bonds | ||
| b. Repair; excision | ||
| c. Restrict the replication of; linking them to lamins | ||
| d. Link RNA primer to; phosphodiester bond at the beginning of the replication |
| a. Ligases; seal fragments of; sites | ||
| b. DNases; cut; developmental stages | ||
| c. Molecular scissors; cut; recognition sites | ||
| d. Polymerases; replicate; locations |
| a. 3'OH of the sugar | ||
| b. 2'OH of the sugar | ||
| c. Terminal phosphate group | ||
| d. Chain terminating polymerase |
| a. 16 | ||
| b. 32 | ||
| c. 64 | ||
| d. 128 |
| a. Polymerase chain reaction-DNA amplification | ||
| b. Ion exchange chromatography-purified RNA | ||
| c. Restriction enzyme digestion-DNA fragments | ||
| d. Ligation-joined DNA fragments |
| a. Reporter genes; cloning site; disruption | ||
| b. Antibiotic resistance genes; cloning site; inhibition | ||
| c. Multicloning sites; restriction enzyme recognition site; amplification | ||
| d. PCR sites; restriction enzyme recognition site; amplification |
| a. Ion exchange chromatography | ||
| b. Affinity chromatography | ||
| c. Ultracentrifugation | ||
| d. 2D gelelectrophoresis |
| a. Charge | ||
| b. Charge and size | ||
| c. Size | ||
| d. Shape |
| a. Knock-out and knock-in | ||
| b. Transposon induced | ||
| c. Mutagen induced | ||
| d. Knock over |
| a. Southern | ||
| b. Western | ||
| c. Northern | ||
| d. Protein |
| a. From one species to another; within a species | ||
| b. Within a species; from different species | ||
| c. And produces new strains slowly; and gets the result within a generation | ||
| d. but the produced strains are not homogenous; and easily gets clones |
| a. Escherichia coli | ||
| b. Saccharomyces cerevisiae | ||
| c. Caenorhabditis elegans | ||
| d. Drosophila melanogaster |
| a. Escherichia coli | ||
| b. Saccharomyces cerevisiae | ||
| c. Caenorhabditis elegans | ||
| d. Drosophila melanogaster |
| a. Escherichia coli | ||
| b. Saccharomyces cerevisiae | ||
| c. Caenorhabditis elegans | ||
| d. Penicillium chrysogenum |
| a. Arabidopsis thaliana | ||
| b. Zea mays | ||
| c. Oryza sativa | ||
| d. Allium cepa |
| a. Escherichia coli | ||
| b. Saccharomyces cerevisiae | ||
| c. Caenorhabditis elegans | ||
| d. Penicillium chrysogenum |