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 |