|
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 |