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 ![]() |