複選題

13. Which of the following factor(s) are involved in dissociating improper complexes between 40S subunits and mRNA?
(A) eIF1
(B) eIF1A
(C) eIF4A
(D) eIF4E
(E) eIF4G

9. Which of the following factor(s) mediates the binding of the Shine-Dalgarno sequence with the complementary sequence of the 16S rRNA? (A) IF-2 (B) IF-3 (C) EF-Tu (D) EF-G (E) RRF

10. Which of the following descriptions is NOT correct for comparison of protein translation between eukaryotes and bacteria? (A) Bacterial translation begins with methionine (B) Bacterial translation requires Shine-Dalgarno sequence to show ribosomes where to start (C) Eukaryotic mRNA has caps at 5'end (D) Eukaryotic initiating tRNA is not same as tRNA for interior (E) Eukaryotic translation requires Kozak sequence to show ribosomes where to start

複選題11. Which of the following factor(s) can bind Pab1p, a poly[A]-binding protein? (A) eIF1 (B) eIF1A (C) eIF4A (D) eIF4E (E) eIF4G

12. Which of the following factor(s) has an RNA helicase activity in translation initiation complex? (A) eIF1 (B) eIF1A (C) eIF4A (D) eIF4E (E) eIF4G

14. Which of the following descriptions is NOT correct for the peptidyl transferase in ribosome? (A) The peptidyl transferase resides on the 50S ribosomal particle (B) The peptidyl transferase activity is GTP-dependent (C) Minimum components necessary for its activity are 23S rRNA and proteins L2 and L3 (D) 23S rRNA is at the catalytic center of peptidyl transferase (E) puromycin can be its substrate

複選題15. Which of the following description about histone is (are) correct? (A) The molecular mass of Histone H4 is bigger than the other types of histones. (B) Histones H2A/H2B and H3/H4 dimerize through the non-covalent interaction of a highly conserved structural motif found in each core histone. (C) The histone H3 is extreme highly conserved from pea to cow, which differs by only two residues. (D) Histones H1 and H5 bind as monomers to nucleosomes and internucleosomal linker DNA to facilitate higher-order DNA compaction. (E) The heterogeneity of histone proteins is due to alternative splicing.

複選題16. Which of the following description about histones modification is (are) correct? (A) Histone acetylation specifically occurs in the nucleus. (B) The bromodomain domain of HAT(histone acetyltransferase) recognizes acetylated lysine residues on the N-terminal tails of histones. (C) The type B HAT does not contain the bromodomain. (D) The SANT domain of the type A HAT binds to DNA instead of histone. (E) HDAC deacetylates lysine on the N-terminal tail of core histone, leading to activation of gene transcription.

複選題17. Which of the following description about RNA polymerase II (Pol II) is (are) correct? (A) Pol II is a multiprotein complex that transcribes DNA into precursors of mRNA and microRNA. (B) The C-terminal domain (CTD) of the RNA polymerase binding protein (Rpb1) subunit of Pol II interacts with the splicing factor and stimulates splicing of substrates in organisms that use exon definition. (C) The facilitates chromatin transcription (FACT) complex is a histone chaperone comprising Spt16 and SSRP1, which is involved in transcription elongation by RNA polymerases II. (D) The CTD of the Rbpl subunit is involved in capping and splicing but not in polyadenylation. (E) The cotranscriptional cleavage (CoTC) element is essential for transcription termination.

複選題18. Which of the following description about polyadenylation is (are) correct? (A) The polyA binding protein I (PAB I) binds to mRNA Poly( A ), which recruits polysomes and enhances the translatability of mRNA. (B) Continuously translating mRNA to protein causes Poly( A ) turnover, leading to mRNA degradation. (C) PAB II is critical for the initiation of polyadenylation. (D) Occurrence of pre-mRNA cleavage triggers the assembling the of precleavage complex bound to the cleavage site. (E) The cleavage and polyadenylation specificity factor (CPSF) is required for both initiation and elongation phases of Poly( A ).

複選題19. Which of the following description about RNA editing is (are) correct? (A) RNA editing occurs in kinetoplasts. (B) RNA editing proceeds in a 5'→3' direction (C) gRNAs form wobble base pairs with pre-mRNA and direct both insertion and deletion of UMPs in pre-mRNA (D) The cytidine deaminases acting on RNA (CDAR) carries out C to G transversion for RNA editing. (E) Endonuclease, terminal uridylyl transferase (TUTase), and ligase are required for removing UTP from pre-mRNA.