MCQs Flashcards
The rules used to determine the link between the nucleotide sequence of a gene and the amino acid sequence of the protein specified by that gene is referred to as: A. secondary structure guidelines B. R group rules C. codon assignments steps D. the genetic code E. Chargaff’s rules
D. the genetic code
Which of the following is incorrect?
A. the amino terminus of a protein corresponds to the 3′ end of a gene
B. a codon always contains a triplet of nucleotides
C. the order of nucleotides in a prokaryotic gene correlates precisely with the order of amino acids in the corresponding protein
D. a deletion of one or two nucleotides in the coding region of a gene will disrupt the codons downstream of the deletion and give rise to a non-functional protein
E. through wobble, it is possible for one tRNA to read two or possibly three codons.
A. the amino terminus of a protein corresponds to the 3′ end of a gene
In terms of actual gene coding sequences, how much bigger is the human genome than the Escherichia coli genome? A. 10,000 x B. 5,000 x C. 1,000 x D. 500 x E. 50 x.
E. 50 x.
In the context of prokaryotic gene expression, which of the following is the most appropriate definition of an operator?
A. a cluster of genes that are regulated by a single promotor
B. a DNA-binding protein that regulates gene expression
C. a non-coding regulatory DNA sequence that is bound by RNA polymerase
D. a non-coding regulatory DNA sequence that is bound by a repressor protein
E. a section of DNA transcribed but not translated.
D. a non-coding regulatory DNA sequence that is bound by a repressor protein
A frameshift mutation could be caused by a:
A. a transitional base substitution
B. a transversional base substitution
C. a deletion of 3 base pairs
D. an insertion of 3 base pairs
E. a deletion or insertion of 1 or 2 base pairs.
E. a deletion or insertion of 1 or 2 base pairs.
Bacteriophage mediated gene transfer amongst bacteria is known as: A. transformation B. transduction C. translocation D. transcription E. translation.
B. transduction
In female mammals, one X chromosome is largely inactivated. The inactivated X chromosome has:
A. higher levels of acetylation of histone proteins
B. lower levels of acetylation of histone proteins
C. a lack of associated histone proteins
D. lower levels of DNA methylation
E. higher levels of DNA methylation.
E. higher levels of DNA methylation.
Eukaryote gene enhancer sequences are:
A. located either side of a gene, at some distance from a gene, or even within a gene
B. located downstream of the genes which they regulate
C. located upstream of the genes which they regulate
D. situated at a fixed distance from the site where transcription is initiated
E. able only to affect the expression of a single specific gene.
A. located either side of a gene, at some distance from a gene, or even within a gene
Changes in chromatin organisation (chromatin remodelling) may be required for various processes in eukaryotes. Which?
A. DNA repair, replication, recombination, and transcription
B. DNA repair, replication, and recombination, but not transcription
C. DNA repair and replication, but not recombination or transcription
D. DNA repair, but not replication, recombination, or transcription
E. DNA transcription only
A. DNA repair, replication, recombination, and transcription
The anterior-posterior axis in the early Drosophila embryo is established by concentration gradients of which proteins? A. NOS and BCD proteins B. NOS and HB-M proteins C. BCD and HB-M proteins D. BCD and CACT proteins E. HB-M and CACT proteins.
C. BCD and HB-M proteins
In humans, HOX genes are found:
A. spread throughout the genome and located on most chromosomes
B. organised in four clusters located on four different chromosomes
C. organised in four clusters, two clusters located on each of two different chromosomes
D. closely linked together in a cluster on a single chromosome
E. spread throughout the length of a single chromosome.
B. organised in four clusters located on four different chromosomes
12. Mutations can occur at the level of: A. DNA bases B. an individual gene C. chromosomes D. the whole genome E. all of the above.
E. all of the above.
- Apoptosis or programmed cell death occurs:
A. at single cell level
B. in a group of cells
C. either at a single cell level or in a group of cells
D. at tissue level
E. at the organ level.
A. at single cell level
DNA repair using a homologous recombination (HR) process takes place:
A. shortly after S and G2 phases of the cell cycle
B. only in the S phase of the cell cycle
C. in the mitotic phase of the cell cycle
D. in the G1 phase of the cell cycle
E. at any stage of the cell cycle.
A. shortly after S and G2 phases of the cell cycle
Xeroderma pigmentosum :
A. is an autosomal recessive disease
B. individuals are sensitive to sun/UV light
C. individuals are deficient in DNA repair process
D. all of the above
E. none of the above.
D. all of the above