Biology
Molecular Biology and Genetics
717 Questions
Molecular biology and genetics explore the structure and function of DNA, RNA, genetic mutations, and heredity. Understanding these building blocks of life is essential for most biology examinations. Review these practice questions to test your molecular genetics knowledge.
DNA structure and basesGenetic mutationsNucleic acids compositionDNA sequencing and replication
Molecular Biology and Genetics Questions
D
Correct answer
Explanation
Correct answer. A is incorrect and R is correct.
DNA shows hyperchromicity on heating. Heat denaturation of DNA causes the double helix structure to unwind to form single-stranded DNA. When DNA in solution is heated above its melting temperature, the double-stranded DNA unwinds to form single-stranded DNA. The bases become unstacked and can thus, absorb more light.
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nucleoside + phosphoric acid
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nucleoside + sulphuric acid
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nucleoside + nitric acid
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nucleoside + citric acid
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NA
A
Correct answer
Explanation
It is the correct answer as nucleotides are monomeric units of nucleic acids. Each nucletode consists of a nucleoside linked with phosphoric acid. Nucleoside is a combination of a nitrogen base and a pentose sugar.
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Beta glycosidic linkage
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Nitrogenous base
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Phosphoric acid
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Pentose sugar
C
Correct answer
Explanation
Phosphoric acid is not present in a nucleoside.
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Acriflavin
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Acyclovir
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Agent orange
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Albomycin
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Naphthol blue black
A
Correct answer
Explanation
Acriflavin is an acridine dye that is known to create frame shift mutations, caused by a deletion or insertion in a DNA sequence that shifts the reading frame sequence.
C
Correct answer
Explanation
ATP (Adenosine Triphosphate) contains 3 phosphate molecules in its structure: adenine-ribose-phosphate-phosphate-phosphate. The 'Tri' in Triphosphate means 'three'. Breaking the bond to the third (terminal) phosphate releases energy for cellular work. ADP (Adenosine Diphosphate) has only 2 phosphates.
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The noncoding regions are under poor evolutionary pressure and negative selection.
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Prevents frameshift mutation.
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Controls the flow of transcription.
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Acts as genetic switches.
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The amount of noncoding DNA varies greatly among species.
A
Correct answer
Explanation
Many noncoding DNA sequences have important biological functions as indicated by comparative genomics studies that report some regions of noncoding DNA that are highly conserved, sometimes on time-scales representing hundreds of millions of years, implying that these noncoding regions are under strong evolutionary pressure and positive selection.
B
Correct answer
Explanation
AGC and U are present in RNA.
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GTA ATCGATCTAUAC
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AUCGUAGUACUG
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GTAATGATGGUACUG
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GUAUUCGUACUACUG
D
Correct answer
Explanation
If the base sequence of the template strand of DNA is CATAAGCATGATGAC, the sequence of RNA strand which is complimentary with the DNA will be GUAUUCGUACUACUG as per Chargaff base pair rule.
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phosphate-diester bonds
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covalent bonds
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hydrogen bonds
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ionic bonds
C
Correct answer
Explanation
The two strands of DNA are linked by hydrogen bonds formed in between nitrogen bases.
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9 base pairs
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12 base pairs
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15 base pairs
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10 base pairs
B
Correct answer
Explanation
One codon contains 3 base pairs. Therefore, 4 codon contains 12 base pairs.
C
Correct answer
Explanation
Total number of base pairs in one full turn of B-DNA is 10.
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3000 base pairs
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1 million base pairs
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2.4million base pairs
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1.2 million base pairs
C
Correct answer
Explanation
The number of nucleotides in the gene which code for dystrophin protein is 2.4 million base pairs.
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frameshift mutation
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neutral mutation
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silent mutation
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conditional mutation
A
Correct answer
Explanation
Frameshift mutation is a mutation caused by insertion or deletion of a number of nucleotides that is not evenly divisible by three from a DNA sequence. Due to the triplet nature of gene expression by codons, the insertion or deletion can disrupt the reading frame, or the grouping of the codons, resulting in a completely different translation from the original. The earlier in the sequence the deletion or insertion occurs, the more altered the protein produced is.
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point mutation
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insertions
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deletions
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amplifications
B
Correct answer
Explanation
Insertions add one or more extra nucleotides into the DNA. They are usually caused by transposable elements, or errors during replication of repeating elements, e.g. AT repeats. Insertions in the coding region of a gene may alter splicing of the mRNA (splice site mutation), or cause a shift in the reading frame (frameshift), both of which can significantly alter the gene product.
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nucleosides
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nucleotides
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nucleobases
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nucleic acid analogues
D
Correct answer
Explanation
Nucleic acid analogues are compounds structurally similar (analog) to naturally occurring RNA and DNA, used in medicine and in molecular biology research.