Explore topic-wise InterviewSolutions in .

This section includes InterviewSolutions, each offering curated multiple-choice questions to sharpen your knowledge and support exam preparation. Choose a topic below to get started.

1.

How does polymorphism arise?(a) Mutations(b) Recombination(c) Diploidy(d) HaploidyThe question was posed to me in class test.The origin of the question is Molecular Basis of Inheritance topic in portion Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct answer is (a) MUTATIONS

To elaborate: POLYMORPHISM arises DUE to mutations. It can also be known as the discontinuous variation that is seen among the INDIVIDUALS of a species.

2.

How DNA can be as a useful tool in the forensic applications?(a) Showing the same degree of polymorphism with hair follicles(b) Showing different degrees of polymorphism with saliva(c) By not possessing any hereditable information(d) By the presence of lysozymes in itThis question was posed to me in final exam.My question is based upon Molecular Basis of Inheritance in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer» CORRECT answer is (a) Showing the same degree of polymorphism with hair follicles

Best EXPLANATION: The DOUBLE helical structure of the DNA present on SALIVA, hair follicles, BONES, blood and sperm serve as a useful took in the forensic studies. This can be done as the DNA from an individual’s tissue shows the same degree of polymorphism. These polymorphic characters are inheritable from parents to their children.
3.

The sequences of satellite DNA do not code for proteins.(a) True(b) FalseI got this question during an online exam.Query is from Molecular Basis of Inheritance topic in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct answer is (a) True

The explanation: The small peaks formed by the DNA when kept in the DENSITY gradient centrifugation are CALLED as satellite DNA. These DNA sequences do not code for proteins. On the contrary, they form a large PORTION in the GENOME of humans.

4.

What are the small peaks achieved by the repetitive DNA during the density gradient centrifugation process of DNA finger printing known as?(a) Non repetitive DNA(b) Trough(c) Satellite DNA(d) Histone DNAThe question was asked in an online interview.I'd like to ask this question from Molecular Basis of Inheritance in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer» RIGHT choice is (C) Satellite DNA

Easiest explanation: The genomic DNA forms a high peak in the density GRADIENT centrifugation. Whereas, the various small peaks which are formed are collectively CALLED as the satellite DNA.
5.

What are the differences in the specific regions of DNA sequence called during DNA finger printing?(a) Non repetitive DNA(b) Repetitive DNA(c) Satellite DNA(d) Histone DNAI have been asked this question in examination.Origin of the question is Molecular Basis of Inheritance in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct option is (b) Repetitive DNA

The best explanation: In DNA finger printing, the differences in the SPECIFIC regions of the DNA sequence are called as Repetitive DNA. In this part, a small structure of the DNA is repeated many TIMES. These repetitive STRUCTURES can be separated from the bulk genomic DNA. This is done by observing the different peaks ACHIEVED by them during the density gradient centrifugation.

6.

Repeated sequence makes a large portion of the human genome.(a) True(b) FalseThe question was posed to me in unit test.The above asked question is from Molecular Basis of Inheritance in division Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct option is (a) True

To explain I WOULD SAY: DNA contains many repeated sequences in it. Sometimes it is noted to have more than hundreds or THOUSANDS of sequences in them. These sequences MIGHT not POSSESS any direct coding functions in them. This altogether makes the large portion of the human genome.

7.

How many nucleotides are present in the human genome?(a) 3164.7 million(b) 2015.9 million(c) 1982.0 million(d) 3247.9 millionThe question was posed to me during an interview.The query is from Molecular Basis of Inheritance topic in division Molecular Basis of Inheritance of Biology – Class 12

Answer»

Right ANSWER is (a) 3164.7 million

Best explanation: NUCLEOTIDES are the organic carbon molecules. They contain both a NUCLEOSIDE and a PHOSPHATE group. Inside the human genome, there is a total of 3164.7 million nucleotides.

8.

Based on whose principle were the DNA molecules fragmented in the year 1977?(a) Maurice Wilkins(b) Rosalind Franklin(c) James Watson(d) Frederick SangerI have been asked this question in my homework.This intriguing question originated from Molecular Basis of Inheritance in portion Molecular Basis of Inheritance of Biology – Class 12

Answer» RIGHT choice is (d) Frederick Sanger

For EXPLANATION: The double helical STRUCTURE of the DNA molecule was first fragmented by Frederick Sanger in the 1977. These fragments were then sequenced using automated DNA sequencers. These DNA sequencers operated based on the PRINCIPLE of Frederick Sanger.
9.

How are the genetic and the physical maps assigned on the genome?(a) Based on microsatellites(b) Based on macrosatellites(c) Based on kinetochores(d) Based on centromeresThis question was posed to me at a job interview.Question is from Molecular Basis of Inheritance topic in division Molecular Basis of Inheritance of Biology – Class 12

Answer»

The CORRECT answer is (a) Based on microsatellites

The explanation: The genetic and the physical maps on the GENOME are assigned based on microsatellites. They are also assigned based on the act of polymorphism at the restriction endonuclease recognition SITES. The repetitive DNA SEQUENCES are called as microsatellites.

10.

Which of the following is a suitable vector for the process of cloning in Human Genome Project (HGP)?(a) PAC (Protozoal Artificial Chromosomes)(b) FAC (Fungal Artificial Chromosomes)(c) VAC (Viral Artificial Chromosomes)(d) YAC (Yeast Artificial Chromosomes)This question was posed to me in a job interview.The origin of the question is Molecular Basis of Inheritance topic in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer»

Right answer is (d) YAC (Yeast Artificial Chromosomes)

For explanation: Both BAC (Bacterial Artificial Chromosomes) and YAC (Yeast Artificial Chromosomes) ACT as a suitable vector for the process of cloning in HGP WHEREAS BACTERIA and yeast act as the HOST for cloning in HGP.

11.

Which of the following is a suitable host for the process of cloning in Human Genome Project (HGP)?(a) Virus(b) All types of fungi(c) Bacteria(d) ProtozoanThe question was asked by my school teacher while I was bunking the class.The query is from Molecular Basis of Inheritance topic in portion Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct option is (c) Bacteria

For explanation I would say: Bacteria and yeast are the most COMMONLY used hosts for the process of cloning in Human Genome PROJECT. Not all types of FUNGI can be used for this process. But yeast and BACTERIUM can be employed.

12.

Which of the following methodology is used to identify all the genes that are expressed as RNA in Human Genome Project (HGP)?(a) Sequence Annotation(b) Expressed Sequence Tags(c) Karyotyping(d) AmmonificationI got this question during an online interview.My enquiry is from Molecular Basis of Inheritance in section Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct ANSWER is (b) Expressed Sequence Tags

To explain: The methodologies for the HGP are INVOLVED in two major processes. ONE among them is ESTs (Expressed Sequence Tags). It is USED to identify all the genes that are expressed as RNA in HGP.

13.

What is the regulation of a lac operon by a repressor known as?(a) Neutral regulation(b) Positive regulation(c) Mixed regulation(d) Negative regulationThis question was posed to me in an international level competition.I need to ask this question from Molecular Basis of Inheritance in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer»

The correct OPTION is (d) Negative REGULATION

Easiest explanation: The regulation of a LAC operon by the repressor is known as negative regulation. At rare occasions, lac OPERONS are ALSO observed to be under the control of positive regulation. In negative regulation, the operon cannot transcribe the RNA polymerase enzyme.

14.

Which of the following is the necessary condition for the entry of lactose into the cell?(a) High level expression of lac operon(b) Low level expression of lac operon(c) Absence of lac operon in the cell(d) Absence of proteins in the cellThe question was asked in exam.The doubt is from Molecular Basis of Inheritance topic in section Molecular Basis of Inheritance of Biology – Class 12

Answer» CORRECT OPTION is (b) Low level EXPRESSION of lac OPERON

To explain: The action of the enzyme protease helps LACTOSE to enter into the cell. But this can be achieved only if a low-level expression of the lac operon is present inside the cell. Otherwise, lactose cannot enter the cell.
15.

Which of the following is responsible for the switching on and off of the lac operon?(a) Lactose(b) Ethanol(c) Malate(d) FructoseI had been asked this question during an internship interview.Asked question is from Molecular Basis of Inheritance topic in section Molecular Basis of Inheritance of Biology – Class 12

Answer»

The correct OPTION is (a) Lactose

For explanation I would say: The substrate for the enzyme β-galactosidase is lactose. The lac operon can EITHER be in its SWITCHED on or off position. This OPERATION is being regulated by lactose which is also known as the inducer.

16.

How many structural genes are present in a lac operon?(a) One(b) Five(c) Three(d) SevenI had been asked this question during an interview for a job.Origin of the question is Molecular Basis of Inheritance in section Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct option is (c) Three

Easiest EXPLANATION: A lac OPERON consists of one regulatory gene (i) and three structural GENES (z, y and a). The “i” in regulatory gene is DERIVED from the word “inhibitor”.

17.

What does the structural gene (y) of a lac operon code for?(a) β-galactosidase(b) Transacetylase(c) Permease(d) GlucagonI have been asked this question in semester exam.The above asked question is from Molecular Basis of Inheritance topic in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct ANSWER is (C) Permease

Explanation: The structural gene (z) of the lac operon codes for β-galactosidase. It is RESPONSIBLE for the hydrolysis of polysaccharides. The ‘y’ genes CODE for permease. It increases the permeability of a CELL to β-galactosidase. The ‘a’ genes code for transacetylase.

18.

Which polycistronic structural gene is regulated by a common promoter and regulatory gene?(a) Trp operon(b) Lac operon(c) Ara operon(d) His operonI had been asked this question in an internship interview.This intriguing question originated from Molecular Basis of Inheritance in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer»

The correct answer is (B) Lac operon

The BEST I can explain: Lac (lactose) operon has a polycistronic STRUCTURAL gene which is regulated by a common promoter and regulatory gene. It is MAINLY present in prokaryotes like bacteria. This TYPE of an arrangement is called as an operon in general.

19.

What happens when the small subunit of the ribosome encounters an mRNA?(a) Separation of the small and the larger subunit of the ribosome(b) Translation of the central dogma of DNA(c) Joining of the small and the larger subunit of the ribosome(d) Transcription of the central dogma of DNAThis question was posed to me in a job interview.My question is based upon Molecular Basis of Inheritance in portion Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct ANSWER is (b) Translation of the central dogma of DNA

For explanation: The central dogma of DNA occurs in its 2 STAGES. They are TRANSCRIPTION and translation. When the small subunit of the ribosome encounters an mRNA, the PROCESS of translation commences. The process of translation from the mRNA to the proteins occur.

20.

Regulatory protein can act both as an activator and a repressor.(a) True(b) FalseThe question was posed to me in an interview for job.The query is from Molecular Basis of Inheritance topic in section Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct option is (a) True

Easiest explanation: The regulatory PROTEINS have the ability to act both as an ACTIVATOR and a repressor. They will be positive when they are ACTIVATORS. They will be negative when they are REPRESSORS.

21.

In which of the following levels can gene expression not be exerted?(a) Transitional level(b) Transcriptional level(c) Reverse transcriptional level(d) Processing levelThe question was posed to me during an online interview.This is a very interesting question from Molecular Basis of Inheritance topic in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer»

The correct answer is (c) Reverse TRANSCRIPTIONAL level

The EXPLANATION: In eukaryotes, the REGULATION of gene expression occurs at various LEVELS. They are transcriptional level, processing level, transport of mRNA from the NUCLEUS to the cytoplasm and translational level.

22.

Where are the untranslated regions (UTRs) present?(a) At both the 5’ and the 3’ ends(b) At only the 5’ end(c) At only the 3’ end(d) Outer to the 5’ and the 3’ endI have been asked this question by my college professor while I was bunking the class.My question comes from Molecular Basis of Inheritance topic in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer» CORRECT option is (a) At both the 5’ and the 3’ ends

To explain I would say: The untranslated regions (UTRs) are the additional sequences of the mRNA which aren’t TRANSLATED during the process of translation into PROTEINS. This REGION is present at both the 5’ and the 3’ end. They are required so that an efficient process of translation OCCURS.
23.

Which of the following cell organelle is responsible for the synthesis of proteins?(a) Lysosomes(b) Mitochondria(c) Nucleus(d) RibosomesI had been asked this question in class test.Asked question is from Molecular Basis of Inheritance in division Molecular Basis of Inheritance of Biology – Class 12

Answer»

Right choice is (d) Ribosomes

The explanation is: Lysosomes help in the BREAK down and digestion of the worn out or dead cell components. Mitochondria is known as the power house of the cell for the production of ATP MOLECULES. Nucleus helps in CARRYING the information from one GENERATION to the next generation. Ribosomes help in the SYNTHESIS of proteins.

24.

How many types of proteins are present inside a single ribosome?(a) 40(b) 60(c) 80(d) 100I had been asked this question by my college director while I was bunking the class.Asked question is from Molecular Basis of Inheritance topic in section Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct answer is (c) 80

The explanation: Ribosomes consists of structural RNAS and they also POSSESS about 80 different TYPES of PROTEINS in them. A RIBOSOME can either be in its active state or inactive state. While it is in its inactive state, it will exist as 2 subunits.

25.

What is the process of activation of amino acids in the presence of ATP and its linkage to their cognate tRNA known as?(a) Charging of tRNA(b) Charging of ATP(c) Aminoacetylation of tRNA(d) Aminoacetylation of ATPThe question was asked in final exam.This intriguing question comes from Molecular Basis of Inheritance topic in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer»

Right choice is (a) Charging of tRNA

To explain: In order to FORM a peptide BOND, a certain quantity of energy is required. The first phase in this process is known as charging of tRNA. It is also known as Aminoacylation of tRNA. In this process, the amino ACIDS are activated in the presence of ATP and are linked to their cognate tRNA.

26.

The presence of a catalyst would decrease the rate of formation of a peptide bond.(a) True(b) FalseThe question was asked in an online interview.Enquiry is from Molecular Basis of Inheritance in section Molecular Basis of Inheritance of Biology – Class 12

Answer» RIGHT ANSWER is (b) False

To explain: When TWO molecules of charged tRNAs are brought close to one ANOTHER, the formation of a peptide bond between these two molecules will be highly favoured (energetically). So the presence of a catalyst would INCREASE the rate of peptide bond formation.
27.

What is the process of polymerisation of polypeptides to amino acids known as?(a) Transcription(b) Translation(c) Reverse transcription(d) Reverse translationThis question was addressed to me in an online quiz.I need to ask this question from Molecular Basis of Inheritance in portion Molecular Basis of Inheritance of Biology – Class 12

Answer»

The correct choice is (b) Translation

For explanation I would say: There are certain sequences for the bases PRESENT in the mRNA. The order and sequence of the AMINO acids are defined by them. And so, transcription is a PROCESS where the POLYMERISATION of the polypeptide leads to the formation of amino acids.

28.

What does the anticodon loop of the tRNA contain?(a) A site for binding the amino acids(b) Bases that are complementary to the code(c) They have UAA codons(d) They have UAG codonsI got this question in my homework.My question is from tRNA-Adapter Molecule in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer»

The CORRECT answer is (B) Bases that are complementary to the code

For explanation I would say: The stop codons are UAA, UAG and UGA. These codons are absent in the tRNA molecules. tRNA POSSESSES an AMINO acid acceptor end which is the site for binding the amino acids. FINALLY, the anticodon loop of the tRNA contains bases that are complementary to the codes.

29.

Which of the following is an adapter molecule?(a) mRNA(b) rRNA(c) cRNA(d) tRNAThe question was posed to me in an online interview.This is a very interesting question from tRNA-Adapter Molecule topic in section Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct CHOICE is (d) TRNA

Best explanation: The tRNA was known by the name sRNA in its early DAYS. sRNA stands for soluble RNA. This was even before the postulation of the genetic code.But, the role of tRNA as an ADAPTER was assigned much later.

30.

Who came up with the idea of “adapter molecule”?(a) James Watson(b) Francis Crick(c) Gregor Mendel(d) Charles DarwinThe question was asked in an interview for internship.My query is from tRNA-Adapter Molecule topic in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct answer is (b) FRANCIS Crick

The explanation is: Amino acids do not have any structural specialties to read a CODE. Francis Crick came up with an IDEOLOGY that an adapter molecule will be PRESENT. This adapter molecule will be capable of both reading the code and ALSO on binding itself to the specific amino acid.

31.

Amino acids have no structural specialities to read a code in a unique mode.(a) True(b) FalseI got this question in my homework.My question comes from tRNA-Adapter Molecule topic in division Molecular Basis of Inheritance of Biology – Class 12

Answer»

The correct OPTION is (a) True

For EXPLANATION I would say: In the earlier days, Francis Crick FELT that a mechanism has to be there to read the codes. This was because amino acids possess no structural specialities to do that. And so, he POSTULATED that there had to be an ADAPTER molecule.

32.

When is a codon said to be unambiguous?(a) When it codes for 2 amino acids(b) When it codes for 1 amino acids(c) When it codes for 3 amino acids(d) When it codes for 4 amino acidsThis question was posed to me during an online interview.The query is from Molecular Basis of Inheritance topic in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer»

The correct choice is (B) When it codes for 1 amino acids

Explanation: One codon codes for only one amino acid. And so, the CODING is said to be unambiguous and specific. In some cases, one amino acid is coded more than once by MANY codons. These are CALLED are degenerates.

33.

How many codons code for an amino acid?(a) 3(b) 8(c) 90(d) 61The question was posed to me in a job interview.Origin of the question is Molecular Basis of Inheritance in section Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct option is (d) 61

Explanation: There are a total of 64 codons. Among these 64 codons, 61 codons are responsible for CODING the amino acids. The remaining 3 codons do not take PART in producing the amino acids. On the other hand, they are responsible for stopping the PRODUCTION of amino acids. Hence, they are CALLED as “STOP Codons”.

34.

How many bases are required for coding 20 amino acids?(a) 1(b) 2(c) 3(d) 4I had been asked this question in homework.Origin of the question is Molecular Basis of Inheritance in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct answer is (d) 4

For explanation I would SAY: George GAMOW who was a physicist mentioned that to be able to CODE for 20 amino acids, we require 4 bases. The code should also be MADE up of 3 NUCLEOTIDES. The code should be made up of bases in a particular combination.

35.

Which of the following refers to a proposition which directs the sequence of amino acids during protein synthesis?(a) DNA fingerprinting(b) Genetic Code(c) Transcription(d) EndolysisThis question was addressed to me in an online interview.My question comes from Molecular Basis of Inheritance topic in division Molecular Basis of Inheritance of Biology – Class 12

Answer»

Correct ANSWER is (b) Genetic CODE

The explanation: The change in NUCLEIC acids is responsible for the change in AMINO acids in the protein. This observation LED to the proposition of genetic code. Genetic code is responsible for directing the sequence of amino acids during protein synthesis.

36.

What is the approximate count of the total number of adenylate residues that are added to the 3’-end of the hnRNA during the process of tailing?(a) 100-200(b) 200-300(c) 300-400(d) 500-700This question was addressed to me by my school principal while I was bunking the class.This interesting question is from Molecular Basis of Inheritance topic in division Molecular Basis of Inheritance of Biology – Class 12

Answer»

Right ANSWER is (b) 200-300

For explanation I WOULD say: During the additional process of tailing that is undergone by the hnRNA, adenylate RESIDUES are added to it. An approximate count of 200-300 adenylate residues are added to it at the 3’-end of the hnRNA.

37.

Which of the following process represents the domination of the RNA-world?(a) Splicing(b) Trailing(c) Tailing(d) CappingThe question was asked in an internship interview.This question is from Molecular Basis of Inheritance in chapter Molecular Basis of Inheritance of Biology – Class 12

Answer»

The correct OPTION is (a) Splicing

To elaborate: The ancient FEATURE of a genome is represented by its split-gene ARRANGEMENTS. The presence of introns is a reminiscent of its antiquity. And so, the PROCESS of splicing gives a representation about the DOMINATION of the world of RNA (RNA-world).

38.

Which of the following types of RNA undergoes an additional process of capping and tailing during transcription?(a) sRNA(b) hnRNA(c) 5srRNA(d) snRNAI have been asked this question in homework.The origin of the question is Molecular Basis of Inheritance in portion Molecular Basis of Inheritance of Biology – Class 12

Answer» CORRECT answer is (B) hnRNA

To EXPLAIN: hnRNA undergoes the process of splicing. But in addition to that, it also undergoes the processes of capping and tailing. In splicing, the INTRONS are removed and the exons are arranged together.
39.

Which of the following is the unusual nucleotide that is added to the 5’-end of the hnRNA during capping?(a) Methyl Guanosine Triphosphate(b) Adenine(c) Guanine(d) Adenosine TriphosphateThe question was posed to me during an online exam.My question is taken from Molecular Basis of Inheritance in section Molecular Basis of Inheritance of Biology – Class 12

Answer» CORRECT answer is (a) Methyl Guanosine Triphosphate

Best EXPLANATION: In addition to the SPLICING process that the hnRNA undergoes, it also undergoes the processes of capping and TAILING. During the process of capping, the unusual nucleotide (i.e) Methyl Guanosine Triphosphate is ADDED to the 5’-end of the hnRNA.
40.

What is the name of the process where the introns are removed and the exons are joined together in a defined order?(a) Trailing(b) Capping(c) Tailing(d) SplicingThe question was posed to me by my school principal while I was bunking the class.The question is from Molecular Basis of Inheritance in division Molecular Basis of Inheritance of Biology – Class 12

Answer»

The correct CHOICE is (d) SPLICING

Explanation: The primary TRANSCRIPT CONSISTS of both the exons and the introns, and they are non-functional. And so, the introns are removed and the exons are ARRANGED in a well-defined manner. This process is called as splicing.

41.

What is the role of RNA polymerase III?(a) Transcription of rRNAs(b) Transcription of mRNAs(c) Transcription of tRNAs(d) Transcription of hnRNAThis question was posed to me in an international level competition.My enquiry is from Molecular Basis of Inheritance in division Molecular Basis of Inheritance of Biology – Class 12

Answer» CORRECT choice is (c) Transcription of tRNAs

To EXPLAIN I WOULD say: rRNAs are TRANSCRIBED with the help of RNA polymerase I. RNA polymerase II is responsible for the transcription of mRNA, which is the heterogeneous nuclear RNA (hnRNA). RNA polymerase III transcribes the tRNAs, 5srRNAs and SNRNAS.
42.

Which of the following stage is catalyzed by the RNA polymerase enzyme?(a) Initiation(b) Elongation(c) Termination(d) MonocistronicThe question was asked in an interview for internship.My question is based upon Types of RNA and Process of Transcription in Prokaryotes topic in portion Molecular Basis of Inheritance of Biology – Class 12

Answer»

The CORRECT option is (b) Elongation

For EXPLANATION I would say: There are three stages in the transcription process. They are initiation, elongation and termination. Among these three, the stage of elongation is catalyzed by the RNA POLYMERASE ENZYME.

43.

What happens when the polymerase enzyme reaches the terminator region during transcription?(a) The nascent RNA falls off(b) The nascent DNA falls off(c) The nascent protein falls off(d) The nascent enzyme falls offThis question was posed to me by my college director while I was bunking the class.Asked question is from Types of RNA and Process of Transcription in Prokaryotes topic in division Molecular Basis of Inheritance of Biology – Class 12

Answer» CORRECT CHOICE is (a) The nascent RNA falls off

To explain I would say: During the termination stage of transcription process, the nascent RNA falls off. This is observed when the polymerase enzyme reaches the terminator region. Following this, the RNA polymerase enzyme also falls off.
44.

Which of the following enzyme binds to the promoter and initiates the process of transcription?(a) DNA polymerase(b) Lipase(c) RNA polymerase(d) LysozymeThis question was addressed to me during an interview for a job.My question comes from Types of RNA and Process of Transcription in Prokaryotes in section Molecular Basis of Inheritance of Biology – Class 12

Answer»

The correct choice is (c) RNA polymerase

The explanation is: The RNA polymerase BINDS to the promoter REGION of the DNA molecule. After the attachment of the RNA polymerase enzyme to the promoter, the process of transcription is being INITIATED.

45.

What is the role of tRNA?(a) It provides the template strand(b) It brings the amino acids and reads the genetic code(c) It plays a catalytic role during translation(d) It plays a structural role during translationThis question was posed to me in an online interview.The question is from Types of RNA and Process of Transcription in Prokaryotes in portion Molecular Basis of Inheritance of Biology – Class 12

Answer»

Right ANSWER is (b) It brings the AMINO ACIDS and reads the genetic code

The explanation is: The role of mRNA is to PROVIDE the template strand. The role of TRNA is to bring the amino acids and read the genetic code. rRNA plays the structural and catalytic role during the process of translation.

46.

Which of the following is not a type of RNA?(a) mRNA(b) tRNA(c) rRNA(d) sRNAI have been asked this question by my college professor while I was bunking the class.This question is from Types of RNA and Process of Transcription in Prokaryotes topic in portion Molecular Basis of Inheritance of Biology – Class 12

Answer» RIGHT answer is (d) sRNA

To explain: There are THREE DIFFERENT types of RNA. They are mRNA (messenger RNA), rRNA (ribosomal RNA) and tRNA (transfer RNA). sRNA is a small ribosomal RNA. They are produced by the bacterium. The three different types of RNA are required for the synthesis of PROTEIN.
47.

The genes in eukaryotic organisms are split.(a) True(b) FalseThis question was addressed to me during a job interview.Asked question is from Transcription Unit and the Gene topic in portion Molecular Basis of Inheritance of Biology – Class 12

Answer» CORRECT CHOICE is (a) True

The best I can explain: The presence of monocistronic structural genes results in the formation of INTERRUPTED coding sequences. The monocistronic structural genes are present in the EUKARYOTES. So, their genes are split.
48.

Which of the following is polycistronic?(a) Bacteria(b) Rats(c) Snakes(d) HamsterThis question was posed to me in my homework.This is a very interesting question from Transcription Unit and the Gene topic in division Molecular Basis of Inheritance of Biology – Class 12

Answer» CORRECT answer is (a) BACTERIA

To explain: The polycistronic organisms can code for more than one polypeptide sequence as individuals inside the RNA MOLECULE. EXAMPLES of such are the bacteria and prokaryotes.
49.

What is a cistron?(a) A gene coding for RNA(b) A segment of DNA responsible for producing the nuclear coat(c) A segment of DNA coding for polypeptides(d) A gene coding for the template strand of DNAI got this question in my homework.Question is from Transcription Unit and the Gene in section Molecular Basis of Inheritance of Biology – Class 12

Answer»

Right option is (c) A segment of DNA CODING for polypeptides

For explanation I WOULD say: A CISTRON is the segment of a DNA. It is responsible for coding polypeptide chains. This is seen during the process of protein SYNTHESIS.

50.

Which of the following is monocistronic?(a) Fungi(b) Eukaryotes(c) Bacteria(d) VirusI got this question during an interview.Question is taken from Transcription Unit and the Gene topic in section Molecular Basis of Inheritance of Biology – Class 12

Answer»

Right option is (b) Eukaryotes

The best I can explain: Cistrons are the segments of the DNA HELICAL STRUCTURE which code for polypeptide chains. The structural gene in the transcription UNIT can be either monocistronic or POLYCISTRONIC. The monocistronic genes are mostly present in eukaryotes.