NCERT Class 12 Biology Solutions: Chapter 6 - Molecular Basis of Inheritance
Group the following as nitrogenous bases and nucleosides
Adenine, Cytidine, Thymine, Guanosine, Uracil, and Cytosine.
Solution: Nitrogenous bases present in the list are adenine, thymine, uracil, and cytosine. Nucleosides present in the list are cytidine and guanosine.
If a double-stranded DNA has 20 percent of cytosine, calculate the percent of adenine in the DNA.
Solution: According to Chargaff’s rule, the DNA molecule should have an equal ratio of pyrimidine (cytosine and thymine) and purine (adenine and guanine).
% A = % T and % G = % C
If dsDNA has 20% of cytosine, then according to the law, it would have 20% of guanine. Thus, percentage of G + C content = 40%
The remaining 60% represents both A + T molecule.
Since adenine and guanine are always present in equal numbers, the percentage of adenine molecule is 30%.
If the sequence of one strand of DNA is written as follows:
5'-ATGCATGCATGCATGCATGCATGCATGC-3'. Write down the sequence of a complementary strand in 5'→3' direction
The DNA strands are complementary to each other with respect to base sequence. Hence, if the sequence of one strand of DNA is
5'- ATGCATGCATGCATGCATGCATGCATGC – 3’
Then, the sequence of a complementary strand in 5' to 3' direction will be
3'- TACGTACGTACGTACGTACGTACGTACG − 5’
Therefore, the sequence of nucleotides on DNA polypeptide in 5' to 3' direction is
5'- GCATGCATGCATGCATGCATGCATGCAT− 3’
If the sequence of the coding strand in a transcription unit is written as follows:
5'-ATGCATGCATGCATGCATGCATGCATGC-3'. Write down the sequence of mRNA.
Solution: If the coding strand in a transcription unit is
A sequence of mRNA is the same as the coding strand of DNA.
However, in mRNA, thymine is replaced by uracil. Hence, the sequence of mRNA will be
5’ − AUGCAUGCAUGCAUGCAUGCAUGCAUGC-3’
Which property of DNA double helix led Watson and Crick to hypothesize semiconservative mode of DNA replication? Explain.
Solution: Watson and Crick observed that the two strands of DNA are complementary to each other with respect to their base sequences. This arrangement led to the hypothesis that DNA replication is semiconservative. It means that the double stranded DNA molecule separates and then, each of the separated strand acts as a template for the synthesis of a new complementary strand. As a result, each DNA molecule would have one parental strand and a newly synthesized daughter strand. As only one parental strand is conserved in each daughter molecule, it is known as semi-conservative mode of replication.
Depending upon the chemical nature of the template (DNA or RNA) and the nature of nucleic acids synthesized from it (DNA or RNA), list the types of nucleic acid polymerases.
Solution: There are two different types of nucleic acid polymerases.
- DNA-dependent DNA polymerases: The DNA-dependent DNA polymerases use a DNA template for synthesizing a new strand of DNA.
- DNA-dependent RNA polymerase: Whereas DNA-dependent RNA polymerases use a DNA template strand for synthesizing RNA.
How did Hershey and Chase differentiate between DNA and protein in their experiment while proving that DNA is the genetic material?
Solution: Hershey and Chase worked with bacteriophage and E.Coli to prove that DNA is the genetic material. Some bacteriophages are grown on a medium containing radioactive phosphorus to identify DNA and some on a medium containing radioactive sulfur to identify the protein. Then, these radioactively labeled phages were allowed to infect E.coli bacteria. After infecting, the protein coat of the bacteriophage was separated from the bacterial cell by blending and then subjected to the process of centrifugation. Since the protein coat was lighter, it was found in the supernatant while the infected bacteria got settled at the bottom of the centrifuge tube. Hence, it was proved that DNA is the genetic material as it was transferred from virus to bacteria.
Differentiate between the following:
(a) Repetitive DNA and Satellite DNA
(b) mRNA and tRNA
(c) Template strand and Coding strand
(a) Repetitive DNA and satellite DNA
(b) mRNA and tRNA
(c) Template strand and coding strand
List two essential roles of the ribosome during translation.
The important functions of the ribosome during translation are as follows.
- Ribosome acts as the site where protein synthesis takes place from individual amino acids. The smaller subunit of ribosome comes in contact with mRNA and forms a protein synthesizing complex whereas the larger subunit of ribosome acts as an amino acid binding site.
- Ribosome acts as a catalyst for forming peptide bond. For example, 23s r-RNA in bacteria acts as a ribozyme.
In the medium where coli was growing, lactose was added, which induced the lac operon. Then, why does lac operon shut down sometime after the addition of lactose in the medium?
Solution: Lac operon is a segment of DNA that is made up of three adjacent structural genes, namely, an operator gene, a promoter gene, and a regulator gene. It works in a coordinated manner to metabolize lactose into glucose and galactose.
In lac operon, lactose acts as an inducer. It binds to the repressor and inactivates it. Once the lactose binds to the repressor, RNA polymerase binds to the promoter region. Hence, three structural genes express their product and respective enzymes are produced. These enzymes act on lactose so that lactose is metabolized into glucose and galactose.
After sometime, when the level of inducer decreases as it is completely metabolized by enzymes, it causes the synthesis of the repressor from regulator gene. The repressor binds to the operator gene and prevents RNA polymerase from transcribing the operon. Hence, the transcription is stopped.
- Explain (in one or two lines) the function of the followings:
Promoter is a region of DNA that helps in initiating the process of transcription. It serves as the binding site for RNA polymerase.
tRNA or transfer RNA is a small RNA that reads the genetic code present on mRNA. It carries specific amino acid to mRNA on ribosome during translation of proteins.
Exons are coding sequences of DNA in eukaryotes that transcribe for proteins.
Why is the Human Genome project called a mega project?
Solution: Human genome project was considered to be a mega project because it had a specific goal to sequence every base pair present in the human genome. It took around 13 years for its completion and got completed in year 2006. It was a large scale project, which aimed at developing new technology and generating new information in the field of genomic studies.
What is DNA fingerprinting? Mention its application.
Solution: DNA fingerprinting is a technique used to identify and analyse the variations in various individuals at the level of DNA. It is based on variability and polymorphism in DNA sequences.
- It is used in forensic sciences to identify potential crime suspects.
- It is used to establish paternity.
- It is used to identify and protect commercial varieties of crops and livestock.
- It is used to find out the evolutionary history of an organism.
Briefly describe the following:
Transcription is the process of synthesis of RNA from DNA template. A segment of DNA gets copied into mRNA during the process.
The three important events that occur during the process of transcription are as follows.
Initiation: The DNA-dependent RNA polymerase and certain initiation factors (σ) bind at the double stranded DNA at the promoter region of the template strand and initiate the process of transcription.
Elongation: RNA polymerase moves along the DNA and leads to the unwinding of DNA duplex into two separate strands. Then, one of the strands, called sense strand, acts as a template for mRNA synthesis. The enzyme, RNA polymerase, utilizes nucleoside triphosphates (dNTPs) as raw material and polymerizes them to form mRNA according to the complementary bases present on the template DNA.
Termination: This process of opening of helix and elongation of the polynucleotide chain continues until the enzyme reaches the terminator region. As RNA polymerase reaches the terminator region, the newly synthesized mRNA transcripted along with enzyme is released. Another factor called terminator factor (ρ) is required for the termination of the transcription.
Polymorphism is a form of genetic variation in which distinct nucleotide sequence can exist at a particular site in a DNA molecule. It arises due to mutation either in somatic cell or in the germ cells. The germ cell mutation can be transmitted from parents to their offsprings. This results in accumulation of various mutations in a population, leading to variation and polymorphism in the population. This plays a very important role in the process of evolution and speciation.
The translation is the process of polymerizing amino acid to form a polypeptide chain. The triplet sequence of base pairs in mRNA defines the order and sequence of amino acids in a polypeptide chain.
The process of translation involves three steps.
- Initiation: During the initiation of the translation, tRNA gets charged when the amino acid binds to it using ATP. The start (initiation) codon (AUG) present on mRNA is recognized only by the charged tRNA. The ribosome acts as an actual site for the process of translation and contains two separate sites in a large subunit for the attachment of subsequent amino acids. The small subunit of ribosome binds to mRNA at the initiation codon (AUG) followed by the large subunit. Then, it initiates the process of translation.
- Elongation: During the elongation process, the ribosome moves one codon downstream along with mRNA so as to leave the space for binding of another charged tRNA. The amino acid brought by tRNA gets linked with the previous amino acid through a peptide bond and this process continues resulting in the formation of a polypeptide chain.
- Termination: When the ribosome reaches one or more STOP codon (VAA, UAG, and UGA), the process of translation gets terminated. The polypeptide chain is released and the ribosomes get detached from mRNA.
Bioinformatics is the application of computational and statistical techniques to the field of molecular biology. The field of bioinformatics developed after the completion of the human genome project (HGP). This is because an enormous amount of data has been generated during the process of HGP that has to be managed and stored for easy access and interpretation for future use by various scientists. Hence, bioinformatics involves the creation of biological databases that store the vast information of biology.
It involves the development of certain tools for easy and efficient access to the information and its utilization. Bioinformatics has developed new algorithms and statistical methods to find out the relationship between the data, to predict protein structure and their functions, and to cluster the protein sequences into their related families.
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