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NCERT Exemplar solutions for बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ chapter 6 - Molecular Basis of Inheritance [Latest edition]

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NCERT Exemplar solutions for बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ chapter 6 - Molecular Basis of Inheritance - Shaalaa.com
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Solutions for Chapter 6: Molecular Basis of Inheritance

Below listed, you can find solutions for Chapter 6 of CBSE, Karnataka Board PUC NCERT Exemplar for बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२.


MULTIPLE CHOICE QUESTIONSVERY SHORT ANSWERSHORT ANSWERLONG ANSWER
MULTIPLE CHOICE QUESTIONS [Pages 36 - 40]

NCERT Exemplar solutions for बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ 6 Molecular Basis of Inheritance MULTIPLE CHOICE QUESTIONS [Pages 36 - 40]

1.Page 36

In a DNA strand the nucleotides are linked together by ______.

  • phosphodiester bonds

  • glycosidic bonds

  • peptide bonds

  • hydrogen bonds

2.Page 36

A nucleoside differs from a nucleotide. It lacks the ______.

  • phosphate group

  • hydroxyl group

  • sugar

  • base

3.Page 36

Both deoxyribose and ribose belong to a class of sugars called ______.

  • pentoses

  • polysaccharides

  • hexoses

  • trioses

4.Page 36

The fact that a purine base always paired through hydrogen bonds with a pyrimidine base leads to, in the DNA double helix ______.

  • uniform width throughout DNA

  • uniform length in all DNA

  • the semiconservative nature

  • the antiparallel nature

5.Page 36

The net electric charge on DNA and histones is ______.

  • negative and positive, respectively

  • both negative

  • both positive

  • zero

6.Page 37

The promoter site and the terminator site for transcription are located at ______.

  • 5' (upstream) end and 3' (downstream) end, respectively of thetranscription unit

  • the 5' (upstream) end

  • the 3' (downstream) end

  • 3' (downstream) end and 5' (upstream) end, respectively of the transcription unit

7.Page 37

Which of the following statements is the most appropriate for sickle cell anaemia?

  • It cannot be treated with iron supplements

  • It is a molecular disease

  • It confers resistance to acquiring malaria

  • All of the above

8.Page 37

Which of the following is true with respect to AUG?

  • It codes for methionine only

  • It is an initiation codon

  • It codes for methionine in both prokaryotes and eukaryotes

  • All of the above

9.Page 37

The first genetic material could be ______.

  • RNA

  • DNA

  • carbohydrates

  • protein

10.Page 37

With regard to mature mRNA in eukaryotes.

  • exons appear but introns do not appear in the mature RNA

  • exons and introns do not appear in the mature RNA

  • introns appear but exons do not appear in the mature RNA

  • both exons and introns appear in the mature RNA

11.Page 37

The human chromosome with the highest and least number of genes in them are respectively ______.

  • Chromosome 1 and Y

  • Chromosome 1 and X

  • Chromosome X and Y

  • Chromosome 21 and Y

12.Page 38

Who amongst the following scientists had no contribution in the development of the double helix model for the structure of DNA?

  • Meselson and Stahl

  • Erwin Chargaff

  • Maurice Wilkins

  • Rosalind Franklin

13.Page 38

DNA is a polymer of nucleotides which are linked to each other by 3’-5’ phosphodiester bond. To prevent polymerisation of nucleotides, which of the following modifications would you choose?

  • Remove/Replace 3' OH group in deoxy ribose

  • Remove/Replace 2' OH group with some other group in deoxy ribose

  • Both ‘B’ and ‘C’

  • Replace purine with pyrimidines

14.Page 38

Discontinuous synthesis of DNA occurs in one strand, because ______.

  • DNA dependent DNA polymearse catalyses polymerisation only in one direction (5' → 3')

  • DNA molecule being synthesised is very long

  • it is a more efficient process

  • DNA ligase has to have a role

15.Page 38

Which of the following steps in transcription is catalysed by RNA polymerse?

  • Elongation

  • Initiation

  • Termination

  • All of the above

16.Page 38

Control of gene expression in prokaryotes takes place at the level of ______.

  • Transcription

  • Translation

  • DNA-replication

  • None of the above

17.Page 38

Which of the following statements is correct about the role of regulatory proteins in transcription in prokaryotes?

  • They only increase expression

  • They only decrease expression

  • They interact with RNA polymerase but do not affect the expression

  • They can act both as activators and as repressors

18.Page 39

Which was the last human chromosome to be completely sequenced?

  • Chromosome 1

  • Chromosome 11

  • Chromosome 21

  • Chromosome x

19.Page 39

Which of the following are the functions of RNA?

  • It is a constituent component of ribosomes

  • It carries amino acids to ribosomes

  • It is a carrier of genetic information from DNA to ribosomes synthesising polypeptides

  • All of the above

20.Page 39

While analysing the DNA of an organism a total number of 5386 nucleotides were found out of which the proportion of different bases were: Adenine = 29%, Guanine = 17%, Cytosine = 32%, Thymine = 17%. Considering the Chargaff’s rule it can be concluded that ______.

  • It is single stranded DNA

  • it is a double stranded circular DNA

  • It is a double stranded linear DNA

  • No conclusion can be drawn

21.Page 39

In some viruses, DNA is synthesised by using RNA as template. Such a DNA is called ______.

  • cDNA

  • rDNA

  • B-DNA

  • A-DNA

22.Page 39

If Meselson and Stahl's experiment is continued for four generations in bacteria, the ratio of `15_N/15_N:15_N/14_N:14_N/14_N` containing DNA in the fourth generation would be ______.

  • 0 : 1 : 7

  • 0 : 1 : 3

  • 1 : 4 : 0

  • 1 : 1 : 0

23.Page 39

If the sequence of nitrogen bases of the coding strand of DNA in a transcription unit is 5’ - ATGAATG - 3’ the sequence of bases in its RNA transcript would be ______.

  • 5’ - AUGAAUG - 3’

  • 5’ - UACUUAC - 3’

  • 5’ - CAUUCAU - 3’

  • 5’ - GUAAGUA - 3’

24.Page 40

The RNA polymerase holoenzyme transcribes ______.

  • the structural gene and the terminator region

  • the structural gene only

  • the promoter and the terminator region

  • the promoter, structural gene, and the terminator region

25.Page 40

If the base sequence of a codon in mRNA is 5'-AUG-3', the sequence of tRNA pairing with it must be ______.

  • 5' - CAU - 3'

  • 5' - AUG - 3'

  • 5' - GUA - 3'

  • 5' - UAC - 3'

26.Page 40

The amino acid attaches to the tRNA at its ______.

  • 3' - end

  • 5' - end

  • Anti codon site

  • DHU loop

27.Page 40

To initiate translation, the mRNA first binds to ______.

  • The smaller ribosomal sub-unit

  • The larger ribosomal sub-unit

  • The whole ribosome

  • No such specificity exists

28.Page 40

In E.coli, the lac operon gets switched on when ______.

  • lactose is present and it binds to the repressor.

  • repressor binds to operator.

  • RNA polymerase binds to the operator.

  • lactose is present and it binds to RNA polymerase.

VERY SHORT ANSWER [Pages 40 - 41]

NCERT Exemplar solutions for बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ 6 Molecular Basis of Inheritance VERY SHORT ANSWER [Pages 40 - 41]

1.Page 40

What is the function of histones in DNA packaging?

2.Page 40

Distinguish between heterochromatin and euchromatin. Which of the two is transcriptionally active?

3.Page 41

The enzyme DNA polymerase in E.coli is a DNA dependent polymerase and also has the ability to proof-read the DNA strand being synthesised. Explain. Discuss the dual polymerase.

4.Page 41

What is the cause of discontinuous synthesis of DNA on one of the parental strands of DNA? What happens to these short stretches of synthesised DNA?

5.aPage 41

Given below is the sequence of coding strand of DNA in a transcription unit 3 'A A T G C A G C T A T T A G G – 5’ write the sequence of its complementary strand

5.bPage 41

Given below is the sequence of coding strand of DNA in a transcription unit 3 'A A T G C A G C T A T T A G G – 5’ write the sequence of the mRNA

6.Page 41

What is DNA polymorphism? Why is it important to study it?

7.Page 41

Based on your understanding of genetic code, explain the formation of any abnormal hemoglobin molecule. What are the known consequences of such a change?

8.Page 41

Sometimes cattle or even human beings give birth to their young ones that are having extremely different sets of organs like limbs/position of eye(s) etc. Comment.

9.Page 41

In a nucleus, the number of ribonucleoside triphosphates is 10 times the number of deoxy x10 ribonucleoside triphosphates, but only deoxy ribonucleotides are added during the DNA replication. Suggest a mechanism.

10.Page 41

Name a few enzymes involved in DNA replication other than DNA polymerase and ligase. Name the key functions for each of them.

11.Page 41

Name any three viruses which have RNA as the genetic material.

SHORT ANSWER [Pages 41 - 43]

NCERT Exemplar solutions for बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ 6 Molecular Basis of Inheritance SHORT ANSWER [Pages 41 - 43]

1.Page 41

Define transformation in Griffith's experiment. Discuss how it helps in the identification of DNA as the genetic material.

2.Page 41

Who revealed biochemical nature of the transforming principle? How was it done?

3.Page 41

Discuss the significance of heavy isotope of nitrogen in the Meselson and Stahl’s experiment.

4.Page 42

Define a cistron. Giving examples differentiate between monocistronic and polycistronic transcription unit.

5.Page 42

Give any six features of the human genome.

6.Page 42

During DNA replication, why is it that the entire molecule does not open in one go? Explain replication fork. What are the two functions that the monomers (dNTPs) play?

7.Page 42

Retroviruses do not follow central Dogma. Comment.

8.Page 42

In an experiment, DNA is treated with a compound which tends to place itself amongst the stacks of nitrogenous base pairs. As a result of which, the distance between two consecutive base increases, from 0.34nm to 0.44 nm. Calculate the length of DNA double helix (which has 2 × 109 bp) in the presence of saturating amount of this compound.

9.Page 42

What would happen if histones were to be mutated and made rich in acidic amino acids such as aspartic acid and glutamic acid in place of basic amino acids such as lysine and arginine?

10.Page 42

Recall the experiments done by Frederick Griffith, Avery, MacLeod and McCarty, where DNA was speculated to be the genetic material. If RNA, instead of DNA was the genetic material, would the heat killed strain of Pneumococcus have transformed the R-strain into virulent strain? Explain.

11.Page 42

You are repeating the Hershey-Chase experiment and are provided with two isotopes: 32P and 15N (in place of 35S in the original experiment). How do you expect your results to be different?

12.Page 42

There is only one possible sequence of amino acids when deduced from a given nucleotides. But multiple nucleotides sequence can be deduced from a single amino acid sequence. Explain this phenomena.

13.Page 42

A single base mutation in a gene may not ‘always’ result in loss or gain of function. Do you think the statement is correct? Defend your answer.

14.Page 42

A low level of expression of the lac operon occurs at all times. Can you explain the logic behind this phenomenon?

15.Page 42

How has the sequencing of human genome opened new windows for treatment of various genetic disorders. Discuss amongst your classmates.

16.Page 42

The total number of genes in humans is far less (< 25,000) than the previous estimate (upto 1,40,000 gene). Comment.

17.Page 42

Now, sequencing of total genomes getting is getting less expensive day by the day. Soon it may be affordable for a common man to get his genome sequenced. What in your opinion could be the advantage and disadvantage of this development?

18.Page 43

Would it be appropriate to use DNA probes such as VNTR in DNA finger printing of a bacteriaphage?

19.Page 43

During in vitro synthesis of DNA, a researcher used 2’, 3’ – dideoxy cytidine triphosphate as raw nucleotide in place of 2’-deoxy cytidine. What would be the consequence?

20.Page 43

What background information did Watson and Crick had available with them for developing a model of DNA? What was their own contribution?

21.(i)Page 43

What are the functions of methylated guanasine cap?

21.(ii)Page 43

What are the functions of poly-A “tail” in a mature on RNA?

22.Page 43

Do you think that the alternate splicing of exons may enable a structural gene to code for several isoproteins from one and the same gene? If yes, how? If not, why so?

23.Page 43

Comment on the utility of variability in number of tandem repeats during DNA finger printing.

LONG ANSWER [Page 43]

NCERT Exemplar solutions for बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ 6 Molecular Basis of Inheritance LONG ANSWER [Page 43]

1.Page 43

Give an account of Hershey and Chase experiment. What did it conclusively prove? If both DNA and proteins contained phosphorus and sulphur do you think the result would have been the same?

2.Page 43

During the course of evolution why DNA was chosen over RNA as genetic material? Give reasons by first discussing the desired criteria in a molecule that can act as genetic material and in the light of biochemical differences between DNA and RNA.

3.Page 43

Give an account of post transcriptional modifications of a eukaryotic mRNA.

4.Page 43

Discuss the process of translation in detail.

5.Page 43

Define an operon. giving an example, explain an Inducible operon.

6.Page 43

‘There is a paternity dispute for a child’. Which technique can solve the problem. Discuss the principle involved.

7.Page 43

Give an account of the methods used in sequencing the human genome.

8.Page 43

List the various markers that are used in DNA finger printing.

9.Page 43

Replication was allowed to take place in the presence of radioactive deoxynucleotides precursors in E.coli that was a mutant for DNA ligase. Newly synthesised radioactive DNA was purified and strands were separated by denaturation. These were centrifuged using density gradient centrifugation. Which of the following would be a correct result?

Solutions for 6: Molecular Basis of Inheritance

MULTIPLE CHOICE QUESTIONSVERY SHORT ANSWERSHORT ANSWERLONG ANSWER
NCERT Exemplar solutions for बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ chapter 6 - Molecular Basis of Inheritance - Shaalaa.com

NCERT Exemplar solutions for बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ chapter 6 - Molecular Basis of Inheritance

Shaalaa.com has the CBSE, Karnataka Board PUC Mathematics बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ CBSE, Karnataka Board PUC solutions in a manner that help students grasp basic concepts better and faster. The detailed, step-by-step solutions will help you understand the concepts better and clarify any confusion. NCERT Exemplar solutions for Mathematics बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ CBSE, Karnataka Board PUC 6 (Molecular Basis of Inheritance) include all questions with answers and detailed explanations. This will clear students' doubts about questions and improve their application skills while preparing for board exams.

Further, we at Shaalaa.com provide such solutions so students can prepare for written exams. NCERT Exemplar textbook solutions can be a core help for self-study and provide excellent self-help guidance for students.

Concepts covered in बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ chapter 6 Molecular Basis of Inheritance are Deoxyribonucleic Acid (DNA), Structure of Polynucleotide Chain, Packaging of DNA Helix, Search for Genetic Material, Griffith’s Experiment, Avery, McCarty and MacLeod’s Experiment, The Hershey-Chase Experiment, Properties of Genetic Material, The RNA World, DNA Replication, Conservative Replication, Dispersive Replication, Semi-Conservative Replication, Meselson and Stahl’s Experiment, Enzymes used in DNA Replication, Mechanism of DNA Replication, Reverse Transcription (Teminism), Transcription, Transcription Unit and the Gene, Process of Transcription in Bacteria, Process of Transcription in Eukaryotes, Genetic Code, Characteristics of the Genetic Code, Mutations and Genetic Code, tRNA – the Adapter Molecule, Translation, Regulation of Gene Expression, The Lac Operon, Human Genome Project, DNA Fingerprinting, Protein Synthesis.

Using NCERT Exemplar बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ solutions Molecular Basis of Inheritance exercise by students is an easy way to prepare for the exams, as they involve solutions arranged chapter-wise and also page-wise. The questions involved in NCERT Exemplar Solutions are essential questions that can be asked in the final exam. Maximum CBSE, Karnataka Board PUC बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ students prefer NCERT Exemplar Textbook Solutions to score more in exams.

Get the free view of Chapter 6, Molecular Basis of Inheritance बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ additional questions for Mathematics बायोलॉजी एक्सेम्पलार [इंग्रजी] इयत्ता १२ CBSE, Karnataka Board PUC, and you can use Shaalaa.com to keep it handy for your exam preparation.

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