Tag: asexual modes of reproduction

Questions Related to asexual modes of reproduction

Morphallaxis is reported in

  1. Porifers

  2. Coelenterates and flatworms

  3. Nemarteans and some ascidians

  4. All the above


Correct Option: D
Explanation:

The reconstruction of an entire animal from a small fragment by reorganizing the existing cells, is called Morphallaxis. The regenerated animal is far smaller than the original one after the completion of the process. It grows to attain the normal size. It is reported in Porifers, Coelenterates, flatworms, Nemarteans, and some ascidians.

So, the correct option is ‘Porifers, Coelenterates, flatworms, Nemarteans, and some ascidians’.

Formation of whole body from a fragment is

  1. Morphallaxis

  2. Epimorphosis

  3. Epigenesis

  4. Auxetic growth


Correct Option: D
Explanation:

A. Morphallaxis - The reconstruction of an entire animal from a small fragment by reorganizing the existing cells, is called Morphallaxis.

B.Epimorphosis - The regeneration of tissues or organs through the dedifferentiation of existing, differentiated adult tissues

C.Epigenesis - The theory, now generally held, that an embryo develops progressively from an undifferentiated egg cell.

D. Auxetic growth – Growth takes place by the influence of auxins.

So, the correct option is ‘Auxetic growth’.

Regeneration was first discovered in

  1. Planaria

  2. Hydra

  3. Sponges

  4. Salamander


Correct Option: B
Explanation:

Formation of new cells or tissues in the body organs is called Regeneration. It is first discovered in hydra by Abraham Trembley.

So, the correct option is ‘Hydra’.

Enzyme' Taq polymerase' used in PCR, has been isolated from bacterium _________________.

  1. Agrobacterium tumefaciens

  2. Thermus aquaticus

  3. Streptomyces albus

  4. Escherichia coli


Correct Option: B
Explanation:

The final step of PCR is the extension, wherein Taq DNA polymerase is isolated from a thermophilic bacterium Thermus aquaticus.

The polymerase chain reaction is a technique used for ____________.

  1. Amplification of DNA

  2. Amplification of enzymes

  3. Amplification of proteins

  4. All of these


Correct Option: A
Explanation:

Polymerase chain reaction is a technique used for amplification of DNA fragments. Its amplification cycle involve three steps - denaturation, annealing and polymerisation which are repeated for 'n', cycles.

Which of the following statements are correct for the enzyme Taq polymerase?


(i) It remains active during the high temperature-induced denaturation of dsDNA.

(ii) It requires primers for carrying out the process of polymerisation.
(iii) It synthesizes the RNA region between the primers, using $dNTPs$ and $Mg^{2+}$ _______________.

  1. (i) and (ii)

  2. (ii) and (iii)

  3. (i), (ii) and (iii)

  4. None of these


Correct Option: A
Explanation:

The final step of PCR is the extension, wherein Taq DNA polymerase (isolated from a thermophilic bacterium Thermus aquaticus) synthesizes the DNA region between the primers, using dNTPs (deoxynucleoside triphosphates) and $Mg^{2+}$. The primers are extended towards each other so that the DNA segment lying between the two primers is copied. The optimum temperature for this polymerisation step is $72^o$$C$. Taq polymerase remains active during high temperature-induced denaturation of double-stranded DNA.

Process used for amplification or multiplication of DNA in DNA fingerprinting is

  1. Polymerase chain reaction

  2. Southern blotting

  3. Northern blotting

  4. None of these


Correct Option: A
Explanation:

Process used for amplification or multiplication of DNA in DNA fingerprinting is Polymerase chain reaction (PCR) .It is done in invitro system.

So, the correct option is 'Option A' . 

Primers are

  1. Chemically synthesised oligonucleotides that are complementary to the regions of DNA

  2. Chemically synthesised oligonucleotides that are not complementary to the regions of DNA

  3. Chemically synthesised, autonomously replicating circular DNA molecules

  4. Specific sequences present on recombinant DNA


Correct Option: A
Explanation:
Primers are small, chemically synthesised oligonucleotides that are complementary to the sequences, present at 3' end of the template DNA. They hybridise to the target DNA region, one to each strand of the double helix. These primers are oriented with their ends facing each other allowing synthesis of the DNA towards one another.
So, the correct answer is 'Chemically synthesised oligonucleotides that are complementary to the regions of DNA'.

Given table gives an account of differences between PCR and gene cloning. Which of the, following points shows the incorrect difference?

  Parameter PCR Gene cloning
1 Efficient More Less
2 Apparatus Requirement DNA Restriction enzyme, ligase, vector, bacterial cell
3 Manipulation In vitro In vitro and in vivo
4 Cost More Less
5 Automation Yes No
6 Error probability Less More
7 Time for a typical experiment 2-4 days 4 hours
8 Application More Less


  1. 1 and 3

  2. 4 and 6

  3. 4 and 7

  4. 4, 7 and 8


Correct Option: C
Explanation:

The cost of gene cloning is far more than PCR because gene cloning requires many intricate steps. PCR takes less than 4 hours while gene cloning can take days.

In a polymerase chain reaction, temperature required for the steps (i) Denaturation,(ii) Annealing, and (iii) Extension are respectively.

  1. (i) $94^o$$C$ (ii) $40^o$$C$ (iii) $72^o$$C$

  2. (i) $40^o$$C$ (ii) $72^o$$C$ (iii) $94^o$$C$

  3. (i) $94^o$$C$ (ii) $72^o$$C$ (iii) $40^o$$C$

  4. (i) $72^o$$C$ (ii) $94^o$$C$ (iii) $40^o$$C$


Correct Option: A
Explanation:
  • At the start of PCR, the DNA from which a segment is to be amplified, an excess of the two primer molecules, the four deoxynucleoside triphosphates and the DNA polymerase are mixed in the reaction mixture that has appropriate quantities of $Mg^{2+}$. 
  • The reaction mixture is first heated to a temperature between $90-$$98^oC$ (commonly $94^oC$) that ensures DNA denaturation. Every single strand of the target DNA then acts as a template for DNA synthesis. This is the denaturation step. The duration of this step in the first cycle of PCR is usually 2 min at  $94^oC$
  • The mixture is now cooled to a temperature (generally $40-60^oC$) that permits annealing of the primer to the complementary sequences in the DNA. This step is called annealing. The duration of the annealing step is usually 1 min.
  • The primers are extended towards each other so that the DNA segment lying between the two primers is copied, this is ensured by employing primers complementary to the 3': ends of the segment to be amplified. The duration of primer extension is usually 2 min at $72^oC$.