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40

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

Explanation

In Griffith's experiment, transformation can be defined as a change in the genetic constitution of an organism by picking out up DNA from the environment (from dead organisms).

Transformation helps in identification of DNA as a genetic material. When heat was used to kill the virulent bacteria, they died but not their genetic material (DNA). This DNA when picked up by non-virulent bacteria made them capable of causing infection.

Since, ability to cause infection could be passed on by these organisms to their progeny, it was concluded that DNA was the material that was inherited.

41

$$ \text { Who revealed biochemical nature of the transforming principle? } $$

Explanation

Oswald, Avery, Colin MacLeod and Maclyn McCarty revealed biochemical nature of the transforming principle.

They reported Griffith's experiment in an in vitro system in order to determine biochemical nature of transforming principle.

They reported that DNA from the heat-killed S-type bacteria caused the transformation of non-virulent R-type bacteria into virulent S-type bacteria. They also discovered that proteases and RNase did not affect transformation while DNase inhibited the process. They concluded that DNA is the hereditary material.

42

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

Explanation

They performed experiments on $E$. coli to prove that DNA replication is semi-conservative. They first grew the bacteria in a medium containing ${ }^{15} \mathrm{NH}_4 \mathrm{Cl}$ (in which ${ }^{15} \mathrm{~N}$ is the heavy istope of nitrogen) for many generations.

Then they transferred the cells into a medium with normal ${ }^{14} \mathrm{NH}_4 \mathrm{Cl}$ (in which ${ }^{14} \mathrm{~N}$ is the lighter isotope) and took the samples at various definite time intervals as the cells multiplied. The extracted DNAs were centrifuged and measured to get their densities.

The DNA extracted from the culture after one generation of transfer from then ${ }^{15} \mathrm{~N}$ mediun to ${ }^{14} \mathrm{~N}$ mediun, (i.e., after 20 minutes E.coli divides every 20 minutes) showed an intermediate hybrid density, i.e., both heavy and light nitrogen, which proved the semi-conservative nature of DNA.

43

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

Explanation

A cistron is stretch of base sequences that codes for one polypeptide chain including adjacent control regions. It may also code for a tRNA, rRNA molecule or may perform other specific functions including regulating functions of other cistrons.

This term has replaced the definition of a gene. Monocistronic transcription unit will have all the regulatory and coding sequences for a single polypeptide, whereas polycistronic may have coding sequences for more than one polypeptide.

In eukaryotic cells almost all the messenger RNAs are monocistronic. In prokaryotes, lac operon coding sequence would be an example of polycistronic DNA region.

44

$$ \text { Give any six features of the human genome. } $$

Explanation

Salient features of human genome

(i) The human genome contains 3164.7 million nucleotide bases.

(ii) The average gene consists of 30000 the largest know human gene being dystrophin at 2.4 Million bases.

(iii) The total number of genes is estimated to be 30000 and $99.9 \%$ nucleotide bases are exactly the same in all people.

(iv) The functions are unknown for over $50 \%$ of the discovered genes.

(v) Less than $2 \%$ of the genome codes for proteins.

(vi) The human genome contains large repeated sequences.

(vii) The repeated sequence is thought to have no direct coding functions but they throw light on chromosome structures, dynamics and evolution.

viii) Chromosome I has most genes (2968) and the Y has the fewest genes (231).

(ix) Scientists have identified about 1.4 million locations where single base DNA sequence differences called SNPs or Single Nucleotide Polymorphisms occur in humans.