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31. Define gene mutation. Describe the kinds of gene mutations. 32. Define chromatin. What are chromosomes?...

31. Define gene mutation. Describe the kinds of gene mutations.

32. Define chromatin. What are chromosomes? What are nucleosomes? How many chromosomes do humans have (diploid number)?

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31. A gene mutation is a permanent modification in a gene sequence, such that the sequence varies from generally found sequence in compare to other people.

Gene mutations have two categories-

Hereditary mutations or germline mutations inherit from parents and remain heritable throughout the generations.

Second kind is Acquired (or somatic) mutations that occur through environmental factors, errors in DNA amplification, protein formation or transcription, and induce by chemicals.

32. Chromatin is the complex form of macromolecules DNA, protein, and RNA. Chromatin is a very crucial structure present in the cell. It helps in compaction of large DNA molecule into nucleus, reopen when requires and prevention of the DNA.

The eukaryotic chromatin needs an important part of chromatin- the histone protein. The chromosome is an invisible thread like structure that made of complex by the histone protein with the DNA molecule. Each chromosome segregates in centromere and the short arm knows as p arm while the long arm as q arm.

Nucleosomes are the coiled structure of DNA around the histone protein, through them DNA is capable to arrange in very compact and dense structure- the chromosome.

Human have 23 pairs of chromosomes that are showing the diploid number of chromosome.

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