Answer:
Pressure :)))))))........
Watson and Crick's model explained mutability because bases pairs can suffer changes (mutations) during DNA replication. Moreover, this model also explained stability because DNA strands are held together by hydrogen bonds.
Deoxyribonucleic acid (DNA) is a double helix molecule composed of two long chains of four types of nucleotides, each containing one different nitrogenous base, i.e., Adenine, Guanine, Cytosine and Thymine.
In Watson and Crick's model, both DNA strands are held together by hydrogen bonds between nitrogenous bases on opposite DNA strands, thereby providing stability to the DNA molecule.
In DNA, Guanine always pairs with Cytosine by three hydrogen bonds, while Adenine always pairs with Thymine by two hydrogen bonds.
Moreover, Watson and Crick suggested that mutations could occur as a consequence of a base occurring very infrequently in one of the less likely tautomeric forms during DNA replication, thereby also explaining the mutability of life.
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Different types of blood contact different kinds of antigens and antibodies. For example, Type A blood has A antigens and B antibodies, antibodies being the thing that fights B antigens. Type B blood has B antigens and A antibodies. So if someone with type B gets transfused with Type A blood, the person's antibodies will attack the new blood.
Based on the above information, the mutation type is frameshift mutation.
It is a genetic mutation caused by indels of various nucleotides in a DNA succession that is not detachable by three. The additions and erasures cause an adjustment in the length of a quality, which causes a movement in the codon perusing outline. A frameshift mutation happens when a protein is radically modified as a result of an addition or an erasure. Tay-Sachs illness is a human issue caused by a frameshift change.
