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∙ 14y agoMutation occurs where one DNA nucleotide base is changed in the process of DNA replication. These mutations may or may not cause genetic disorders or other observable changes in the organism, but they play a huge role in evolution, cancer, and immune system development.
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∙ 9y agoThe substitution of one base for another during DNA replication is an example of a point mutation. This type of mutation can result in changes to the amino acid sequence of a protein, which can impact its structure and function.
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∙ 12y agoThe substitution of one base for another during DNA replication is an example of a point mutation. Depending on the substitution, this could be harmless, or it could cause a genetic disorder, such as sickle cell anemia.
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∙ 9y agoWhen a mistake happens in the process of copying DNA, the result is called a Mutation.
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∙ 14y agomutations
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∙ 14y agoMutation
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∙ 14y agoA mutation
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∙ 10y agomutation
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∙ 12y agoA mutation
One common example of a substitution mutation is a point mutation where one nucleotide base is replaced by another. This can lead to changes in the amino acid sequence of a protein during translation. An example would be a mutation where a Cytosine (C) is substituted for a Thymine (T) in the DNA sequence.
During replication, enzymes called helicases unwind and separate the DNA strands by breaking the hydrogen bonds between the base pairs. This process creates a replication fork where new complementary strands are synthesized.
DNA replication is the second part of inter-phase where the cell makes an exact copy of the DNA in its cell. Please see the answer to the related question below..
DNA is copied during a process called DNA replication. This process occurs in the nucleus of a cell and involves making an exact copy of the original DNA molecule. DNA replication is essential for cell division and passing genetic information from one generation to the next.
The sites where DNA replication and separation occur are called the replication fork, which is formed during DNA replication when the double-stranded DNA is unwound, and the centromere, which is the region of a chromosome where sister chromatids are held together before separation during cell division.
Mutations
Substitution mutations are typically caused by errors during DNA replication, where a wrong nucleotide is incorporated into the DNA sequence. This can also be caused by exposure to mutagens, such as certain chemicals or radiation, which can lead to changes in the DNA nucleotide sequence.
The specific type of mutation resulting from a mistake during DNA replication will depend on the nature of the mistake and the type of nucleotide substitution that occurred. Some possible types of mutations include point mutations (such as a substitution, insertion, or deletion of a single nucleotide), frameshift mutations, or silent mutations.
One common example of a substitution mutation is a point mutation where one nucleotide base is replaced by another. This can lead to changes in the amino acid sequence of a protein during translation. An example would be a mutation where a Cytosine (C) is substituted for a Thymine (T) in the DNA sequence.
A cell's DNA is copied during replication.
I can find no reference to a molecule used in "pf" replication. Do you have another term in mind? Please resubmit your question if you do.
The difference between between replication and replication is that replication is the series of copies, and repetition is the series of repeats.
During replication, enzymes called helicases unwind and separate the DNA strands by breaking the hydrogen bonds between the base pairs. This process creates a replication fork where new complementary strands are synthesized.
dna is that because the structures of what is does. and how it reacts
because it just is
DNA is made during replication. RNA is made during transcription. Proteins are made during translation.
DNA replication is the second part of inter-phase where the cell makes an exact copy of the DNA in its cell. Please see the answer to the related question below..