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Eukaryotes initiate DNA replication at multiple points in the chromosome, so replication forks meet and terminate at many points in the chromosome. Because eukaryotes have linear chromosomes, DNA replication is unable to reach the very end of the chromosomes. Due to this problem, DNA is lost in each replication cycle from the end of the chromosome.
Their repeated nature allows a unique form of mutation: the number of copies can increase or decrease when strand slippage occurs during DNA replication. (Regular point mutation still happens and could be more frequent than slippage.) [7] Their copy number not only have use in forensics and ancestry testing, [8] but are also linked to diseases. [9]
Other effects of point mutations, or single nucleotide polymorphisms in DNA, depend on the location of the mutation within the gene. For example, if the mutation occurs in the region of the gene responsible for coding, the amino acid sequence of the encoded protein may be altered, causing a change in the function, protein localization ...
Tandem repeats can occur through different mechanisms. For example, slipped strand mispairing, (also known as replication slippage), is a mutation process which occurs during DNA replication. It involves denaturation and displacement of the DNA strands, resulting in mispairing of the complementary bases.
The presence of repeated sequence DNA makes it easier for areas of homology to align, thereby controlling when and where recombination occurs. In addition to playing an important role in recombination, tandem repeats also play important structural roles in the genome. For example, telomeres are composed mainly of tandem TTAGGG repeats. [15]
Recurrent evolution also referred to as repeated [1] [2] or replicated [3] evolution is the repeated evolution of a particular trait, character, or mutation. [4] Most evolution is the result of drift, often interpreted as the random chance of some alleles being passed down to the next generation and others not.
During DNA replication, the replisome will unwind the parental duplex DNA into a two single-stranded DNA template replication fork in a 5' to 3' direction. The leading strand is the template strand that is being replicated in the same direction as the movement of the replication fork.
A postzygotic mutation (or post-zygotic mutation) is a change in an organism's genome that is acquired during its lifespan, instead of being inherited from its parent(s) through fusion of two haploid gametes. Mutations that occur after the zygote has formed can be caused by a variety of sources that fall under two classes: spontaneous mutations ...