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Genetic Drifts: What Is Proteomics?

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Question #5 (1 Point)
What is proteomics? With modern advances to genome sequencing, whole genomes can now be used to rapidly identify protein encoding sequences from a small amount of amino acid sequences. This has led to a field of study called proteomics, which encompasses the study of proteins, protein complexes, and protein-protein interactions. As an example when one isolated protein is found to interact with a complex of proteins known to be part of an enzyme complex, it could be inferred that the isolated protein may be part of the enzyme complex as well. Some of the techniques involved for studying proteomics are interaction assays that allow for the rapid identification and purification of proteins. A genome wide protein-protein …show more content…

It is defined as the random change in the predominate alleles over time. Some major examples that show genetic drifts occur when a small population establishes a new population. Such events are known as the founder effect in which at times a small portion of a population split from the main group and become isolated from each other. The small population now contains a small subset of alleles that the original population had. The subsequent generations will have a change in allele frequencies without selection since the having fewer genetic variation. Likewise population bottlenecks may occur where a large portion of the population dies off thus leaving a small subset of individuals to breed causing a random change in allele frequencies without influence of …show more content…

This would occur by the genomic restructuring mechanism recombination has, particularly in areas with repeated sequences. Recombination of transposable elements, which many contain repeated sequences, as well as other repeat sequences found in the genome, may be one of the main mechanisms by which genetic regions are rearranged, lost, or duplicated. Recombination can result in the following: translocations, in which repeated sequences on two different chromosomes are swapped with a region of another chromosome, possibly lead to a change in the copy number of genes; deletions, in which a loss of a region of a genome occurs, usually decreasing fitness and are selected against over time; duplications, which result in the presence of extra copies of specific regions of the genome; inversions, which lead to a change in the order in which they are found, resulting in alterations in gene expression without changing the copy number of

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