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what is the expected functional consequence of movement of a transposable element within the genome?

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A transposable element is a segment of DNA that can move or “jump” from one location in the genome to another. This phenomenon, known as transposition, is an important process in the evolution of many organisms, and it can have a variety of functional consequences.

The most common outcome of transposition is the alteration or disruption of gene expression. Transposable elements can insert themselves into gene coding regions, causing a change in the sequence of the gene and potentially altering its expression. This can result in the production of an aberrant protein, or it can prevent the production of a functional protein altogether. In either case, this alteration of gene expression can lead to changes in the function of the organism.

Transposable elements can also affect gene expression indirectly. For example, they can insert themselves into regulatory sequences, such as promoters or enhancers, and alter the binding of transcription factors that control gene expression. This can result in changes in gene expression without altering the coding sequence of the gene.

In addition to altering gene expression, transposition can also lead to genetic rearrangements. Transposition can cause deletions, inversions, or duplications of a gene, as well as large-scale chromosomal rearrangements. These rearrangements can have a variety of functional consequences, including the activation or inactivation of specific genes.

Finally, transposition can lead to the formation of novel genetic elements. Transposable elements can generate new combinations of genetic sequences, which can lead to the creation of new genes or regulatory sequences. This can result in new functions for the organism, and can be an important source of evolutionary innovation.

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