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Snezhnost [94]
3 years ago
10

Frameshift mutation are the result of what occurrence?​

Biology
1 answer:
Alisiya [41]3 years ago
7 0

Explanation:

A frameshift mutation (also called a framing error or a reading frame shift) is a genetic mutation caused by indels (insertions or deletions) of a number of nucleotides in a DNA sequence that is not divisible by three. Due to the triplet nature of gene expression by codons, the insertion or deletion can change the reading frame (the grouping of the codons), resulting in a completely different translation from the original. The earlier in the sequence the deletion or insertion occurs, the more altered the protein. A frameshift mutation is not the same as a single-nucleotide polymorphism in which a nucleotide is replaced, rather than inserted or deleted. A frameshift mutation will in general cause the reading of the codons after the mutation to code for different amino acids. The frameshift mutation will also alter the first stop codon ("UAA", "UGA" or "UAG") encountered in the sequence. The polypeptide being created could be abnormally short or abnormally long, and will most likely not be functional.

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3 0
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A daughter cell that matures to the inside of the vascular cambium becomes<u> secondary xylem</u> and a daughter cell that matures to the outside of the vascular cambium becomes <u>secondary phloem.</u>

<u />

  • The cambium divides its cells to create secondary xylem and phloem. As secondary phloem and xylem tissue builds up, the stem becomes thicker and develops wood and bark.
  • The kind of xylem produced by secondary growth is known as secondary xylem. In contrast, during primary growth, the primary xylem develops.
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  • The procambium, which is found between the xylem axis and the phloem pole, develops into the cambium in the root.
  • A pattern resembling the arrangement of secondary stem is produced when xylem forms in the core and phloem on the perimeter of secondary development.

learn more about vascular cambium here: brainly.com/question/859907

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