Just some queries in regards to mutations. Could someone check my expression:
What occurs in translocation mutations:
A section of a chromosome breaks off and attaches to a non-homologous chromosome.
What occurs in inversion mutations:
A segment of a chromosome breaks off, flips around, and reattaches to the same chromosome.
What occurs in deletion mutations:
A segment of a chromosome is lost; genetic material is lost.
What occurs in a duplication mutation:
A section of a chromosome is repeated, resulting in an addition of genetic material.
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Explaining a non-sense mutation:
* As a result of the insertion/deletion/substitution of the base, a premature stop codon is present in the mRNA transcript of the gene, and a polypeptide with a shortened amino acid sequence is synthesised.
Explaining a missense mutation:
As a result of the base substitution mutation, a different amino acid is coded for at position ____. Thus, a polypeptide with an altered primary structure is produced.
Explaining a silent mutation:
Because the genetic code is redundant, and the amino acid ____ is coded for by different codons, the substitution mutation has no effect on the amino acid sequence of the polypeptide.
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Explaining the effects of a Frameshift mutation:
When a base is added or deleted, all triplets beyond the mutation are altered. As a result, a dysfunctional polypeptide with a different amino acid sequence is produced.
Explaining a frameshift mutation:
- When a base is inserted or deleted, all bases beyond this mutation point are displaced one position. The reading template is frameshifted, triplets are altered and a dysfunctional polypeptide is synthesised.
^^ Is this fine?! Thank you! (:
And can someone PLEASE explain to me translocations in regards to gamete formation? Also, how do I know whether an extra X chromosome is a result of non-disjunction occurring in the mother or the father during meiosis? Thanks