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What kind of mutation would changing CGT ACG GCT AC to CCT ACG GCT AC be?

The mutation changing CGT ACG GCT AC to CCT ACG GCT AC is a point mutation, specifically a missense mutation. This occurs because the first codon changes from CGT, which codes for the amino acid arginine (Arg), to CCT, which codes for proline (Pro). This alteration results in a different amino acid being incorporated into the protein, potentially affecting its function.


GGCAGTTCATGC What would be the sequence of bases on the complimentary stand?

Ccg tca agt acg


How can you complete the complementary strand for the base sequence acg tag gct tca gct?

TGC ATC CGA AGT CGA


Base Sequence CGT ACG GCT AC WHAT WOULD BE the base sequence formed by transcription?

During transcription, the DNA sequence is converted into a complementary RNA sequence. For the given DNA base sequence CGT ACG GCT AC, the corresponding RNA sequence would be GCA UGC CGA UG. This involves replacing thymine (T) with uracil (U) in RNA.


What would happen if a mutation occurred and DNA became ACT instead of ACG?

If a mutation resulted in the DNA sequence changing from ACG to ACT, it would alter the corresponding mRNA and potentially change the amino acid sequence during protein synthesis. ACG codes for the amino acid threonine, while ACT codes for the amino acid threonine as well. Therefore, in this specific case, the mutation might not have a significant effect on the resulting protein due to the redundancy of the genetic code, where multiple codons can code for the same amino acid. However, the impact of a mutation can vary greatly depending on the specific sequence and context within a gene.