In complementary base pairing, the G pairs with C, and A pairs with T. Given that this be the rule, the complementary nucleotides for your sequence would be as follows: CGATTAACGTAGGCA.
With regards to proofreading, mutations in cell division occur once in around every 100,000 base pairs. If this happens, the enzyme that pairs the nucleotides to form DNA, called DNA polymerase, detects the error and moves back along the strand, it then cuts the incorrect nucleotide and replaces it with the correct one, fixing the error and continuing with the DNA synthesis.
This process corrects the majority of errors in DNA synthesis, but some errors can still be missed by the DNA polymerase, this is then rectified by a protein complex which binds to the incorrect pairing until anther complex, comes along and cuts that particular section of DNA out, which is then replaced by a new section of correct nucleotides synthesized by the polymerase enzyme, the two sections at either end that were cut is then sealed by ligase, an enzyme which essentially "glues" the DNA stands back together.
My apologies for the long answer, I hope I answered your question and that you understand it well enough.
Answer:
A. All offspring will be affected by the dominant traits
D colors of UV rays separate base on on their wavelength
The percentage of the white salamander population is 16%.
<h3>Hardy-Weinberg Equilibrium Equation</h3>
The genotypic frequencies within a population can be expressed by the binomial (p + q)² = 1, which can be developed and represented by the following equation:
p = frequency of the dominant allele;
q = frequency of the recessive allele;
p² = frequency of the zygous dominant genotype;
2pq = frequency of the heterozygous genotype;
q² = frequency of the zygous recessive genotype.
Also according to the equation presented (p² + 2pq + q² = 1), we will have the following distribution of genotypes:
- CC = 0.36 = 36%
- Cc = 0.48 = 48%
- cc = 0.16 = 16%
Learn more about recessive allele in brainly.com/question/844145
