Answer:
If the sequence of one strand on DNA is CTA GCT CCA, the
complementary strand is GAT CGA GGT.
Explanation:
The DNA molecule has four nitrogenous bases in its structure, two purines —adenine and guanine— and two pyrimidines, cytosine and thymine.
The two DNA strands are linked by hydrogen bonds established between their complementary nitrogenous bases, where a purine is complemented by a pyrimidine.
In the case of DNA, adenine is complemented by thymine and cytosine is complemented by guanine:
<em>A=T</em>
<em>C≡G</em>
In the sequence belonging to a DNA strand CTA GCT CCA, the strand that is complementary would be GAT CGA GGT.
Not the same and they is not in a relationship
Answer:
Each mutant would be mated to wild type and to every other mutant to create diploid strains. The diploids would be assayed for growth at permissive and restrictive temperature. Diploids formed by mating a mutant to a wild type that can grow at restrictive temperatures identify the mutation as recessive. Only recessive mutations can be studied using complementation analysis. Diploids formed by mating two recessive mutants identify mutations in the same gene if the diploid cannot grow at restrictive temperature (non-complementation), and they identify mutations in different genes if the diploids can grow at restrictive temperature (complementation).
Explanation:
Recessive mutations are those whose phenotypic effects are only visible in homo-zygous individuals. Moreover, a complementation test is a genetic technique used to determine if two different mutations associated with a phenotype colocalize in the same <em>locus</em> (i.e., they are alleles of the same gene) or affect two different <em>loci</em>. In diploid (2n) organisms, this test is performed by crossing two homo-zygous recessive mutants and then observing whether offspring have the wild-type phenotype. When two different recessive mutations localize in different <em>loci</em>, they can be considered as 'complementary' since the heterozygote condition may rescue the function lost in homo-zygous recessive mutants. In consequence, when two recessive mutations are combined in the same genetic background (i.e., in the same individual) and they produce the same phenotype, it is possible to determine that both mutations are alleles of the same gene/<em>locus</em>.
Answer:
b to help organize data and record info.
