Passing genes to GENErations
Answer: alternative D.
Explanation: For the DNA to have the double strand structure, it is necessary to copy the sequence of the existing DNA strand in a complementary sequence of nucleotides, forming hydrogen bonds between them. The mRNA also uses this strategy when reading the DNA strand during the transcription, in order for the translation to begin.
Macromolecules. would be the answer hope this helps
A patient who suffer visual
agnosia will probably show an inability to identify or recognize common objects
in a plain view and they cannot interpret visual information. This is due to
the damage in anterior cortex like the temporal lobes and posterior occipital
of the brain. Additionally, visual agnosia is diagnosed by assessing the
patient’s ability to name and describe the use of visually presented objects
The recombination frequency of the two gene pairs is 3%.
The number of recombinant offspring(r.o.) / total number of offspring x 100% = recombination frequency(θ):
r.o./total x 100% = θ
30/100 x 100% = 3%
Recombinant offspring are children that have a different allele combination to their parents.
For example, say a mother has a haploid cell with the alleles AB and the father has a haploid cell with the alleles ab. These combine to make a diploid cell with the sequence Aa+Bb.
Formation of Recombinant Offspring :
Recombination can happen in two different ways; independent assortment and crossing over.
- Independent assortment is when the maternal and parental DNA are mixed during meiosis, creating a new gene sequence.
- Crossing over happens during the first stage of meiosis when the two homologous chromosomes are paired and a portion breaks off on the same loci then reconnects to a different end. Crossing over can only happen when there isn't a physical linkage of the parental alleles.
Recombination frequency (θ) is the frequency with which a single chromosomal crossover will take place between two genes during meiosis. A centimorgan (cM) is a unit that describes a recombination frequency of 1%. In this way we can measure the genetic distance between two loci, based upon their recombination frequency. This is a good estimate of the real distance. Double crossovers would turn into no recombination. In this case we cannot tell if crossovers took place. If the loci we're analysing are very close (less than 7 cM) a double crossover is very unlikely. When distances become higher, the likelihood of a double crossover increases. As the likelihood of a double crossover increases we systematically underestimate the genetic distance between two loci.
When two genes are close together on the same chromosome, they do not assort independently and are said to be linked. Whereas genes located on different chromosomes assort independently and have a recombination frequency of 50%, linked genes have a recombination frequency that is less than 50%.
To learn more about Recombination frequency : brainly.com/question/7299933
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