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xxMikexx [17]
3 years ago
5

In the Hardy-Weinberg equation shown below, p is the frequency of the dominat allele, and q is the recessive allele

Biology
2 answers:
Anvisha [2.4K]3 years ago
7 0

Answer:

Option D

Explanation:

Because of blah blah blah.

Lemur [1.5K]3 years ago
3 0

Answer:

Option D- frequency of the heterozygous qenotype

Explanation:

In the Hardy-Weinberg equilibrium , 2pq stands for the genotype frequency of heterozygotes (Aa) in a population at the state of equilibrium. dominant homozygotes (AA) is represented by the p-square and q- square represents the recessive homozygotes (aa) frequency. p represents the allele frequency of A Allele and q stands for the allele frequency of the allele a. Summation of the terms gives an equal to 1(100%). The sum of all of these terms is always equal to due to the fact that the 3 frequencies in the equation are the available or possible allele combinations.

Hardy-Weinberg is relevant for it helps us in comparison of a population's actual genetic structure as time goes on along with the genetic structure we are to get if really population was in Hardy-Weinberg equilibrium state that is population was not evolving.

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Match the scientist(s) with their contribution to what we now know about DNA.
Lerok [7]

Hi,

Here are the answers:

1) Rosalind Franklin and Maurice Wilkens

<u><em>Found DNA to be a helix structure because of their x-ray crystallography </em></u>

During 1953, Rosalind Franklin and Maurice Wilkens attempted to explore the structure of DNA by firing the x-rays on the fibres of DNA. X-rays were scattered when they hit the DNA and later detected on the photographic film. The image on photographic film indicated that DNA had a helical structure. This served as a basis for further analysis of DNA structure by coming scientists, most importantly Watson and Crick.

*********************************


2) Alfred Hershey and Martha Chase:  

<u><em>Conclusively proved DNA is the hereditary molecule with their work with bacteriophages. </em></u>

Harshey and Chase, did experimentation on a bacteriophage called T2. During their experiment, they infected some bacteria E-coli with T2. They used radioactively labelled S and P atoms in the protein coat and DNA of virus respectively. When the virus infected bacteriophage, they found that the radioactively labelled P atoms were found in bacteriophage but S were not found. Now, as we know that S- Sulphur atoms become part of protein coat of virus and when virus infects bacteria, protein remains outside. Only DNA containing P-Phosphorus is injected in bacteria. They, proved that hereditary molecule was DNA and not proteins. Their experimentation was a great breakthrough in the field of Biology and it paved the paths for better understanding of DNA by coming generation of scientists.

******************************


3) Avery, McLoed and McCarty:  

<u><em>Determined Griffith's transforming factor was DNA </em></u>

Avery, McLoed and McCarty proceeded the experimentation of a scientist Griffith. Griffith used two strains of bacteria <em>Steptococcus pneumonia</em> for his experimentation i.e S strain and R strain. S strain bacteria had capsule of polysaccharide around them and they produced smooth colonies while R strain did not have and produce rough colonies. Griffith killed S strain bacteria and injected in mice, but mice stayed alive. This depicted that polysaccharide coat was not responsible for the death of mice.

He then injected the mice with live S strains along with some dead R strains. The mice died of pneumonia. So Griffith thought that something was transferred from dead R strains into the S strains due to which they became infectious.

In 1944, Avery, McLoed and McCarty, continued his experimentation and proved that the molecule that was transferred from R strain to S stain was DNA and DNA is basically the transforming factor.

**********************************


4) James Watson and Frances Crick:  

<u><em>Determined DNA to be double helix structure </em></u>

In 1953, using the work of Rosalind and Franklin, two scientists  James Watson and Frances Crick got successful in creating a perfect three dimensional structure of a DNA molecule. They described their model as double helix that is composed of backbones of sugar and phosphate molecules that are held together through bonding between nitrogenous bases. They also proposed  that there exists hydrogen bonding between nitrogenous bases, purines and pyrimidines.

**********************************


5) Erwin Chargaff:  

<u><em>Determined base pair ruling and that percentages of bases is species specific. </em></u>

Erwin Chargaff studied the DNA of different living organisms and gave out a rule called Chargaff's rule. His rule also contributed and helped in the understanding and preparation of DNA structure by Watson and Crick. According to his rule, In the DNA of any cell at any time, the amount of guanine units is equal to the amount of cytosine units, and the amount of adenine units is equal to the amount of thymine units. This gave an important clue about the complementary bonding of bases i.e Adenine always pairs with Thymine and Guanine always pairs with Cytosine.

Hope it helps! :)


8 0
4 years ago
If a mutation occurs in a body cell and the mutation changes the phenotype of the individual, what will happen to the offspring
denis-greek [22]

Answer:

The correct option is B. The offspring will inherit neither the genotype nor the phenotype change.

Explanation:

Any changes which occur in the DNA sequence of a person are termed as mutations.

Mutations will only be transferred to offsprings if the mutated gene or sequence gets incorporated into the genome of the mutated person.

In the above scenario, the mutation is just changing the person's phenotype and it has not been incorporated in the genotype of the affected person. Hence, the offsprings will not inherit the mutation, nether in their genotype nor the phenotype.

3 0
3 years ago
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