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4.Monohybrid Cross: Count the yellow and purple kernels for 3 ears of corn from the “3:1” collection. These are the result ...

ion. These are the result of a monohybrid cross (two heterozygous parents) and we expect a ratio of 3 dominant phenotypes to 1 recessive phenotype.
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5.In mice, grey coat colour, G, is dominant to white, g, and long tail, T, is dominant to short tail, ...

t. What is the genotypic and phenotypic ratio if a female mouse that is heterozygous for colour and short-tailed is crossed with a male mouse that is homozygous dominant for colour and is heterozygous for tail length?
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6.I was looking at my notes on protein structure and I am trying to understand quaternary structures for proteins. I ...

or proteins. I understand that primary, secondary, and tertiary structures are encoded by one gene each. However, I am not entirely sure if quaternary structures are encoded by one or multiple different genes. The reasons why I am a little confused is for two reasons. Firstly, quaternary structures are made up of more than one protein subunit (i.e. multiple polypeptides). Secondly, as I understand, Hemoglobin, for example, has different subunits, each of which is encoded by a different gene. Does this necessarily mean that all quaternary structures are composed of proteins encoded from different, separate genes? If quaternary subunits are encoded by different, separate genes, can those different genes be located on different loci, or are all of the subunits necessarily encoded by the different gene but its mRNA molecule is spliced differently?
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7.Monohybrid Cross: Count the yellow and purple kernels for 3 ears of corn from the “3:1” collection. These are the result ...

ion. These are the result of a monohybrid cross (two heterozygous parents) and we expect a ratio of 3 dominant phenotypes to 1 recessive phenotype. II. Test Cross: Count the yellow and purple kernels for 3 ears of corn from the “1:1” collection. These are the result of a test cross (two heterozygous parents) and we expect a ratio of 1 dominant phenotype to 1 recessive phenotype. III. Dihybrid Cross: Count the kernels for 3 ears of corn from the “9:3:3:1” collection. These are the result of a dihybrid cross (two heterozygous parents for two traits) and we expect a ratio of 9 dominant/dominant: 3 dominant/recessive: 3 recessive/dominant: 1 recessive/recessive.
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Principles of heredity: 

 

There are mainly three principles of heredity, the principle of segregation, the principle of dominance, the principle of independent assortment. Heredity is defined when characters are transferred from one generation to the next.

 

Principles of heredity Sample Questions:

 

Question 1: What is the reason for down syndrome in humans?

 

Answer: Because of the extra copy of chromosome number 21
( Trisomy-21).

Explanation: Down syndrome is caused by aneuploidy in humans because of the trisomy at chromosome number 21. In this disease, there is an asymmetrical skull, mental retardation, and decreased muscle tone.

 

 

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Question 2: Which organism is used as a model organism in genetic studies?

 

Answer: Drosophila melanogaster.

Explanation: This organism is used in the laboratory because it has a short life cycle and clear differentiation of sexes and produces a large number of offspring in a single reproduction.

 

 

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Question 3: The human skin color is an example of which type of inheritance?

 

Answer: Polygenic inheritance.

Explanation: Polygenic inheritance means which is controlled by more than two genes in cumulative form. In the case of human skin color, the three genes A, B, C control the clour of human skin in additive form.

 

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Question 4: What is the reason for sickle cell anemia disease?

 

Answer: Missense mutation.

Explanation: The sickle cell anemia disease is caused by the change of amino acid from glutamic acid to valine because of the change of one base pair in the codon, in this, the shape of RBC is sickle-shaped which is insufficient to carry oxygen in the blood.

 

 

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Question 5: What is the phenotypic and genotypic ratio in incomplete dominance?

 

Answer: 1:2:1

Explanation: The incomplete dominance is the limitation of mendelian inheritance where two alleles express incompletely and produce a new phenotype, it is also called partial dominance.

 

 

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Question 6: The scientist who discovered the concept of linkage in drosophila.
 

Answer: T.H Morgan.

Explanation: Morgan discovered linkage first time in drosophila, linkage is the phenomenon in which two genes are linked together and pass on to the next generation in linked form.

 

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Question 7: Hemophilia-B is the disease caused by the deficiency of which clotting factor?

 

Answer: Deficiency of factor (ix)

Explanation: Hemophilia is a disease in which the blood loses the ability to clot because of the lack of clotting factors and there is a lot of blood loss during any injury.

 

 

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Question 8: Who has given the law of dominance?

 

Answer: Gregor Johann Mendel discovered the law of dominance.

Explanation: Law of dominance means the one allele is dominant over the other allele and the allele control the characters of the individuals.

 

 

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Question 9: Color blindness in humans shows which kind of linkage?


Answer: It is an x-linked disorder.

Explanation: Color blindness is the x-linked disorder which is when there are two copies of x-chromosomes that carry the disease. It found more in males as compared to females because males carry only one copy of the x-chromosome and females have two copies.                                                                                                                                                            

 

 

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Question 10: Which syndrome is caused by the presence of an additional copy of the x-chromosome?

 

Answer: Kleinfelter’s syndrome.

Explanation: In this type of disorder, the x-character increases so it affects males, the males develop more feminine characters, such as the development of breasts and poor muscle growth.

 

 

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