Autosomal dominant
Sex-linked dominant
Sex-limited recessive
Sex-linked recessive
Based on the information provided, the most likely mode of inheritance for this disease is:
Sex-linked recessive
Here's the reasoning:
The man and woman do not show signs of the disease, which suggests they are carriers (heterozygous) for the disease gene.
Three out of the five sons are affected by the disease, while none of the daughters are affected. This pattern is consistent with X-linked recessive inheritance.
In X-linked recessive inheritance, the gene responsible for the disease is located on the X chromosome. Males have only one X chromosome, so if they inherit a copy of the disease gene, they will express the disease because there is no corresponding healthy allele on the Y chromosome to mask the effect. Females, on the other hand, have two X chromosomes, so they can be carriers without expressing the disease if they have one normal allele to compensate for the mutated one. This pattern explains why none of the daughters are affected (they received a normal X chromosome from the unaffected mother) and why three out of the five sons are affected (they inherited the X chromosome carrying the disease gene from their carrier mother).
So, based on the inheritance pattern observed in the family, X-linked recessive is the most likely mode of inheritance for this disease.
So, the correct option is (D): Sex-linked recessive
The sequence of nitrogenous bases in a segment of a coding strand of DNA is
5' – AATGCTAGGCAC – 3'. Choose the option that shows the correct sequence of nitrogenous bases in the mRNA transcribed by the DNA.
1. Perform a cross between two sickle cell carriers. What ratio is obtained between carrier, disease free and diseased individuals in F1 progeny? Name the nitrogenous base substituted, in the haemoglobin molecule in this disease.
2. Explain the difference in inheritance pattern of flower colour in garden pea plant and snap-dragon plant with the help of monohybrid crosses.
OR,
Explain with the help of well-labelled diagrams how lac operon operates in E. coli :
1. In presence of an inducer.
2. In absence of an inducer.
Study the pedigree chart given below, showing the inheritance pattern of blood group in a family:
Answer the following questions:
(a) Give the possible genotypes of individual 1 and 2.
(b) Which antigen or antigens will be present on the plasma membranes of the R.B.Cs of individuals ‘5’ and ‘8’?
The current passing through the battery in the given circuit, is:
A bob of heavy mass \(m\) is suspended by a light string of length \(l\). The bob is given a horizontal velocity \(v_0\) as shown in figure. If the string gets slack at some point P making an angle \( \theta \) from the horizontal, the ratio of the speed \(v\) of the bob at point P to its initial speed \(v_0\) is :
A full wave rectifier circuit with diodes (\(D_1\)) and (\(D_2\)) is shown in the figure. If input supply voltage \(V_{in} = 220 \sin(100 \pi t)\) volt, then at \(t = 15\) msec:
A Mutation is a change in the sequence of our DNA base pairs caused by numerous environmental stimuli such as UV light or mistakes during DNA replication. Germline mutations take place in the eggs and sperm and can be passed onto offspring, whereas somatic mutations take place in body cells and are not passed on.
There are three types of mutations, which are as follows:
It refers to any change in DNA sequence that has no effect on the amino acid sequence in a protein or the functions that a protein performs. There is no phenotypic indication that a mutation has occurred.
When there is a change in the sequence of base pairs due to a point mutation, that results in a stop codon. This leads to a protein that is either shortened or non-functional.
A missense mutation occurs when a point mutation causes a change in the codon, which then codes for another amino acid.
When DNA copies incorrectly, the majority of mutations occur. Evolution occurs as a result of all of these mutations. DNA makes a copy of itself during cell division. When a copy of DNA isn't flawless, it's called a mutation since it differs somewhat from the original DNA.
When certain chemicals or radiations are used to break down DNA, it causes the DNA to break down. The thymine dimers are broken by UV radiation, resulting in altered DNA.