Answer:
See the explanation
Explanation:
Answer 1.
As given that in F1 all are short and white then it can be said according to Mendel's law that short and white are dominant over tall and purple.
Let S for short s for tall and W for white and w for purple allele.
So the genotype of short purple will be Ssww or SSww. So In first case Ssww self crossed then resultant offsprings will be,
................ Sw .................... sw
Sw ........ SSww ............. Ssww
sw ........ Ssww .............. ssww (tall and purple)
So from this 1/4 will be tall and purple while 3/4 will be short and purple.
In second case SSww only short purple progeny will appear.
Answer 2.
2. a) The female progeny will not show any trait because there are two X chromosome in females , so female offspring can be carrier but not show any trait in case of X- linked trait.
2. b) Half of male offsprings show trait because X is inherited from mother. So the chance of having X-linked recessive allele is 1/2.
2. c) The chance of having X linked affect allele in daughter is 1/2. So the chance of inheriting that X to son will be 1/2 so in total there is chance of 1/4 that son will be affected.
2. d) the chance of first child show this trait will be 1/4 in case of male offspring while 0 in case of female offspring.
Hope this helps!
Answer:
Methionine- Serine- Histidine- Aspartate- Glycine- stop
Explanation:
Translation, which occurs in the ribosomes, is the second stage of protein synthesis where mRNA transcript is used to synthesize a peptide chain that eventually forms a protein. The mRNA sequence is read in a group of three nucleotide called CODON. Each codon specifies a particular amino acid, which is read and added to the growing peptide chain.
In this question, a DNA sequence reds 3'- TACAGGGTGCTACCCACT-5, the
mRNA sequence from this DNA during transcription will be:
AUG UCC CAC GAU GGG UGA
From this mRNA sequence, the peptide chain that will result following translation is:
Methionine- Serine- Histidine- Aspartate- Glycine- stop
Answer: Option C
Explanation:
Color blindness is a common hereditary condition which means it usually passes from parents. Red green color blindness is passed on from the mother to the son.
The chromosome number 23 is the sex chromosome also responsible for colorblindness. As it is sex linked the son can receive the recessive allele from the mother.
The mother of the child had a recessive allele which she transferred into her son. As it is sex inherited disease the son is affected by gene carried from mother.
ANSWER: MITRAL VALVE STENOSIS
EXPLANATION:
The child have the risk of having MITRAL VALVE STENOSIS. It is also referred to as mitral stenosis.
Mitral valve stenosis occurs as results of the mitral valve opening narrowing. Which effect to less blood flowing through it.
The mitral valve is located between two chambers (the atrium and the ventricle) on the left side of your heart.
However, Mitral valve stenosis can lead to different health issues, including blood clots, difficulty breathing, fatigue, and heart failure.
Mitral valve stenosis is specifically caused by rheumatic fever (a childhood disease). This rheumatic fever occurs has a result of the body's immune response to an infection associated with the streptococcal bacteria.
Acute rheumatic fever affects the joints and the heart greatly. It causes joints inflammation temporarily and in severe case causes chronic disability.
Nevertheless, this cardiac complication have treatment and it is based on whether the affected individuals shows symptoms. Medications like blood thinners or anticoagulants (to reduce the risk of blood clots), diuretics, antiarrhythmics (to cure abnormal heart rhythms), beta-blockers (to slow your heart) etc, are being administered based on the level of the complication.
All bacteria are prokaryotic!
