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Archy [21]
3 years ago
14

Sickle cell disease is a recessive trait which causes a deformation in red blood cells due to a mutation in the gene that codes

for hemoglobin. Consider a father and a mother BOTH with the genotype Hh, where H is the normal hemoglobin gene, and h is the gene that codes for the defective hemoglobin. What percent of their children will have the genotype hh, which means they will have the full-blown disease?
Biology
1 answer:
Ugo [173]3 years ago
7 0

Answer: Sickle cell disease is caused by a mutation in the hemoglobin-Beta gene found on chromosome 11. Hemoglobin transports oxygen from the lungs to other parts of the body. Red blood cells with normal hemoglobin (hemoglobin-A) are smooth and round and glide through blood vessels.

Explanation:

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Two species of frogs belonging to the same genus occasionally mate, but the embryos stop developing after a day and then die. th
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These two frog species separate by reduced hybrid viability. In reduced hybrid viability gene of different parent species may interact and impair the hybrid's development while in a reduced hybrid fertility a viable individual is sterile often due to the inability to produce normal gametes in meiosis. Hybrid breakdown; the first generation are viable and fertile, but when they mate the offspring are feeble and sterile.
7 0
3 years ago
An example of an epigenetic change is
Oksana_A [137]

Answer:

The correct answer is option d.

Explanation:

An illustration of epigenetic change is a microbe, which can stimulate modifications in the host DNA, causing suppression of defenses or weakening of individual cells. Epigenetic changes modify the physical composition of DNA.  

One of the examples of epigenetic change is DNA methylation. DNA methylation refers to the supplementation of methyl group, which inhibits some of the genes from getting expressed. One of the conditions of DNA methylation is cancer.  

In the majority of cancer, the tumor cells go through global hypomethylation. The tumor suppressed genes seem to turn highly methylated in the conditions of cancer.  

5 0
3 years ago
Explain what it means for a section of DNA to be considered a molecular clock. Be sure to discuss the importance of neutral muta
IceJOKER [234]
  <span>Neutral mutations are neither harmful nor beneficial. 

Therefore, they are invisible to natural selection. (Since they neither improve nor worsen one individual's chances of survival and reproduction over another.) 

However neutral mutations can still spread into the population by just random replications and matings. This is called genetic drift. 

In other words, they are 'silent'. They are mutations that exist and propagate in populations, but seem to have no effect at all. 

The reason they can become important to evolution is that a day can come when they *do* have an effect. In other words, even though an individual mutation may have no immediate effect on survival or reproduction, a *combination* of neutral mutations may provide some new benefit or harm ... at which point natural selection *will* act on that combination. 
</span>

I hope my answer has come to your help. Thank you for posting your question here in Brainly. We hope to answer more of your questions and inquiries soon. Have a nice day ahead!
6 0
3 years ago
A gene on human chromosome 15 is expressed throughout the body. However, in the brain, only the maternal copy of the gene is exp
lord [1]

Answer:

C) Through genomic imprinting, methylation regulates expression of the paternal copy of the gene in the brain.

Explanation:

The pattern of gene expression wherein either paternal or maternal gene is expressed in specific cells while the other one is prevented from expression is known as genomic imprinting.

In the given example, the maternal copy of the gene on chromosome 15 is expressed in brain cells while its paternal copy is not expressed in these cells. Hence, the pattern of expression of this gene is regulated through genome imprinting. One of the mechanism is methylation of cytidine residues of CpG islands of the DNA that are more frequently present within promoters of the genes.

When the cytidine residues of these sequences are methylated into 5-methylcytidine, the transcription factors do not bind to these promoters preventing the expression of these genes.

Hence, methylation of cytidine residue in CpG islands of the promoters of the gene present on chromosome 15 could have silenced its expression in brain cells.

6 0
3 years ago
Please help please thank you
Misha Larkins [42]

Answer:

Hi there!

The correct answer is igneous rock.

Igneous rocks they are most likely to experience brittle deformation is termed as breaking of rocks.

5 0
3 years ago
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