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kari74 [83]
3 years ago
14

Speculate as to how the information obtained from the sequencing of the human genome might be used to someday eliminate inborn e

rrors of metabolism
Biology
1 answer:
Katena32 [7]3 years ago
5 0

Answer:

Explanation:

Sequencing the human genome is the function of the human genome project with the goal of determining the base pairs/order of DNA nucleotides that make up human genome, and also identifying and mapping all of the genes of the human genome both from the physical level and its functions in molecular medicine. The benefits in this field could allow for better diagnosis of disease, early detection of certain diseases, and gene therapy and control systems for drugs.

Inborn errors of metabolism are rare genetic (inherited) disorders where the body cannot properly digest and turn food into energy through the normal pathway. The disorders are usually caused by mutations in specific enzymes that help in the break down of these foods.

Through the study of the human genome, sequences involved in these mutations giving rise to these disorders are identified and mapped to their variuos locations. This can help in the early diagnosis of the disorders and effective control system for drugs and gene therapy against these disorders.  

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Several assumptions can be made using these results. The one of the main assumption is that these result prove the higher similarity among identical twins then of those who are fraternal. This is because the identical twins share mostly same amount of genome from both parents as a single zygote that is fertilized by one sperm divides into two. On the other hand, all fraternal are dizygotic. It means that there were two eggs that were fertilized by two totally different sperms. They do not share any of characteristics but may share some with parents.  

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