Genetics and Human Welfare

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Genetics and Human welfare

Introduction
Human genetics can be considered as basic and a practical science. In the view of basic science it can be described as the branch of science that deals with laws of storage, transference, and understanding of information for development and normal working of the living. In this way, human genetics involves most worth-studying creature organism i.e. the human being. Human genetics is a practical science as its results are not only confined to theoretical level but of practical use as well. Its value for human wellbeing is bound to have consequences for theoretical research as well, since it effects the selection of problems by human geneticists, their beneficial results which allow the financers to invest. Because of its hypothetical and practical importance, human genetics offers temptation and human satisfaction unmatched by work in fields that are either primarily hypothetical or entirely practical.

In human genetics 1st step is to isolate gene and clone it. Then desired products can be obtained.

Cloned genes and production of chemicals
Cloned Genes can be used for
1. Production of Human Hormones
2. Vaccines
3. Commercial Chemicals

1. Production of Human Hormones

a. Human genes for peptide hormone
In the humans, peptide hormones are secreted from secretory cells of gland after gene expression of peptide hormone genes in these cells .e.g. insulin and other Human Growth Hormones

Insulin
Insulin is released from the Islets of Langerhans of pancreas gland located in abdomen, a peptide (protein) hormone. Insulin is a necessary for the diabetics whose normal function for glucose (carbohydrate) metabolism generally fails. Its precursor is proinsulin a pro-hormone in beta cells of pancrea...

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... 1st seven amino acids of b-galactosidase to fuse with that of growth hormone inhibitory hormone i.e. Somatostatin. Somatostatin was not detected in transformed bacteria the possible explanation was that it degraded in E. coli bacteria. So the other plasmid was genetically formed to prevent the degradation which had mutually a promoter of the lac operon and another lacL region. The gene for beta-galactosidase is lacZ. This time plasmid was sliced close to c-terminus of beta-galactosidase gene the fusion peptide thud obtained had piece of beta-galactosidase at N-terminus joined to Somatostatin by methionine. Cyanogen bromide used to cleave only carboxyl side of methionine. Thus, the somatostatin was synthesized. Nowadays it is possible to inhibit the destruction of protein in escherichia coli by expressing of viral enzyme inhibitor gene i.e. protease inhibitor gene.

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