Question

Why are recombinant DNA technology and nucleus transplantation technology still dangerous?

Why are recombinant DNA technology and nucleus transplantation technology still dangerous?

Homework Answers

Answer #1

Recombinant DNA technology and nucleus transplantation technology (cloning) are extremely dangerous since they are able to modify, in a very short time, the ecological balance that evolution has taken millions of years to create on the planet.

During the evolutionary process, under the slow and gradual effect of mutations, genetic recombinations and natural selection, species emerged, were modified, and genetic heritages were formed.

With genetic engineering, however, humans can mix and modify genes, making changes with unpredictable long-term consequences, risking the creation of new plant or animal diseases, new types of cancers and new disease outbreaks. It is a field as potentially dangerous as the manipulation of nuclear energy.

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Why are recombinant DNA technology and nucleus transplantation technology still dangerous?
Why are recombinant DNA technology and nucleus transplantation technology still dangerous?
Describe the process of making Insulin from recombinant DNA technology.
Describe the process of making Insulin from recombinant DNA technology.
Match the following terms with their description: DNA technology, recombinant DNA, genetic engineering, plasmid, biotechnology, DNA...
Match the following terms with their description: DNA technology, recombinant DNA, genetic engineering, plasmid, biotechnology, DNA cloning - Production of multiple identical copies of a piece of DNA ________________ - A set of techniques for manipulating DNA ________________ - The use of organisms or their products for human purposes ________________ - A round bacterial chromosome _________ - DNA combined from two different sources _______________ - Purposefully altering genes for human purposes __________________
25. In recombinant DNA, a DNA probe is used to: transfer DNA into a cell synthesise...
25. In recombinant DNA, a DNA probe is used to: transfer DNA into a cell synthesise DNA for cloning separate pieces of DNA find a specific nucleotide sequence
Utilizing recombinant DNA technology methods, a DNA sequence coding for the KDEL peptide region characteristic of...
Utilizing recombinant DNA technology methods, a DNA sequence coding for the KDEL peptide region characteristic of ER resident proteins was engineered into a gene for a protein that is destined to be secreted out of a cell (eg., Insulin protein that is secreted by pancreatic acinar cells). The hybrid secretory protein coding gene bearing the KDEL coding sequence was introduced into cultured pancreatic cells. You would expect: a.       the hybrid secretory protein would be secreted out of the cell and...
You identify a gene from E. coli that is very small. Using recombinant DNA technology, you...
You identify a gene from E. coli that is very small. Using recombinant DNA technology, you managed to clone the whole piece of DNA that contains all codons (including stop and start codons) for protein synthesis. Using automated sequencing, you obtain the following sequence: 5’-TTAATATCAAGCTGATTCAGGCCCAAACATCCT-3’ A. Using the above sequence for reference, write out the mRNA transcript (be sure to label the 5' and 3' ends). B. Translate the protein that is coded for by the mRNA strand. C. How...
Describe the technique of Recombinant DNA, application and commercial value of their product.
Describe the technique of Recombinant DNA, application and commercial value of their product.
which of the following is NOT used to generate a recombinant DNA molecule ? 1) DNA...
which of the following is NOT used to generate a recombinant DNA molecule ? 1) DNA ligase 2) RNA polymerase 3) restriction endonuclease A mature mRNA is shorter than its corresponding gene because? 1)the mature mRNA contains only exons 2) not all segments of the gene are transcribed into RNA 3) DNA is double stranded and RNA is single stranded 4)the poly(A) tail has been spliced  
What would be a suitable process for introductions a piece of recombinant DNA into a bacterium...
What would be a suitable process for introductions a piece of recombinant DNA into a bacterium that is too large for a plasmid vector? Electrophoresis Conjugation Transduction Transformation
explain the process of how recombinant dna technique is used to produce human insulin genes with...
explain the process of how recombinant dna technique is used to produce human insulin genes with bacteria.
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT