Scientist where intending to clone humans

  • Thread starter Thread starter gunblaze
  • Start date Start date
  • Tags Tags
    Scientist
AI Thread Summary
The discussion centers on the implications and potential side effects of human cloning. Clones are likened to identical twins, possessing separate identities and minds. Concerns are raised about the technical challenges of cloning, particularly regarding cell damage during the process and the biological age of the clone. If a clone is created from an older cell, it may inherit age-related issues, as seen in Dolly the sheep, who developed diseases associated with aging. The debate includes whether cloning affects telomere length and if that contributes to health problems. Additionally, the accumulation of DNA mutations over time is highlighted as a significant concern, potentially impacting the viability and health of clones. Overall, while cloning holds scientific interest, the risks and ethical considerations remain complex and unresolved.
gunblaze
Messages
187
Reaction score
0
there is one period where i heard scientist where intending to clone humans...right?

what i would like to noe is whether does cloning have any side-effects? would both clones be still of the same age? is there any danger in life when cloning?

About the side-effects...eg: would both clones have the same mindset... do the same things at the same time?

I would appreciate all replies...also, pls correct me if anything is wrong!
 
Biology news on Phys.org
Hi Gunblaze, this post would actually belong in the Biology forum. To answer you question simply: clones are just like identical twins, separate people with separate minds.

The side-effect would be the technical difficulties that scientists are facing to perform the procedure safely. The cells can be damaged during the procedure and no one really knows whether the cells are reset correctly. There has been some debate about the biological age of the clone, but I think the clock is reset so the age would be too.
 
In case anyone is interested, I found a bunch of pictures of clones on the internet. I guess its up to the viewer to decide if these clones consider themselves individuals:

VangViengLandscape03.jpg

6561.jpg

http://www.askadavid.org/photos/photos54/banana_trees.jpg
http://www.oldkoloahouse.com/banana%20tree%202.jpg
http://www.princeton.edu/~jhalderm/pics/2000-08=bermuda/m/banana.jpg
http://www.oxfam.org.uk/coolplanet/kidsweb/banana/images/grow3.jpg
 
Last edited by a moderator:
A major problem, besides the ones that Monique mentioned is age of the cloned cell.

If a newborn is cloned there is not a problem. But if a cell from a 50 year old person is cloned, then that cell is 50 years old. This could cause problems for the cloned person. Much like that of Dolly, who several months after birth experienced diseases related to old age, such as arthritus.

Nautica
 
But in Dolly it was not proven to be an aging effect of the clone right?
 
Not proven. But, it wouldn't stand to reason, that if you clone a cell that is 50 years old, you are starting with a 50 year old cell, which would be near its programed death. Right?

Nautica
 
That would be debatable.. is arthritis programmable in a cell? Does decreased telomere length cause arthritis? Are the telomeres really shorter in clones? Are the short telomeres thát short that after 3 months it develops arthritis?

I'm mentioning it, since I've never seen a report how much the telomeres are shortned in clones, or how much they vary from human to human for instance. Also, it might be that during the cloning process the telomeres are lengthened.
 
Technically the telomere length migth not be a problem. Telomerase can be activated in vitro and a cell line can become immortal (i.e. cancerous). All you have to do is inactivated the telomerase before you transfert the nucleus.

The major I would be concern with would be DNA damage/mutation. Depending where you are taking the cell from this migth be an issue of major concern. As you cell divide, damage will acumulate and migth participates in the aging process.

The only thing we know about dolly is that she die prematurly. The rest is just speculation.
 
I agree it is speculation. But, after 1000's of replications, I just do not see how a cell could be as "perfect" as the original, nor after 10^6,s years of selection, do I see how any of these mutations could be anything but deleterious.

This is what you are cloning. The problem should be obvious, reguardless of the reduction in telomeres.

Maybe, when we figure out a cause and/or a cure for Progeria, we will come closer to being able to clone an older individual.

Either way, the point is mute at the present time.

Nautica
 
  • #10
Ok, so accumulation of mutations in somatic cells would be the problem and also the genetic imprinting that is present in the genome.
 
Back
Top