Clone telomeres behave normally

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In summary, a team of researchers in Germany has discovered that early embryo telomerase-dependent length resetting between the morula and blastocyst stages prevents cloned embryos from having short telomeres, which can typically be associated with aging. The study was coauthored by Heiner Niemann, a professor at Institut für Tierzucht, and published in PNAS Early Edition. Previous concerns about cloned animals exhibiting premature aging due to shortened telomeres were later disproved by studies in cattle and mice.
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Early embryo telomerase-dependent length resetting means clones won't have short telomeres | By Cathy Holding

A team of researchers at Hannover Medical School, Germany, has found a telomerase-dependent telomere length–resetting event between the morula and blastocyst embryonic stages that they say keeps cloned embryo telomere length normal.

Because telomeres—the structures located at the end of chromosomes—lose a piece of their sequences with each cell division, short telomeres are usually correlated with age, said Heiner Niemann, professor and head of the Department of Biotechnology at the Institut für Tierzucht, Neustadt, Germany, who coauthored the study, published in the May 17 PNAS Early Edition, with Sonja Schaetzlein and colleagues.

Scientists had earlier looked at telomere lengths in cloned animals because there was some concern that such animals may exhibit premature aging. “There was quite an uproar with Dolly [the first sheep clone] in that when they measured telomere length, they were indeed obviously shortened compared to age-matched controls,” Niemann said. However, later studies in cloned cattle and mice showed telomeres to be of normal length, he said.

http://www.biomedcentral.com/news/20040518/01
 
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Yeah, I thought so. Telomeres also have nothing to do with Progeria, as once thought.
 
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Thank you for sharing this interesting article. It is reassuring to hear that cloned telomeres behave normally and that early embryo telomerase-dependent length resetting helps maintain normal telomere length in clones. This finding addresses concerns about premature aging in cloned animals and provides further support for the safety and viability of cloning technology. It is also interesting to note that earlier studies showed shortened telomeres in cloned animals, but subsequent studies have shown normal telomere length. This highlights the importance of continued research and the need to not jump to conclusions based on limited data. Overall, this study adds to our understanding of telomere dynamics and the potential applications of telomerase in maintaining healthy telomeres.
 

1. What are telomeres?

Telomeres are repetitive sequences of DNA located at the ends of chromosomes. They act as protective caps and help maintain the stability of the genome by preventing the loss of genetic information during cell division.

2. How do telomeres behave normally in clones?

Telomeres in clones behave in the same way as in non-cloned individuals. They shorten with each round of cell division, but are replenished by the enzyme telomerase. This allows the cells to continue dividing and maintain their normal function.

3. Can telomeres be cloned?

No, telomeres cannot be cloned because they are a natural part of the genetic material and cannot be artificially replicated in a laboratory setting.

4. Do cloned telomeres have any abnormal behavior?

Studies have shown that cloned telomeres behave normally and do not exhibit any abnormal behavior. This is because the telomeres in cloned cells are identical to those in non-cloned cells.

5. How do telomeres affect aging in clones?

Telomeres play a role in the aging process by gradually shortening with each cell division. However, cloned telomeres behave in the same way as non-cloned telomeres and do not have a significant impact on the aging process in clones.

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