The following sections of this BookRags Literature Study Guide is offprint from Gale's For Students Series: Presenting Analysis, Context, and Criticism on Commonly Studied Works: Introduction, Author Biography, Plot Summary, Characters, Themes, Style, Historical Context, Critical Overview, Criticism and Critical Essays, Media Adaptations, Topics for Further Study, Compare & Contrast, What Do I Read Next?, For Further Study, and Sources.
(c)1998-2002; (c)2002 by Gale. Gale is an imprint of The Gale Group, Inc., a division of Thomson Learning, Inc. Gale and Design and Thomson Learning are trademarks used herein under license.
The following sections, if they exist, are offprint from Beacham's Encyclopedia of Popular Fiction: "Social Concerns", "Thematic Overview", "Techniques", "Literary Precedents", "Key Questions", "Related Titles", "Adaptations", "Related Web Sites". (c)1994-2005, by Walton Beacham.
The following sections, if they exist, are offprint from Beacham's Guide to Literature for Young Adults: "About the Author", "Overview", "Setting", "Literary Qualities", "Social Sensitivity", "Topics for Discussion", "Ideas for Reports and Papers". (c)1994-2005, by Walton Beacham.
All other sections in this Literature Study Guide are owned and copyrighted by BookRags, Inc.
Telomeres are specialized DNA regions that consist of short, tandemly repeated sequences at the ends of linear chromosomes. Telomeres are found in all eukaryotes and are essential for normal cell growth. During DNA replication, telomeres complete the synthesis of chromosomes that otherwise would have been lost or recombined with other chromosomes during replication. However, there is still some shortening of the telomere with each DNA replication that is theorized to be equivalent to cell aging.
In 1973, Aleksei M. Olovnikov, a scientist at the Institute of Biochemical Physics in the Russian Academy of Sciences in Moscow, proposed the telomere theory of aging. Olovnikov claimed that during DNA synthesis, DNA polymerase fails to replicate all of the nucleic acids resulting in shortened chromosomes with each successive generation. Eventually, the cell will no longer divide and after enough critical regions have been deleted, the cell cycle will arrest.
Telomeres are synthesized by the enzyme telomerase, a reverse transcriptase that contains its own RNA template complementary to the telomere. After DNA replication, the RNA primer is removed leaving a gap at the end of the newly synthesized strand of DNA. In order to fill in the gap, the enzyme telomerase catalyzes the extension of the template strand at the end. This extension of DNA forms a hairpin loop that attaches to the end nucleotide on the newly synthesized strand, thus completing the telomere.
The existence and persistence of telomerase in normal cells is under active study. Telomerase is one of the factors believed to control the length of telomeres that act as a biological clock for the cell. Telomerase is not active all the time, nor is it found in every cell of the body. Researchers have discovered that if the action of telomerase is interrupted, the telomere will be abnormally short and the aging process of the cell accelerates, resulting in cell death much earlier than normal. Likewise, scientists theorize that the uninhibited action of telomerase can lead to cell immortality. Cancer cells have been found to have active telomerase that increases cell proliferation by extending telomeres. Researchers claim that when newly formed tumor cells arise, they turn on a gene for telomerase. However, some cancer cells have been found to extend their telomeres without turning on this gene. By understanding the role of telomeres and telomerase, scientists hope to one day predict and treat the onset of disease.