Telomeres, Telomerase, Stress, and Aging
نویسندگان
چکیده
Why should a behavioral scientist study telomeres? Mainte nance of telomeres, the natural ends of linear chromosomes, is a fundamental biological mechanism of all eukaryotic cells, from protozoa to humans. Gradual shortening of telomeres after each cell division eventually can lead to loss of cellular division capacity and cell death, and contribute to genomic instability, a characteristic of cancer. Telomeres and telomerase, the enzyme that adds nucleotides to telomere ends, have been linked to human aging and aging related diseases (Aubert & Lansdorp, 2008). Further, lifestyle and psychological state are increasingly being associated with telomere length and telom erase activity changes. Thus, telomere length and telomerase activity emerge as new biomarkers for cellular aging and may serve as surrogate markers for factors that contribute to aging and aging related diseases. Therefore, scientists interested in understanding early onset of aging related diseases, as well as longevity, may want to include this measure of cell aging. This chapter gives the behavioral scientist a general understanding of the telomere/telomerase maintenance system, from its molecular basis, to clinical observations, to measurement. It addresses such questions as: Why do telomeres shorten? What are the consequences of telomere shortening? How are telomeres and telomerase related to cancer and diseases of aging? And, lastly and most relevant to behavioral scientists, what environmental (nongenetic) factors modulate telomere length? For detailed discussion of each topic, readers are encouraged to read the literature cited in this chapter.
منابع مشابه
Telomeres and aging.
Telomeres play a central role in cell fate and aging by adjusting the cellular response to stress and growth stimulation on the basis of previous cell divisions and DNA damage. At least a few hundred nucleotides of telomere repeats must "cap" each chromosome end to avoid activation of DNA repair pathways. Repair of critically short or "uncapped" telomeres by telomerase or recombination is limit...
متن کاملChronic stress elevates telomerase activity in rats.
The enzyme telomerase lengthens telomeres-protective structures containing repetitive DNA sequences at chromosome ends. Telomere shortening is associated with diseases of ageing in mammals. Chronic stress has been related to shorter immune-cell telomeres, but telomerase activity under stress may be low, permitting telomere loss, or high, partially attenuating it. We developed an experimental mo...
متن کاملTelomeres, stem cells, and hematology.
Telomeres are highly dynamic structures that adjust the cellular response to stress and growth stimulation based on previous cell divisions. This critical function is accomplished by progressive telomere shortening and DNA damage responses activated by chromosome ends without sufficient telomere repeats. Repair of critically short telomeres by telomerase or recombination is limited in most soma...
متن کاملCould serum levels of telomerase be considered as an oxidative stress marker in COPD?
Telomeres are specialized regions of repetitive sequences that found at each end of chromosomes and have an important function in protecting the genomic integrity. In the absence of telomerase functioning in the proliferating cells, every mitotic division progressively shorten telomeres which ultimately leads to senescence of the cells. Therefore, shortening of telomeres’ length is recognized a...
متن کاملCharacterization of telomeric defects and signal transduction pathways in Dyskeratosis Congenita cells
Telomere attrition is a natural process that occurs due to inadequate telomere maintenance. Once at a critically short threshold, telomeres signal the cell to cease division and enter a cell fate termed senescence. Telomeres can be elongated by the enzyme telomerase, which adds de novo telomere repeats to the ends of chromosomes. Mutations in the telomerase complex or telomere-related genes giv...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2009