Blood cell telomere lengths and shortening rates of chimpanzee and human females

Objectives Slower rates of aging distinguish humans from our nearest living cousins. Chimpanzees rarely survive their forties while large fractions of women are postmenopausal even in high‐mortality hunter–gatherer populations. Cellular and molecular mechanisms for these somatic aging differences re...

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Veröffentlicht in:American journal of human biology 2014-07, Vol.26 (4), p.452-460
Hauptverfasser: Tackney, Justin, Cawthon, Richard M., Coxworth, James E., Hawkes, Kristen
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container_title American journal of human biology
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creator Tackney, Justin
Cawthon, Richard M.
Coxworth, James E.
Hawkes, Kristen
description Objectives Slower rates of aging distinguish humans from our nearest living cousins. Chimpanzees rarely survive their forties while large fractions of women are postmenopausal even in high‐mortality hunter–gatherer populations. Cellular and molecular mechanisms for these somatic aging differences remain to be identified, though telomeres might play a role. To find out, we compared telomere lengths across age‐matched samples of female chimpanzees and women. Methods We used a monochrome multiplex quantitative polymerase chain reaction to assay canonical telomere repeats in blood cells from captive female chimpanzees (65 individuals; age: 6.2–56.7 years) and compared them to the same measure in human females (43 individuals; age: 7.4–57.3 years). Results Our samples showed little difference in attrition rates between the species (∼0.022 T/S per year for chimpanzees and ∼0.012 T/S per year for humans with overlapping 95% confidence intervals), but telomeres were twice as long in chimpanzees as in humans (T/S ratios = 2.70 and 1.26, respectively). Conclusions Based on the longevity differences, we initially hypothesized that telomere shortening rates would be faster in chimpanzees than in humans. Instead, it is shorter telomere length that appears to be the derived state in humans. This comparison indicates that better characterization of physiological aging in our closest living relatives will be indispensable for understanding the evolution of distinctive human longevity. Am. J. Hum. Biol. 26:452–460, 2014. © 2014 Wiley Periodicals, Inc.
doi_str_mv 10.1002/ajhb.22538
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Chimpanzees rarely survive their forties while large fractions of women are postmenopausal even in high‐mortality hunter–gatherer populations. Cellular and molecular mechanisms for these somatic aging differences remain to be identified, though telomeres might play a role. To find out, we compared telomere lengths across age‐matched samples of female chimpanzees and women. Methods We used a monochrome multiplex quantitative polymerase chain reaction to assay canonical telomere repeats in blood cells from captive female chimpanzees (65 individuals; age: 6.2–56.7 years) and compared them to the same measure in human females (43 individuals; age: 7.4–57.3 years). Results Our samples showed little difference in attrition rates between the species (∼0.022 T/S per year for chimpanzees and ∼0.012 T/S per year for humans with overlapping 95% confidence intervals), but telomeres were twice as long in chimpanzees as in humans (T/S ratios = 2.70 and 1.26, respectively). Conclusions Based on the longevity differences, we initially hypothesized that telomere shortening rates would be faster in chimpanzees than in humans. Instead, it is shorter telomere length that appears to be the derived state in humans. This comparison indicates that better characterization of physiological aging in our closest living relatives will be indispensable for understanding the evolution of distinctive human longevity. Am. J. Hum. 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J. Hum. Biol</addtitle><description>Objectives Slower rates of aging distinguish humans from our nearest living cousins. Chimpanzees rarely survive their forties while large fractions of women are postmenopausal even in high‐mortality hunter–gatherer populations. Cellular and molecular mechanisms for these somatic aging differences remain to be identified, though telomeres might play a role. To find out, we compared telomere lengths across age‐matched samples of female chimpanzees and women. Methods We used a monochrome multiplex quantitative polymerase chain reaction to assay canonical telomere repeats in blood cells from captive female chimpanzees (65 individuals; age: 6.2–56.7 years) and compared them to the same measure in human females (43 individuals; age: 7.4–57.3 years). Results Our samples showed little difference in attrition rates between the species (∼0.022 T/S per year for chimpanzees and ∼0.012 T/S per year for humans with overlapping 95% confidence intervals), but telomeres were twice as long in chimpanzees as in humans (T/S ratios = 2.70 and 1.26, respectively). Conclusions Based on the longevity differences, we initially hypothesized that telomere shortening rates would be faster in chimpanzees than in humans. Instead, it is shorter telomere length that appears to be the derived state in humans. This comparison indicates that better characterization of physiological aging in our closest living relatives will be indispensable for understanding the evolution of distinctive human longevity. Am. J. Hum. 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subjects Adolescent
Adult
Animals
Child
Cohort Studies
Cross-Sectional Studies
Female
Humans
Leukocytes - cytology
Middle Aged
Multiplex Polymerase Chain Reaction
Pan troglodytes - genetics
Telomere - genetics
Telomere Shortening
Young Adult
title Blood cell telomere lengths and shortening rates of chimpanzee and human females
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