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Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2018-03, Vol.373 (1741), p.20160451
Ort / Verlag
England
Erscheinungsjahr
2018
Quelle
MEDLINE
Beschreibungen/Notizen
The strengths and limitations of the major methods developed to measure telomere lengths (TLs) in cells and tissues are presented in this review. These include Q-PCR (
uantitative
olymerase
hain
eaction), TRF (
erminal
estriction
ragment) analysis, a variety of Q-FISH (
uantitative
luorescence
n
itu
ybridization) methods, STELA (
ingle
lomere
ength
nalysis) and TeSLA (
lomere
hortest
ength
ssay). For each method, we will cover information about validation studies, including reproducibility in independent laboratories, accuracy, reliability and sensitivity for measuring not only the average but also the shortest telomeres. There is substantial evidence that it is the shortest telomeres that trigger DNA damage responses leading to replicative senescence in mammals. However, the most commonly used TL measurement methods generally provide information on average or relative TL, but it is the shortest telomeres that leads to telomere dysfunction (identified by TIF,
elomere dysfunction
nduced
oci) and limit cell proliferation in the absence of a telomere maintenance mechanism, such as telomerase. As the length of the shortest telomeres is a key biomarker determining cell fate and the onset of senescence, a new technique (TeSLA) that provides quantitative information about all the shortest telomeres will be highlighted.This article is part of the theme issue 'Understanding diversity in telomere dynamics'.