Nucleic Acids Research, Vol 25, Issue 15 3051-3058, Copyright © 1997 by Oxford University Press
GM Coviello-McLaughlin and KR Prowse
Telomere shortening has been causally implicated in replicative senescence
in humans. To examine the relationship between telomere length and ageing
in mice, we have utilized Mus spretus as a model species because it has
telomere lengths of approximately the same length as humans. Telomere
length and telomerase were analyzed from liver, kidney, spleen, brain and
testis from >180 M.spretus male and female mice of different ages.
Although telomere lengths for each tissue were heterogeneous, significant
changes in telomere lengths were found in spleen and brain, but not in
liver, testis or kidney. Telomerase activity was abundant in liver and
testis, but weak to non- detectable in spleen, kidney and brain. Gender
differences in mean terminal restriction fragment length were discovered in
tissues from M.spretus and from M.spretus xC57BL/6 F1 mice, in which a M.
spretus - sized telomeric smear could be measured. The comparison of the
rank order of tissue telomere lengths within individual M. spretus showed
that certain tissues tended to be longer than the others, and this ranking
also extended to tissues of the M.spretus xC57BL/6 F1 mice. These data
suggest that telomere lengths within individual tissues are regulated
independently and are genetically controlled.
ARTICLES
Telomere length regulation during postnatal development and ageing in Mus spretus
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