Higher transcriptome stability during aging in long-lived giant mole-rats compared to short-lived rats
Higher transcriptome stability during aging in long-lived giant mole-rats compared to short-lived rats
复制标题
与短命大鼠相比,长寿巨鼹鼠在衰老过程中转录组稳定性更高
DOI:
10.1101/251777
复制
发表时间:
--
期刊:
影响因子:
--
通讯作者:
Dammann P
中科院分区:
文献类型:
--
作者:
Sahm A;Bens M;Henning Y;Vole C;Groth M;Schwab M;Platzer M;Szafranski K;Dammann P
Many aging-associated physiological changes are known to come up in short‐ and long-lived species with a different trajectory and emerging evidence suggests that large parts of life history trait differences between species are based on inter-species variation in gene expression. Little information is yet available, however, about transcriptome changes during aging when comparing mammals with different lifespans. For this reason, we studied the transcriptomes of five tissues and two age cohorts in two similar sized rodent species with very different lifespans: rat (Rattus norvegicus) and giant mole-rat (Fukomys mechowii) with maximum lifespans of 3.8 and >20 years, respectively. Our results show that giant mole-rats exhibit higher transcriptome stability during aging than the rat. While well-known aging signatures (e.g. up-regulation of pro-inflammatory genes) were detected in all rat tissues, they showed up only in one giant mole-rat tissue. Furthermore, many differentially expressed genes that were found in both species, were regulated in opposite directions during aging. This suggests that expression changes that cause aging in short-lived species are counteracted in long-lived species. Taken together, transcriptome stability may be one key causal factor of the long life‐ and healthspan of giant mole-rats and maybe of African mole-rats in general.
影响因子:
3.7
作者:
Dammann P;Šumbera R;Massmann C;Scherag A;Burda H
通讯作者:
Burda H
DOI:
--
发表时间:
2016
期刊:
Veterinary Pathology-Supplement
影响因子:
--
作者:
M. Delaney;M. Kinsel;P. Treuting
通讯作者:
P. Treuting
影响因子:
1.5
作者:
R. Ettlin;P. Stirnimann;D. Prentice
通讯作者:
D. Prentice