RNA sequencing reveals differential expression of mitochondrial and oxidation reduction genes in the long-lived naked mole-rat when compared to mice.
RNA sequencing reveals differential expression of mitochondrial and oxidation reduction genes in the long-lived naked mole-rat when compared to mice.
复制标题
DOI:
10.1371/journal.pone.0026729
复制
发表时间:
2011
期刊:
影响因子:
3.7
通讯作者:
Church GM
中科院分区:
文献类型:
--
作者:
Yu C;Li Y;Holmes A;Szafranski K;Faulkes CG;Coen CW;Buffenstein R;Platzer M;de Magalhães JP;Church GM
The naked mole-rat (Heterocephalus glaber) is a long-lived, cancer resistant rodent and there is a great interest in identifying the adaptations responsible for these and other of its unique traits. We employed RNA sequencing to compare liver gene expression profiles between naked mole-rats and wild-derived mice. Our results indicate that genes associated with oxidoreduction and mitochondria were expressed at higher relative levels in naked mole-rats. The largest effect is nearly 300-fold higher expression of epithelial cell adhesion molecule (Epcam), a tumour-associated protein. Also of interest are the protease inhibitor, alpha2-macroglobulin (A2m), and the mitochondrial complex II subunit Sdhc, both ageing-related genes found strongly over-expressed in the naked mole-rat. These results hint at possible candidates for specifying species differences in ageing and cancer, and in particular suggest complex alterations in mitochondrial and oxidation reduction pathways in the naked mole-rat. Our differential gene expression analysis obviated the need for a reference naked mole-rat genome by employing a combination of Illumina/Solexa and 454 platforms for transcriptome sequencing and assembling transcriptome contigs of the non-sequenced species. Overall, our work provides new research foci and methods for studying the naked mole-rat's fascinating characteristics.
登录
查看更多内容
DOI:
10.1083/jcb.139.5.1337
发表时间:
1997-12-01
期刊:
The Journal of cell biology
影响因子:
--
作者:
Litvinov SV;Balzar M;Winter MJ;Bakker HA;Briaire-de Bruijn IH;Prins F;Fleuren GJ;Warnaar SO
通讯作者:
Warnaar SO
影响因子:
3.7
作者:
de Candia P;Blekhman R;Chabot AE;Oshlack A;Gilad Y
通讯作者:
Gilad Y
影响因子:
7.8
作者:
Harper, James M.;Leathers, Charles W.;Austad, Steven N.
通讯作者:
Austad, Steven N.
影响因子:
30.8
作者:
Blacker, D;Wilcox, MA;Tanzi, RE
通讯作者:
Tanzi, RE
影响因子:
--
作者:
Hulbert, A. J.
通讯作者:
Hulbert, A. J.