Budovskaya Yelena V, Wu Kendall, Southworth Lucinda K, Jiang Min, Tedesco Patricia, Johnson Thomas E, Kim Stuart K
Department of Developmental Biology, Stanford University Medical Center, Stanford, CA 94305, USA.
Cell. 2008 Jul 25;134(2):291-303. doi: 10.1016/j.cell.2008.05.044.
To define the C. elegans aging process at the molecular level, we used DNA microarray experiments to identify a set of 1294 age-regulated genes and found that the GATA transcription factors ELT-3, ELT-5, and ELT-6 are responsible for age regulation of a large fraction of these genes. Expression of elt-5 and elt-6 increases during normal aging, and both of these GATA factors repress expression of elt-3, which shows a corresponding decrease in expression in old worms. elt-3 regulates a large number of downstream genes that change expression in old age, including ugt-9, col-144, and sod-3. elt-5(RNAi) and elt-6(RNAi) worms have extended longevity, indicating that elt-3, elt-5, and elt-6 play an important functional role in the aging process. These results identify a transcriptional circuit that guides the rapid aging process in C. elegans and indicate that this circuit is driven by drift of developmental pathways rather than accumulation of damage.
为了在分子水平上定义秀丽隐杆线虫的衰老过程,我们利用DNA微阵列实验鉴定出一组1294个随年龄变化而调节的基因,并发现GATA转录因子ELT-3、ELT-5和ELT-6负责这些基因中很大一部分的年龄调节。在正常衰老过程中,elt-5和elt-6的表达增加,并且这两种GATA因子均抑制elt-3的表达,elt-3在老龄线虫中的表达相应降低。elt-3调节大量在老年时表达发生变化的下游基因,包括ugt-9、col-144和sod-3。elt-5(RNA干扰)和elt-6(RNA干扰)线虫的寿命延长,这表明elt-3、elt-5和elt-6在衰老过程中发挥重要的功能作用。这些结果确定了一个指导秀丽隐杆线虫快速衰老过程的转录回路,并表明该回路是由发育途径的漂移而非损伤积累驱动的。