Zhao Po, Seo Jinwook, Wang Zuyi, Wang Yue, Shneiderman Ben, Hoffman Eric P
Research Center for Genetic Medicine, Children's National Medical Center, Washington, DC 20010, USA.
C R Biol. 2003 Oct-Nov;326(10-11):1049-65. doi: 10.1016/j.crvi.2003.09.035.
A published set of downstream targets of MyoD defined in a well-controlled in vitro experiment was filtered for relevance to muscle regeneration using a 27-time-point in vivo murine regeneration series. Using interactive hierarchical and Bayes soft clustering, only a minority of the targets defined in vitro can be confirmed in vivo (approximately 50% of induced transcripts, and none of repressed transcripts). This approach provided strong support that 18 targets including of MyoD are biologically relevant during myoblast differentiation.
在一项严格控制的体外实验中定义的一组已发表的MyoD下游靶点,通过一个27个时间点的体内小鼠再生系列,筛选其与肌肉再生的相关性。使用交互式层次聚类和贝叶斯软聚类,体外定义的靶点中只有少数能在体内得到证实(约50%的诱导转录本,而抑制转录本无一得到证实)。这种方法有力地支持了包括MyoD在内的18个靶点在成肌细胞分化过程中具有生物学相关性。