Epigenetics Laboratory, Queensland Institute of Medical Research, Herston, Brisbane, QLD 4006, Australia.
G3 (Bethesda). 2012 Nov;2(11):1393-6. doi: 10.1534/g3.112.004036. Epub 2012 Nov 1.
We have used a forward genetic screen to identify genes required for transgene silencing in the mouse. Previously these genes were found using candidate-based sequencing, a slow and labor-intensive process. Recently, whole-exome deep sequencing has accelerated our ability to find the causative point mutations, resulting in the discovery of novel and sometimes unexpected genes. Here we report the identification of translation initiation factor 3, subunit H (eIF3h) in two modifier of murine metastable epialleles (Mommes) lines. Mice carrying mutations in this gene have not been reported previously, and a possible involvement of eIF3h in transcription or epigenetic regulation has not been considered.
我们使用正向遗传学筛选来鉴定小鼠中转基因沉默所需的基因。之前,这些基因是通过候选测序发现的,这是一个缓慢且劳动密集型的过程。最近,全外显子深度测序加速了我们发现致病点突变的能力,从而发现了新的、有时是意想不到的基因。在这里,我们报告了在两个修饰鼠不稳定表等位基因(Mommes)系中鉴定到翻译起始因子 3 亚基 H(eIF3h)。携带该基因突变的小鼠以前尚未报道过,eIF3h 可能参与转录或表观遗传调控也尚未被考虑。