A forward genetic screen identifies eukaryotic translation initiation factor 3, subunit H (eIF3h), as an enhancer of variegation in the mouse.

A forward genetic screen identifies eukaryotic translation initiation factor 3, subunit H (eIF3h), as an enhancer of variegation in the mouse.
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DOI:
10.1534/g3.112.004036
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发表时间:
2012-11
期刊:
G3 (Bethesda, Md.)
影响因子:
--
通讯作者:
Whitelaw E
Whitelaw E
中科院分区:
其他
文献类型:
--
作者:
Daxinger L;Oey H;Apedaile A;Sutton J;Ashe A;Whitelaw E

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我们使用正向遗传筛选来鉴定小鼠转基因沉默所需的基因。此前,这些基因是通过基于候选的测序发现的,这是一个缓慢且劳动密集型的过程。最近,全外显子组深度测序加速了我们寻找致病点突变的能力,从而发现了新的、有时是意想不到的基因。在此,我们报告了在小鼠亚稳态表观等位基因 (Mommes) 系的两个修饰因子中翻译起始因子 3、H 亚基 (eIF3h) 的鉴定。此前尚未报道携带该基因突变的小鼠,并且尚未考虑 eIF3h 可能参与转录或表观遗传调控。
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.
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